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X-linked inheritance of Fanconi anemia complementation group B.
Meetei AR, Levitus M, Xue Y, Medhurst AL, Zwaan M, Ling C, Rooimans MA, Bier P, Hoatlin M, Pals G, de Winter JP, Wang W, Joenje H. Meetei AR, et al. Nat Genet. 2004 Nov;36(11):1219-24. doi: 10.1038/ng1458. Epub 2004 Oct 24. Nat Genet. 2004. PMID: 15502827
A novel ubiquitin ligase is deficient in Fanconi anemia.
Meetei AR, de Winter JP, Medhurst AL, Wallisch M, Waisfisz Q, van de Vrugt HJ, Oostra AB, Yan Z, Ling C, Bishop CE, Hoatlin ME, Joenje H, Wang W. Meetei AR, et al. Nat Genet. 2003 Oct;35(2):165-70. doi: 10.1038/ng1241. Epub 2003 Sep 14. Nat Genet. 2003. PMID: 12973351
Evidence for subcomplexes in the Fanconi anemia pathway.
Medhurst AL, Laghmani el H, Steltenpool J, Ferrer M, Fontaine C, de Groot J, Rooimans MA, Scheper RJ, Meetei AR, Wang W, Joenje H, de Winter JP. Medhurst AL, et al. Among authors: meetei ar. Blood. 2006 Sep 15;108(6):2072-80. doi: 10.1182/blood-2005-11-008151. Epub 2006 May 23. Blood. 2006. PMID: 16720839 Free PMC article.
Impaired FANCD2 monoubiquitination and hypersensitivity to camptothecin uniquely characterize Fanconi anemia complementation group M.
Singh TR, Bakker ST, Agarwal S, Jansen M, Grassman E, Godthelp BC, Ali AM, Du CH, Rooimans MA, Fan Q, Wahengbam K, Steltenpool J, Andreassen PR, Williams DA, Joenje H, de Winter JP, Meetei AR. Singh TR, et al. Among authors: meetei ar. Blood. 2009 Jul 2;114(1):174-80. doi: 10.1182/blood-2009-02-207811. Epub 2009 May 7. Blood. 2009. PMID: 19423727 Free PMC article.
41 results