BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Lammi L, Arte S, Somer M, Jarvinen H, Lahermo P, Thesleff I, Pirinen S, Nieminen P. Mutations in AXIN2 cause familial tooth agenesis and predispose to colorectal cancer. Am J Hum Genet. 2004;74:1043-1050. [PMID: 15042511 DOI: 10.1086/386293] [Cited by in Crossref: 419] [Cited by in F6Publishing: 346] [Article Influence: 24.6] [Reference Citation Analysis]
Number Citing Articles
1 Kim R, Yu T, Li J, Prochazka J, Sharir A, Green JBA, Klein OD. Early perturbation of Wnt signaling reveals patterning and invagination-evagination control points in molar tooth development. Development 2021;148:dev199685. [PMID: 34195802 DOI: 10.1242/dev.199685] [Reference Citation Analysis]
2 Macklin-Mantia SK, Hines SL, Chaichana KL, Donaldson AM, Ko SL, Zhai Q, Samadder NJ, Riegert-Johnson DL. Case report expanding the germline AXIN2- related phenotype to include olfactory neuroblastoma and gastric adenoma. BMC Med Genet 2020;21:161. [PMID: 32807118 DOI: 10.1186/s12881-020-01103-0] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
3 Shim JS, Kim B, Park HC, Ryu JJ. Temporal Control of WNT Activity Regulates Tooth Number in Fish. J Dent Res 2019;98:339-46. [PMID: 30513239 DOI: 10.1177/0022034518811322] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
4 Gokkaya B, Kargul B. Prevalence and Pattern of Non-Syndromic Hypodontia in a Group of Turkish Children. Acta Stomatol Croat 2016;50:58-64. [PMID: 27688427 DOI: 10.15644/asc50/1/8] [Cited by in Crossref: 4] [Cited by in F6Publishing: 1] [Article Influence: 0.8] [Reference Citation Analysis]
5 Valle L, de Voer RM, Goldberg Y, Sjursen W, Försti A, Ruiz-Ponte C, Caldés T, Garré P, Olsen MF, Nordling M, Castellvi-Bel S, Hemminki K. Update on genetic predisposition to colorectal cancer and polyposis. Mol Aspects Med 2019;69:10-26. [PMID: 30862463 DOI: 10.1016/j.mam.2019.03.001] [Cited by in Crossref: 39] [Cited by in F6Publishing: 27] [Article Influence: 19.5] [Reference Citation Analysis]
6 Yin W, Bian Z. The Gene Network Underlying Hypodontia. J Dent Res 2015;94:878-85. [PMID: 25910507 DOI: 10.1177/0022034515583999] [Cited by in Crossref: 59] [Cited by in F6Publishing: 46] [Article Influence: 9.8] [Reference Citation Analysis]
7 Suomalainen M, Thesleff I. Patterns of Wnt pathway activity in the mouse incisor indicate absence of Wnt/beta-catenin signaling in the epithelial stem cells. Dev Dyn. 2010;239:364-372. [PMID: 19806668 DOI: 10.1002/dvdy.22106] [Cited by in Crossref: 19] [Cited by in F6Publishing: 48] [Article Influence: 1.7] [Reference Citation Analysis]
8 Arte S, Parmanen S, Pirinen S, Alaluusua S, Nieminen P. Candidate gene analysis of tooth agenesis identifies novel mutations in six genes and suggests significant role for WNT and EDA signaling and allele combinations. PLoS One 2013;8:e73705. [PMID: 23991204 DOI: 10.1371/journal.pone.0073705] [Cited by in Crossref: 66] [Cited by in F6Publishing: 55] [Article Influence: 8.3] [Reference Citation Analysis]
9 Kettunen P, Kivimäe S, Keshari P, Klein OD, Cheyette BN, Luukko K. Dact1-3 mRNAs exhibit distinct expression domains during tooth development. Gene Expr Patterns 2010;10:140-3. [PMID: 20170752 DOI: 10.1016/j.gep.2010.02.002] [Cited by in Crossref: 12] [Cited by in F6Publishing: 8] [Article Influence: 1.1] [Reference Citation Analysis]
10 Malmgren B, Andersson K, Lindahl K, Kindmark A, Grigelioniene G, Zachariadis V, Dahllöf G, Åström E. Tooth agenesis in osteogenesis imperfecta related to mutations in the collagen type I genes. Oral Dis 2017;23:42-9. [DOI: 10.1111/odi.12568] [Cited by in Crossref: 25] [Cited by in F6Publishing: 20] [Article Influence: 5.0] [Reference Citation Analysis]
11 Papagerakis P, Lin HK, Lee KY, Hu Y, Simmer JP, Bartlett JD, Hu JC. Premature stop codon in MMP20 causing amelogenesis imperfecta. J Dent Res 2008;87:56-9. [PMID: 18096894 DOI: 10.1177/154405910808700109] [Cited by in Crossref: 52] [Cited by in F6Publishing: 45] [Article Influence: 4.0] [Reference Citation Analysis]
12 Park MK, Shin MK, Kim SO, Lee HS, Lee JH, Jung HS, Song JS. Prevalence of delayed tooth development and its relation to tooth agenesis in Korean children. Arch Oral Biol 2017;73:243-7. [PMID: 27810381 DOI: 10.1016/j.archoralbio.2016.10.024] [Cited by in Crossref: 9] [Cited by in F6Publishing: 2] [Article Influence: 1.8] [Reference Citation Analysis]
13 Chang SC, Lan YT, Lin PC, Yang SH, Lin CH, Liang WY, Chen WS, Jiang JK, Lin JK. Patterns of germline and somatic mutations in 16 genes associated with mismatch repair function or containing tandem repeat sequences. Cancer Med 2020;9:476-86. [PMID: 31769227 DOI: 10.1002/cam4.2702] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
14 Menezes R, Marazita ML, Mchenry TG, Cooper ME, Bardi K, Brandon C, Letra A, Martin RA, Vieira AR. AXIS inhibition protein 2, orofacial clefts and a family history of cancer. The Journal of the American Dental Association 2009;140:80-4. [DOI: 10.14219/jada.archive.2009.0022] [Cited by in Crossref: 56] [Cited by in F6Publishing: 44] [Article Influence: 4.7] [Reference Citation Analysis]
15 Regier DS, Hart TC. Genetics. Dental Clinics of North America 2016;60:943-9. [DOI: 10.1016/j.cden.2016.03.005] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 0.6] [Reference Citation Analysis]
16 Yusof KM, Makpol S, Fen LS, Jamal R, Wan Ngah WZ. Suppression of colorectal cancer cell growth by combined treatment of 6-gingerol and γ-tocotrienol via alteration of multiple signalling pathways. J Nat Med 2019;73:745-60. [DOI: 10.1007/s11418-019-01323-6] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
17 Song S, Han D, Qu H, Gong Y, Wu H, Zhang X, Zhong N, Feng H. EDA gene mutations underlie non-syndromic oligodontia. J Dent Res 2009;88:126-31. [PMID: 19278982 DOI: 10.1177/0022034508328627] [Cited by in Crossref: 50] [Cited by in F6Publishing: 41] [Article Influence: 4.2] [Reference Citation Analysis]
18 Polakis P. Drugging Wnt signalling in cancer. EMBO J 2012;31:2737-46. [PMID: 22617421 DOI: 10.1038/emboj.2012.126] [Cited by in Crossref: 158] [Cited by in F6Publishing: 146] [Article Influence: 17.6] [Reference Citation Analysis]
19 Andrade Filho PA, Letra A, Cramer A, Prasad JL, Garlet GP, Vieira AR, Ferris RL, Menezes R. Insights from studies with oral cleft genes suggest associations between WNT-pathway genes and risk of oral cancer. J Dent Res 2011;90:740-6. [PMID: 21393552 DOI: 10.1177/0022034511401622] [Cited by in Crossref: 34] [Cited by in F6Publishing: 34] [Article Influence: 3.4] [Reference Citation Analysis]
20 Esteban-Jurado C, Garre P, Vila M, Lozano JJ, Pristoupilova A, Beltrán S, Abulí A, Muñoz J, Balaguer F, Ocaña T, Castells A, Piqué JM, Carracedo A, Ruiz-Ponte C, Bessa X, Andreu M, Bujanda L, Caldés T, Castellví-Bel S. New genes emerging for colorectal cancer predisposition. World J Gastroenterol 2014;20:1961-71. [PMID: 24587672 DOI: 10.3748/wjg.v20.i8.1961] [Cited by in CrossRef: 25] [Cited by in F6Publishing: 23] [Article Influence: 4.2] [Reference Citation Analysis]
21 Handrigan GR, Richman JM. A network of Wnt, hedgehog and BMP signaling pathways regulates tooth replacement in snakes. Developmental Biology 2010;348:130-41. [DOI: 10.1016/j.ydbio.2010.09.003] [Cited by in Crossref: 59] [Cited by in F6Publishing: 53] [Article Influence: 5.4] [Reference Citation Analysis]
22 Mazzoni SM, Petty EM, Stoffel EM, Fearon ER. An AXIN2 Mutant Allele Associated With Predisposition to Colorectal Neoplasia Has Context-Dependent Effects on AXIN2 Protein Function. Neoplasia 2015;17:463-72. [PMID: 26025668 DOI: 10.1016/j.neo.2015.04.006] [Cited by in Crossref: 11] [Cited by in F6Publishing: 10] [Article Influence: 2.2] [Reference Citation Analysis]
23 Valle L. Recent Discoveries in the Genetics of Familial Colorectal Cancer and Polyposis. Clinical Gastroenterology and Hepatology 2017;15:809-19. [DOI: 10.1016/j.cgh.2016.09.148] [Cited by in Crossref: 43] [Cited by in F6Publishing: 36] [Article Influence: 10.8] [Reference Citation Analysis]
24 Yu HM, Jin Y, Fu J, Hsu W. Expression of Gpr177, a Wnt trafficking regulator, in mouse embryogenesis. Dev Dyn 2010;239:2102-9. [PMID: 20549736 DOI: 10.1002/dvdy.22336] [Cited by in Crossref: 28] [Cited by in F6Publishing: 26] [Article Influence: 2.5] [Reference Citation Analysis]
25 Bengoa-vergniory N, Kypta RM. Canonical and noncanonical Wnt signaling in neural stem/progenitor cells. Cell Mol Life Sci 2015;72:4157-72. [DOI: 10.1007/s00018-015-2028-6] [Cited by in Crossref: 81] [Cited by in F6Publishing: 67] [Article Influence: 13.5] [Reference Citation Analysis]
26 Mostowska A, Hozyasz KK, Wójcicki P, Lasota A, Dunin-Wilczyńska I, Jagodziński PP. Association of DVL2 and AXIN2 gene polymorphisms with cleft lip with or without cleft palate in a Polish population. Birth Defects Res A Clin Mol Teratol 2012;94:943-50. [PMID: 22887353 DOI: 10.1002/bdra.23056] [Cited by in Crossref: 14] [Cited by in F6Publishing: 13] [Article Influence: 1.6] [Reference Citation Analysis]
27 Dinckan N, Du R, Akdemir ZC, Bayram Y, Jhangiani SN, Doddapaneni H, Hu J, Muzny DM, Guven Y, Aktoren O, Kayserili H, Boerwinkle E, Gibbs RA, Posey JE, Lupski JR, Uyguner ZO, Letra A. A biallelic ANTXR1 variant expands the anthrax toxin receptor associated phenotype to tooth agenesis. Am J Med Genet A 2018;176:1015-22. [PMID: 29436111 DOI: 10.1002/ajmg.a.38625] [Cited by in Crossref: 8] [Cited by in F6Publishing: 4] [Article Influence: 2.7] [Reference Citation Analysis]
28 Dobbins SE, Broderick P, Chubb D, Kinnersley B, Sherborne AL, Houlston RS. Undefined familial colorectal cancer and the role of pleiotropism in cancer susceptibility genes. Fam Cancer 2016;15:593-9. [PMID: 27356891 DOI: 10.1007/s10689-016-9914-4] [Cited by in Crossref: 8] [Cited by in F6Publishing: 6] [Article Influence: 2.0] [Reference Citation Analysis]
29 Chia IV, Costantini F. Mouse axin and axin2/conductin proteins are functionally equivalent in vivo. Mol Cell Biol 2005;25:4371-6. [PMID: 15899843 DOI: 10.1128/MCB.25.11.4371-4376.2005] [Cited by in Crossref: 79] [Cited by in F6Publishing: 49] [Article Influence: 4.9] [Reference Citation Analysis]
30 Kapadia H, Mues G, D'souza R. Genes affecting tooth morphogenesis. Orthod Craniofac Res 2007;10:237-44. [DOI: 10.1111/j.1601-6343.2007.00407.x] [Cited by in Crossref: 63] [Cited by in F6Publishing: 45] [Article Influence: 4.5] [Reference Citation Analysis]
31 Behrens J. The role of the Wnt signalling pathway in colorectal tumorigenesis. Biochem Soc Trans. 2005;33:672-675. [PMID: 16042571 DOI: 10.1042/BST0330672] [Cited by in Crossref: 97] [Cited by in F6Publishing: 50] [Article Influence: 6.1] [Reference Citation Analysis]
32 Mostowska A, Biedziak B, Jagodzinski PP. Axis inhibition protein 2 (AXIN2) polymorphisms may be a risk factor for selective tooth agenesis. J Hum Genet. 2006;51:262-266. [PMID: 16432638 DOI: 10.1007/s10038-005-0353-6] [Cited by in Crossref: 67] [Cited by in F6Publishing: 55] [Article Influence: 4.5] [Reference Citation Analysis]
33 Koch A, Hrychyk A, Hartmann W, Waha A, Mikeska T, Waha A, Schüller U, Sörensen N, Berthold F, Goodyer CG, Wiestler OD, Birchmeier W, Behrens J, Pietsch T. Mutations of the Wnt antagonist AXIN2 (Conductin) result in TCF-dependent transcription in medulloblastomas. Int J Cancer 2007;121:284-91. [PMID: 17373666 DOI: 10.1002/ijc.22675] [Cited by in Crossref: 42] [Cited by in F6Publishing: 34] [Article Influence: 3.0] [Reference Citation Analysis]
34 Sameer AS. Colorectal cancer: a researcher’s perspective of the molecular angel’s gone eccentric in the Vale of Kashmir. Tumor Biol 2013;34:1301-15. [DOI: 10.1007/s13277-013-0692-4] [Cited by in Crossref: 13] [Cited by in F6Publishing: 9] [Article Influence: 1.6] [Reference Citation Analysis]
35 Slavkin HC. Revising the scope of practice for oral health professionals. The Journal of the American Dental Association 2014;145:228-30. [DOI: 10.14219/jada.2014.11] [Cited by in Crossref: 10] [Cited by in F6Publishing: 6] [Article Influence: 1.4] [Reference Citation Analysis]
36 Wang X, Goode EL, Fredericksen ZS, Vierkant RA, Pankratz VS, Liu-Mares W, Rider DN, Vachon CM, Cerhan JR, Olson JE, Couch FJ. Association of genetic variation in genes implicated in the beta-catenin destruction complex with risk of breast cancer. Cancer Epidemiol Biomarkers Prev 2008;17:2101-8. [PMID: 18708403 DOI: 10.1158/1055-9965.EPI-08-0134] [Cited by in Crossref: 55] [Cited by in F6Publishing: 36] [Article Influence: 4.2] [Reference Citation Analysis]
37 Segditsas S, Tomlinson I. Colorectal cancer and genetic alterations in the Wnt pathway. Oncogene 2006;25:7531-7. [DOI: 10.1038/sj.onc.1210059] [Cited by in Crossref: 393] [Cited by in F6Publishing: 365] [Article Influence: 26.2] [Reference Citation Analysis]
38 Magruder S, Carter E, Williams MA, English J, Akyalcin S, Letra A. Further evidence for the role of WNT10A, WNT10B and GREM2 as candidate genes for isolated tooth agenesis. Orthod Craniofac Res 2018;21:258-63. [DOI: 10.1111/ocr.12248] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 1.3] [Reference Citation Analysis]
39 Xuan K, Jin F, Liu YL, Yuan LT, Wen LY, Yang FS, Wang XJ, Wang GH, Jin Y. Identification of a novel missense mutation of MSX1 gene in Chinese family with autosomal-dominant oligodontia. Arch Oral Biol 2008;53:773-9. [PMID: 18374898 DOI: 10.1016/j.archoralbio.2008.02.012] [Cited by in Crossref: 35] [Cited by in F6Publishing: 31] [Article Influence: 2.7] [Reference Citation Analysis]
40 Sarkar T, Bansal R, Das P. Whole genome sequencing reveals novel non-synonymous mutation in ectodysplasin A (EDA) associated with non-syndromic X-linked dominant congenital tooth agenesis. PLoS One 2014;9:e106811. [PMID: 25203534 DOI: 10.1371/journal.pone.0106811] [Cited by in Crossref: 8] [Cited by in F6Publishing: 4] [Article Influence: 1.1] [Reference Citation Analysis]
41 Yang Y, Luo L, Xu J, Zhu P, Xue W, Wang J, Li W, Wang M, Cheng K, Liu S, Tang Z, Ring BZ, Su L. Novel EDA p.Ile260Ser mutation linked to non-syndromic hypodontia. J Dent Res 2013;92:500-6. [PMID: 23625373 DOI: 10.1177/0022034513487557] [Cited by in Crossref: 11] [Cited by in F6Publishing: 8] [Article Influence: 1.4] [Reference Citation Analysis]
42 Galluccio G, Castellano M, La Monaca C. Genetic basis of non-syndromic anomalies of human tooth number. Arch Oral Biol 2012;57:918-30. [PMID: 22325622 DOI: 10.1016/j.archoralbio.2012.01.005] [Cited by in Crossref: 42] [Cited by in F6Publishing: 28] [Article Influence: 4.7] [Reference Citation Analysis]
43 Liu H, Zhang J, Song S, Zhao H, Han D, Feng H. A case-control study of the association between tooth-development gene polymorphisms and non-syndromic hypodontia in the Chinese Han population. Eur J Oral Sci 2012;120:378-85. [DOI: 10.1111/j.1600-0722.2012.00986.x] [Cited by in Crossref: 8] [Cited by in F6Publishing: 7] [Article Influence: 0.9] [Reference Citation Analysis]
