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For: Ma K, Qiu L, Mrasek K, Zhang J, Liehr T, Quintana LG, Li Z. Common fragile sites: genomic hotspots of DNA damage and carcinogenesis. Int J Mol Sci 2012;13:11974-99. [PMID: 23109895 DOI: 10.3390/ijms130911974] [Cited by in Crossref: 43] [Cited by in F6Publishing: 43] [Article Influence: 4.3] [Reference Citation Analysis]
Number Citing Articles
1 Wu X, Guo M, Cui J, Cai H, Wang SM. Heterozygotic Brca1 mutation initiates mouse genome instability at embryonic stage. Oncogenesis 2022;11. [DOI: 10.1038/s41389-022-00417-3] [Reference Citation Analysis]
2 Aksoy Yasar FB, Shingu T, Zamler DB, Zaman MF, Chien DL, Zhang Q, Ren J, Hu J. Quaking but not parkin is the major tumor suppressor in 6q deleted region in glioblastoma. Front Cell Dev Biol 2022;10:931387. [DOI: 10.3389/fcell.2022.931387] [Reference Citation Analysis]
3 Xu N, Yao Z, Shang G, Ye D, Wang H, Zhang H, Qu Y, Xu F, Wang Y, Qin Z, Zhu J, Zhang F, Feng J, Tian S, Liu Y, Zhao J, Hou J, Guo J, Hou Y, Ding C. Integrated proteogenomic characterization of urothelial carcinoma of the bladder. J Hematol Oncol 2022;15:76. [PMID: 35659036 DOI: 10.1186/s13045-022-01291-7] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
4 Janjetovic S, Hinke J, Balachandran S, Akyüz N, Behrmann P, Bokemeyer C, Dierlamm J, Murga Penas EM. Non-Random Pattern of Integration for Epstein-Barr Virus with Preference for Gene-Poor Genomic Chromosomal Regions into the Genome of Burkitt Lymphoma Cell Lines. Viruses 2022;14:86. [PMID: 35062290 DOI: 10.3390/v14010086] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
5 St Germain C, Zhao H, Barlow JH. Transcription-Replication Collisions-A Series of Unfortunate Events. Biomolecules 2021;11:1249. [PMID: 34439915 DOI: 10.3390/biom11081249] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
6 Hadi K, Yao X, Behr JM, Deshpande A, Xanthopoulakis C, Tian H, Kudman S, Rosiene J, Darmofal M, DeRose J, Mortensen R, Adney EM, Shaiber A, Gajic Z, Sigouros M, Eng K, Wala JA, Wrzeszczyński KO, Arora K, Shah M, Emde AK, Felice V, Frank MO, Darnell RB, Ghandi M, Huang F, Dewhurst S, Maciejowski J, de Lange T, Setton J, Riaz N, Reis-Filho JS, Powell S, Knowles DA, Reznik E, Mishra B, Beroukhim R, Zody MC, Robine N, Oman KM, Sanchez CA, Kuhner MK, Smith LP, Galipeau PC, Paulson TG, Reid BJ, Li X, Wilkes D, Sboner A, Mosquera JM, Elemento O, Imielinski M. Distinct Classes of Complex Structural Variation Uncovered across Thousands of Cancer Genome Graphs. Cell 2020;183:197-210.e32. [PMID: 33007263 DOI: 10.1016/j.cell.2020.08.006] [Cited by in Crossref: 30] [Cited by in F6Publishing: 45] [Article Influence: 30.0] [Reference Citation Analysis]
7 Zhu Y, Gujar AD, Wong CH, Tjong H, Ngan CY, Gong L, Chen YA, Kim H, Liu J, Li M, Mil-Homens A, Maurya R, Kuhlberg C, Sun F, Yi E, deCarvalho AC, Ruan Y, Verhaak RGW, Wei CL. Oncogenic extrachromosomal DNA functions as mobile enhancers to globally amplify chromosomal transcription. Cancer Cell 2021;39:694-707.e7. [PMID: 33836152 DOI: 10.1016/j.ccell.2021.03.006] [Cited by in Crossref: 1] [Cited by in F6Publishing: 29] [Article Influence: 1.0] [Reference Citation Analysis]
