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For: Bult CJ, Blake JA, Smith CL, Kadin JA, Richardson JE; Mouse Genome Database Group. Mouse Genome Database (MGD) 2019. Nucleic Acids Res 2019;47:D801-6. [PMID: 30407599 DOI: 10.1093/nar/gky1056] [Cited by in Crossref: 271] [Cited by in F6Publishing: 219] [Article Influence: 135.5] [Reference Citation Analysis]
Number Citing Articles
1 Stacy A, Andrade-Oliveira V, McCulloch JA, Hild B, Oh JH, Perez-Chaparro PJ, Sim CK, Lim AI, Link VM, Enamorado M, Trinchieri G, Segre JA, Rehermann B, Belkaid Y. Infection trains the host for microbiota-enhanced resistance to pathogens. Cell 2021;184:615-627.e17. [PMID: 33453153 DOI: 10.1016/j.cell.2020.12.011] [Cited by in Crossref: 18] [Cited by in F6Publishing: 21] [Article Influence: 18.0] [Reference Citation Analysis]
2 Brennan JA, Chen Q, Gams A, Dyavanapalli J, Mendelowitz D, Peng W, Efimov IR. Evidence of Superior and Inferior Sinoatrial Nodes in the Mammalian Heart. JACC Clin Electrophysiol 2020;6:1827-40. [PMID: 33357580 DOI: 10.1016/j.jacep.2020.09.012] [Cited by in Crossref: 12] [Cited by in F6Publishing: 8] [Article Influence: 6.0] [Reference Citation Analysis]
3 Aponte JD, Katz DC, Roth DM, Vidal-García M, Liu W, Andrade F, Roseman CC, Murray SA, Cheverud J, Graf D, Marcucio RS, Hallgrímsson B. Relating multivariate shapes to genescapes using phenotype-biological process associations for craniofacial shape. Elife 2021;10:e68623. [PMID: 34779766 DOI: 10.7554/eLife.68623] [Reference Citation Analysis]
4 Tansley S, Uttam S, Ureña Guzmán A, Yaqubi M, Pacis A, Parisien M, Deamond H, Wong C, Rabau O, Brown N, Haglund L, Ouellet J, Santaguida C, Ribeiro-da-Silva A, Tahmasebi S, Prager-Khoutorsky M, Ragoussis J, Zhang J, Salter MW, Diatchenko L, Healy LM, Mogil JS, Khoutorsky A. Single-cell RNA sequencing reveals time- and sex-specific responses of mouse spinal cord microglia to peripheral nerve injury and links ApoE to chronic pain. Nat Commun 2022;13:843. [PMID: 35149686 DOI: 10.1038/s41467-022-28473-8] [Reference Citation Analysis]
5 Hillman P, Baker C, Hebert L, Brown M, Hixson J, Ashley-Koch A, Morrison AC, Northrup H, Au KS. Identification of novel candidate risk genes for myelomeningocele within the glucose homeostasis/oxidative stress and folate/one-carbon metabolism networks. Mol Genet Genomic Med 2020;8:e1495. [PMID: 32960507 DOI: 10.1002/mgg3.1495] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
6 de Souza ID, Reis CF, Morais DAA, Fernandes VGS, Cavalcante JVF, Dalmolin RJS. Ancestry analysis indicates two different sets of essential genes in eukaryotic model species. Funct Integr Genomics 2021;21:523-31. [PMID: 34279742 DOI: 10.1007/s10142-021-00794-9] [Reference Citation Analysis]
7 Baldarelli RM, Smith CM, Finger JH, Hayamizu TF, McCright IJ, Xu J, Shaw DR, Beal JS, Blodgett O, Campbell J, Corbani LE, Frost PJ, Giannatto SC, Miers DB, Kadin JA, Richardson JE, Ringwald M. The mouse Gene Expression Database (GXD): 2021 update. Nucleic Acids Res 2021;49:D924-31. [PMID: 33104772 DOI: 10.1093/nar/gkaa914] [Cited by in Crossref: 3] [Cited by in F6Publishing: 6] [Article Influence: 3.0] [Reference Citation Analysis]