44 Majid S, Saini S, Dahiya R. Wnt signaling pathways in urological cancers: past decades and still growing. Mol Cancer 2012;11:7. [PMID: 22325146 DOI: 10.1186/1476-4598-11-7] [Cited by in Crossref: 37] [Cited by in F6Publishing: 37] [Article Influence: 4.1] [Reference Citation Analysis]
45 Pinho T, Silva-fernandes A, Bousbaa H, Maciel P. Mutational analysis of MSX1 and PAX9 genes in Portuguese families with maxillary lateral incisor agenesis. European Journal of Orthodontics 2010;32:582-8. [DOI: 10.1093/ejo/cjp155] [Cited by in Crossref: 20] [Cited by in F6Publishing: 12] [Article Influence: 1.8] [Reference Citation Analysis]
46 Doering JA, Tang S, Peng H, Eisner BK, Sun J, Giesy JP, Wiseman S, Hecker M. High Conservation in Transcriptomic and Proteomic Response of White Sturgeon to Equipotent Concentrations of 2,3,7,8-TCDD, PCB 77, and Benzo[a]pyrene. Environ Sci Technol 2016;50:4826-35. [DOI: 10.1021/acs.est.6b00490] [Cited by in Crossref: 20] [Cited by in F6Publishing: 16] [Article Influence: 4.0] [Reference Citation Analysis]
47 Kretzschmar K, Clevers H. Wnt/β-catenin signaling in adult mammalian epithelial stem cells. Dev Biol 2017;428:273-82. [PMID: 28526587 DOI: 10.1016/j.ydbio.2017.05.015] [Cited by in Crossref: 77] [Cited by in F6Publishing: 59] [Article Influence: 19.3] [Reference Citation Analysis]
48 Mostowska A, Biedziak B, Dunin-Wilczynska I, Komorowska A, Jagodzinski PP. Polymorphisms in CHDH gene and the risk of tooth agenesis. Birth Defects Res A Clin Mol Teratol 2011;91:169-76. [PMID: 21308979 DOI: 10.1002/bdra.20771] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 0.4] [Reference Citation Analysis]
49 Schaal U, Grenz S, Merkel S, Rau TT, Hadjihannas MV, Kremmer E, Chudasama P, Croner RS, Behrens J, Stürzl M. Expression and localization of axin 2 in colorectal carcinoma and its clinical implication. Int J Colorectal Dis. 2013;28:1469-1478. [PMID: 23702820 DOI: 10.1007/s00384-013-1709-6] [Cited by in Crossref: 11] [Cited by in F6Publishing: 10] [Article Influence: 1.4] [Reference Citation Analysis]
50 McGee-Lawrence ME, Carpio LR, Bradley EW, Dudakovic A, Lian JB, van Wijnen AJ, Kakar S, Hsu W, Westendorf JJ. Runx2 is required for early stages of endochondral bone formation but delays final stages of bone repair in Axin2-deficient mice. Bone 2014;66:277-86. [PMID: 24973690 DOI: 10.1016/j.bone.2014.06.022] [Cited by in Crossref: 31] [Cited by in F6Publishing: 25] [Article Influence: 4.4] [Reference Citation Analysis]
51 Rohlin A, Rambech E, Kvist A, Törngren T, Eiengård F, Lundstam U, Zagoras T, Gebre-Medhin S, Borg Å, Björk J, Nilbert M, Nordling M. Expanding the genotype-phenotype spectrum in hereditary colorectal cancer by gene panel testing. Fam Cancer 2017;16:195-203. [PMID: 27696107 DOI: 10.1007/s10689-016-9934-0] [Cited by in Crossref: 30] [Cited by in F6Publishing: 21] [Article Influence: 7.5] [Reference Citation Analysis]
52 Lorans M, Dow E, Macrae FA, Winship IM, Buchanan DD. Update on Hereditary Colorectal Cancer: Improving the Clinical Utility of Multigene Panel Testing. Clin Colorectal Cancer 2018;17:e293-305. [PMID: 29454559 DOI: 10.1016/j.clcc.2018.01.001] [Cited by in Crossref: 34] [Cited by in F6Publishing: 18] [Article Influence: 11.3] [Reference Citation Analysis]
53 Catón J, Tucker AS. Current knowledge of tooth development: patterning and mineralization of the murine dentition. J Anat 2009;214:502-15. [PMID: 19422427 DOI: 10.1111/j.1469-7580.2008.01014.x] [Cited by in Crossref: 96] [Cited by in F6Publishing: 69] [Article Influence: 8.7] [Reference Citation Analysis]
54 Heald B, Hampel H, Church J, Dudley B, Hall MJ, Mork ME, Singh A, Stoffel E, Stoll J, You YN, Yurgelun MB, Kupfer SS; Collaborative Group of the Americas on Inherited Gastrointestinal Cancer. Collaborative Group of the Americas on Inherited Gastrointestinal Cancer Position statement on multigene panel testing for patients with colorectal cancer and/or polyposis. Fam Cancer 2020;19:223-39. [PMID: 32172433 DOI: 10.1007/s10689-020-00170-9] [Cited by in Crossref: 9] [Cited by in F6Publishing: 5] [Article Influence: 9.0] [Reference Citation Analysis]
55 Han Y, Zhou L, Ma L, Li D, Xu M, Yuan H, Ma J, Zhang W, Jiang H, Wu Y, Wang L, Pan Y. The axis inhibition protein 2 polymorphisms and non-syndromic orofacial clefts susceptibility in a Chinese Han population. J Oral Pathol Med 2014;43:554-60. [DOI: 10.1111/jop.12162] [Cited by in Crossref: 13] [Cited by in F6Publishing: 10] [Article Influence: 1.9] [Reference Citation Analysis]
56 Dong Y, Zhang N, Zhao S, Chen X, Li F, Tao X. miR-221-3p and miR-15b-5p promote cell proliferation and invasion by targeting Axin2 in liver cancer. Oncol Lett 2019;18:6491-500. [PMID: 31814849 DOI: 10.3892/ol.2019.11056] [Cited by in Crossref: 3] [Cited by in F6Publishing: 9] [Article Influence: 1.5] [Reference Citation Analysis]
57 Lima LS, Silverio MDO, Swerts MSO, Aquino SND, Martelli DRB, Martelli-junior H. Frequency of Cancer in First-Degree Relatives of Patients with Cleft Lip and/or Palate in the Brazilian Population. Braz Dent J 2013;24:200-3. [DOI: 10.1590/0103-6440201302191] [Cited by in Crossref: 8] [Cited by in F6Publishing: 5] [Article Influence: 1.0] [Reference Citation Analysis]
58 Ng LF, Kaur P, Bunnag N, Suresh J, Sung ICH, Tan QH, Gruber J, Tolwinski NS. WNT Signaling in Disease. Cells. 2019;8:826. [PMID: 31382613 DOI: 10.3390/cells8080826] [Cited by in Crossref: 55] [Cited by in F6Publishing: 37] [Article Influence: 27.5] [Reference Citation Analysis]
59 Lee KE, Ko J, Shin TJ, Hyun HK, Lee SH, Kim JW. Oligodontia and curly hair occur with ectodysplasin-a mutations. J Dent Res 2014;93:371-5. [PMID: 24487376 DOI: 10.1177/0022034514522059] [Cited by in Crossref: 11] [Cited by in F6Publishing: 9] [Article Influence: 1.6] [Reference Citation Analysis]
60 Sharma M, Pruitt K. Wnt Pathway: An Integral Hub for Developmental and Oncogenic Signaling Networks. Int J Mol Sci 2020;21:E8018. [PMID: 33126517 DOI: 10.3390/ijms21218018] [Cited by in Crossref: 12] [Cited by in F6Publishing: 10] [Article Influence: 12.0] [Reference Citation Analysis]
61 Bock NC, Lenz S, Ruiz-Heiland G, Ruf S. Nonsyndromic oligodontia : Does the Tooth Agenesis Code (TAC) enable prediction of the causative mutation? J Orofac Orthop 2017;78:112-20. [PMID: 28204848 DOI: 10.1007/s00056-016-0056-y] [Cited by in Crossref: 5] [Cited by in F6Publishing: 1] [Article Influence: 1.3] [Reference Citation Analysis]
62 Hu JC, Yamakoshi Y, Yamakoshi F, Krebsbach PH, Simmer JP. Proteomics and genetics of dental enamel. Cells Tissues Organs 2005;181:219-31. [PMID: 16612087 DOI: 10.1159/000091383] [Cited by in Crossref: 42] [Cited by in F6Publishing: 41] [Article Influence: 2.8] [Reference Citation Analysis]
63 Tanahashi J, Daa T, Yada N, Kashima K, Kondoh Y, Yokoyama S. Mutational analysis of Wnt signaling molecules in ameloblastoma with aberrant nuclear expression of β-catenin: Wnt signaling molecules in ameloblastoma. Journal of Oral Pathology & Medicine 2008;37:565-70. [DOI: 10.1111/j.1600-0714.2008.00645.x] [Cited by in Crossref: 18] [Cited by in F6Publishing: 17] [Article Influence: 1.4] [Reference Citation Analysis]
64 Parveen N, Hussain MU, Pandith AA, Mudassar S. Diversity of axin in signaling pathways and its relation to colorectal cancer. Med Oncol 2011;28:259-67. [DOI: 10.1007/s12032-010-9722-x] [Cited by in Crossref: 14] [Cited by in F6Publishing: 11] [Article Influence: 1.3] [Reference Citation Analysis]
65 Mikkola ML, Millar SE. The Mammary Bud as a Skin Appendage: Unique and Shared Aspects of Development. J Mammary Gland Biol Neoplasia 2006;11:187-203. [DOI: 10.1007/s10911-006-9029-x] [Cited by in Crossref: 95] [Cited by in F6Publishing: 86] [Article Influence: 6.3] [Reference Citation Analysis]
66 Zhao JJ, Carrasco RD. Crosstalk between microRNA30a/b/c/d/e-5p and the canonical Wnt pathway: implications for multiple myeloma therapy. Cancer Res. 2014;74:5351-5358. [PMID: 25228654 DOI: 10.1158/0008-5472.can-14-0994] [Cited by in Crossref: 13] [Cited by in F6Publishing: 13] [Article Influence: 1.9] [Reference Citation Analysis]
67 Mues G, Tardivel A, Willen L, Kapadia H, Seaman R, Frazier-Bowers S, Schneider P, D'Souza RN. Functional analysis of Ectodysplasin-A mutations causing selective tooth agenesis. Eur J Hum Genet 2010;18:19-25. [PMID: 19623212 DOI: 10.1038/ejhg.2009.127] [Cited by in Crossref: 41] [Cited by in F6Publishing: 36] [Article Influence: 3.7] [Reference Citation Analysis]
68 MacDonald BT, Tamai K, He X. Wnt/beta-catenin signaling: components, mechanisms, and diseases. Dev Cell. 2009;17:9-26. [PMID: 19619488 DOI: 10.1016/j.devcel.2009.06.016s1534-5807(09)00257-3] [Reference Citation Analysis]
69 Ritwik P, Chrisentery-singleton TE. Oral and dental considerations in pediatric cancers. Cancer Metastasis Rev 2020;39:43-53. [DOI: 10.1007/s10555-020-09842-5] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 5.0] [Reference Citation Analysis]
70 Renkonen ET, Nieminen P, Abdel-Rahman WM, Moisio AL, Järvelä I, Arte S, Järvinen HJ, Peltomäki P. Adenomatous polyposis families that screen APC mutation-negative by conventional methods are genetically heterogeneous. J Clin Oncol 2005;23:5651-9. [PMID: 16110024 DOI: 10.1200/JCO.2005.14.712] [Cited by in Crossref: 56] [Cited by in F6Publishing: 26] [Article Influence: 3.5] [Reference Citation Analysis]
71 Shimizu T, Maeda T. Prevalence and genetic basis of tooth agenesis. Japanese Dental Science Review 2009;45:52-8. [DOI: 10.1016/j.jdsr.2008.12.001] [Cited by in Crossref: 45] [Cited by in F6Publishing: 9] [Article Influence: 3.8] [Reference Citation Analysis]
72 Pedone E, Marucci L. Role of β-Catenin Activation Levels and Fluctuations in Controlling Cell Fate. Genes (Basel) 2019;10:E176. [PMID: 30823613 DOI: 10.3390/genes10020176] [Cited by in Crossref: 16] [Cited by in F6Publishing: 12] [Article Influence: 8.0] [Reference Citation Analysis]
73 Liu F, Millar SE. Wnt/beta-catenin signaling in oral tissue development and disease. J Dent Res. 2010;89:318-330. [PMID: 20200414 DOI: 10.1177/0022034510363373] [Cited by in Crossref: 135] [Cited by in F6Publishing: 123] [Article Influence: 12.3] [Reference Citation Analysis]
74 Tallón-Walton V, Manzanares-Céspedes MC, Carvalho-Lobato P, Valdivia-Gandur I, Arte S, Nieminen P. Exclusion of PAX9 and MSX1 mutation in six families affected by tooth agenesis. A genetic study and literature review. Med Oral Patol Oral Cir Bucal 2014;19:e248-54. [PMID: 24316698 DOI: 10.4317/medoral.19173] [Cited by in Crossref: 9] [Cited by in F6Publishing: 4] [Article Influence: 1.3] [Reference Citation Analysis]
75 Ritwik P, Patterson KK. Diagnosis of Tooth Agenesis in Childhood and Risk for Neoplasms in Adulthood. Ochsner J 2018;18:345-50. [PMID: 30559619 DOI: 10.31486/toj.18.0060] [Cited by in Crossref: 9] [Cited by in F6Publishing: 5] [Article Influence: 3.0] [Reference Citation Analysis]
76 Jass JR. Hereditary Non-Polyposis Colorectal Cancer: the rise and fall of a confusing term. World J Gastroenterol. 2006;12:4943-4950. [PMID: 16937488 DOI: 10.3748/wjg.v12.i31.4943] [Cited by in CrossRef: 102] [Cited by in F6Publishing: 76] [Article Influence: 7.3] [Reference Citation Analysis]
77 Hu J, Simmer J. Developmental biology and genetics of dental malformations. Orthod Craniofac Res 2007;10:45-52. [DOI: 10.1111/j.1601-6343.2007.00384.x] [Cited by in Crossref: 53] [Cited by in F6Publishing: 45] [Article Influence: 3.8] [Reference Citation Analysis]
78 Nie J, Liu L, Xing G, Zhang M, Wei R, Guo M, Li X, Xie P, Li L, He F, Han W, Zhang L. CKIP-1 acts as a colonic tumor suppressor by repressing oncogenic Smurf1 synthesis and promoting Smurf1 autodegradation. Oncogene 2014;33:3677-87. [DOI: 10.1038/onc.2013.340] [Cited by in Crossref: 32] [Cited by in F6Publishing: 27] [Article Influence: 4.0] [Reference Citation Analysis]
79 Schneikert J, Behrens J. The canonical Wnt signalling pathway and its APC partner in colon cancer development. Gut 2007;56:417-25. [PMID: 16840506 DOI: 10.1136/gut.2006.093310] [Cited by in Crossref: 190] [Cited by in F6Publishing: 159] [Article Influence: 12.7] [Reference Citation Analysis]
80 Hayano S, Kurosaka H, Yanagita T, Kalus I, Milz F, Ishihara Y, Islam MN, Kawanabe N, Saito M, Kamioka H, Adachi T, Dierks T, Yamashiro T. Roles of heparan sulfate sulfation in dentinogenesis. J Biol Chem 2012;287:12217-29. [PMID: 22351753 DOI: 10.1074/jbc.M111.332924] [Cited by in Crossref: 28] [Cited by in F6Publishing: 15] [Article Influence: 3.1] [Reference Citation Analysis]
81 Mitsiadis T, Luder H. Genetic basis for tooth malformations: from mice to men and back again. Clinical Genetics 2011;80:319-29. [DOI: 10.1111/j.1399-0004.2011.01762.x] [Cited by in Crossref: 32] [Cited by in F6Publishing: 25] [Article Influence: 3.2] [Reference Citation Analysis]
82 Peres RC, Line SR. Analysis of MMP-9 and TIMP-2 gene promoter polymorphisms in individuals with hypodontia. Braz Dent J 2005;16:231-6. [DOI: 10.1590/s0103-64402005000300011] [Cited by in Crossref: 8] [Article Influence: 0.5] [Reference Citation Analysis]
83 Haga S, Nakaoka H, Yamaguchi T, Yamamoto K, Kim Y, Samoto H, Ohno T, Katayama K, Ishida H, Park S, Kimura R, Maki K, Inoue I. A genome-wide association study of third molar agenesis in Japanese and Korean populations. J Hum Genet 2013;58:799-803. [DOI: 10.1038/jhg.2013.106] [Cited by in Crossref: 11] [Cited by in F6Publishing: 9] [Article Influence: 1.4] [Reference Citation Analysis]
84 Kapadia H, Mues G, D'souza R. Genes affecting tooth morphogenesis. Orthod Craniofac Res 2007;10:105-13. [DOI: 10.1111/j.1601-6343.2007.00395.x] [Cited by in Crossref: 26] [Cited by in F6Publishing: 20] [Article Influence: 1.9] [Reference Citation Analysis]
85 Küchler EC, Sabóia TM, Vieira TC, Lips A, Tannure PN, Deeley K, Reis MF, Ho B, Rey AC, Costa MC, Granjeiro JM, Vieira AR. Studies of genes involved in craniofacial development and tumorigenesis: FGF3 contributes to isolated oral clefts and may interact with PAX9. Acta Odontologica Scandinavica 2014;72:1070-8. [DOI: 10.3109/00016357.2014.903514] [Cited by in Crossref: 8] [Cited by in F6Publishing: 7] [Article Influence: 1.1] [Reference Citation Analysis]
86 Mitsui SN, Yasue A, Masuda K, Naruto T, Minegishi Y, Oyadomari S, Noji S, Imoto I, Tanaka E. Novel human mutation and CRISPR/Cas genome-edited mice reveal the importance of C-terminal domain of MSX1 in tooth and palate development. Sci Rep 2016;6:38398. [PMID: 27917906 DOI: 10.1038/srep38398] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 1.2] [Reference Citation Analysis]