8 Quistrebert J, Orlova M, Kerner G, Ton LT, Luong NT, Danh NT, Vincent QB, Jabot-Hanin F, Seeleuthner Y, Bustamante J, Boisson-Dupuis S, Huong NT, Ba NN, Casanova JL, Delacourt C, Hoal EG, Alcaïs A, Thai VH, Thành LT, Abel L, Schurr E, Cobat A. Genome-wide association study of resistance to Mycobacterium tuberculosis infection identifies a locus at 10q26.2 in three distinct populations. PLoS Genet 2021;17:e1009392. [PMID: 33661925 DOI: 10.1371/journal.pgen.1009392] [Cited by in Crossref: 1] [Cited by in F6Publishing: 4] [Article Influence: 1.0] [Reference Citation Analysis]
9 Ukadike KC, Mustelin T. Implications of Endogenous Retroelements in the Etiopathogenesis of Systemic Lupus Erythematosus. J Clin Med 2021;10:856. [PMID: 33669709 DOI: 10.3390/jcm10040856] [Reference Citation Analysis]
10 Lee JJ, Lee J, Lee H. Alternative paths to telomere elongation. Semin Cell Dev Biol 2021;113:88-96. [PMID: 33293233 DOI: 10.1016/j.semcdb.2020.11.003] [Cited by in Crossref: 4] [Cited by in F6Publishing: 6] [Article Influence: 2.0] [Reference Citation Analysis]
11 Iourov IY, Vorsanova SG, Yurov YB, Zelenova MA, Kurinnaia OS, Vasin KS, Kutsev SI. The Cytogenomic "Theory of Everything": Chromohelkosis May Underlie Chromosomal Instability and Mosaicism in Disease and Aging. Int J Mol Sci 2020;21:E8328. [PMID: 33171981 DOI: 10.3390/ijms21218328] [Cited by in Crossref: 6] [Cited by in F6Publishing: 9] [Article Influence: 3.0] [Reference Citation Analysis]
12 Li X, Pei Y, Zhang Y, Liu Y, Fu W, Li J, You H, Huang J. Single-Molecule Mechanical Unfolding of AT-Rich Chromosomal Fragile Site DNA Hairpins: Resolving the Thermodynamic and Kinetic Effects of a Single G-T Mismatch. J Phys Chem B 2020;124:9365-70. [PMID: 32970435 DOI: 10.1021/acs.jpcb.0c06954] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
13 Shu Z, Li Z, Huang H, Chen Y, Fan J, Yu L, Wu Z, Tian L, Qi Q, Peng S, Wei C, Xie Z, Li X, Feng Q, Sheng H, Li G, Wei D, Shan C, Chen G. Cell-cycle-dependent phosphorylation of RRM1 ensures efficient DNA replication and regulates cancer vulnerability to ATR inhibition. Oncogene 2020;39:5721-33. [PMID: 32712628 DOI: 10.1038/s41388-020-01403-y] [Cited by in Crossref: 5] [Cited by in F6Publishing: 8] [Article Influence: 2.5] [Reference Citation Analysis]
14 Kim C, Sung S, Kim J, Lee J. Repair and Reconstruction of Telomeric and Subtelomeric Regions and Genesis of New Telomeres: Implications for Chromosome Evolution. Bioessays 2020;42:e1900177. [PMID: 32236965 DOI: 10.1002/bies.201900177] [Cited by in Crossref: 1] [Cited by in F6Publishing: 3] [Article Influence: 0.5] [Reference Citation Analysis]
15 Liehr T. From Human Cytogenetics to Human Chromosomics. Int J Mol Sci 2019;20:E826. [PMID: 30769866 DOI: 10.3390/ijms20040826] [Cited by in Crossref: 6] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
16 Weise A, Mrasek K, Pentzold C, Liehr T. Chromosomes in the DNA era: Perspectives in diagnostics and research. Medizinische Genetik 2019;31:8-19. [DOI: 10.1007/s11825-019-0236-4] [Cited by in Crossref: 3] [Article Influence: 1.0] [Reference Citation Analysis]