8 [DOI: 10.1101/2020.09.16.300632] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
9 Brosens E, Brouwer RWW, Douben H, van Bever Y, Brooks AS, Wijnen RMH, van IJcken WFJ, Tibboel D, Rottier RJ, de Klein A. Heritability and De Novo Mutations in Oesophageal Atresia and Tracheoesophageal Fistula Aetiology. Genes (Basel) 2021;12:1595. [PMID: 34680991 DOI: 10.3390/genes12101595] [Reference Citation Analysis]
10 Choi J, Jang YJ, Dabrowska C, Iich E, Evans KV, Hall H, Janes SM, Simons BD, Koo BK, Kim J, Lee JH. Release of Notch activity coordinated by IL-1β signalling confers differentiation plasticity of airway progenitors via Fosl2 during alveolar regeneration. Nat Cell Biol 2021;23:953-66. [PMID: 34475534 DOI: 10.1038/s41556-021-00742-6] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
11 Chen JJ, Nathaniel DL, Raghavan P, Nelson M, Tian R, Tse E, Hong JY, See SK, Mok SA, Hein MY, Southworth DR, Grinberg LT, Gestwicki JE, Leonetti MD, Kampmann M. Compromised function of the ESCRT pathway promotes endolysosomal escape of tau seeds and propagation of tau aggregation. J Biol Chem 2019;294:18952-66. [PMID: 31578281 DOI: 10.1074/jbc.RA119.009432] [Cited by in Crossref: 37] [Cited by in F6Publishing: 21] [Article Influence: 12.3] [Reference Citation Analysis]
12 Panov J, Simchi L, Feuermann Y, Kaphzan H. Bioinformatics Analyses of the Transcriptome Reveal Ube3a-Dependent Effects on Mitochondrial-Related Pathways. Int J Mol Sci 2020;21:E4156. [PMID: 32532103 DOI: 10.3390/ijms21114156] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
13 Del Gobbo GF, Yin Y, Choufani S, Butcher EA, Wei J, Rajcan-Separovic E, Bos H, von Dadelszen P, Weksberg R, Robinson WP, Yuen RKC. Genomic imbalances in the placenta are associated with poor fetal growth. Mol Med 2021;27:3. [PMID: 33413077 DOI: 10.1186/s10020-020-00253-4] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
14 Kasak L, Laan M. Monogenic causes of non-obstructive azoospermia: challenges, established knowledge, limitations and perspectives. Hum Genet 2021;140:135-54. [DOI: 10.1007/s00439-020-02112-y] [Cited by in Crossref: 18] [Cited by in F6Publishing: 14] [Article Influence: 9.0] [Reference Citation Analysis]
15 Payseur BA, Jing P. Genomic Targets of Positive Selection in Giant Mice from Gough Island. Mol Biol Evol 2021;38:911-26. [PMID: 33022034 DOI: 10.1093/molbev/msaa255] [Reference Citation Analysis]
16 Shichkova P, Coggan JS, Markram H, Keller D. A Standardized Brain Molecular Atlas: A Resource for Systems Modeling and Simulation. Front Mol Neurosci 2021;14:604559. [PMID: 34858137 DOI: 10.3389/fnmol.2021.604559] [Reference Citation Analysis]
17 Gurumurthy CB, Saunders TL, Ohtsuka M. Designing and generating a mouse model: frequently asked questions. J Biomed Res 2021;35:76-90. [PMID: 33797414 DOI: 10.7555/JBR.35.20200197] [Reference Citation Analysis]
