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The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J.
Levitus M, Waisfisz Q, Godthelp BC, de Vries Y, Hussain S, Wiegant WW, Elghalbzouri-Maghrani E, Steltenpool J, Rooimans MA, Pals G, Arwert F, Mathew CG, Zdzienicka MZ, Hiom K, De Winter JP, Joenje H. Levitus M, et al. Among authors: de vries y, de winter jp. Nat Genet. 2005 Sep;37(9):934-5. doi: 10.1038/ng1625. Epub 2005 Aug 21. Nat Genet. 2005. PMID: 16116423
Multiple TPR motifs characterize the Fanconi anemia FANCG protein.
Blom E, van de Vrugt HJ, de Vries Y, de Winter JP, Arwert F, Joenje H. Blom E, et al. Among authors: de vries y, de winter jp. DNA Repair (Amst). 2004 Jan 5;3(1):77-84. doi: 10.1016/j.dnarep.2003.09.007. DNA Repair (Amst). 2004. PMID: 14697762
Fanconi anemia is associated with a defect in the BRCA2 partner PALB2.
Xia B, Dorsman JC, Ameziane N, de Vries Y, Rooimans MA, Sheng Q, Pals G, Errami A, Gluckman E, Llera J, Wang W, Livingston DM, Joenje H, de Winter JP. Xia B, et al. Among authors: de vries y, de winter jp. Nat Genet. 2007 Feb;39(2):159-61. doi: 10.1038/ng1942. Epub 2006 Dec 31. Nat Genet. 2007. PMID: 17200672
Genetic subtyping of Fanconi anemia by comprehensive mutation screening.
Ameziane N, Errami A, Léveillé F, Fontaine C, de Vries Y, van Spaendonk RM, de Winter JP, Pals G, Joenje H. Ameziane N, et al. Among authors: de vries y, de winter jp. Hum Mutat. 2008 Jan;29(1):159-66. doi: 10.1002/humu.20625. Hum Mutat. 2008. PMID: 17924555
Mice with a targeted disruption of the Fanconi anemia homolog Fanca.
Cheng NC, van de Vrugt HJ, van der Valk MA, Oostra AB, Krimpenfort P, de Vries Y, Joenje H, Berns A, Arwert F. Cheng NC, et al. Among authors: de vries y. Hum Mol Genet. 2000 Jul 22;9(12):1805-11. doi: 10.1093/hmg/9.12.1805. Hum Mol Genet. 2000. PMID: 10915769
102 results