17 Irony-Tur Sinai M, Kerem B. Genomic instability in fragile sites-still adding the pieces. Genes Chromosomes Cancer 2019;58:295-304. [PMID: 30525255 DOI: 10.1002/gcc.22715] [Cited by in Crossref: 12] [Cited by in F6Publishing: 10] [Article Influence: 3.0] [Reference Citation Analysis]
18 Ochoa B, Chico Y, Martínez MJ. Insights Into SND1 Oncogene Promoter Regulation. Front Oncol 2018;8:606. [PMID: 30619748 DOI: 10.3389/fonc.2018.00606] [Cited by in Crossref: 9] [Cited by in F6Publishing: 12] [Article Influence: 2.3] [Reference Citation Analysis]
19 Wilhelm K, Pentzold C, Schoener S, Arakelyan A, Hakobyan A, Mrasek K, Weise A. Fragile Sites as Drivers of Gene and Genome Evolution. Curr Genet Med Rep 2018;6:136-43. [DOI: 10.1007/s40142-018-0154-9] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
20 Herrero MJ, Gitton Y. The untold stories of the speech gene, the FOXP2 cancer gene. Genes Cancer 2018;9:11-38. [PMID: 29725501 DOI: 10.18632/genesandcancer.169] [Cited by in Crossref: 15] [Cited by in F6Publishing: 19] [Article Influence: 3.8] [Reference Citation Analysis]
21 Shi X, Qin T, Liu W, Zhang X, Li L, Huo J, Zhou K, Yang D, Zhang Y, Wang C. Selective anticancer activity of the novel steroidal dihydropyridine spirooxindoles against human esophageal EC109 cells. Biomed Pharmacother 2017;96:1186-92. [PMID: 29196102 DOI: 10.1016/j.biopha.2017.11.100] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 0.4] [Reference Citation Analysis]
22 Savić I, Ćirović D, Bugarski-Stanojević V. Exceptional Chromosomal Evolution and Cryptic Speciation of Blind Mole Rats Nannospalax leucodon (Spalacinae, Rodentia) from South-Eastern Europe. Genes (Basel) 2017;8:E292. [PMID: 29068425 DOI: 10.3390/genes8110292] [Cited by in Crossref: 6] [Cited by in F6Publishing: 3] [Article Influence: 1.2] [Reference Citation Analysis]
23 Lessler J, Azman AS, McKay HS, Moore SM. What is a Hotspot Anyway? Am J Trop Med Hyg 2017;96:1270-3. [PMID: 28719289 DOI: 10.4269/ajtmh.16-0427] [Cited by in Crossref: 38] [Cited by in F6Publishing: 37] [Article Influence: 7.6] [Reference Citation Analysis]
24 Jahid S, Sun J, Gelincik O, Blecua P, Edelmann W, Kucherlapati R, Zhou K, Jasin M, Gümüş ZH, Lipkin SM. Inhibition of colorectal cancer genomic copy number alterations and chromosomal fragile site tumor suppressor FHIT and WWOX deletions by DNA mismatch repair. Oncotarget 2017;8:71574-86. [PMID: 29069730 DOI: 10.18632/oncotarget.17776] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 0.8] [Reference Citation Analysis]
25 Fragkos M, Naim V. Rescue from replication stress during mitosis. Cell Cycle 2017;16:613-33. [PMID: 28166452 DOI: 10.1080/15384101.2017.1288322] [Cited by in Crossref: 34] [Cited by in F6Publishing: 30] [Article Influence: 6.8] [Reference Citation Analysis]
26 Filipović J, Joksić G, Vujić D, Joksić I, Mrasek K, Weise A, Liehr T. First molecular-cytogenetic characterization of Fanconi anemia fragile sites in primary lymphocytes of FA-D2 patients in different stages of the disease. Mol Cytogenet 2016;9:70. [PMID: 27625703 DOI: 10.1186/s13039-016-0280-6] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 0.8] [Reference Citation Analysis]