18 Starcher AE, Peissig K, Stanton JB, Churchill GA, Cai D, Maxwell JT, Grider A, Love K, Chen SY, Coleman AE, Strauss E, Pazdro R. A systems approach using Diversity Outbred mice distinguishes the cardiovascular effects and genetics of circulating GDF11 from those of its homolog, myostatin. G3 (Bethesda) 2021:jkab293. [PMID: 34510201 DOI: 10.1093/g3journal/jkab293] [Reference Citation Analysis]
19 Foong D, Liyanage L, Zhou J, Zarrouk A, Ho V, O'Connor MD. Single-cell RNA sequencing predicts motility networks in purified human gastric interstitial cells of Cajal. Neurogastroenterol Motil 2021;:e14303. [PMID: 34913225 DOI: 10.1111/nmo.14303] [Reference Citation Analysis]
20 Ke L, Yang DC, Wang Y, Ding Y, Gao G. AnnoLnc2: the one-stop portal to systematically annotate novel lncRNAs for human and mouse. Nucleic Acids Res 2020;48:W230-8. [PMID: 32406920 DOI: 10.1093/nar/gkaa368] [Cited by in Crossref: 10] [Cited by in F6Publishing: 9] [Article Influence: 5.0] [Reference Citation Analysis]
21 Shohat S, Shifman S. Genes essential for embryonic stem cells are associated with neurodevelopmental disorders. Genome Res 2019;29:1910-8. [PMID: 31649057 DOI: 10.1101/gr.250019.119] [Cited by in Crossref: 5] [Cited by in F6Publishing: 2] [Article Influence: 1.7] [Reference Citation Analysis]
22 Ietswaart R, Gyori BM, Bachman JA, Sorger PK, Churchman LS. GeneWalk identifies relevant gene functions for a biological context using network representation learning. Genome Biol 2021;22:55. [PMID: 33526072 DOI: 10.1186/s13059-021-02264-8] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
23 Doshida Y, Sano H, Iwabuchi S, Aigaki T, Yoshida M, Hashimoto S, Ishigami A. Age-associated changes in the transcriptomes of non-cultured adipose-derived stem cells from young and old mice assessed via single-cell transcriptome analysis. PLoS One 2020;15:e0242171. [PMID: 33237970 DOI: 10.1371/journal.pone.0242171] [Reference Citation Analysis]
24 [DOI: 10.1101/534834] [Cited by in Crossref: 12] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
25 Long H, Reeves R, Simon MM. Mouse genomic and cellular annotations. Mamm Genome. [DOI: 10.1007/s00335-021-09936-7] [Reference Citation Analysis]
26 Luo Y, Hitz BC, Gabdank I, Hilton JA, Kagda MS, Lam B, Myers Z, Sud P, Jou J, Lin K, Baymuradov UK, Graham K, Litton C, Miyasato SR, Strattan JS, Jolanki O, Lee JW, Tanaka FY, Adenekan P, O'Neill E, Cherry JM. New developments on the Encyclopedia of DNA Elements (ENCODE) data portal. Nucleic Acids Res 2020;48:D882-9. [PMID: 31713622 DOI: 10.1093/nar/gkz1062] [Cited by in Crossref: 12] [Cited by in F6Publishing: 11] [Article Influence: 6.0] [Reference Citation Analysis]
27 Zhu Z, Guan Z, Liu G, Wang Y, Zhang Z. SGID: a comprehensive and interactive database of the silkworm. Database (Oxford) 2019;2019:baz134. [PMID: 31836898 DOI: 10.1093/database/baz134] [Cited by in Crossref: 6] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
