de Wind N - Search Results

1

Functional analysis helps to clarify the clinical importance of unclassified variants in DNA mismatch repair genes.

Ou J, Niessen RC, Lützen A, Sijmons RH, Kleibeuker JH, de Wind N, Rasmussen LJ, Hofstra RM. Ou J, et al. Among authors: de wind n. Hum Mutat. 2007 Nov;28(11):1047-54. doi: 10.1002/humu.20580. Hum Mutat. 2007. PMID: 17594722 Review.

2

HNPCC-like cancer predisposition in mice through simultaneous loss of Msh3 and Msh6 mismatch-repair protein functions.

de Wind N, Dekker M, Claij N, Jansen L, van Klink Y, Radman M, Riggins G, van der Valk M, van't Wout K, te Riele H. de Wind N, et al. Nat Genet. 1999 Nov;23(3):359-62. doi: 10.1038/15544. Nat Genet. 1999. PMID: 10545954

3

The crystal structure of DNA mismatch repair protein MutS binding to a G x T mismatch.

Lamers MH, Perrakis A, Enzlin JH, Winterwerp HH, de Wind N, Sixma TK. Lamers MH, et al. Among authors: de wind n. Nature. 2000 Oct 12;407(6805):711-7. doi: 10.1038/35037523. Nature. 2000. PMID: 11048711

4

Mismatch repair: praying for genome stability.

de Wind N, Hays JB. de Wind N, et al. Curr Biol. 2001 Jul 24;11(14):R545-8. doi: 10.1016/s0960-9822(01)00338-4. Curr Biol. 2001. PMID: 11509249 Free article. No abstract available.

5

Mismatch repair protein Msh2 contributes to UVB-induced cell cycle arrest in epidermal and cultured mouse keratinocytes.

van Oosten M, Stout GJ, Backendorf C, Rebel H, de Wind N, Darroudi F, van Kranen HJ, de Gruijl FR, Mullenders LH. van Oosten M, et al. Among authors: de wind n, de gruijl fr. DNA Repair (Amst). 2005 Jan 2;4(1):81-9. doi: 10.1016/j.dnarep.2004.08.008. DNA Repair (Amst). 2005. PMID: 15533840

6

Spontaneous and mutagen-induced loss of DNA mismatch repair in Msh2-heterozygous mammalian cells.

Borgdorff V, van Hees-Stuivenberg S, Meijers CM, de Wind N. Borgdorff V, et al. Among authors: de wind n. Mutat Res. 2005 Jul 1;574(1-2):50-7. doi: 10.1016/j.mrfmmm.2005.01.021. Epub 2005 Apr 20. Mutat Res. 2005. PMID: 15914206

7

Functional analysis of HNPCC-related missense mutations in MSH2.

Lützen A, de Wind N, Georgijevic D, Nielsen FC, Rasmussen LJ. Lützen A, et al. Among authors: de wind n. Mutat Res. 2008 Oct 14;645(1-2):44-55. doi: 10.1016/j.mrfmmm.2008.08.015. Epub 2008 Sep 4. Mutat Res. 2008. PMID: 18822302

8

Sequence variant classification and reporting: recommendations for improving the interpretation of cancer susceptibility genetic test results.

Plon SE, Eccles DM, Easton D, Foulkes WD, Genuardi M, Greenblatt MS, Hogervorst FB, Hoogerbrugge N, Spurdle AB, Tavtigian SV; IARC Unclassified Genetic Variants Working Group. Plon SE, et al. Hum Mutat. 2008 Nov;29(11):1282-91. doi: 10.1002/humu.20880. Hum Mutat. 2008. PMID: 18951446 Free PMC article.

9

Tumor characteristics as an analytic tool for classifying genetic variants of uncertain clinical significance.

Hofstra RM, Spurdle AB, Eccles D, Foulkes WD, de Wind N, Hoogerbrugge N, Hogervorst FB; IARC Unclassified Genetic Variants Working Group. Hofstra RM, et al. Among authors: de wind n. Hum Mutat. 2008 Nov;29(11):1292-303. doi: 10.1002/humu.20894. Hum Mutat. 2008. PMID: 18951447 Free PMC article.

10

Assessment of functional effects of unclassified genetic variants.

Couch FJ, Rasmussen LJ, Hofstra R, Monteiro AN, Greenblatt MS, de Wind N; IARC Unclassified Genetic Variants Working Group. Couch FJ, et al. Among authors: de wind n. Hum Mutat. 2008 Nov;29(11):1314-26. doi: 10.1002/humu.20899. Hum Mutat. 2008. PMID: 18951449 Free PMC article.

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