Godthelp BC - Search Results

1

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: godthelp bc. Nat Genet. 2005 Sep;37(9):934-5. doi: 10.1038/ng1625. Epub 2005 Aug 21. Nat Genet. 2005. PMID: 16116423

2

Reduced fertility and hypersensitivity to mitomycin C characterize Fancg/Xrcc9 null mice.

Koomen M, Cheng NC, van de Vrugt HJ, Godthelp BC, van der Valk MA, Oostra AB, Zdzienicka MZ, Joenje H, Arwert F. Koomen M, et al. Among authors: godthelp bc. Hum Mol Genet. 2002 Feb 1;11(3):273-81. doi: 10.1093/hmg/11.3.273. Hum Mol Genet. 2002. PMID: 11823446

3

Impaired DNA damage-induced nuclear Rad51 foci formation uniquely characterizes Fanconi anemia group D1.

Godthelp BC, Artwert F, Joenje H, Zdzienicka MZ. Godthelp BC, et al. Oncogene. 2002 Jul 25;21(32):5002-5. doi: 10.1038/sj.onc.1205656. Oncogene. 2002. PMID: 12118380

4

Inducibility of nuclear Rad51 foci after DNA damage distinguishes all Fanconi anemia complementation groups from D1/BRCA2.

Godthelp BC, Wiegant WW, Waisfisz Q, Medhurst AL, Arwert F, Joenje H, Zdzienicka MZ. Godthelp BC, et al. Mutat Res. 2006 Feb 22;594(1-2):39-48. doi: 10.1016/j.mrfmmm.2005.07.008. Epub 2005 Sep 8. Mutat Res. 2006. PMID: 16154163

5

Warsaw breakage syndrome, a cohesinopathy associated with mutations in the XPD helicase family member DDX11/ChlR1.

van der Lelij P, Chrzanowska KH, Godthelp BC, Rooimans MA, Oostra AB, Stumm M, Zdzienicka MZ, Joenje H, de Winter JP. van der Lelij P, et al. Among authors: godthelp bc. Am J Hum Genet. 2010 Feb 12;86(2):262-6. doi: 10.1016/j.ajhg.2010.01.008. Epub 2010 Feb 4. Am J Hum Genet. 2010. PMID: 20137776 Free PMC article.

6

Cellular characterization of cells from the Fanconi anemia complementation group, FA-D1/BRCA2.

Godthelp BC, van Buul PP, Jaspers NG, Elghalbzouri-Maghrani E, van Duijn-Goedhart A, Arwert F, Joenje H, Zdzienicka MZ. Godthelp BC, et al. Mutat Res. 2006 Oct 10;601(1-2):191-201. doi: 10.1016/j.mrfmmm.2006.07.003. Epub 2006 Aug 21. Mutat Res. 2006. PMID: 16920162

7

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: godthelp bc. 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.

8

The cellular phenotype of Roberts syndrome fibroblasts as revealed by ectopic expression of ESCO2.

van der Lelij P, Godthelp BC, van Zon W, van Gosliga D, Oostra AB, Steltenpool J, de Groot J, Scheper RJ, Wolthuis RM, Waisfisz Q, Darroudi F, Joenje H, de Winter JP. van der Lelij P, et al. Among authors: godthelp bc. PLoS One. 2009 Sep 7;4(9):e6936. doi: 10.1371/journal.pone.0006936. PLoS One. 2009. PMID: 19738907 Free PMC article.

9

Mammalian Rad51C contributes to DNA cross-link resistance, sister chromatid cohesion and genomic stability.

Godthelp BC, Wiegant WW, van Duijn-Goedhart A, Schärer OD, van Buul PP, Kanaar R, Zdzienicka MZ. Godthelp BC, et al. Nucleic Acids Res. 2002 May 15;30(10):2172-82. doi: 10.1093/nar/30.10.2172. Nucleic Acids Res. 2002. PMID: 12000837 Free PMC article.

10

Chinese hamster cell mutant, V-C8, a model for analysis of Brca2 function.

Wiegant WW, Overmeer RM, Godthelp BC, van Buul PP, Zdzienicka MZ. Wiegant WW, et al. Among authors: godthelp bc. Mutat Res. 2006 Aug 30;600(1-2):79-88. doi: 10.1016/j.mrfmmm.2006.03.001. Epub 2006 Apr 27. Mutat Res. 2006. PMID: 16643964

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