87 Adachi J, Aoki Y, Tatematsu T, Goto H, Nakayama A, Nishiyama T, Takahashi K, Sana M, Ota A, Machida J, Nagao T, Tokita Y. Novel MSX1 frameshift mutation in a Japanese family with nonsyndromic oligodontia. Hum Genome Var 2021;8:29. [PMID: 34285200 DOI: 10.1038/s41439-021-00161-x] [Reference Citation Analysis]
88 Cadigan KM, Peifer M. Wnt signaling from development to disease: insights from model systems. Cold Spring Harb Perspect Biol 2009;1:a002881. [PMID: 20066091 DOI: 10.1101/cshperspect.a002881] [Cited by in Crossref: 197] [Cited by in F6Publishing: 185] [Article Influence: 17.9] [Reference Citation Analysis]
89 Salahshor S, Woodgett JR. The links between axin and carcinogenesis. J Clin Pathol. 2005;58:225-236. [PMID: 15735151 DOI: 10.1136/jcp.2003.009506] [Cited by in Crossref: 158] [Cited by in F6Publishing: 151] [Article Influence: 9.9] [Reference Citation Analysis]
90 Ahtiainen L, Uski I, Thesleff I, Mikkola ML. Early epithelial signaling center governs tooth budding morphogenesis. J Cell Biol 2016;214:753-67. [PMID: 27621364 DOI: 10.1083/jcb.201512074] [Cited by in Crossref: 35] [Cited by in F6Publishing: 24] [Article Influence: 8.8] [Reference Citation Analysis]
91 Fan H, Ye X, Shi L, Yin W, Hua B, Song G, Shi B, Bian Z. Mutations in the EDA gene are responsible for X-linked hypohidrotic ectodermal dysplasia and hypodontia in Chinese kindreds. European Journal of Oral Sciences 2008;116:412-7. [DOI: 10.1111/j.1600-0722.2008.00555.x] [Cited by in Crossref: 23] [Cited by in F6Publishing: 20] [Article Influence: 1.8] [Reference Citation Analysis]
92 Yang L, Wang G, Zhao X, Ye S, Shen P, Wang W, Zheng S. A Novel WRN Frameshift Mutation Identified by Multiplex Genetic Testing in a Family with Multiple Cases of Cancer. PLoS One 2015;10:e0133020. [PMID: 26241669 DOI: 10.1371/journal.pone.0133020] [Cited by in Crossref: 7] [Cited by in F6Publishing: 5] [Article Influence: 1.2] [Reference Citation Analysis]
93 Mostowska A, Biedziak B, Zadurska M, Bogdanowicz A, Olszewska A, Cieślińska K, Firlej E, Jagodziński P. GREM2 nucleotide variants and the risk of tooth agenesis. Oral Dis 2018;24:591-9. [DOI: 10.1111/odi.12793] [Cited by in Crossref: 6] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
94 Nikopensius T, Annilo T, Jagomägi T, Gilissen C, Kals M, Krjutškov K, Mägi R, Eelmets M, Gerst-talas U, Remm M, Saag M, Hoischen A, Metspalu A. Non-syndromic Tooth Agenesis Associated with a Nonsense Mutation in Ectodysplasin-A (EDA). J Dent Res 2013;92:507-11. [DOI: 10.1177/0022034513487210] [Cited by in Crossref: 14] [Cited by in F6Publishing: 9] [Article Influence: 1.8] [Reference Citation Analysis]
95 Vink CP, Ockeloen CW, ten Kate S, Koolen DA, Ploos van Amstel JK, Kuijpers-Jagtman AM, van Heumen CC, Kleefstra T, Carels CE. Variability in dentofacial phenotypes in four families with WNT10A mutations. Eur J Hum Genet 2014;22:1063-70. [PMID: 24398796 DOI: 10.1038/ejhg.2013.300] [Cited by in Crossref: 23] [Cited by in F6Publishing: 13] [Article Influence: 3.3] [Reference Citation Analysis]
96 Mongin C, Coulet F, Lefevre JH, Colas C, Svrcek M, Eyries M, Lahely Y, Fléjou JF, Soubrier F, Parc Y. Unexplained polyposis: a challenge for geneticists, pathologists and gastroenterologists. Clin Genet. 2012;81:38-46. [PMID: 21476993 DOI: 10.1111/j.1399-0004.2011.01676.x] [Cited by in Crossref: 34] [Cited by in F6Publishing: 30] [Article Influence: 3.4] [Reference Citation Analysis]
97 Stavropoulos D, Bartzela T, Bronkhorst E, Mohlin B, Hagberg C. Dental agenesis patterns of permanent teeth in Apert syndrome: Dental agenesis in Apert syndrome. European Journal of Oral Sciences 2011;119:198-203. [DOI: 10.1111/j.1600-0722.2011.00821.x] [Cited by in Crossref: 16] [Cited by in F6Publishing: 14] [Article Influence: 1.6] [Reference Citation Analysis]
98 Wei Z, Zhong M, Guo Y, Wang Y, Ren M, Wang Z. Expression of β-catenin and AXIN2 in ameloblastomas. Contemp Oncol (Pozn) 2013;17:250-6. [PMID: 24596510 DOI: 10.5114/wo.2013.35278] [Cited by in Crossref: 2] [Cited by in F6Publishing: 5] [Article Influence: 0.3] [Reference Citation Analysis]
99 Küchler E, Lips A, Tannure P, Ho B, Costa M, Granjeiro J, Vieira A. Tooth Agenesis Association with Self-reported Family History of Cancer. J Dent Res 2013;92:149-55. [DOI: 10.1177/0022034512468750] [Cited by in Crossref: 24] [Cited by in F6Publishing: 17] [Article Influence: 2.7] [Reference Citation Analysis]
100 Swinnen S, Bailleul-Forestier I, Arte S, Nieminen P, Devriendt K, Carels C. Investigating the etiology of multiple tooth agenesis in three sisters with severe oligodontia. Orthod Craniofac Res 2008;11:24-31. [PMID: 18199077 DOI: 10.1111/j.1601-6343.2008.00410.x] [Cited by in Crossref: 15] [Cited by in F6Publishing: 11] [Article Influence: 1.2] [Reference Citation Analysis]
101 Pereira TV, Salzano FM, Mostowska A, Trzeciak WH, Ruiz-Linares A, Chies JA, Saavedra C, Nagamachi C, Hurtado AM, Hill K, Castro-de-Guerra D, Silva-Júnior WA, Bortolini MC. Natural selection and molecular evolution in primate PAX9 gene, a major determinant of tooth development. Proc Natl Acad Sci U S A 2006;103:5676-81. [PMID: 16585527 DOI: 10.1073/pnas.0509562103] [Cited by in Crossref: 31] [Cited by in F6Publishing: 26] [Article Influence: 2.1] [Reference Citation Analysis]
102 Hartmann C. A Wnt canon orchestrating osteoblastogenesis. Trends Cell Biol 2006;16:151-8. [PMID: 16466918 DOI: 10.1016/j.tcb.2006.01.001] [Cited by in Crossref: 213] [Cited by in F6Publishing: 203] [Article Influence: 14.2] [Reference Citation Analysis]
103 Moon RT, Kohn AD, De Ferrari GV, Kaykas A. WNT and beta-catenin signalling: diseases and therapies. Nat Rev Genet. 2004;5:691-701. [PMID: 15372092 DOI: 10.1038/nrg1427] [Cited by in Crossref: 1308] [Cited by in F6Publishing: 1221] [Article Influence: 76.9] [Reference Citation Analysis]
104 Beard C, Purvis R, Winship IM, Macrae FA, Buchanan DD. Phenotypic confirmation of oligodontia, colorectal polyposis and cancer in a family carrying an exon 7 nonsense variant in the AXIN2 gene. Familial Cancer 2019;18:311-5. [DOI: 10.1007/s10689-019-00120-0] [Cited by in Crossref: 8] [Cited by in F6Publishing: 2] [Article Influence: 4.0] [Reference Citation Analysis]
105 Wong SW, Liu HC, Han D, Chang HG, Zhao HS, Wang YX, Feng HL. A novel non-stop mutation in MSX1 causing autosomal dominant non-syndromic oligodontia. Mutagenesis 2014;29:319-23. [PMID: 24914010 DOI: 10.1093/mutage/geu019] [Cited by in Crossref: 21] [Cited by in F6Publishing: 21] [Article Influence: 3.0] [Reference Citation Analysis]
106 Bonczek O, Krejci P, Izakovicova-Holla L, Cernochova P, Kiss I, Vojtesek B. Tooth agenesis: What do we know and is there a connection to cancer? Clin Genet 2021;99:493-502. [PMID: 33249565 DOI: 10.1111/cge.13892] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
107 Ishimoto K, Hayano S, Yanagita T, Kurosaka H, Kawanabe N, Itoh S, Ono M, Kuboki T, Kamioka H, Yamashiro T. Topical application of lithium chloride on the pulp induces dentin regeneration. PLoS One 2015;10:e0121938. [PMID: 25812134 DOI: 10.1371/journal.pone.0121938] [Cited by in Crossref: 25] [Cited by in F6Publishing: 21] [Article Influence: 4.2] [Reference Citation Analysis]
108 Phan M, Conte F, Khandelwal KD, Ockeloen CW, Bartzela T, Kleefstra T, van Bokhoven H, Rubini M, Zhou H, Carels CE. Tooth agenesis and orofacial clefting: genetic brothers in arms? Hum Genet 2016;135:1299-327. [PMID: 27699475 DOI: 10.1007/s00439-016-1733-z] [Cited by in Crossref: 30] [Cited by in F6Publishing: 21] [Article Influence: 6.0] [Reference Citation Analysis]
109 Gomes RR, da Fonseca JA, Paula LM, Faber J, Acevedo AC. Prevalence of hypodontia in orthodontic patients in Brasilia, Brazil. Eur J Orthod 2010;32:302-6. [PMID: 19837747 DOI: 10.1093/ejo/cjp107] [Cited by in Crossref: 43] [Cited by in F6Publishing: 23] [Article Influence: 3.6] [Reference Citation Analysis]
110 Square TA, Sundaram S, Mackey EJ, Miller CT. Distinct tooth regeneration systems deploy a conserved battery of genes. Evodevo 2021;12:4. [PMID: 33766133 DOI: 10.1186/s13227-021-00172-3] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
111 Mostowska A, Zadurska M, Rakowska A, Lianeri M, Jagodziński PP. Novel PAX9 mutation associated with syndromic tooth agenesis. Eur J Oral Sci 2013;121:403-11. [DOI: 10.1111/eos.12071] [Cited by in Crossref: 14] [Cited by in F6Publishing: 11] [Article Influence: 1.8] [Reference Citation Analysis]
112 Olsen AK, Coskun M, Bzorek M, Kristensen MH, Danielsen ET, Jørgensen S, Olsen J, Engel U, Holck S, Troelsen JT. Regulation of APC and AXIN2 expression by intestinal tumor suppressor CDX2 in colon cancer cells. Carcinogenesis 2013;34:1361-9. [DOI: 10.1093/carcin/bgt037] [Cited by in Crossref: 34] [Cited by in F6Publishing: 31] [Article Influence: 4.3] [Reference Citation Analysis]
113 Chen X, Liu J, Li N, Wang Y, Zhou N, Zhu L, Shi Y, Wu Y, Xiao J, Liu C. Mesenchymal Wnt/β-catenin signaling induces Wnt and BMP antagonists in dental epithelium. Organogenesis 2019;15:55-67. [PMID: 31240991 DOI: 10.1080/15476278.2019.1633871] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
114 Fekonja A, Cretnik A, Zerdoner D, Takac I. Hypodontia phenotype in patients with epithelial ovarian cancer. Radiol Oncol 2015;49:65-70. [PMID: 25810703 DOI: 10.2478/raon-2014-0034] [Cited by in Crossref: 4] [Cited by in F6Publishing: 7] [Article Influence: 0.7] [Reference Citation Analysis]
115 Marvin ML, Mazzoni SM, Herron CM, Edwards S, Gruber SB, Petty EM. AXIN2-associated autosomal dominant ectodermal dysplasia and neoplastic syndrome. Am J Med Genet A. 2011;155A:898-902. [PMID: 21416598 DOI: 10.1002/ajmg.a.33927] [Cited by in Crossref: 53] [Cited by in F6Publishing: 46] [Article Influence: 5.3] [Reference Citation Analysis]
116 Luo J, Chen J, Deng ZL, Luo X, Song WX, Sharff KA, Tang N, Haydon RC, Luu HH, He TC. Wnt signaling and human diseases: what are the therapeutic implications? Lab Invest 2007;87:97-103. [PMID: 17211410 DOI: 10.1038/labinvest.3700509] [Cited by in Crossref: 116] [Cited by in F6Publishing: 108] [Article Influence: 8.3] [Reference Citation Analysis]
117 Williams MA, Biguetti C, Romero-Bustillos M, Maheshwari K, Dinckan N, Cavalla F, Liu X, Silva R, Akyalcin S, Uyguner ZO, Vieira AR, Amendt BA, Fakhouri WD, Letra A. Colorectal Cancer-Associated Genes Are Associated with Tooth Agenesis and May Have a Role in Tooth Development. Sci Rep 2018;8:2979. [PMID: 29445242 DOI: 10.1038/s41598-018-21368-z] [Cited by in Crossref: 12] [Cited by in F6Publishing: 10] [Article Influence: 4.0] [Reference Citation Analysis]
118 Mitsui S, Yasue A, Masuda K, Watanabe K, Horiuchi S, Imoto I, Tanaka E. Novel PAX9 Mutations Cause Non-syndromic Tooth Agenesis. J Dent Res 2014;93:245-9. [DOI: 10.1177/0022034513519801] [Cited by in Crossref: 15] [Cited by in F6Publishing: 13] [Article Influence: 2.1] [Reference Citation Analysis]
119 Medina MCG, Bastos RTDRM, Mecenas P, Pinheiro JJV, Normando D. Association between tooth agenesis and cancer: a systematic review. J Appl Oral Sci 2021;29:e20200955. [PMID: 34378652 DOI: 10.1590/1678-7757-2020-0955] [Reference Citation Analysis]
120 Dreesen K, Swinnen S, Devriendt K, Carels C. Tooth agenesis patterns and phenotype variation in a cohort of Belgian patients with hypodontia and oligodontia clustered in 79 families with their pedigrees. Eur J Orthod 2014;36:99-106. [PMID: 23598609 DOI: 10.1093/ejo/cjt021] [Cited by in Crossref: 10] [Cited by in F6Publishing: 9] [Article Influence: 1.3] [Reference Citation Analysis]
121 Cobourne MT, Sharpe PT. Diseases of the tooth: the genetic and molecular basis of inherited anomalies affecting the dentition: Diseases of the tooth. WIREs Dev Biol 2013;2:183-212. [DOI: 10.1002/wdev.66] [Cited by in Crossref: 39] [Cited by in F6Publishing: 23] [Article Influence: 4.3] [Reference Citation Analysis]
122 Fekonja A. Comparison of Mesiodistal Crown Dimension and Arch Width in Subjects with and without Hypodontia: Comparison of Mesiodistal Crown Dimension and Arch Width. J Esthet Restor Dent 2013;25:203-10. [DOI: 10.1111/jerd.12026] [Cited by in Crossref: 7] [Cited by in F6Publishing: 2] [Article Influence: 0.9] [Reference Citation Analysis]
123 Daw EM, Saliba C, Grech G, Camilleri S. A novel PAX9 mutation causing oligodontia. Archives of Oral Biology 2017;84:100-5. [DOI: 10.1016/j.archoralbio.2017.09.018] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 1.3] [Reference Citation Analysis]
124 Mendoza-Fandino GA, Gee JM, Ben-Dor S, Gonzalez-Quevedo C, Lee K, Kobayashi Y, Hartiala J, Myers RM, Leal SM, Allayee H, Patel PI. A novel g.-1258G>A mutation in a conserved putative regulatory element of PAX9 is associated with autosomal dominant molar hypodontia. Clin Genet 2011;80:265-72. [PMID: 21443745 DOI: 10.1111/j.1399-0004.2010.01529.x] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 0.7] [Reference Citation Analysis]
125 Abid MF, Simpson M, Petridis C, Cobourne M, Sharpe P. Non-syndromic severe hypodontia caused by a novel frameshift insertion mutation in the homeobox of the MSX1 gene. Archives of Oral Biology 2017;75:8-13. [DOI: 10.1016/j.archoralbio.2016.11.018] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 1.3] [Reference Citation Analysis]
126 Lindor NM, Win AK, Gallinger S, Daftary D, Thibodeau SN, Silva R, Letra A. Colorectal cancer and self-reported tooth agenesis. Hered Cancer Clin Pract 2014;12:7. [PMID: 24607150 DOI: 10.1186/1897-4287-12-7] [Cited by in Crossref: 10] [Cited by in F6Publishing: 10] [Article Influence: 1.4] [Reference Citation Analysis]
127 Al-Ani AH, Antoun JS, Thomson WM, Merriman TR, Farella M. Maternal Smoking during Pregnancy Is Associated with Offspring Hypodontia. J Dent Res 2017;96:1014-9. [PMID: 28535361 DOI: 10.1177/0022034517711156] [Cited by in Crossref: 12] [Cited by in F6Publishing: 7] [Article Influence: 3.0] [Reference Citation Analysis]
128 Goto H, Kimura M, Machida J, Ota A, Nakashima M, Tsuchida N, Adachi J, Aoki Y, Tatematsu T, Takahashi K, Sana M, Nakayama A, Suzuki S, Nagao T, Matsumoto N, Tokita Y. A novel LRP6 variant in a Japanese family with oligodontia. Hum Genome Var 2021;8:30. [PMID: 34285199 DOI: 10.1038/s41439-021-00162-w] [Reference Citation Analysis]
129 Adaimy L, Chouery E, Megarbane H, Mroueh S, Delague V, Nicolas E, Belguith H, de Mazancourt P, Megarbane A. Mutation in WNT10A is associated with an autosomal recessive ectodermal dysplasia: the odonto-onycho-dermal dysplasia. Am J Hum Genet 2007;81:821-8. [PMID: 17847007 DOI: 10.1086/520064] [Cited by in Crossref: 159] [Cited by in F6Publishing: 129] [Article Influence: 11.4] [Reference Citation Analysis]
