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Page 1
Disruption of mouse Cenpj, a regulator of centriole biogenesis, phenocopies Seckel syndrome.
McIntyre RE, Lakshminarasimhan Chavali P, Ismail O, Carragher DM, Sanchez-Andrade G, Forment JV, Fu B, Del Castillo Velasco-Herrera M, Edwards A, van der Weyden L, Yang F; Sanger Mouse Genetics Project; Ramirez-Solis R, Estabel J, Gallagher FA, Logan DW, Arends MJ, Tsang SH, Mahajan VB, Scudamore CL, White JK, Jackson SP, Gergely F, Adams DJ. McIntyre RE, et al. PLoS Genet. 2012;8(11):e1003022. doi: 10.1371/journal.pgen.1003022. Epub 2012 Nov 15. PLoS Genet. 2012. PMID: 23166506 Free PMC article.
BRCTx is a novel, highly conserved RAD18-interacting protein.
Adams DJ, van der Weyden L, Gergely FV, Arends MJ, Ng BL, Tannahill D, Kanaar R, Markus A, Morris BJ, Bradley A. Adams DJ, et al. Among authors: gergely fv. Mol Cell Biol. 2005 Jan;25(2):779-88. doi: 10.1128/MCB.25.2.779-788.2005. Mol Cell Biol. 2005. PMID: 15632077 Free PMC article.
CCDC61/VFL3 Is a Paralog of SAS6 and Promotes Ciliary Functions.
Ochi T, Quarantotti V, Lin H, Jullien J, Rosa E Silva I, Boselli F, Barnabas DD, Johnson CM, McLaughlin SH, Freund SMV, Blackford AN, Kimata Y, Goldstein RE, Jackson SP, Blundell TL, Dutcher SK, Gergely F, van Breugel M. Ochi T, et al. Structure. 2020 Jun 2;28(6):674-689.e11. doi: 10.1016/j.str.2020.04.010. Epub 2020 May 5. Structure. 2020. PMID: 32375023 Free PMC article.
WDR62 is associated with the spindle pole and is mutated in human microcephaly.
Nicholas AK, Khurshid M, Désir J, Carvalho OP, Cox JJ, Thornton G, Kausar R, Ansar M, Ahmad W, Verloes A, Passemard S, Misson JP, Lindsay S, Gergely F, Dobyns WB, Roberts E, Abramowicz M, Woods CG. Nicholas AK, et al. Nat Genet. 2010 Nov;42(11):1010-4. doi: 10.1038/ng.682. Epub 2010 Oct 3. Nat Genet. 2010. PMID: 20890279 Free PMC article.
Centrosomal TACCtics.
Gergely F. Gergely F. Bioessays. 2002 Oct;24(10):915-25. doi: 10.1002/bies.10162. Bioessays. 2002. PMID: 12325124 Review.
51 results