28 Stanzick KJ, Li Y, Schlosser P, Gorski M, Wuttke M, Thomas LF, Rasheed H, Rowan BX, Graham SE, Vanderweff BR, Patil SB, Robinson-Cohen C, Gaziano JM, O'Donnell CJ, Willer CJ, Hallan S, Åsvold BO, Gessner A, Hung AM, Pattaro C, Köttgen A, Stark KJ, Heid IM, Winkler TW; VA Million Veteran Program. Discovery and prioritization of variants and genes for kidney function in >1.2 million individuals. Nat Commun 2021;12:4350. [PMID: 34272381 DOI: 10.1038/s41467-021-24491-0] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
29 Cheong A, Archambault D, Degani R, Iverson E, Tremblay KD, Mager J. Nuclear-encoded mitochondrial ribosomal proteins are required to initiate gastrulation. Development 2020;147:dev188714. [PMID: 32376682 DOI: 10.1242/dev.188714] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 3.0] [Reference Citation Analysis]
30 Birling MC, Yoshiki A, Adams DJ, Ayabe S, Beaudet AL, Bottomley J, Bradley A, Brown SDM, Bürger A, Bushell W, Chiani F, Chin HG, Christou S, Codner GF, DeMayo FJ, Dickinson ME, Doe B, Donahue LR, Fray MD, Gambadoro A, Gao X, Gertsenstein M, Gomez-Segura A, Goodwin LO, Heaney JD, Hérault Y, de Angelis MH, Jiang ST, Justice MJ, Kasparek P, King RE, Kühn R, Lee H, Lee YJ, Liu Z, Lloyd KCK, Lorenzo I, Mallon AM, McKerlie C, Meehan TF, Fuentes VM, Newman S, Nutter LMJ, Oh GT, Pavlovic G, Ramirez-Solis R, Rosen B, Ryder EJ, Santos LA, Schick J, Seavitt JR, Sedlacek R, Seisenberger C, Seong JK, Skarnes WC, Sorg T, Steel KP, Tamura M, Tocchini-Valentini GP, Wang CL, Wardle-Jones H, Wattenhofer-Donzé M, Wells S, Wiles MV, Willis BJ, Wood JA, Wurst W, Xu Y, Teboul L, Murray SA; International Mouse Phenotyping Consortium (IMPC). A resource of targeted mutant mouse lines for 5,061 genes. Nat Genet 2021;53:416-9. [PMID: 33833456 DOI: 10.1038/s41588-021-00825-y] [Cited by in Crossref: 7] [Cited by in F6Publishing: 8] [Article Influence: 7.0] [Reference Citation Analysis]
31 Luo L, Ambrozkiewicz MC, Benseler F, Chen C, Dumontier E, Falkner S, Furlanis E, Gomez AM, Hoshina N, Huang WH, Hutchison MA, Itoh-Maruoka Y, Lavery LA, Li W, Maruo T, Motohashi J, Pai EL, Pelkey KA, Pereira A, Philips T, Sinclair JL, Stogsdill JA, Traunmüller L, Wang J, Wortel J, You W, Abumaria N, Beier KT, Brose N, Burgess HA, Cepko CL, Cloutier JF, Eroglu C, Goebbels S, Kaeser PS, Kay JN, Lu W, Luo L, Mandai K, McBain CJ, Nave KA, Prado MAM, Prado VF, Rothstein J, Rubenstein JLR, Saher G, Sakimura K, Sanes JR, Scheiffele P, Takai Y, Umemori H, Verhage M, Yuzaki M, Zoghbi HY, Kawabe H, Craig AM. Optimizing Nervous System-Specific Gene Targeting with Cre Driver Lines: Prevalence of Germline Recombination and Influencing Factors. Neuron 2020;106:37-65.e5. [PMID: 32027825 DOI: 10.1016/j.neuron.2020.01.008] [Cited by in Crossref: 34] [Cited by in F6Publishing: 29] [Article Influence: 17.0] [Reference Citation Analysis]
32 Yao X, Glessner JT, Li J, Qi X, Hou X, Zhu C, Li X, March ME, Yang L, Mentch FD, Hain HS, Meng X, Xia Q, Hakonarson H, Li J. Integrative analysis of genome-wide association studies identifies novel loci associated with neuropsychiatric disorders. Transl Psychiatry 2021;11:69. [PMID: 33479212 DOI: 10.1038/s41398-020-01195-5] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