130 Sabóia TM, Reis MF, Martins ÂM, Romanos HF, Tannure PN, Granjeiro JM, Vieira AR, Antunes LS, Küchler EC, Costa MC. DLX1 and MMP3 contribute to oral clefts with and without positive family history of cancer. Arch Oral Biol 2015;60:223-8. [PMID: 25463899 DOI: 10.1016/j.archoralbio.2014.10.002] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 1.0] [Reference Citation Analysis]
131 Bonds J, Pollan-White S, Xiang L, Mues G, D'Souza R. Is there a link between ovarian cancer and tooth agenesis? Eur J Med Genet 2014;57:235-9. [PMID: 24631698 DOI: 10.1016/j.ejmg.2014.02.013] [Cited by in Crossref: 17] [Cited by in F6Publishing: 16] [Article Influence: 2.4] [Reference Citation Analysis]
132 Rivera B, Perea J, Sánchez E, Villapún M, Sánchez-Tomé E, Mercadillo F, Robledo M, Benítez J, Urioste M. A novel AXIN2 germline variant associated with attenuated FAP without signs of oligondontia or ectodermal dysplasia. Eur J Hum Genet 2014;22:423-6. [PMID: 23838596 DOI: 10.1038/ejhg.2013.146] [Cited by in Crossref: 23] [Cited by in F6Publishing: 19] [Article Influence: 2.9] [Reference Citation Analysis]
133 Yin W, Bian Z. Hypodontia, a prospective predictive marker for tumor? Oral Dis 2016;22:265-73. [DOI: 10.1111/odi.12400] [Cited by in Crossref: 8] [Cited by in F6Publishing: 7] [Article Influence: 1.6] [Reference Citation Analysis]
134 Song S, Zhao R, He H, Zhang J, Feng H, Lin L. WNT10A variants are associated with non-syndromic tooth agenesis in the general population. Hum Genet 2014;133:117-24. [PMID: 24043634 DOI: 10.1007/s00439-013-1360-x] [Cited by in Crossref: 46] [Cited by in F6Publishing: 32] [Article Influence: 5.8] [Reference Citation Analysis]
135 Katoh M, Katoh M. Molecular genetics and targeted therapy of WNT-related human diseases (Review). Int J Mol Med. 2017;40:587-606. [PMID: 28731148 DOI: 10.3892/ijmm.2017.3071] [Cited by in Crossref: 37] [Cited by in F6Publishing: 53] [Article Influence: 9.3] [Reference Citation Analysis]
136 Xie X, Zhou Z, Song Y, Zhang X, Dang C, Zhang H. Mist1 Inhibits Epithelial-Mesenchymal Transition in Gastric Adenocarcinoma via Downregulating the Wnt/β-catenin Pathway. J Cancer 2021;12:4574-84. [PMID: 34149921 DOI: 10.7150/jca.59138] [Reference Citation Analysis]
137 Barker N, Clevers H. Mining the Wnt pathway for cancer therapeutics. Nat Rev Drug Discov. 2006;5:997-1014. [PMID: 17139285 DOI: 10.1038/nrd2154] [Cited by in Crossref: 538] [Cited by in F6Publishing: 476] [Article Influence: 38.4] [Reference Citation Analysis]
138 Fleischmannova J, Matalova E, Tucker AS, Sharpe PT. Mouse models of tooth abnormalities. Eur J Oral Sci 2008;116:1-10. [PMID: 18186725 DOI: 10.1111/j.1600-0722.2007.00504.x] [Cited by in Crossref: 54] [Cited by in F6Publishing: 45] [Article Influence: 4.2] [Reference Citation Analysis]
139 Liang J, Song G, Li Q, Bian Z. Novel missense mutations in PAX9 causing oligodontia. Arch Oral Biol 2012;57:784-9. [PMID: 22277187 DOI: 10.1016/j.archoralbio.2011.12.005] [Cited by in Crossref: 17] [Cited by in F6Publishing: 16] [Article Influence: 1.9] [Reference Citation Analysis]
140 Buchert M, Athineos D, Abud HE, Burke ZD, Faux MC, Samuel MS, Jarnicki AG, Winbanks CE, Newton IP, Meniel VS, Suzuki H, Stacker SA, Näthke IS, Tosh D, Huelsken J, Clarke AR, Heath JK, Sansom OJ, Ernst M. Genetic dissection of differential signaling threshold requirements for the Wnt/beta-catenin pathway in vivo. PLoS Genet 2010;6:e1000816. [PMID: 20084116 DOI: 10.1371/journal.pgen.1000816] [Cited by in Crossref: 67] [Cited by in F6Publishing: 59] [Article Influence: 6.1] [Reference Citation Analysis]
141 Gaczkowska A, Abdalla EM, Dowidar KM, Elhady GM, Jagodzinski PP, Mostowska A. De novo EDA mutations: Variable expression in two Egyptian families. Arch Oral Biol 2016;68:21-8. [PMID: 27054699 DOI: 10.1016/j.archoralbio.2016.03.015] [Cited by in Crossref: 7] [Cited by in F6Publishing: 4] [Article Influence: 1.4] [Reference Citation Analysis]
142 Gillespie J, Ross RL, Corinaldesi C, Esteves F, Derrett-Smith E, McDermott MF, Doody GM, Denton CP, Emery P, Del Galdo F. Transforming Growth Factor β Activation Primes Canonical Wnt Signaling Through Down-Regulation of Axin-2. Arthritis Rheumatol 2018;70:932-42. [PMID: 29409120 DOI: 10.1002/art.40437] [Cited by in Crossref: 11] [Cited by in F6Publishing: 10] [Article Influence: 3.7] [Reference Citation Analysis]
143 Järvinen E, Salazar-Ciudad I, Birchmeier W, Taketo MM, Jernvall J, Thesleff I. Continuous tooth generation in mouse is induced by activated epithelial Wnt/beta-catenin signaling. Proc Natl Acad Sci U S A 2006;103:18627-32. [PMID: 17121988 DOI: 10.1073/pnas.0607289103] [Cited by in Crossref: 274] [Cited by in F6Publishing: 236] [Article Influence: 18.3] [Reference Citation Analysis]
144 Wang Y, Cao J, Liu W, Zhang J, Wang Z, Zhang Y, Hou L, Chen S, Hao P, Zhang L, Zhuang M, Yu Y, Li D, Fan G. Protein tyrosine phosphatase receptor type R (PTPRR) antagonizes the Wnt signaling pathway in ovarian cancer by dephosphorylating and inactivating β-catenin. J Biol Chem 2019;294:18306-23. [PMID: 31653698 DOI: 10.1074/jbc.RA119.010348] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.5] [Reference Citation Analysis]
145 De Coster PJ, Mortier G, Marks LA, Martens LC. Cranial suture biology and dental development: genetic and clinical perspectives. J Oral Pathol Med 2007;36:447-55. [PMID: 17686002 DOI: 10.1111/j.1600-0714.2007.00553.x] [Cited by in Crossref: 27] [Cited by in F6Publishing: 22] [Article Influence: 1.9] [Reference Citation Analysis]
146 Kwon HE, Jiang R. Development of Teeth ☆. Reference Module in Biomedical Sciences. Elsevier; 2018. [DOI: 10.1016/b978-0-12-801238-3.64113-2] [Cited by in Crossref: 3] [Article Influence: 1.0] [Reference Citation Analysis]
147 Machida J, Goto H, Tatematsu T, Shibata A, Miyachi H, Takahashi K, Izumi H, Nakayama A, Shimozato K, Tokita Y. WNT10A variants isolated from Japanese patients with congenital tooth agenesis. Hum Genome Var 2017;4:17047. [PMID: 29367877 DOI: 10.1038/hgv.2017.47] [Cited by in Crossref: 7] [Cited by in F6Publishing: 4] [Article Influence: 1.8] [Reference Citation Analysis]
148 Mostowska A, Biedziak B, Zadurska M, Dunin-wilczynska I, Lianeri M, Jagodzinski P. Nucleotide variants of genes encoding components of the Wnt signalling pathway and the risk of non-syndromic tooth agenesis: Risk of non-syndromic tooth agenesis. Clin Genet 2013;84:429-40. [DOI: 10.1111/cge.12061] [Cited by in Crossref: 38] [Cited by in F6Publishing: 30] [Article Influence: 4.2] [Reference Citation Analysis]
149 Iavazzo C, Papakiritsis M, Gkegkes ID. Hypodontia and ovarian cancer: A systematic review. J Turk Ger Gynecol Assoc 2016;17:41-4. [PMID: 27026778 DOI: 10.5152/jtgga.2015.15174] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 0.6] [Reference Citation Analysis]
150 Ishida K, Yuge Y, Hanaoka M, Yasukawa M, Minami Y, Ogawa M, Masumoto K, Shigeyoshi Y, Saito M, Tsuji T. Gadd45g regulates dental epithelial cell proliferation through p38 MAPK-mediated p21 expression. Genes Cells 2013;18:660-71. [DOI: 10.1111/gtc.12067] [Cited by in Crossref: 9] [Cited by in F6Publishing: 8] [Article Influence: 1.1] [Reference Citation Analysis]
151 Kettunen P, Spencer-dene B, Furmanek T, Kvinnsland IH, Dickson C, Thesleff I, Luukko K. Fgfr2b mediated epithelial–mesenchymal interactions coordinate tooth morphogenesis and dental trigeminal axon patterning. Mechanisms of Development 2007;124:868-83. [DOI: 10.1016/j.mod.2007.09.003] [Cited by in Crossref: 35] [Cited by in F6Publishing: 28] [Article Influence: 2.5] [Reference Citation Analysis]
152 Klein OD, Oberoi S, Huysseune A, Hovorakova M, Peterka M, Peterkova R. Developmental disorders of the dentition: an update. Am J Med Genet C Semin Med Genet. 2013;163C:318-332. [PMID: 24124058 DOI: 10.1002/ajmg.c.31382] [Cited by in Crossref: 68] [Cited by in F6Publishing: 40] [Article Influence: 8.5] [Reference Citation Analysis]
153 Arai K. Tooth agenesis patterns in Japanese orthodontic patients with nonsyndromic oligodontia. American Journal of Orthodontics and Dentofacial Orthopedics 2019;156:238-47. [DOI: 10.1016/j.ajodo.2018.09.015] [Cited by in Crossref: 5] [Cited by in F6Publishing: 1] [Article Influence: 2.5] [Reference Citation Analysis]
154 Isman E, Nergiz S, Acar H, Sari Z. PAX9 polymorphisms and susceptibility with sporadic tooth agenesis in Turkish populations: a case-control study. BMC Genomics 2013;14:733. [PMID: 24160254 DOI: 10.1186/1471-2164-14-733] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 0.3] [Reference Citation Analysis]
155 Nusse R, Clevers H. Wnt/β-Catenin Signaling, Disease, and Emerging Therapeutic Modalities. Cell 2017;169:985-99. [PMID: 28575679 DOI: 10.1016/j.cell.2017.05.016] [Cited by in Crossref: 1477] [Cited by in F6Publishing: 1255] [Article Influence: 369.3] [Reference Citation Analysis]
156 de la Chapelle A. Genetic predisposition to colorectal cancer. Nat Rev Cancer. 2004;4:769-780. [PMID: 15510158 DOI: 10.1038/nrc1453] [Cited by in Crossref: 410] [Cited by in F6Publishing: 351] [Article Influence: 24.1] [Reference Citation Analysis]
157 Jara-Espejo M, Hawkins MTR, Fogalli GB, Line SRP. Folding Stability of Pax9 Intronic G-Quadruplex Correlates with Relative Molar Size in Eutherians. Mol Biol Evol 2021;38:1860-73. [PMID: 33355664 DOI: 10.1093/molbev/msaa331] [Reference Citation Analysis]
158 Wang Z, Li Z, Ji H. Direct targeting of β-catenin in the Wnt signaling pathway: Current progress and perspectives. Med Res Rev 2021;41:2109-29. [PMID: 33475177 DOI: 10.1002/med.21787] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 6.0] [Reference Citation Analysis]
159 Kim S, Choi E, Song K, Kim S, Seo E, Jho E, Kee S. Axin localizes to mitotic spindles and centrosomes in mitotic cells. Experimental Cell Research 2009;315:943-54. [DOI: 10.1016/j.yexcr.2009.01.013] [Cited by in Crossref: 28] [Cited by in F6Publishing: 28] [Article Influence: 2.3] [Reference Citation Analysis]
160 Matalova E, Fleischmannova J, Sharpe PT, Tucker AS. Tooth agenesis: from molecular genetics to molecular dentistry. J Dent Res 2008;87:617-23. [PMID: 18573979 DOI: 10.1177/154405910808700715] [Cited by in Crossref: 117] [Cited by in F6Publishing: 76] [Article Influence: 9.0] [Reference Citation Analysis]
161 Tarapore RS, Siddiqui IA, Mukhtar H. Modulation of Wnt/β-catenin signaling pathway by bioactive food components. Carcinogenesis 2012;33:483-91. [PMID: 22198211 DOI: 10.1093/carcin/bgr305] [Cited by in Crossref: 77] [Cited by in F6Publishing: 70] [Article Influence: 7.7] [Reference Citation Analysis]
162 Townsend G, Harris EF, Lesot H, Clauss F, Brook A. Morphogenetic fields within the human dentition: a new, clinically relevant synthesis of an old concept. Arch Oral Biol 2009;54 Suppl 1:S34-44. [PMID: 18760768 DOI: 10.1016/j.archoralbio.2008.06.011] [Cited by in Crossref: 56] [Cited by in F6Publishing: 35] [Article Influence: 4.3] [Reference Citation Analysis]
163 Yu M, Wang H, Fan Z, Xie C, Liu H, Liu Y, Han D, Wong SW, Feng H. BMP4 mutations in tooth agenesis and low bone mass. Arch Oral Biol 2019;103:40-6. [PMID: 31128441 DOI: 10.1016/j.archoralbio.2019.05.012] [Cited by in Crossref: 7] [Cited by in F6Publishing: 4] [Article Influence: 3.5] [Reference Citation Analysis]
164 Jobbágy-óvári G, Páska C, Stiedl P, Trimmel B, Hontvári D, Soós B, Hermann P, Tóth Z, Kerekes-máthé B, Nagy D, Szántó I, Nagy Á, Martonosi M, Nagy K, Hadadi É, Szalai C, Hullám G, Temesi G, Antal P, Varga G, Tarján I. Complex analysis of multiple single nucleotide polymorphisms as putative risk factors of tooth agenesis in the Hungarian population. Acta Odontologica Scandinavica 2013;72:216-27. [DOI: 10.3109/00016357.2013.822547] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 0.5] [Reference Citation Analysis]
165 Gui B, Yu C, Li X, Zhao S, Zhao H, Yan Z, Cheng X, Lin J, Zheng H, Shao J, Zhao Z, Zhao L, Niu Y, Zhao Z, Wang H, Xie B, Wei X, Gui C, Li C, Chen S, Wang Y, Song Y, Gong C, Zhang TJ, Fan X, Wu Z, Chen Y, Wu N. Heterozygous Recurrent Mutations Inducing Dysfunction of ROR2 Gene in Patients With Short Stature. Front Cell Dev Biol 2021;9:661747. [PMID: 33937263 DOI: 10.3389/fcell.2021.661747] [Reference Citation Analysis]
166 McGee-Lawrence ME, Li X, Bledsoe KL, Wu H, Hawse JR, Subramaniam M, Razidlo DF, Stensgard BA, Stein GS, van Wijnen AJ, Lian JB, Hsu W, Westendorf JJ. Runx2 protein represses Axin2 expression in osteoblasts and is required for craniosynostosis in Axin2-deficient mice. J Biol Chem 2013;288:5291-302. [PMID: 23300083 DOI: 10.1074/jbc.M112.414995] [Cited by in Crossref: 27] [Cited by in F6Publishing: 19] [Article Influence: 3.4] [Reference Citation Analysis]
167 Cohen Jr. MM. The new bone biology: Pathologic, molecular, and clinical correlates. Am J Med Genet 2006;140A:2646-706. [DOI: 10.1002/ajmg.a.31368] [Cited by in Crossref: 209] [Cited by in F6Publishing: 163] [Article Influence: 13.9] [Reference Citation Analysis]
168 Jussila M, Juuri E, Thesleff I. Tooth Morphogenesis and Renewal. In: Huang GT, Thesleff I, editors. Stem Cells in Craniofacial Development and Regeneration. Hoboken: John Wiley & Sons, Inc.; 2013. pp. 109-34. [DOI: 10.1002/9781118498026.ch6] [Cited by in Crossref: 13] [Cited by in F6Publishing: 3] [Article Influence: 1.6] [Reference Citation Analysis]
169 Peterlongo P, Howe LR, Radice P, Sala P, Hong YJ, Hong SI, Mitra N, Offit K, Ellis NA. Germline mutations of AXIN2 are not associated with nonsyndromic colorectal cancer. Hum Mutat. 2005;25:498-500. [PMID: 15841489 DOI: 10.1002/humu.20189] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 0.5] [Reference Citation Analysis]
170 Ye X, Attaie AB. Genetic Basis of Nonsyndromic and Syndromic Tooth Agenesis. J Pediatr Genet 2016;5:198-208. [PMID: 27895972 DOI: 10.1055/s-0036-1592421] [Cited by in Crossref: 18] [Cited by in F6Publishing: 13] [Article Influence: 3.6] [Reference Citation Analysis]
171 Sato A, Arai K. Estimation of tooth agenesis risks between tooth types in orthodontic patients with non-syndromic oligodontia. Orthodontic Waves 2019;78:49-55. [DOI: 10.1016/j.odw.2019.04.001] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.5] [Reference Citation Analysis]
172 Yan C, Ji Y, Huang T, Yu F, Gao Y, Gu Y, Qi Q, Du J, Dai J, Ma H, Jin G. An esophageal adenocarcinoma susceptibility locus at 9q22 also confers risk to esophageal squamous cell carcinoma by regulating the function of BARX1. Cancer Lett 2018;421:103-11. [PMID: 29454095 DOI: 10.1016/j.canlet.2018.02.019] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 2.0] [Reference Citation Analysis]
173 Yang L, Liang J, Yue H, Bian Z. Two novel mutations in MSX1 causing oligodontia. PLoS One 2020;15:e0227287. [PMID: 31914153 DOI: 10.1371/journal.pone.0227287] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]
