de Wind N - Search Results

1

A cell-free assay for the functional analysis of variants of the mismatch repair protein MLH1.

Drost M, Zonneveld Je, van Dijk L, Morreau H, Tops CM, Vasen HF, Wijnen JT, de Wind N. Drost M, et al. Among authors: de wind n. Hum Mutat. 2010 Mar;31(3):247-53. doi: 10.1002/humu.21180. Hum Mutat. 2010. PMID: 20020535

2

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

3

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

4

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.

5

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

6

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.

7

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.

8

Deciphering the colon cancer genes--report of the InSiGHT-Human Variome Project Workshop, UNESCO, Paris 2010.

Kohonen-Corish MR, Macrae F, Genuardi M, Aretz S, Bapat B, Bernstein IT, Burn J, Cotton RG, den Dunnen JT, Frebourg T, Greenblatt MS, Hofstra R, Holinski-Feder E, Lappalainen I, Lindblom A, Maglott D, Møller P, Morreau H, Möslein G, Sijmons R, Spurdle AB, Tavtigian S, Tops CM, Weber TK, de Wind N, Woods MO; Contributors to the InSiGHT-HVP Workshop. Kohonen-Corish MR, et al. Among authors: de wind n. Hum Mutat. 2011 Apr;32(4):491-4. doi: 10.1002/humu.21450. Epub 2011 Mar 8. Hum Mutat. 2011. PMID: 21387463

9

Transient suppression of MLH1 allows effective single-nucleotide substitution by single-stranded DNA oligonucleotides.

Dekker M, de Vries S, Aarts M, Dekker R, Brouwers C, Wiebenga O, de Wind N, Cantelli E, Tonelli R, Te Riele H. Dekker M, et al. Among authors: de wind n, de vries s. Mutat Res. 2011 Oct 1;715(1-2):52-60. doi: 10.1016/j.mrfmmm.2011.07.008. Epub 2011 Jul 27. Mutat Res. 2011. PMID: 21801734

10

A rapid and cell-free assay to test the activity of lynch syndrome-associated MSH2 and MSH6 missense variants.

Drost M, Zonneveld JB, van Hees S, Rasmussen LJ, Hofstra RM, de Wind N. Drost M, et al. Among authors: de wind n. Hum Mutat. 2012 Mar;33(3):488-94. doi: 10.1002/humu.22000. Epub 2011 Dec 29. Hum Mutat. 2012. PMID: 22102614

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