27 Baldazzi C, Luatti S, Zuffa E, Papayannidis C, Ottaviani E, Marzocchi G, Ameli G, Bardi MA, Bonaldi L, Paolini R, Gurrieri C, Rigolin GM, Cuneo A, Martinelli G, Cavo M, Testoni N. Complex chromosomal rearrangements leading to MECOM overexpression are recurrent in myeloid malignancies with various 3q abnormalities. Genes Chromosomes Cancer 2016;55:375-88. [PMID: 26815134 DOI: 10.1002/gcc.22341] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
28 Roszik J, Wu CJ, Siroy AE, Lazar AJ, Davies MA, Woodman SE, Kwong LN. Somatic Copy Number Alterations at Oncogenic Loci Show Diverse Correlations with Gene Expression. Sci Rep 2016;6:19649. [PMID: 26787600 DOI: 10.1038/srep19649] [Cited by in Crossref: 10] [Cited by in F6Publishing: 7] [Article Influence: 1.7] [Reference Citation Analysis]
29 Osborn MJ, Webber BR, Knipping F, Lonetree CL, Tennis N, DeFeo AP, McElroy AN, Starker CG, Lee C, Merkel S, Lund TC, Kelly-Spratt KS, Jensen MC, Voytas DF, von Kalle C, Schmidt M, Gabriel R, Hippen KL, Miller JS, Scharenberg AM, Tolar J, Blazar BR. Evaluation of TCR Gene Editing Achieved by TALENs, CRISPR/Cas9, and megaTAL Nucleases. Mol Ther 2016;24:570-81. [PMID: 26502778 DOI: 10.1038/mt.2015.197] [Cited by in Crossref: 108] [Cited by in F6Publishing: 118] [Article Influence: 15.4] [Reference Citation Analysis]
30 Song F, Zhang J, Qiu L, Zhao Y, Xing P, Lu J, Chen K, Li Z. A functional genetic variant in fragile-site gene FATS modulates the risk of breast cancer in triparous women. BMC Cancer 2015;15:559. [PMID: 26223354 DOI: 10.1186/s12885-015-1570-9] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 0.4] [Reference Citation Analysis]
31 Xi G, Liu Z. Coumarin sharing the benzene ring with quinoline for quenching radicals and inhibiting DNA oxidation. European Journal of Medicinal Chemistry 2015;95:416-23. [DOI: 10.1016/j.ejmech.2015.03.061] [Cited by in Crossref: 8] [Cited by in F6Publishing: 10] [Article Influence: 1.1] [Reference Citation Analysis]
32 Gallo LH, Nelson KN, Meyer AN, Donoghue DJ. Functions of Fibroblast Growth Factor Receptors in cancer defined by novel translocations and mutations. Cytokine Growth Factor Rev 2015;26:425-49. [PMID: 26003532 DOI: 10.1016/j.cytogfr.2015.03.003] [Cited by in Crossref: 70] [Cited by in F6Publishing: 72] [Article Influence: 10.0] [Reference Citation Analysis]
33 Ambroziak W, Koziorowski D, Duszyc K, Górka-Skoczylas P, Potulska-Chromik A, Sławek J, Hoffman-Zacharska D. Genomic instability in the PARK2 locus is associated with Parkinson's disease. J Appl Genet 2015;56:451-61. [PMID: 25833766 DOI: 10.1007/s13353-015-0282-9] [Cited by in Crossref: 19] [Cited by in F6Publishing: 16] [Article Influence: 2.7] [Reference Citation Analysis]
34 Burton DG, Faragher RG. Cellular senescence: from growth arrest to immunogenic conversion. Age (Dordr) 2015;37:27. [PMID: 25787341 DOI: 10.1007/s11357-015-9764-2] [Cited by in Crossref: 46] [Cited by in F6Publishing: 51] [Article Influence: 6.6] [Reference Citation Analysis]