174 Wang Z, Liu CH, Huang S, Chen J. Wnt Signaling in vascular eye diseases. Prog Retin Eye Res 2019;70:110-33. [PMID: 30513356 DOI: 10.1016/j.preteyeres.2018.11.008] [Cited by in Crossref: 33] [Cited by in F6Publishing: 20] [Article Influence: 11.0] [Reference Citation Analysis]
175 Letra A, Bjork B, Cooper ME, Szabo-Rogers H, Deleyiannis FW, Field LL, Czeizel AE, Ma L, Garlet GP, Poletta FA, Mereb JC, Lopez-Camelo JS, Castilla EE, Orioli IM, Wendell S, Blanton SH, Liu K, Hecht JT, Marazita ML, Vieira AR, Silva RM. Association of AXIN2 with non-syndromic oral clefts in multiple populations. J Dent Res 2012;91:473-8. [PMID: 22370446 DOI: 10.1177/0022034512440578] [Cited by in Crossref: 25] [Cited by in F6Publishing: 22] [Article Influence: 2.8] [Reference Citation Analysis]
176 Otero L, Lacunza E, Vasquez V, Arbelaez V, Cardier F, González F. Variations in AXIN2 predict risk and prognosis of colorectal cancer. BDJ Open 2019;5:13. [PMID: 31632692 DOI: 10.1038/s41405-019-0022-z] [Cited by in Crossref: 10] [Cited by in F6Publishing: 6] [Article Influence: 5.0] [Reference Citation Analysis]
177 Ci Y, Li X, Chen M, Zhong J, North BJ, Inuzuka H, He X, Li Y, Guo J, Dai X. SCFβ-TRCP E3 ubiquitin ligase targets the tumor suppressor ZNRF3 for ubiquitination and degradation. Protein Cell 2018;9:879-89. [PMID: 29497989 DOI: 10.1007/s13238-018-0510-2] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 2.3] [Reference Citation Analysis]
178 Suryadeva S, Khan MB. Role of homeobox genes in tooth morphogenesis: a review. J Clin Diagn Res 2015;9:ZE09-12. [PMID: 25859538 DOI: 10.7860/JCDR/2015/11067.5606] [Cited by in Crossref: 2] [Cited by in F6Publishing: 8] [Article Influence: 0.3] [Reference Citation Analysis]
179 Li S, Li J, Cheng J, Zhou B, Tong X, Dong X, Wang Z, Hu Q, Chen M, Hua ZC. Non-syndromic tooth agenesis in two Chinese families associated with novel missense mutations in the TNF domain of EDA (ectodysplasin A). PLoS One 2008;3:e2396. [PMID: 18545687 DOI: 10.1371/journal.pone.0002396] [Cited by in Crossref: 24] [Cited by in F6Publishing: 20] [Article Influence: 1.8] [Reference Citation Analysis]
180 Johnson PM, Gallinger S, McLeod RS. Surveillance colonoscopy in individuals at risk for hereditary nonpolyposis colorectal cancer: an evidence-based review. Dis Colon Rectum 2006;49:80-93; discussion 94-5. [PMID: 16284887 DOI: 10.1007/s10350-005-0228-0] [Cited by in Crossref: 18] [Cited by in F6Publishing: 11] [Article Influence: 1.2] [Reference Citation Analysis]
181 Mostowska A, Biedziak B, Trzeciak WH. A novel c.581C>T transition localized in a highly conserved homeobox sequence of MSX1: is it responsible for oligodontia? J Appl Genet 2006;47:159-64. [PMID: 16682758 DOI: 10.1007/BF03194616] [Cited by in Crossref: 34] [Cited by in F6Publishing: 10] [Article Influence: 2.3] [Reference Citation Analysis]
182 Wong S, Liu H, Bai B, Chang H, Zhao H, Wang Y, Han D, Feng H. Novel missense mutations in the AXIN2 gene associated with non-syndromic oligodontia. Arch Oral Biol 2014;59:349-53. [PMID: 24581859 DOI: 10.1016/j.archoralbio.2013.12.009] [Cited by in Crossref: 16] [Cited by in F6Publishing: 13] [Article Influence: 2.0] [Reference Citation Analysis]
183 Polakis P. The many ways of Wnt in cancer. Curr Opin Genet Dev. 2007;17:45-51. [PMID: 17208432 DOI: 10.1016/j.gde.2006.12.007] [Cited by in Crossref: 631] [Cited by in F6Publishing: 583] [Article Influence: 45.1] [Reference Citation Analysis]
184 Bailleul-forestier I, Molla M, Verloes A, Berdal A. The genetic basis of inherited anomalies of the teeth. European Journal of Medical Genetics 2008;51:273-91. [DOI: 10.1016/j.ejmg.2008.02.009] [Cited by in Crossref: 101] [Cited by in F6Publishing: 63] [Article Influence: 7.8] [Reference Citation Analysis]
185 Obara N, Suzuki Y, Takeda M. Gene expression of β–catenin is up-regulated in inner dental epithelium and enamel knots during molar tooth morphogenesis in the mouse. Cell Tissue Res 2006;325:197-201. [DOI: 10.1007/s00441-005-0136-6] [Cited by in Crossref: 20] [Cited by in F6Publishing: 19] [Article Influence: 1.3] [Reference Citation Analysis]
186 Zhong Z, Ethen NJ, Williams BO. WNT signaling in bone development and homeostasis. Wiley Interdiscip Rev Dev Biol 2014;3:489-500. [PMID: 25270716 DOI: 10.1002/wdev.159] [Cited by in Crossref: 77] [Cited by in F6Publishing: 58] [Article Influence: 11.0] [Reference Citation Analysis]
187 Armstrong J, Seehra J, Andiappan M, Jones AG, Papageorgiou SN, Cobourne MT. Palatal rugae morphology is associated with variation in tooth number. Sci Rep 2020;10:19074. [PMID: 33154503 DOI: 10.1038/s41598-020-76240-w] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
188 Kimura M, Machida J, Yamaguchi S, Shibata A, Tatematsu T, Miyachi H, Jezewski PA, Nakayama A, Higashi Y, Shimozato K, Tokita Y. Novel nonsense mutation in MSX1 in familial nonsyndromic oligodontia: subcellular localization and role of homeodomain/MH4. Eur J Oral Sci 2014;122:15-20. [PMID: 24329876 DOI: 10.1111/eos.12105] [Cited by in Crossref: 20] [Cited by in F6Publishing: 19] [Article Influence: 2.5] [Reference Citation Analysis]
189 Liu H, Ding T, Zhan Y, Feng H. A Novel AXIN2 Missense Mutation Is Associated with Non-Syndromic Oligodontia. PLoS One 2015;10:e0138221. [PMID: 26406231 DOI: 10.1371/journal.pone.0138221] [Cited by in Crossref: 12] [Cited by in F6Publishing: 10] [Article Influence: 2.0] [Reference Citation Analysis]
190 Vijayan V, Ummer R, Weber R, Silva R, Letra A. Association of WNT Pathway Genes With Nonsyndromic Cleft Lip With or Without Cleft Palate. Cleft Palate Craniofac J 2018;55:335-41. [PMID: 29437498 DOI: 10.1177/1055665617732782] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 1.3] [Reference Citation Analysis]
191 Hakim SG, Kosmehl H, Sieg P, Trenkle T, Jacobsen H, Attila Benedek G, Ribbat J, Driemel O. Altered expression of cell–cell adhesion molecules β-catenin/E-cadherin and related Wnt-signaling pathway in sporadic and syndromal keratocystic odontogenic tumors. Clin Oral Invest 2011;15:321-8. [DOI: 10.1007/s00784-010-0388-8] [Cited by in Crossref: 26] [Cited by in F6Publishing: 25] [Article Influence: 2.4] [Reference Citation Analysis]
192 Lei Z, Yang L, Lei Y, Yang Y, Zhang X, Song Q, Chen G, Liu W, Wu H, Guo J. High dose lithium chloride causes colitis through activating F4/80 positive macrophages and inhibiting expression of Pigr and Claudin-15 in the colon of mice. Toxicology 2021;457:152799. [PMID: 33901603 DOI: 10.1016/j.tox.2021.152799] [Reference Citation Analysis]
193 Brečević L, Rinčić M, Krsnik Ž, Sedmak G, Hamid AB, Kosyakova N, Galić I, Liehr T, Borovečki F. Association of new deletion/duplication region at chromosome 1p21 with intellectual disability, severe speech deficit and autism spectrum disorder-like behavior: an all-in approach to solving the DPYD enigma. Transl Neurosci 2015;6:59-86. [PMID: 28123791 DOI: 10.1515/tnsci-2015-0007] [Cited by in Crossref: 6] [Cited by in F6Publishing: 4] [Article Influence: 1.0] [Reference Citation Analysis]
194 Carinci F, Piattelli A, Guida L, Perrotti V, Laino G, Oliva A, Annunziata M, Palmieri A, Pezzetti F. Effects of Emdogain on osteoblast gene expression. Oral Dis 2006;12:329-42. [PMID: 16700745 DOI: 10.1111/j.1601-0825.2005.01204.x] [Cited by in Crossref: 33] [Cited by in F6Publishing: 23] [Article Influence: 2.2] [Reference Citation Analysis]
195 He F, Chen H, Yang P, Wu Q, Zhang T, Wang C, Wei J, Chen Z, Hu H, Li W, Cao J. Gankyrin sustains PI3K/GSK-3β/β-catenin signal activation and promotes colorectal cancer aggressiveness and progression. Oncotarget 2016;7:81156-71. [PMID: 27835604 DOI: 10.18632/oncotarget.13215] [Cited by in Crossref: 21] [Cited by in F6Publishing: 20] [Article Influence: 7.0] [Reference Citation Analysis]
196 Mostowska A, Biedziak B, Jagodzinski PP. Novel MSX1 mutation in a family with autosomal-dominant hypodontia of second premolars and third molars. Arch Oral Biol 2012;57:790-5. [PMID: 22297032 DOI: 10.1016/j.archoralbio.2012.01.003] [Cited by in Crossref: 27] [Cited by in F6Publishing: 29] [Article Influence: 3.0] [Reference Citation Analysis]
197 Hansen L, Kreiborg S, Jarlov H, Niebuhr E, Eiberg H. A novel nonsense mutation in PAX9 is associated with marked variability in number of missing teeth. Eur J Oral Sci 2007;115:330-3. [PMID: 17697174 DOI: 10.1111/j.1600-0722.2007.00457.x] [Cited by in Crossref: 25] [Cited by in F6Publishing: 24] [Article Influence: 1.8] [Reference Citation Analysis]
198 Koizumi Y, Kawashima N, Yamamoto M, Takimoto K, Zhou M, Suzuki N, Saito M, Harada H, Suda H. Wnt11 expression in rat dental pulp and promotional effects of Wnt signaling on odontoblast differentiation: Odontoblast differentiation by Wnt. Congenital Anomalies 2013;53:101-8. [DOI: 10.1111/cga.12011] [Cited by in Crossref: 20] [Cited by in F6Publishing: 17] [Article Influence: 2.5] [Reference Citation Analysis]
199 Gerits A, Nieminen P, De Muynck S, Carels C. Exclusion of coding region mutations in MSX1, PAX9 and AXIN2 in eight patients with severe oligodontia phenotype. Orthod Craniofac Res 2006;9:129-36. [PMID: 16918677 DOI: 10.1111/j.1601-6343.2006.00367.x] [Cited by in Crossref: 33] [Cited by in F6Publishing: 27] [Article Influence: 2.2] [Reference Citation Analysis]
200 Nieminen TT, Pavicic W, Porkka N, Kankainen M, Järvinen HJ, Lepistö A, Peltomäki P. Pseudoexons provide a mechanism for allele-specific expression of APC in familial adenomatous polyposis. Oncotarget 2016;7:70685-98. [PMID: 27683109 DOI: 10.18632/oncotarget.12206] [Cited by in Crossref: 9] [Cited by in F6Publishing: 7] [Article Influence: 3.0] [Reference Citation Analysis]
201 Shimizu T, Morita W, Maeda T. Genetic mapping of agenesis of the third molars in mice. Biochem Genet 2013;51:728-36. [PMID: 23736965 DOI: 10.1007/s10528-013-9602-0] [Cited by in Crossref: 7] [Cited by in F6Publishing: 4] [Article Influence: 0.9] [Reference Citation Analysis]
202 AlFawaz S, Plagnol V, Wong FS, Kelsell DP. A novel frameshift MSX1 mutation in a Saudi family with autosomal dominant premolar and third molar agenesis. Arch Oral Biol 2015;60:982-8. [PMID: 25874811 DOI: 10.1016/j.archoralbio.2015.02.023] [Cited by in Crossref: 9] [Cited by in F6Publishing: 8] [Article Influence: 1.5] [Reference Citation Analysis]
203 Juuri E, Balic A. The Biology Underlying Abnormalities of Tooth Number in Humans. J Dent Res 2017;96:1248-56. [DOI: 10.1177/0022034517720158] [Cited by in Crossref: 33] [Cited by in F6Publishing: 16] [Article Influence: 8.3] [Reference Citation Analysis]
204 Dzobo K, Thomford NE, Senthebane DA. Targeting the Versatile Wnt/β-Catenin Pathway in Cancer Biology and Therapeutics: From Concept to Actionable Strategy. OMICS 2019;23:517-38. [PMID: 31613700 DOI: 10.1089/omi.2019.0147] [Cited by in Crossref: 8] [Cited by in F6Publishing: 7] [Article Influence: 4.0] [Reference Citation Analysis]
205 Enzo MV, Rastrelli M, Rossi CR, Hladnik U, Segat D. The Wnt/β-catenin pathway in human fibrotic-like diseases and its eligibility as a therapeutic target. Mol Cell Ther 2015;3:1. [PMID: 26056602 DOI: 10.1186/s40591-015-0038-2] [Cited by in Crossref: 33] [Cited by in F6Publishing: 30] [Article Influence: 5.5] [Reference Citation Analysis]
206 Hahn MM, de Voer RM, Hoogerbrugge N, Ligtenberg MJ, Kuiper RP, van Kessel AG. The genetic heterogeneity of colorectal cancer predisposition - guidelines for gene discovery. Cell Oncol (Dordr) 2016;39:491-510. [PMID: 27279102 DOI: 10.1007/s13402-016-0284-6] [Cited by in Crossref: 22] [Cited by in F6Publishing: 14] [Article Influence: 4.4] [Reference Citation Analysis]
207 Han D, Gong Y, Wu H, Zhang X, Yan M, Wang X, Qu H, Feng H, Song S. Novel EDA mutation resulting in X-linked non-syndromic hypodontia and the pattern of EDA-associated isolated tooth agenesis. Eur J Med Genet 2008;51:536-46. [PMID: 18657636 DOI: 10.1016/j.ejmg.2008.06.002] [Cited by in Crossref: 56] [Cited by in F6Publishing: 43] [Article Influence: 4.3] [Reference Citation Analysis]
208 Regard JB, Zhong Z, Williams BO, Yang Y. Wnt signaling in bone development and disease: making stronger bone with Wnts. Cold Spring Harb Perspect Biol 2012;4:a007997. [PMID: 23209148 DOI: 10.1101/cshperspect.a007997] [Cited by in Crossref: 119] [Cited by in F6Publishing: 103] [Article Influence: 13.2] [Reference Citation Analysis]
209 Roper J, Hung KE. Molecular Mechanisms of Colorectal Carcinogenesis. In: Haigis, Ph.d. KM, editor. Molecular Pathogenesis of Colorectal Cancer. New York: Springer; 2013. pp. 25-65. [DOI: 10.1007/978-1-4614-8412-7_2] [Cited by in Crossref: 4] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
210 Fauzi NH, Ardini YD, Zainuddin Z, Lestari W. A review on non-syndromic tooth agenesis associated with PAX9 mutations. Jpn Dent Sci Rev 2018;54:30-6. [PMID: 29628999 DOI: 10.1016/j.jdsr.2017.08.001] [Cited by in Crossref: 9] [Cited by in F6Publishing: 7] [Article Influence: 2.3] [Reference Citation Analysis]
211 Huang Y, Lu Y, Mues G, Wang S, Bonds J, D'Souza R. Functional evaluation of a novel tooth agenesis-associated bone morphogenetic protein 4 prodomain mutation. Eur J Oral Sci 2013;121:313-8. [PMID: 23841782 DOI: 10.1111/eos.12055] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 0.5] [Reference Citation Analysis]
212 Mazzoni SM, Fearon ER. AXIN1 and AXIN2 variants in gastrointestinal cancers. Cancer Lett. 2014;355:1-8. [PMID: 25236910 DOI: 10.1016/j.canlet.2014.09.018] [Cited by in Crossref: 66] [Cited by in F6Publishing: 58] [Article Influence: 9.4] [Reference Citation Analysis]
213 Jindal A, Vieira AR. Family history of cleft lip and palate in subjects diagnosed with leukemia. Am J Med Genet 2012;158A:678-9. [DOI: 10.1002/ajmg.a.34430] [Cited by in Crossref: 16] [Cited by in F6Publishing: 11] [Article Influence: 1.8] [Reference Citation Analysis]
214 Rafighdoost H, Hashemi M, Danesh H, Bizhani F, Bahari G, Taheri M. Association of single nucleotide polymorphisms in AXIN2, BMP4, and IRF6 with Non-Syndromic Cleft Lip with or without Cleft Palate in a sample of the southeast Iranian population. J Appl Oral Sci 2017;25:650-6. [PMID: 29211286 DOI: 10.1590/1678-7757-2017-0191] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 2.0] [Reference Citation Analysis]
215 Tallón-walton V, Manzanares-céspedes MC, Arte S, Carvalho-lobato P, Valdivia-gandur I, Garcia-susperregui A, Ventura F, Nieminen P. Identification of a novel mutation in the PAX9 gene in a family affected by oligodontia and other dental anomalies. Eur J Oral Sci 2007;115:427-32. [DOI: 10.1111/j.1600-0722.2007.00492.x] [Cited by in Crossref: 26] [Cited by in F6Publishing: 25] [Article Influence: 1.9] [Reference Citation Analysis]
216 Wang J, Jian F, Chen J, Wang H, Lin Y, Yang Z, Pan X, Lai W. Sequence analysis of PAX9, MSX1 and AXIN2 genes in a Chinese oligodontia family. Arch Oral Biol 2011;56:1027-34. [PMID: 21530942 DOI: 10.1016/j.archoralbio.2011.03.023] [Cited by in Crossref: 21] [Cited by in F6Publishing: 22] [Article Influence: 2.1] [Reference Citation Analysis]