33 Bang J, Han M, Yoo TJ, Qiao L, Jung J, Na J, Carlson BA, Gladyshev VN, Hatfield DL, Kim JH, Kim LK, Lee BJ. Identification of Signaling Pathways for Early Embryonic Lethality and Developmental Retardation in Sephs1-/- Mice. Int J Mol Sci 2021;22:11647. [PMID: 34769078 DOI: 10.3390/ijms222111647] [Reference Citation Analysis]
34 Hunter WB, Wintermantel WM. Optimizing Efficient RNAi-Mediated Control of Hemipteran Pests (Psyllids, Leafhoppers, Whitefly): Modified Pyrimidines in dsRNA Triggers. Plants (Basel) 2021;10:1782. [PMID: 34579315 DOI: 10.3390/plants10091782] [Cited by in Crossref: 2] [Article Influence: 2.0] [Reference Citation Analysis]
35 Restrepo CM, Llanes A, Herrera L, Ellis E, Lleonart R, Fernández PL. Gene expression patterns associated with Leishmania panamensis infection in macrophages from BALB/c and C57BL/6 mice. PLoS Negl Trop Dis 2021;15:e0009225. [PMID: 33617537 DOI: 10.1371/journal.pntd.0009225] [Reference Citation Analysis]
36 Novak G, Kyriakis D, Grzyb K, Bernini M, Rodius S, Dittmar G, Finkbeiner S, Skupin A. Single-cell transcriptomics of human iPSC differentiation dynamics reveal a core molecular network of Parkinson's disease. Commun Biol 2022;5:49. [PMID: 35027645 DOI: 10.1038/s42003-021-02973-7] [Reference Citation Analysis]
37 Aschner Y, Correll KA, Beke K, Foster DG, Roybal HM, Nelson MR, Meador CL, Strand M, Anderson KC, Moore CM, Reynolds PR, Kopf KW, Burnham EL, Downey GP. PTPα Promotes Fibroproliferative Responses After Acute Lung Injury. Am J Physiol Lung Cell Mol Physiol 2022. [PMID: 35670474 DOI: 10.1152/ajplung.00436.2021] [Reference Citation Analysis]
38 Deal KK, Chandrashekar AS, Beaman MM, Branch MC, Buehler DP, Conway SJ, Southard-Smith EM. Altered sacral neural crest development in Pax3 spina bifida mutants underlies deficits of bladder innervation and function. Dev Biol 2021;476:173-88. [PMID: 33839113 DOI: 10.1016/j.ydbio.2021.03.024] [Reference Citation Analysis]
39 Jakob L, Müller TA, Rassner M, Kleinfelder H, Veratti P, Mitschke J, Miething C, Oostendorp RAJ, Pfeifer D, Waterhouse M, Duyster J. Murine Oncostatin M Has Opposing Effects on the Proliferation of OP9 Bone Marrow Stromal Cells and NIH/3T3 Fibroblasts Signaling through the OSMR. Int J Mol Sci 2021;22:11649. [PMID: 34769079 DOI: 10.3390/ijms222111649] [Reference Citation Analysis]
40 Dimitrakopoulos GN, Klapa MI, Moschonas NK. PICKLE 3.0: Enriching the human Meta-database with the mouse protein interactome extended via mouse-human orthology. Bioinformatics 2020:btaa1070. [PMID: 33367505 DOI: 10.1093/bioinformatics/btaa1070] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
41 Gagnier L, Belancio VP, Mager DL. Mouse germ line mutations due to retrotransposon insertions. Mob DNA 2019;10:15. [PMID: 31011371 DOI: 10.1186/s13100-019-0157-4] [Cited by in Crossref: 40] [Cited by in F6Publishing: 31] [Article Influence: 13.3] [Reference Citation Analysis]
42 Russkikh N, Antonets D, Shtokalo D, Makarov A, Vyatkin Y, Zakharov A, Terentyev E. Style transfer with variational autoencoders is a promising approach to RNA-Seq data harmonization and analysis. Bioinformatics 2020;36:5076-85. [PMID: 33026062 DOI: 10.1093/bioinformatics/btaa624] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
