Wiegant WW - Search Results

1

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. 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

2

Role of Artemis in DSB repair and guarding chromosomal stability following exposure to ionizing radiation at different stages of cell cycle.

Darroudi F, Wiegant W, Meijers M, Friedl AA, van der Burg M, Fomina J, van Dongen JJ, van Gent DC, Zdzienicka MZ. Darroudi F, et al. Mutat Res. 2007 Feb 3;615(1-2):111-24. doi: 10.1016/j.mrfmmm.2006.11.029. Epub 2006 Dec 12. Mutat Res. 2007. PMID: 17169382

3

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. Among authors: wiegant ww. 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

4

Brca2 (XRCC11) deficiency results in enhanced mutagenesis.

Kraakman-van der Zwet M, Wiegant WW, Zdzienicka MZ. Kraakman-van der Zwet M, et al. Among authors: wiegant ww. Mutagenesis. 2003 Nov;18(6):521-5. doi: 10.1093/mutage/geg032. Mutagenesis. 2003. PMID: 14614187

5

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. Among authors: wiegant ww. 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.

6

Suppression of the DNA repair defects of BRCA2-deficient cells with heterologous protein fusions.

Saeki H, Siaud N, Christ N, Wiegant WW, van Buul PP, Han M, Zdzienicka MZ, Stark JM, Jasin M. Saeki H, et al. Among authors: wiegant ww. Proc Natl Acad Sci U S A. 2006 Jun 6;103(23):8768-73. doi: 10.1073/pnas.0600298103. Epub 2006 May 26. Proc Natl Acad Sci U S A. 2006. PMID: 16731627 Free PMC article.

7

A novel radiosensitive SCID patient with a pronounced G(2)/M sensitivity.

Wiegant WW, Meyers M, Verkaik NS, van der Burg M, Darroudi F, Romeijn R, Bernatowska E, Wolska-Kusnierz B, Mikoluc B, Jaspers NG, Vreeken C, Ijspeert H, Esveldt-van Lange RE, Friedl AA, de Villartay JP, Mullenders LH, van Dongen JJ, van Gent DC, Pastink A, Zdzienicka MZ. Wiegant WW, et al. DNA Repair (Amst). 2010 Apr 4;9(4):365-73. doi: 10.1016/j.dnarep.2009.12.004. Epub 2010 Jan 15. DNA Repair (Amst). 2010. PMID: 20079696

8

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

9

A DNA-PKcs mutation in a radiosensitive T-B- SCID patient inhibits Artemis activation and nonhomologous end-joining.

van der Burg M, Ijspeert H, Verkaik NS, Turul T, Wiegant WW, Morotomi-Yano K, Mari PO, Tezcan I, Chen DJ, Zdzienicka MZ, van Dongen JJ, van Gent DC. van der Burg M, et al. Among authors: wiegant ww. J Clin Invest. 2009 Jan;119(1):91-8. doi: 10.1172/JCI37141. Epub 2008 Dec 15. J Clin Invest. 2009. PMID: 19075392 Free PMC article.

10

A new type of radiosensitive T-B-NK+ severe combined immunodeficiency caused by a LIG4 mutation.

van der Burg M, van Veelen LR, Verkaik NS, Wiegant WW, Hartwig NG, Barendregt BH, Brugmans L, Raams A, Jaspers NG, Zdzienicka MZ, van Dongen JJ, van Gent DC. van der Burg M, et al. Among authors: wiegant ww. J Clin Invest. 2006 Jan;116(1):137-45. doi: 10.1172/JCI26121. Epub 2005 Dec 15. J Clin Invest. 2006. PMID: 16357942 Free PMC article.

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