217 Noroozi N, Dastgheib SA, Lookzadeh MH, Mirjalili SR, Noorishadkam M, Akbarian-Bafghi MJ, Neamatzadeh H. Association of Axis Inhibition Protein 2 Polymorphisms with Non-Syndromic Cleft Lip with or without Cleft Palate in Iranian Children. Fetal Pediatr Pathol 2020;39:29-37. [PMID: 31268379 DOI: 10.1080/15513815.2019.1636430] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
218 Alharatani R, Ververi A, Beleza-Meireles A, Ji W, Mis E, Patterson QT, Griffin JN, Bhujel N, Chang CA, Dixit A, Konstantino M, Healy C, Hannan S, Neo N, Cash A, Li D, Bhoj E, Zackai EH, Cleaver R, Baralle D, McEntagart M, Newbury-Ecob R, Scott R, Hurst JA, Au PYB, Hosey MT, Khokha M, Marciano DK, Lakhani SA, Liu KJ. Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome. Hum Mol Genet 2020;29:1900-21. [PMID: 32196547 DOI: 10.1093/hmg/ddaa050] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 5.0] [Reference Citation Analysis]
219 Aristizabal-pachon AF, Castillo WO. Role of GSK3β in breast cancer susceptibility. CBM 2017;18:169-75. [DOI: 10.3233/cbm-160120] [Cited by in Crossref: 5] [Cited by in F6Publishing: 2] [Article Influence: 1.3] [Reference Citation Analysis]
220 Silvério KG, Davidson KC, James RG, Adams AM, Foster BL, Nociti FH, Somerman MJ, Moon RT. Wnt/β-catenin pathway regulates bone morphogenetic protein (BMP2)-mediated differentiation of dental follicle cells. J Periodontal Res. 2012;47:309-319. [PMID: 22150562 DOI: 10.1111/j.1600-0765.2011.01433.x] [Cited by in Crossref: 39] [Cited by in F6Publishing: 34] [Article Influence: 3.9] [Reference Citation Analysis]
221 Chalabreysse L, Senni F, Bruyère P, Aime B, Ollagnier C, Bozio A, Bouvagnet P. A New Hypo/Oligodontia Syndrome: Carvajal/Naxos Syndrome Secondary to Desmoplakin-dominant Mutations. J Dent Res 2011;90:58-64. [DOI: 10.1177/0022034510383984] [Cited by in Crossref: 30] [Cited by in F6Publishing: 22] [Article Influence: 2.7] [Reference Citation Analysis]
222 Dinckan N, Du R, Petty LE, Coban-Akdemir Z, Jhangiani SN, Paine I, Baugh EH, Erdem AP, Kayserili H, Doddapaneni H, Hu J, Muzny DM, Boerwinkle E, Gibbs RA, Lupski JR, Uyguner ZO, Below JE, Letra A. Whole-Exome Sequencing Identifies Novel Variants for Tooth Agenesis. J Dent Res 2018;97:49-59. [PMID: 28813618 DOI: 10.1177/0022034517724149] [Cited by in Crossref: 21] [Cited by in F6Publishing: 17] [Article Influence: 5.3] [Reference Citation Analysis]
223 Lamba A, Parekh P, Dvorak CC, Karlitz J. Pedigree analysis supports a correlation between an AXIN2 variant and polyposis/colorectal cancer. WJMG 2018;8:1-4. [DOI: 10.5496/wjmg.v8.i1.1] [Reference Citation Analysis]
224 Kim MS, Kim SS, Ahn CH, Yoo NJ, Lee SH. Frameshift mutations of Wnt pathway genes AXIN2 and TCF7L2 in gastric carcinomas with high microsatellite instability. Hum Pathol. 2009;40:58-64. [PMID: 18755497 DOI: 10.1016/j.humpath.2008.06.006] [Cited by in Crossref: 32] [Cited by in F6Publishing: 30] [Article Influence: 2.5] [Reference Citation Analysis]
225 MacDonald BT, Tamai K, He X. Wnt/beta-catenin signaling: components, mechanisms, and diseases. Dev Cell. 2009;17:9-26. [PMID: 19619488 DOI: 10.1016/j.devcel] [Reference Citation Analysis]
226 Pillas D, Hoggart CJ, Evans DM, O'Reilly PF, Sipilä K, Lähdesmäki R, Millwood IY, Kaakinen M, Netuveli G, Blane D, Charoen P, Sovio U, Pouta A, Freimer N, Hartikainen AL, Laitinen J, Vaara S, Glaser B, Crawford P, Timpson NJ, Ring SM, Deng G, Zhang W, McCarthy MI, Deloukas P, Peltonen L, Elliott P, Coin LJ, Smith GD, Jarvelin MR. Genome-wide association study reveals multiple loci associated with primary tooth development during infancy. PLoS Genet 2010;6:e1000856. [PMID: 20195514 DOI: 10.1371/journal.pgen.1000856] [Cited by in Crossref: 47] [Cited by in F6Publishing: 38] [Article Influence: 4.3] [Reference Citation Analysis]
227 Jiang TJ, Wang F, Wang YN, Hu JJ, Ding PR, Lin JZ, Pan ZZ, Chen G, Shao JY, Xu RH, Zhao Q, Wang F. Germline mutational profile of Chinese patients under 70 years old with colorectal cancer. Cancer Commun (Lond) 2020;40:620-32. [PMID: 32914570 DOI: 10.1002/cac2.12093] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 3.0] [Reference Citation Analysis]
228 Mostowska A, Biedziak B, Trzeciak WH. A novel mutation in PAX9 causes familial form of molar oligodontia. Eur J Hum Genet 2006;14:173-9. [PMID: 16333316 DOI: 10.1038/sj.ejhg.5201536] [Cited by in Crossref: 30] [Cited by in F6Publishing: 27] [Article Influence: 2.0] [Reference Citation Analysis]
229 Li S, Wang C, Liu X, Hua S, Liu X. The roles of AXIN2 in tumorigenesis and epigenetic regulation. Fam Cancer 2015;14:325-31. [PMID: 25504512 DOI: 10.1007/s10689-014-9775-7] [Cited by in Crossref: 12] [Cited by in F6Publishing: 10] [Article Influence: 2.4] [Reference Citation Analysis]
230 Järvinen E, Shimomura-Kuroki J, Balic A, Jussila M, Thesleff I. Mesenchymal Wnt/β-catenin signaling limits tooth number. Development 2018;145:dev158048. [PMID: 29437780 DOI: 10.1242/dev.158048] [Cited by in Crossref: 22] [Cited by in F6Publishing: 17] [Article Influence: 7.3] [Reference Citation Analysis]
231 Letra A, Menezes R, Granjeiro JM, Vieira AR. AXIN2 and CDH1 polymorphisms, tooth agenesis, and oral clefts. Birth Defects Res A Clin Mol Teratol 2009;85:169-73. [PMID: 18683894 DOI: 10.1002/bdra.20489] [Cited by in Crossref: 56] [Cited by in F6Publishing: 43] [Article Influence: 4.7] [Reference Citation Analysis]
232 Vieira AR, Modesto A, Meira R, Barbosa AR, Lidral AC, Murray JC. Interferon regulatory factor 6 (IRF6) and fibroblast growth factor receptor 1 (FGFR1) contribute to human tooth agenesis. Am J Med Genet A 2007;143A:538-45. [PMID: 17318851 DOI: 10.1002/ajmg.a.31620] [Cited by in Crossref: 65] [Cited by in F6Publishing: 53] [Article Influence: 4.6] [Reference Citation Analysis]
233 Lam KK, Thean LF, Cheah PY. Advances in colorectal cancer genomics and transcriptomics drive early detection and prevention. Int J Biochem Cell Biol 2021;137:106032. [PMID: 34182137 DOI: 10.1016/j.biocel.2021.106032] [Reference Citation Analysis]
234 Abdalla EM, Mostowska A, Jagodziński PP, Dwidar K, Ismail SR. A novel WNT10A mutation causes non-syndromic hypodontia in an Egyptian family. Archives of Oral Biology 2014;59:722-8. [DOI: 10.1016/j.archoralbio.2014.04.004] [Cited by in Crossref: 12] [Cited by in F6Publishing: 8] [Article Influence: 1.7] [Reference Citation Analysis]
235 Massink MP, Créton MA, Spanevello F, Fennis WM, Cune MS, Savelberg SM, Nijman IJ, Maurice MM, van den Boogaard MJ, van Haaften G. Loss-of-Function Mutations in the WNT Co-receptor LRP6 Cause Autosomal-Dominant Oligodontia. Am J Hum Genet 2015;97:621-6. [PMID: 26387593 DOI: 10.1016/j.ajhg.2015.08.014] [Cited by in Crossref: 63] [Cited by in F6Publishing: 54] [Article Influence: 10.5] [Reference Citation Analysis]
236 Tamura M, Nemoto E. Role of the Wnt signaling molecules in the tooth. Jpn Dent Sci Rev 2016;52:75-83. [PMID: 28408959 DOI: 10.1016/j.jdsr.2016.04.001] [Cited by in Crossref: 20] [Cited by in F6Publishing: 18] [Article Influence: 4.0] [Reference Citation Analysis]
237 Pavicic W, Nieminen TT, Gylling A, Pursiheimo JP, Laiho A, Gyenesei A, Järvinen HJ, Peltomäki P. Promoter-specific alterations of APC are a rare cause for mutation-negative familial adenomatous polyposis. Genes Chromosomes Cancer. 2014;53:857-864. [PMID: 24946964 DOI: 10.1002/gcc.22197] [Cited by in Crossref: 16] [Cited by in F6Publishing: 15] [Article Influence: 2.3] [Reference Citation Analysis]
238 Simmer JP, Papagerakis P, Smith CE, Fisher DC, Rountrey AN, Zheng L, Hu JC. Regulation of dental enamel shape and hardness. J Dent Res 2010;89:1024-38. [PMID: 20675598 DOI: 10.1177/0022034510375829] [Cited by in Crossref: 157] [Cited by in F6Publishing: 116] [Article Influence: 14.3] [Reference Citation Analysis]
239 Cobourne MT. Familial human hypodontia--is it all in the genes? Br Dent J 2007;203:203-8. [PMID: 17721480 DOI: 10.1038/bdj.2007.732] [Cited by in Crossref: 83] [Cited by in F6Publishing: 39] [Article Influence: 5.9] [Reference Citation Analysis]
240 Wu P, Wu X, Jiang TX, Elsey RM, Temple BL, Divers SJ, Glenn TC, Yuan K, Chen MH, Widelitz RB, Chuong CM. Specialized stem cell niche enables repetitive renewal of alligator teeth. Proc Natl Acad Sci U S A 2013;110:E2009-18. [PMID: 23671090 DOI: 10.1073/pnas.1213202110] [Cited by in Crossref: 76] [Cited by in F6Publishing: 61] [Article Influence: 9.5] [Reference Citation Analysis]
241 Schubert SA, Morreau H, de Miranda NFCC, van Wezel T. The missing heritability of familial colorectal cancer. Mutagenesis 2020;35:221-31. [PMID: 31605533 DOI: 10.1093/mutage/gez027] [Cited by in Crossref: 8] [Cited by in F6Publishing: 6] [Article Influence: 8.0] [Reference Citation Analysis]
242 Cardoso J, Boer J, Morreau H, Fodde R. Expression and genomic profiling of colorectal cancer. Biochim Biophys Acta. 2007;1775:103-137. [PMID: 17010523 DOI: 10.1016/j.bbcan.2006.08.004] [Cited by in Crossref: 23] [Cited by in F6Publishing: 48] [Article Influence: 1.5] [Reference Citation Analysis]
243 Kantaputra P, Sripathomsawat W. WNT10A and isolated hypodontia. Am J Med Genet 2011;155:1119-22. [DOI: 10.1002/ajmg.a.33840] [Cited by in Crossref: 64] [Cited by in F6Publishing: 47] [Article Influence: 6.4] [Reference Citation Analysis]
244 Kim JW, Simmer JP, Lin BP, Hu JC. Novel MSX1 frameshift causes autosomal-dominant oligodontia. J Dent Res 2006;85:267-71. [PMID: 16498076 DOI: 10.1177/154405910608500312] [Cited by in Crossref: 76] [Cited by in F6Publishing: 62] [Article Influence: 5.1] [Reference Citation Analysis]
245 Saito-Diaz K, Chen TW, Wang X, Thorne CA, Wallace HA, Page-McCaw A, Lee E. The way Wnt works: components and mechanism. Growth Factors. 2013;31:1-31. [PMID: 23256519 DOI: 10.3109/08977194.2012.752737] [Cited by in Crossref: 141] [Cited by in F6Publishing: 118] [Article Influence: 15.7] [Reference Citation Analysis]
246 Bergendal B, Klar J, Stecksén-Blicks C, Norderyd J, Dahl N. Isolated oligodontia associated with mutations in EDARADD, AXIN2, MSX1, and PAX9 genes. Am J Med Genet A 2011;155A:1616-22. [PMID: 21626677 DOI: 10.1002/ajmg.a.34045] [Cited by in Crossref: 92] [Cited by in F6Publishing: 75] [Article Influence: 9.2] [Reference Citation Analysis]
247 Novellasdemunt L, Antas P, Li VS. Targeting Wnt signaling in colorectal cancer. A Review in the Theme: Cell Signaling: Proteins, Pathways and Mechanisms. Am J Physiol Cell Physiol. 2015;309:C511-C521. [PMID: 26289750 DOI: 10.1152/ajpcell.00117.2015] [Cited by in Crossref: 182] [Cited by in F6Publishing: 160] [Article Influence: 30.3] [Reference Citation Analysis]
248 Moran A, Tippett H, Manoharan A, Cobourne MT. Alteration of palatine ruga pattern in subjects with oligodontia: A pilot study. Am J Orthod Dentofacial Orthop 2016;150:295-302. [PMID: 27476363 DOI: 10.1016/j.ajodo.2015.12.030] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 0.8] [Reference Citation Analysis]
249 Olson HM, Nechiporuk AV. Using Zebrafish to Study Collective Cell Migration in Development and Disease. Front Cell Dev Biol 2018;6:83. [PMID: 30175096 DOI: 10.3389/fcell.2018.00083] [Cited by in Crossref: 20] [Cited by in F6Publishing: 10] [Article Influence: 6.7] [Reference Citation Analysis]
250 Yamaguchi T, Hosomichi K, Yano K, Kim YI, Nakaoka H, Kimura R, Otsuka H, Nonaka N, Haga S, Takahashi M, Shirota T, Kikkawa Y, Yamada A, Kamijo R, Park SB, Nakamura M, Maki K, Inoue I. Comprehensive genetic exploration of selective tooth agenesis of mandibular incisors by exome sequencing. Hum Genome Var 2017;4:17005. [PMID: 28265457 DOI: 10.1038/hgv.2017.5] [Cited by in Crossref: 13] [Cited by in F6Publishing: 8] [Article Influence: 3.3] [Reference Citation Analysis]
251 Sameer AS. Colorectal cancer: molecular mutations and polymorphisms. Front Oncol. 2013;3:114. [PMID: 23717813 DOI: 10.3389/fonc.2013.00114] [Cited by in Crossref: 68] [Cited by in F6Publishing: 57] [Article Influence: 8.5] [Reference Citation Analysis]
252 Solier S, Zhang YW, Ballestrero A, Pommier Y, Zoppoli G. DNA damage response pathways and cell cycle checkpoints in colorectal cancer: current concepts and future perspectives for targeted treatment. Curr Cancer Drug Targets 2012;12:356-71. [PMID: 22385513 DOI: 10.2174/156800912800190901] [Cited by in Crossref: 18] [Cited by in F6Publishing: 19] [Article Influence: 2.0] [Reference Citation Analysis]
253 Clevers H. Wnt/beta-catenin signaling in development and disease. Cell. 2006;127:469-480. [PMID: 17081971 DOI: 10.1016/j.cell.2006.10.018] [Cited by in Crossref: 3754] [Cited by in F6Publishing: 3537] [Article Influence: 250.3] [Reference Citation Analysis]
254 Yue H, Liang J, Yang K, Hua B, Bian Z. Functional analysis of a novel missense mutation in AXIN2 associated with non-syndromic tooth agenesis. Eur J Oral Sci 2016;124:228-33. [PMID: 27090353 DOI: 10.1111/eos.12273] [Cited by in Crossref: 13] [Cited by in F6Publishing: 9] [Article Influence: 2.6] [Reference Citation Analysis]
255 Cheung HW, Cowley GS, Weir BA, Boehm JS, Rusin S, Scott JA, East A, Ali LD, Lizotte PH, Wong TC, Jiang G, Hsiao J, Mermel CH, Getz G, Barretina J, Gopal S, Tamayo P, Gould J, Tsherniak A, Stransky N, Luo B, Ren Y, Drapkin R, Bhatia SN, Mesirov JP, Garraway LA, Meyerson M, Lander ES, Root DE, Hahn WC. Systematic investigation of genetic vulnerabilities across cancer cell lines reveals lineage-specific dependencies in ovarian cancer. Proc Natl Acad Sci U S A 2011;108:12372-7. [PMID: 21746896 DOI: 10.1073/pnas.1109363108] [Cited by in Crossref: 304] [Cited by in F6Publishing: 267] [Article Influence: 30.4] [Reference Citation Analysis]
256 Bergdahl M, Bergdahl J, Nyberg L, Nilsson L. Difference in apolipoprotein E type 4 allele (APOE ɛ4) among dentate and edentulous subjects. Gerodontology 2008;25:179-86. [DOI: 10.1111/j.1741-2358.2008.00225.x] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 0.2] [Reference Citation Analysis]
257 Wright JT, Puranik CP, Farrington F. Oral phenotype and variation in focal dermal hypoplasia. Am J Med Genet 2016;172:52-8. [DOI: 10.1002/ajmg.c.31478] [Cited by in Crossref: 8] [Cited by in F6Publishing: 3] [Article Influence: 1.6] [Reference Citation Analysis]
258 Ogawa T, Kapadia H, Feng JQ, Raghow R, Peters H, D'Souza RN. Functional consequences of interactions between Pax9 and Msx1 genes in normal and abnormal tooth development. J Biol Chem 2006;281:18363-9. [PMID: 16651263 DOI: 10.1074/jbc.M601543200] [Cited by in Crossref: 78] [Cited by in F6Publishing: 38] [Article Influence: 5.2] [Reference Citation Analysis]
259 Nieminen P. Dental Anomalies: Genetics. eLS. Chichester: John Wiley & Sons, Ltd; 2001. [DOI: 10.1002/9780470015902.a0006088.pub2] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.1] [Reference Citation Analysis]