43 Zheng X, Li Z, Wang G, Wang H, Zhou Y, Zhao X, Cheng CY, Qiao Y, Sun F. Sperm epigenetic alterations contribute to inter- and transgenerational effects of paternal exposure to long-term psychological stress via evading offspring embryonic reprogramming. Cell Discov 2021;7:101. [PMID: 34711814 DOI: 10.1038/s41421-021-00343-5] [Reference Citation Analysis]
44 Icick R, Forget B, Cloëz-Tayarani I, Pons S, Maskos U, Besson M. Genetic susceptibility to nicotine addiction: Advances and shortcomings in our understanding of the CHRNA5/A3/B4 gene cluster contribution. Neuropharmacology 2020;177:108234. [PMID: 32738310 DOI: 10.1016/j.neuropharm.2020.108234] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
45 Dan H, Ruan T, Sampogna RV. Circadian Clock Regulation of Developmental Time in the Kidney. Cell Rep 2020;31:107661. [PMID: 32433970 DOI: 10.1016/j.celrep.2020.107661] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
46 Liu L, Wang H, Xu GL, Liu L. Tet1 Deficiency Leads to Premature Ovarian Failure. Front Cell Dev Biol 2021;9:644135. [PMID: 33834024 DOI: 10.3389/fcell.2021.644135] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
47 Cooley LS, Rudewicz J, Souleyreau W, Emanuelli A, Alvarez-Arenas A, Clarke K, Falciani F, Dufies M, Lambrechts D, Modave E, Chalopin-Fillot D, Pineau R, Ambrosetti D, Bernhard JC, Ravaud A, Négrier S, Ferrero JM, Pagès G, Benzekry S, Nikolski M, Bikfalvi A. Experimental and computational modeling for signature and biomarker discovery of renal cell carcinoma progression. Mol Cancer 2021;20:136. [PMID: 34670568 DOI: 10.1186/s12943-021-01416-5] [Reference Citation Analysis]
48 Theis JL, Niaz T, Sundsbak RS, Fogarty ZC, Bamlet WR, Hagler DJ, Olson TM. CELSR1 Risk Alleles in Familial Bicuspid Aortic Valve and Hypoplastic Left Heart Syndrome. Circ Genom Precis Med 2022;15:e003523. [PMID: 35133174 DOI: 10.1161/CIRCGEN.121.003523] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
49 Aviña-Padilla K, Ramírez-Rafael JA, Herrera-Oropeza GE, Muley VY, Valdivia DI, Díaz-Valenzuela E, García-García A, Varela-Echavarría A, Hernández-Rosales M. Evolutionary Perspective and Expression Analysis of Intronless Genes Highlight the Conservation of Their Regulatory Role. Front Genet 2021;12:654256. [PMID: 34306008 DOI: 10.3389/fgene.2021.654256] [Reference Citation Analysis]
50 Adadey SM, Esoh KK, Quaye O, Amedofu GK, Awandare GA, Wonkam A. GJB4 and GJC3 variants in non-syndromic hearing impairment in Ghana. Exp Biol Med (Maywood) 2020;245:1355-67. [PMID: 32524838 DOI: 10.1177/1535370220931035] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
51 Adadey SM, Wonkam-Tingang E, Twumasi Aboagye E, Nayo-Gyan DW, Boatemaa Ansong M, Quaye O, Awandare GA, Wonkam A. Connexin Genes Variants Associated with Non-Syndromic Hearing Impairment: A Systematic Review of the Global Burden. Life (Basel) 2020;10:E258. [PMID: 33126609 DOI: 10.3390/life10110258] [Cited by in Crossref: 2] [Article Influence: 1.0] [Reference Citation Analysis]