35 Shapiro SG, Raghunath S, Williams C, Motsinger-Reif AA, Cullen JM, Liu T, Albertson D, Ruvolo M, Bergstrom Lucas A, Jin J, Knapp DW, Schiffman JD, Breen M. Canine urothelial carcinoma: genomically aberrant and comparatively relevant. Chromosome Res 2015;23:311-31. [PMID: 25783786 DOI: 10.1007/s10577-015-9471-y] [Cited by in Crossref: 37] [Cited by in F6Publishing: 33] [Article Influence: 5.3] [Reference Citation Analysis]
36 Georgakilas AG, Tsantoulis P, Kotsinas A, Michalopoulos I, Townsend P, Gorgoulis VG. Are common fragile sites merely structural domains or highly organized "functional" units susceptible to oncogenic stress? Cell Mol Life Sci 2014;71:4519-44. [PMID: 25238782 DOI: 10.1007/s00018-014-1717-x] [Cited by in Crossref: 40] [Cited by in F6Publishing: 43] [Article Influence: 5.0] [Reference Citation Analysis]
37 Savelyeva L, Brueckner LM. Molecular characterization of common fragile sites as a strategy to discover cancer susceptibility genes. Cell Mol Life Sci 2014;71:4561-75. [PMID: 25231336 DOI: 10.1007/s00018-014-1723-z] [Cited by in Crossref: 12] [Cited by in F6Publishing: 9] [Article Influence: 1.5] [Reference Citation Analysis]
38 Sakellariou D, Chiourea M, Raftopoulou C, Gagos S. Alternative lengthening of telomeres: recurrent cytogenetic aberrations and chromosome stability under extreme telomere dysfunction. Neoplasia 2013;15:1301-13. [PMID: 24339742 DOI: 10.1593/neo.131574] [Cited by in Crossref: 17] [Cited by in F6Publishing: 21] [Article Influence: 2.1] [Reference Citation Analysis]
39 Prada CF, Laissue P. A high resolution map of mammalian X chromosome fragile regions assessed by large-scale comparative genomics. Mamm Genome 2014;25:618-35. [PMID: 25086724 DOI: 10.1007/s00335-014-9537-8] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 0.5] [Reference Citation Analysis]
40 Yan S, Qiu L, Ma K, Zhang X, Zhao Y, Zhang J, Li X, Hao X, Li Z. FATS is an E2-independent ubiquitin ligase that stabilizes p53 and promotes its activation in response to DNA damage. Oncogene 2014;33:5424-33. [PMID: 24240685 DOI: 10.1038/onc.2013.494] [Cited by in Crossref: 13] [Cited by in F6Publishing: 13] [Article Influence: 1.4] [Reference Citation Analysis]
41 Ma K, Wang J, Shen B, Qiu L, Huang X, Li Z. Efficient targeting of FATS at a common fragile site in mice through TALEN-mediated double-hit genome modification. Biotechnol Lett 2014;36:471-9. [PMID: 24158675 DOI: 10.1007/s10529-013-1387-z] [Cited by in Crossref: 6] [Cited by in F6Publishing: 4] [Article Influence: 0.7] [Reference Citation Analysis]
42 Synowiec E, Wojcik KA, Izdebska J, Binczyk E, Blasiak J, Szaflik J, Szaflik JP. Polymorphisms of the homologous recombination gene RAD51 in keratoconus and Fuchs endothelial corneal dystrophy. Dis Markers 2013;35:353-62. [PMID: 24223453 DOI: 10.1155/2013/851817] [Cited by in Crossref: 10] [Cited by in F6Publishing: 13] [Article Influence: 1.1] [Reference Citation Analysis]
43 Barnett RN, Joseph J, Landman U, Schuster GB. Oxidative Thymine Mutation in DNA: Water-Wire-Mediated Proton-Coupled Electron Transfer. J Am Chem Soc 2013;135:3904-14. [DOI: 10.1021/ja311282k] [Cited by in Crossref: 26] [Cited by in F6Publishing: 27] [Article Influence: 2.9] [Reference Citation Analysis]