260 MacDonald BT, Tamai K, He X. Wnt/beta-catenin signaling: Components, mechanisms, and diseases. Dev Cell. 2009;17:9-26. [PMID: 19619488 DOI: 10.1016/j.devcel.2009.06.016] [Cited by in Crossref: 3353] [Cited by in F6Publishing: 3087] [Article Influence: 279.4] [Reference Citation Analysis]
261 Zeng B, Lu H, Xiao X, Yu X, Li S, Zhu L, Yu D, Zhao W. KDF1 is a novel candidate gene of non-syndromic tooth agenesis. Arch Oral Biol 2019;97:131-6. [PMID: 30384154 DOI: 10.1016/j.archoralbio.2018.10.025] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 1.3] [Reference Citation Analysis]
262 Kumari S, Dash D. Regulation of β-catenin stabilization in human platelets. Biochimie 2013;95:1252-7. [DOI: 10.1016/j.biochi.2013.01.021] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 0.6] [Reference Citation Analysis]
263 Baglioni S, Genuardi M. Simple and complex genetics of colorectal cancer susceptibility. Am J Med Genet C Semin Med Genet. 2004;129C:35-43. [PMID: 15264271 DOI: 10.1002/ajmg.c.30023] [Cited by in Crossref: 20] [Cited by in F6Publishing: 18] [Article Influence: 1.2] [Reference Citation Analysis]
264 Grejtakova D, Gabrikova-dojcakova D, Boronova I, Kyjovska L, Hubcejova J, Fecenkova M, Zigova M, Priganc M, Bernasovska J. WNT10A variants in relation to nonsyndromic hypodontia in eastern Slovak population. J Genet 2018;97:1169-77. [DOI: 10.1007/s12041-018-1011-z] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.7] [Reference Citation Analysis]
265 Al-Ani AH, Antoun JS, Thomson WM, Topless R, Merriman TR, Farella M. Common variants of EDA are associated with non-syndromic hypodontia. Orthod Craniofac Res 2021;24:155-63. [PMID: 32772440 DOI: 10.1111/ocr.12419] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
266 Maupin KA, Droscha CJ, Williams BO. A Comprehensive Overview of Skeletal Phenotypes Associated with Alterations in Wnt/β-catenin Signaling in Humans and Mice. Bone Res 2013;1:27-71. [PMID: 26273492 DOI: 10.4248/BR201301004] [Cited by in Crossref: 71] [Cited by in F6Publishing: 37] [Article Influence: 8.9] [Reference Citation Analysis]
267 Qian L, Mahaffey JP, Alcorn HL, Anderson KV. Tissue-specific roles of Axin2 in the inhibition and activation of Wnt signaling in the mouse embryo. Proc Natl Acad Sci U S A 2011;108:8692-7. [PMID: 21555575 DOI: 10.1073/pnas.1100328108] [Cited by in Crossref: 37] [Cited by in F6Publishing: 32] [Article Influence: 3.7] [Reference Citation Analysis]
268 Mu YD, Xu Z, Contreras CI, McDaniel JS, Donly KJ, Chen S. Mutational analysis of AXIN2, MSX1, and PAX9 in two Mexican oligodontia families. Genet Mol Res 2013;12:4446-58. [PMID: 24222224 DOI: 10.4238/2013.October.10.10] [Cited by in Crossref: 10] [Cited by in F6Publishing: 5] [Article Influence: 1.3] [Reference Citation Analysis]
269 Arte S, Awadh W, Nieminen P, Rice DP. Tooth Agenesis. In: Cobourne MT, editor. Orthodontic Management of the Developing Dentition. Cham: Springer International Publishing; 2017. pp. 67-84. [DOI: 10.1007/978-3-319-54637-7_5] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
270 Jussila M, Crespo Yanez X, Thesleff I. Initiation of teeth from the dental lamina in the ferret. Differentiation 2014;87:32-43. [PMID: 24393477 DOI: 10.1016/j.diff.2013.11.004] [Cited by in Crossref: 31] [Cited by in F6Publishing: 27] [Article Influence: 4.4] [Reference Citation Analysis]
271 Masih S, Plumptre LA, Kim Y. One-Carbon Metabolism Nutrients and Epigenetics: A Mechanistic Link Between Aberrant One-Carbon Metabolism and Cancer Risk? In: Maulik N, Karagiannis T, editors. Molecular mechanisms and physiology of disease. New York: Springer; 2014. pp. 277-353. [DOI: 10.1007/978-1-4939-0706-9_11] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.1] [Reference Citation Analysis]
272 Shen W, Wang Y, Liu Y, Liu H, Zhao H, Zhang G, Snead ML, Han D, Feng H. Functional Study of Ectodysplasin-A Mutations Causing Non-Syndromic Tooth Agenesis. PLoS One 2016;11:e0154884. [PMID: 27144394 DOI: 10.1371/journal.pone.0154884] [Cited by in Crossref: 12] [Cited by in F6Publishing: 11] [Article Influence: 2.4] [Reference Citation Analysis]
273 Wang SK, Chan HC, Makovey I, Simmer JP, Hu JC. Novel PAX9 and COL1A2 missense mutations causing tooth agenesis and OI/DGI without skeletal abnormalities. PLoS One 2012;7:e51533. [PMID: 23227268 DOI: 10.1371/journal.pone.0051533] [Cited by in Crossref: 15] [Cited by in F6Publishing: 10] [Article Influence: 1.7] [Reference Citation Analysis]
274 Callahan N, Modesto A, Meira R, Seymen F, Patir A, Vieira AR. Axis inhibition protein 2 (AXIN2) polymorphisms and tooth agenesis. Arch Oral Biol 2009;54:45-9. [PMID: 18790474 DOI: 10.1016/j.archoralbio.2008.08.002] [Cited by in Crossref: 45] [Cited by in F6Publishing: 34] [Article Influence: 3.5] [Reference Citation Analysis]
275 Yu T, Klein OD. Molecular and cellular mechanisms of tooth development, homeostasis and repair. Development. 2020;147. [PMID: 31980484 DOI: 10.1242/dev.184754] [Cited by in Crossref: 27] [Cited by in F6Publishing: 23] [Article Influence: 27.0] [Reference Citation Analysis]
276 Yilmaz E, Mihci E, Guzel Nur B, Alper OM. A novel AXIN2 gene mutation in sagittal synostosis. Am J Med Genet 2018;176:1976-80. [DOI: 10.1002/ajmg.a.40373] [Cited by in Crossref: 7] [Cited by in F6Publishing: 4] [Article Influence: 2.3] [Reference Citation Analysis]
277 Mues G, Kapadia H, Wang Y, D'Souza RN. Genetics and human malformations. J Craniofac Surg 2009;20 Suppl 2:1652-4. [PMID: 19816326 DOI: 10.1097/SCS.0b013e3181b2d3f3] [Cited by in Crossref: 7] [Cited by in F6Publishing: 1] [Article Influence: 0.6] [Reference Citation Analysis]
278 Yuan Q, Zhao M, Tandon B, Maili L, Liu X, Zhang A, Baugh EH, Tran T, Silva RM, Hecht JT, Swindell EC, Wagner DS, Letra A. Role of WNT10A in failure of tooth development in humans and zebrafish. Mol Genet Genomic Med 2017;5:730-41. [PMID: 29178643 DOI: 10.1002/mgg3.332] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 2.0] [Reference Citation Analysis]
279 Li Z, Yu M, Tian W. An inductive signalling network regulates mammalian tooth morphogenesis with implications for tooth regeneration. Cell Prolif 2013;46:501-8. [PMID: 23952789 DOI: 10.1111/cpr.12051] [Cited by in Crossref: 7] [Cited by in F6Publishing: 10] [Article Influence: 0.9] [Reference Citation Analysis]
280 Huysseune A, Soenens M, Elderweirdt F. Wnt signaling during tooth replacement in zebrafish (Danio rerio): pitfalls and perspectives. Front Physiol 2014;5:386. [PMID: 25339911 DOI: 10.3389/fphys.2014.00386] [Cited by in Crossref: 12] [Cited by in F6Publishing: 10] [Article Influence: 1.7] [Reference Citation Analysis]
281 Du R, Dinckan N, Song X, Coban-Akdemir Z, Jhangiani SN, Guven Y, Aktoren O, Kayserili H, Petty LE, Muzny DM, Below JE, Boerwinkle E, Wu N, Gibbs RA, Posey JE, Lupski JR, Letra A, Uyguner ZO. Identification of likely pathogenic and known variants in TSPEAR, LAMB3, BCOR, and WNT10A in four Turkish families with tooth agenesis. Hum Genet 2018;137:689-703. [PMID: 30046887 DOI: 10.1007/s00439-018-1907-y] [Cited by in Crossref: 11] [Cited by in F6Publishing: 5] [Article Influence: 3.7] [Reference Citation Analysis]
282 Bhattacharyya S, Feferman L, Borthakur S, Tobacman JK. Common food additive carrageenan stimulates Wnt/ β-catenin signaling in colonic epithelium by inhibition of nucleoredoxin reduction. Nutr Cancer 2014;66:117-27. [PMID: 24328990 DOI: 10.1080/01635581.2014.852228] [Cited by in Crossref: 12] [Cited by in F6Publishing: 10] [Article Influence: 1.5] [Reference Citation Analysis]
283 Jheon AH, Seidel K, Biehs B, Klein OD. From molecules to mastication: the development and evolution of teeth. Wiley Interdiscip Rev Dev Biol 2013;2:165-82. [PMID: 24009032 DOI: 10.1002/wdev.63] [Cited by in Crossref: 51] [Cited by in F6Publishing: 38] [Article Influence: 5.7] [Reference Citation Analysis]
284 Jussila M, Thesleff I. Signaling networks regulating tooth organogenesis and regeneration, and the specification of dental mesenchymal and epithelial cell lineages. Cold Spring Harb Perspect Biol 2012;4:a008425. [PMID: 22415375 DOI: 10.1101/cshperspect.a008425] [Cited by in Crossref: 136] [Cited by in F6Publishing: 110] [Article Influence: 15.1] [Reference Citation Analysis]
285 Ai D, Fu X, Wang J, Lu MF, Chen L, Baldini A, Klein WH, Martin JF. Canonical Wnt signaling functions in second heart field to promote right ventricular growth. Proc Natl Acad Sci U S A 2007;104:9319-24. [PMID: 17519332 DOI: 10.1073/pnas.0701212104] [Cited by in Crossref: 142] [Cited by in F6Publishing: 128] [Article Influence: 10.1] [Reference Citation Analysis]
286 Sarkar T, Bansal R, Das P. A novel G to A transition at initiation codon and exon-intron boundary of PAX9 identified in association with familial isolated oligodontia. Gene 2017;635:69-76. [PMID: 28847717 DOI: 10.1016/j.gene.2017.08.020] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 1.3] [Reference Citation Analysis]
287 Liang J, Qin C, Yue H, He H, Bian Z. A novel initiation codon mutation of PAX9 in a family with oligodontia. Archives of Oral Biology 2016;61:144-8. [DOI: 10.1016/j.archoralbio.2015.10.022] [Cited by in Crossref: 12] [Cited by in F6Publishing: 13] [Article Influence: 2.4] [Reference Citation Analysis]
288 Yu HM, Jerchow B, Sheu TJ, Liu B, Costantini F, Puzas JE, Birchmeier W, Hsu W. The role of Axin2 in calvarial morphogenesis and craniosynostosis. Development. 2005;132:1995-2005. [PMID: 15790973 DOI: 10.1242/dev.01786] [Cited by in Crossref: 234] [Cited by in F6Publishing: 222] [Article Influence: 14.6] [Reference Citation Analysis]
289 De Coster PJ, Marks LA, Martens LC, Huysseune A. Dental agenesis: genetic and clinical perspectives. J Oral Pathol Med 2009;38:1-17. [PMID: 18771513 DOI: 10.1111/j.1600-0714.2008.00699.x] [Cited by in Crossref: 137] [Cited by in F6Publishing: 87] [Article Influence: 10.5] [Reference Citation Analysis]
290 Williams MA, Letra A. The Changing Landscape in the Genetic Etiology of Human Tooth Agenesis. Genes (Basel) 2018;9:E255. [PMID: 29772684 DOI: 10.3390/genes9050255] [Cited by in Crossref: 16] [Cited by in F6Publishing: 9] [Article Influence: 5.3] [Reference Citation Analysis]
291 Castiglia D, Bernardini S, Alvino E, Pagani E, De Luca N, Falcinelli S, Pacchiarotti A, Bonmassar E, Zambruno G, D'Atri S. Concomitant activation of Wnt pathway and loss of mismatch repair function in human melanoma. Genes Chromosomes Cancer 2008;47:614-24. [PMID: 18384130 DOI: 10.1002/gcc.20567] [Cited by in Crossref: 18] [Cited by in F6Publishing: 16] [Article Influence: 1.4] [Reference Citation Analysis]
292 Zhu M, Ma X, Ding P, Tang H, Peng R, Lu L, Li P, Qiao B, Yang X, Zheng Y, Wang H, Gao Y, Chen F. Novel mutations of AXIN2 identified in a Chinese Congenital Heart Disease Cohort. J Hum Genet 2019;64:427-35. [DOI: 10.1038/s10038-019-0572-x] [Cited by in Crossref: 8] [Cited by in F6Publishing: 5] [Article Influence: 4.0] [Reference Citation Analysis]
293 Leachman SA, Lucero OM, Sampson JE, Cassidy P, Bruno W, Queirolo P, Ghiorzo P. Identification, genetic testing, and management of hereditary melanoma. Cancer Metastasis Rev 2017;36:77-90. [PMID: 28283772 DOI: 10.1007/s10555-017-9661-5] [Cited by in Crossref: 50] [Cited by in F6Publishing: 35] [Article Influence: 12.5] [Reference Citation Analysis]
294 Gkantidis N, Katib H, Oeschger E, Karamolegkou M, Topouzelis N, Kanavakis G. Patterns of non-syndromic permanent tooth agenesis in a large orthodontic population. Arch Oral Biol 2017;79:42-7. [PMID: 28288390 DOI: 10.1016/j.archoralbio.2017.02.020] [Cited by in Crossref: 17] [Cited by in F6Publishing: 10] [Article Influence: 4.3] [Reference Citation Analysis]
295 Kim JH, Liu X, Wang J, Chen X, Zhang H, Kim SH, Cui J, Li R, Zhang W, Kong Y, Zhang J, Shui W, Lamplot J, Rogers MR, Zhao C, Wang N, Rajan P, Tomal J, Statz J, Wu N, Luu HH, Haydon RC, He TC. Wnt signaling in bone formation and its therapeutic potential for bone diseases. Ther Adv Musculoskelet Dis 2013;5:13-31. [PMID: 23514963 DOI: 10.1177/1759720X12466608] [Cited by in Crossref: 167] [Cited by in F6Publishing: 92] [Article Influence: 20.9] [Reference Citation Analysis]
296 Singh D, Khan MA, Siddique HR. Apigenin, A Plant Flavone Playing Noble Roles in Cancer Prevention Via Modulation of Key Cell Signaling Networks. PRA 2020;14:298-311. [DOI: 10.2174/1574892814666191026095728] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 5.0] [Reference Citation Analysis]
297 Lorca V, Garre P. Current status of the genetic susceptibility in attenuated adenomatous polyposis. World J Gastrointest Oncol. 2019;11:1101-1114. [PMID: 31908716 DOI: 10.4251/wjgo.v11.i12.1101] [Cited by in CrossRef: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
298 Li Z, Wang Y, Li Y, Yin W, Mo L, Qian X, Zhang Y, Wang G, Bu F, Zhang Z, Ren X, Zhu B, Niu C, Xiao W, Zhang W. Ube2s stabilizes β-Catenin through K11-linked polyubiquitination to promote mesendoderm specification and colorectal cancer development. Cell Death Dis 2018;9:456. [PMID: 29674637 DOI: 10.1038/s41419-018-0451-y] [Cited by in Crossref: 17] [Cited by in F6Publishing: 17] [Article Influence: 5.7] [Reference Citation Analysis]
299 Bugter JM, Fenderico N, Maurice MM. Mutations and mechanisms of WNT pathway tumour suppressors in cancer. Nat Rev Cancer 2021;21:5-21. [PMID: 33097916 DOI: 10.1038/s41568-020-00307-z] [Cited by in Crossref: 27] [Cited by in F6Publishing: 20] [Article Influence: 27.0] [Reference Citation Analysis]
300 Lohi M, Tucker AS, Sharpe PT. Expression of Axin2 indicates a role for canonical Wnt signaling in development of the crown and root during pre- and postnatal tooth development. Dev Dyn 2009. [DOI: 10.1002/dvdy.22047] [Cited by in Crossref: 15] [Cited by in F6Publishing: 40] [Article Influence: 1.3] [Reference Citation Analysis]
301 Ay A, Gong D, Kahveci T. Network-based Prediction of Cancer under Genetic Storm. Cancer Inform 2014;13:15-31. [PMID: 25368507 DOI: 10.4137/CIN.S14025] [Cited by in F6Publishing: 4] [Reference Citation Analysis]
302 Thesleff I, Nieminen P. Tooth Induction. Encyclopedia of Life Sciences. Chichester: John Wiley & Sons, Ltd; 2001. [DOI: 10.1038/npg.els.0004183] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.1] [Reference Citation Analysis]
303 Valle L, Vilar E, Tavtigian SV, Stoffel EM. Genetic predisposition to colorectal cancer: syndromes, genes, classification of genetic variants and implications for precision medicine. J Pathol 2019;247:574-88. [PMID: 30584801 DOI: 10.1002/path.5229] [Cited by in Crossref: 49] [Cited by in F6Publishing: 30] [Article Influence: 24.5] [Reference Citation Analysis]