52 Verma P, Parte P. Revisiting the Characteristics of Testicular Germ Cell Lines GC-1(spg) and GC-2(spd)ts. Mol Biotechnol 2021. [PMID: 34125394 DOI: 10.1007/s12033-021-00352-5] [Reference Citation Analysis]
53 Choy KHK, Chan SY, Lam W, Jin J, Zheng T, Law TYS, Yu SS, Wang W, Li L, Xie G, Yim HCH, Chen H, Fok EKL. The repertoire of testicular extracellular vesicle cargoes and their involvement in inter-compartmental communication associated with spermatogenesis. BMC Biol 2022;20:78. [PMID: 35351114 DOI: 10.1186/s12915-022-01268-5] [Reference Citation Analysis]
54 Laisk T, Lepamets M, Koel M, Abner E, Mägi R; Estonian Biobank Research Team. Genome-wide association study identifies five risk loci for pernicious anemia. Nat Commun 2021;12:3761. [PMID: 34145262 DOI: 10.1038/s41467-021-24051-6] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
55 Baloghova N, Lidak T, Cermak L. Ubiquitin Ligases Involved in the Regulation of Wnt, TGF-β, and Notch Signaling Pathways and Their Roles in Mouse Development and Homeostasis. Genes (Basel) 2019;10:E815. [PMID: 31623112 DOI: 10.3390/genes10100815] [Cited by in Crossref: 8] [Cited by in F6Publishing: 7] [Article Influence: 2.7] [Reference Citation Analysis]
56 Lines MA, Cuillerier A, Chakraborty P, Naas T, Duque Lasio ML, Michaud J, Pileggi C, Harper ME, Burelle Y, Toler TL, Sondheimer N, Crawford HP, Millan F, Geraghty MT. A recurrent de novo ATP5F1A substitution associated with neonatal complex V deficiency. Eur J Hum Genet 2021;29:1719-24. [PMID: 34483339 DOI: 10.1038/s41431-021-00956-0] [Reference Citation Analysis]
57 Hannigan MM, Hoffman AM, Thompson JW, Zheng T, Nicchitta CV. Quantitative Proteomics Links the LRRC59 Interactome to mRNA Translation on the ER Membrane. Mol Cell Proteomics 2020;19:1826-49. [PMID: 32788342 DOI: 10.1074/mcp.RA120.002228] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
58 Li Q, Chen W, Wang C, Liu Z, Gu Y, Xu X, Xu J, Jiang T, Xu M, Wang Y, Chen C, Zhong Y, Zhang Y, Yao L, Jin G, Hu Z, Zhou P. Whole-exome sequencing reveals common and rare variants in immunologic and neurological genes implicated in achalasia. Am J Hum Genet 2021;108:1478-87. [PMID: 34197731 DOI: 10.1016/j.ajhg.2021.06.004] [Reference Citation Analysis]
59 Breitfeld J, Kehr S, Müller L, Stadler PF, Böttcher Y, Blüher M, Stumvoll M, Kovacs P. Developmentally Driven Changes in Adipogenesis in Different Fat Depots Are Related to Obesity. Front Endocrinol (Lausanne) 2020;11:138. [PMID: 32273869 DOI: 10.3389/fendo.2020.00138] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
60 Ray D, Venkataraghavan S, Zhang W, Leslie EJ, Hetmanski JB, Weinberg SM, Murray JC, Marazita ML, Ruczinski I, Taub MA, Beaty TH. Pleiotropy method reveals genetic overlap between orofacial clefts at multiple novel loci from GWAS of multi-ethnic trios. PLoS Genet 2021;17:e1009584. [PMID: 34242216 DOI: 10.1371/journal.pgen.1009584] [Reference Citation Analysis]
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