304 Mikkola ML. Genetic basis of skin appendage development. Semin Cell Dev Biol 2007;18:225-36. [PMID: 17317239 DOI: 10.1016/j.semcdb.2007.01.007] [Cited by in Crossref: 73] [Cited by in F6Publishing: 60] [Article Influence: 5.2] [Reference Citation Analysis]
305 Polakis P. Wnt signaling in cancer. Cold Spring Harb Perspect Biol. 2012;4. [PMID: 22438566 DOI: 10.1101/cshperspect.a008052] [Cited by in Crossref: 536] [Cited by in F6Publishing: 461] [Article Influence: 59.6] [Reference Citation Analysis]
306 Thesleff I. The genetic basis of tooth development and dental defects. Am J Med Genet 2006;140A:2530-5. [DOI: 10.1002/ajmg.a.31360] [Cited by in Crossref: 210] [Cited by in F6Publishing: 157] [Article Influence: 14.0] [Reference Citation Analysis]
307 Thorne CA, Lafleur B, Lewis M, Hanson AJ, Jernigan KK, Weaver DC, Huppert KA, Chen TW, Wichaidit C, Cselenyi CS, Tahinci E, Meyers KC, Waskow E, Orton D, Salic A, Lee LA, Robbins DJ, Huppert SS, Lee E. A biochemical screen for identification of small-molecule regulators of the Wnt pathway using Xenopus egg extracts. J Biomol Screen 2011;16:995-1006. [PMID: 21859680 DOI: 10.1177/1087057111416657] [Cited by in Crossref: 13] [Cited by in F6Publishing: 12] [Article Influence: 1.3] [Reference Citation Analysis]
308 Fjeld K, Kettunen P, Furmanek T, Kvinnsland IH, Luukko K. Dynamic expression of Wnt signaling-related Dickkopf1, -2, and -3 mRNAs in the developing mouse tooth. Dev Dyn 2005;233:161-6. [DOI: 10.1002/dvdy.20285] [Cited by in Crossref: 54] [Cited by in F6Publishing: 47] [Article Influence: 3.4] [Reference Citation Analysis]
309 Abdel-Rahman WM, Mecklin JP, Peltomäki P. The genetics of HNPCC: application to diagnosis and screening. Crit Rev Oncol Hematol. 2006;58:208-220. [PMID: 16434208 DOI: 10.1016/j.critrevonc.2005.11.001] [Cited by in Crossref: 70] [Cited by in F6Publishing: 61] [Article Influence: 4.7] [Reference Citation Analysis]
310 Xie J, Huang L, Lu YG, Zheng DL. Roles of the Wnt Signaling Pathway in Head and Neck Squamous Cell Carcinoma. Front Mol Biosci 2020;7:590912. [PMID: 33469547 DOI: 10.3389/fmolb.2020.590912] [Reference Citation Analysis]
311 Rey JP, Ellies DL. Wnt modulators in the biotech pipeline. Dev Dyn 2010;239:102-14. [PMID: 20014100 DOI: 10.1002/dvdy.22181] [Cited by in Crossref: 4] [Cited by in F6Publishing: 37] [Article Influence: 0.4] [Reference Citation Analysis]
312 Castelo-branco G, Arenas E. Function of Wnts in Dopaminergic Neuron Development. Neurodegener Dis 2006;3:5-11. [DOI: 10.1159/000092086] [Cited by in Crossref: 44] [Cited by in F6Publishing: 45] [Article Influence: 2.9] [Reference Citation Analysis]
313 Figeac N, Zammit PS. Coordinated action of Axin1 and Axin2 suppresses β-catenin to regulate muscle stem cell function. Cell Signal 2015;27:1652-65. [PMID: 25866367 DOI: 10.1016/j.cellsig.2015.03.025] [Cited by in Crossref: 28] [Cited by in F6Publishing: 23] [Article Influence: 4.7] [Reference Citation Analysis]
314 Chalothorn LA, Beeman CS, Ebersole JL, Kluemper GT, Hicks EP, Kryscio RJ, DeSimone CP, Modesitt SC. Hypodontia as a risk marker for epithelial ovarian cancer: a case-controlled study. J Am Dent Assoc 2008;139:163-9. [PMID: 18245684 DOI: 10.14219/jada.archive.2008.0132] [Cited by in Crossref: 26] [Cited by in F6Publishing: 23] [Article Influence: 2.0] [Reference Citation Analysis]
315 Xin T, Zhang T, Li Q, Yu T, Zhu Y, Yang R, Zhou Y. A novel mutation of MSX1 in oligodontia inhibits odontogenesis of dental pulp stem cells via the ERK pathway. Stem Cell Res Ther 2018;9:221. [PMID: 30134957 DOI: 10.1186/s13287-018-0965-3] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 2.0] [Reference Citation Analysis]
316 Alldredge A, Fuhrmann S. Loss of Axin2 Causes Ocular Defects During Mouse Eye Development. Invest Ophthalmol Vis Sci 2016;57:5253-62. [PMID: 27701636 DOI: 10.1167/iovs.15-18599] [Cited by in Crossref: 14] [Cited by in F6Publishing: 10] [Article Influence: 3.5] [Reference Citation Analysis]
317 Chhabra N, Goswami M, Chhabra A. Genetic basis of dental agenesis--molecular genetics patterning clinical dentistry. Med Oral Patol Oral Cir Bucal 2014;19:e112-9. [PMID: 24121910 DOI: 10.4317/medoral.19158] [Cited by in Crossref: 24] [Cited by in F6Publishing: 16] [Article Influence: 3.4] [Reference Citation Analysis]
318 Nieminen P. Genetic basis of tooth agenesis. J Exp Zool B Mol Dev Evol 2009;312B:320-42. [PMID: 19219933 DOI: 10.1002/jez.b.21277] [Cited by in Crossref: 146] [Cited by in F6Publishing: 109] [Article Influence: 12.2] [Reference Citation Analysis]
319 Kharaishvili G, Simkova D, Makharoblidze E, Trtkova K, Kolar Z, Bouchal J. Wnt signaling in prostate development and carcinogenesis. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub 2011;155:11-8. [PMID: 21475372 DOI: 10.5507/bp.2011.016] [Cited by in Crossref: 23] [Cited by in F6Publishing: 18] [Article Influence: 2.3] [Reference Citation Analysis]
320 Yang J, Wang SK, Choi M, Reid BM, Hu Y, Lee YL, Herzog CR, Kim-Berman H, Lee M, Benke PJ, Lloyd KC, Simmer JP, Hu JC. Taurodontism, variations in tooth number, and misshapened crowns in Wnt10a null mice and human kindreds. Mol Genet Genomic Med 2015;3:40-58. [PMID: 25629078 DOI: 10.1002/mgg3.111] [Cited by in Crossref: 53] [Cited by in F6Publishing: 40] [Article Influence: 7.6] [Reference Citation Analysis]
321 Itasaki N, Hoppler S. Crosstalk between Wnt and bone morphogenic protein signaling: a turbulent relationship. Dev Dyn 2010;239:16-33. [PMID: 19544585 DOI: 10.1002/dvdy.22009] [Cited by in Crossref: 32] [Cited by in F6Publishing: 68] [Article Influence: 2.9] [Reference Citation Analysis]
322 Ruf S, Klimas D, Hönemann M, Jabir S. Genetic background of nonsyndromic oligodontia: a systematic review and meta-analysis. J Orofac Orthop 2013;74:295-308. [PMID: 23828301 DOI: 10.1007/s00056-013-0138-z] [Cited by in Crossref: 34] [Cited by in F6Publishing: 26] [Article Influence: 4.3] [Reference Citation Analysis]
323 Cocos A, Halazonetis DJ. Craniofacial shape differs in patients with tooth agenesis: geometric morphometric analysis. Eur J Orthod 2017;39:345-51. [PMID: 27464525 DOI: 10.1093/ejo/cjw049] [Cited by in Crossref: 6] [Cited by in F6Publishing: 9] [Article Influence: 2.0] [Reference Citation Analysis]
324 Issa YA, Kamal L, Rayyan AA, Dweik D, Pierce S, Lee MK, King MC, Walsh T, Kanaan M. Mutation of KREMEN1, a modulator of Wnt signaling, is responsible for ectodermal dysplasia including oligodontia in Palestinian families. Eur J Hum Genet 2016;24:1430-5. [PMID: 27049303 DOI: 10.1038/ejhg.2016.29] [Cited by in Crossref: 11] [Cited by in F6Publishing: 10] [Article Influence: 2.2] [Reference Citation Analysis]
325 Mumtaz S, Nalbant G, Yıldız Bölükbaşı E, Huma Z, Ahmad N, Tolun A, Malik S. Novel EDAR mutation in tooth agenesis and variable associated features. Eur J Med Genet 2020;63:103926. [PMID: 32325225 DOI: 10.1016/j.ejmg.2020.103926] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
326 Chen D, Xie R, Shu B, Landay AL, Wei C, Reiser J, Spagnoli A, Torquati A, Forsyth CB, Keshavarzian A, Sumner DR. Wnt signaling in bone, kidney, intestine, and adipose tissue and interorgan interaction in aging. Ann N Y Acad Sci 2019;1442:48-60. [PMID: 30101565 DOI: 10.1111/nyas.13945] [Cited by in Crossref: 16] [Cited by in F6Publishing: 13] [Article Influence: 5.3] [Reference Citation Analysis]
327 Lee M, Kim E, Li L, Jung H. Roles of Wnt inhibitory factor 1 during tooth morphogenesis. Cell Tissue Res 2015;362:61-8. [DOI: 10.1007/s00441-015-2170-3] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 1.0] [Reference Citation Analysis]
328 Qin H, Xu HZ, Xuan K. Clinical and genetic evaluation of a Chinese family with isolated oligodontia. Arch Oral Biol 2013;58:1180-6. [PMID: 23731659 DOI: 10.1016/j.archoralbio.2013.04.007] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 0.5] [Reference Citation Analysis]
329 Brook A, Elcock C, Aggarwal M, Lath D, Russell J, Patel P, Smith R. Tooth dimensions in hypodontia with a known PAX9 mutation. Archives of Oral Biology 2009;54:S57-62. [DOI: 10.1016/j.archoralbio.2008.05.017] [Cited by in Crossref: 25] [Cited by in F6Publishing: 17] [Article Influence: 2.1] [Reference Citation Analysis]
330 Prasad MK, Geoffroy V, Vicaire S, Jost B, Dumas M, Le Gras S, Switala M, Gasse B, Laugel-Haushalter V, Paschaki M, Leheup B, Droz D, Dalstein A, Loing A, Grollemund B, Muller-Bolla M, Lopez-Cazaux S, Minoux M, Jung S, Obry F, Vogt V, Davideau JL, Davit-Beal T, Kaiser AS, Moog U, Richard B, Morrier JJ, Duprez JP, Odent S, Bailleul-Forestier I, Rousset MM, Merametdijan L, Toutain A, Joseph C, Giuliano F, Dahlet JC, Courval A, El Alloussi M, Laouina S, Soskin S, Guffon N, Dieux A, Doray B, Feierabend S, Ginglinger E, Fournier B, de la Dure Molla M, Alembik Y, Tardieu C, Clauss F, Berdal A, Stoetzel C, Manière MC, Dollfus H, Bloch-Zupan A. A targeted next-generation sequencing assay for the molecular diagnosis of genetic disorders with orodental involvement. J Med Genet 2016;53:98-110. [PMID: 26502894 DOI: 10.1136/jmedgenet-2015-103302] [Cited by in Crossref: 63] [Cited by in F6Publishing: 50] [Article Influence: 10.5] [Reference Citation Analysis]
331 Dhooge M, Baert-Desurmont S, Corsini C, Caron O, Andrieu N, Berthet P, Bonadona V, Cohen-Haguenauer O, De Pauw A, Delnatte C, Dussart S, Lasset C, Leroux D, Maugard C, Moretta-Serra J, Popovici C, Buecher B, Colas C, Noguès C; GGC-Unicancer Group. National recommendations of the French Genetics and Cancer Group - Unicancer on the modalities of multi-genes panel analyses in hereditary predispositions to tumors of the digestive tract. Eur J Med Genet 2020;63:104080. [PMID: 33039684 DOI: 10.1016/j.ejmg.2020.104080] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 3.0] [Reference Citation Analysis]
332 Makrantonaki E, Brink TC, Zampeli V, Elewa RM, Mlody B, Hossini AM, Hermes B, Krause U, Knolle J, Abdallah M, Adjaye J, Zouboulis CC. Identification of biomarkers of human skin ageing in both genders. Wnt signalling - a label of skin ageing? PLoS One 2012;7:e50393. [PMID: 23226273 DOI: 10.1371/journal.pone.0050393] [Cited by in Crossref: 61] [Cited by in F6Publishing: 42] [Article Influence: 6.8] [Reference Citation Analysis]
333 Jiang X, Tan J, Li J, Kivimäe S, Yang X, Zhuang L, Lee PL, Chan MT, Stanton LW, Liu ET, Cheyette BN, Yu Q. DACT3 is an epigenetic regulator of Wnt/beta-catenin signaling in colorectal cancer and is a therapeutic target of histone modifications. Cancer Cell 2008;13:529-41. [PMID: 18538736 DOI: 10.1016/j.ccr.2008.04.019] [Cited by in Crossref: 158] [Cited by in F6Publishing: 143] [Article Influence: 12.2] [Reference Citation Analysis]
334 Tsuchiya M, Niwa Y, Simizu S. N-glycosylation of R-spondin1 at Asn137 negatively regulates its secretion and Wnt/β-catenin signaling-enhancing activity. Oncol Lett 2016;11:3279-86. [PMID: 27123103 DOI: 10.3892/ol.2016.4425] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 1.8] [Reference Citation Analysis]
335 Clevers H, Nusse R. Wnt/β-catenin signaling and disease. Cell. 2012;149:1192-1205. [PMID: 22682243 DOI: 10.1016/j.cell.2012.05.012] [Cited by in Crossref: 3294] [Cited by in F6Publishing: 2994] [Article Influence: 366.0] [Reference Citation Analysis]
336 Johnson ML, Rajamannan N. Diseases of Wnt signaling. Rev Endocr Metab Disord. 2006;7:41-49. [PMID: 16944325 DOI: 10.1007/s11154-006-9003-3] [Cited by in Crossref: 72] [Cited by in F6Publishing: 72] [Article Influence: 5.1] [Reference Citation Analysis]
337 Berner D, Moser D, Roesti M, Buescher H, Salzburger W. GENETIC ARCHITECTURE OF SKELETAL EVOLUTION IN EUROPEAN LAKE AND STREAM STICKLEBACK: GENETICS OF STICKLEBACK SKELETAL EVOLUTION. Evolution 2014;68:1792-805. [DOI: 10.1111/evo.12390] [Cited by in Crossref: 32] [Cited by in F6Publishing: 27] [Article Influence: 4.6] [Reference Citation Analysis]
338 Andersson K, Malmgren B, Åström E, Nordgren A, Taylan F, Dahllöf G. Mutations in COL1A1/A2 and CREB3L1 are associated with oligodontia in osteogenesis imperfecta. Orphanet J Rare Dis 2020;15:80. [PMID: 32234057 DOI: 10.1186/s13023-020-01361-4] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
339 Kelleher FC, Fennelly D, Rafferty M. Common critical pathways in embryogenesis and cancer. Acta Oncol 2006;45:375-88. [PMID: 16760173 DOI: 10.1080/02841860600602946] [Cited by in Crossref: 82] [Cited by in F6Publishing: 75] [Article Influence: 5.5] [Reference Citation Analysis]
340 Al-muzian L, Almuzian M, Mohammed H, Ulhaq A, Keightley AJ. Are developmentally missing teeth a predictive risk marker of malignant diseases in non-syndromic individuals? A systematic review. J Orthod 2021;48:221-30. [DOI: 10.1177/1465312520984166] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
341 Howe LJ, Hemani G, Lesseur C, Gaborieau V, Ludwig KU, Mangold E, Brennan P, Ness AR, St Pourcain B, Davey Smith G, Lewis SJ. Evaluating shared genetic influences on nonsyndromic cleft lip/palate and oropharyngeal neoplasms. Genet Epidemiol 2020;44:924-33. [PMID: 32710482 DOI: 10.1002/gepi.22343] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
342 Hughes TA, Brady HJ. Regulation of axin2 expression at the levels of transcription, translation and protein stability in lung and colon cancer. Cancer Letters 2006;233:338-47. [DOI: 10.1016/j.canlet.2005.03.026] [Cited by in Crossref: 25] [Cited by in F6Publishing: 21] [Article Influence: 1.7] [Reference Citation Analysis]
343 Salvi A, Giacopuzzi E, Bardellini E, Amadori F, Ferrari L, De Petro G, Borsani G, Majorana A. Mutation analysis by direct and whole exome sequencing in familial and sporadic tooth agenesis. Int J Mol Med 2016;38:1338-48. [PMID: 27665865 DOI: 10.3892/ijmm.2016.2742] [Cited by in Crossref: 9] [Cited by in F6Publishing: 6] [Article Influence: 1.8] [Reference Citation Analysis]
344 Järvinen E, Tummers M, Thesleff I. The role of the dental lamina in mammalian tooth replacement. J Exp Zool B Mol Dev Evol 2009;312B:281-91. [PMID: 19137538 DOI: 10.1002/jez.b.21275] [Cited by in Crossref: 78] [Cited by in F6Publishing: 64] [Article Influence: 6.5] [Reference Citation Analysis]
345 Acevedo AC, da Fonseca JA, Grinham J, Doudney K, Gomes RR, de Paula LM, Stanier P. Autosomal-dominant ankyloglossia and tooth number anomalies. J Dent Res 2010;89:128-32. [PMID: 20042737 DOI: 10.1177/0022034509356401] [Cited by in Crossref: 8] [Cited by in F6Publishing: 7] [Article Influence: 0.7] [Reference Citation Analysis]
346 Vieira AR, Seymen F, Patir A, Menezes R. Evidence of linkage disequilibrium between polymorphisms at the IRF6 locus and isolate tooth agenesis, in a Turkish population. Archives of Oral Biology 2008;53:780-4. [DOI: 10.1016/j.archoralbio.2008.03.006] [Cited by in Crossref: 16] [Cited by in F6Publishing: 14] [Article Influence: 1.2] [Reference Citation Analysis]