Niessen RC - Search Results

1

Mononucleotide precedes dinucleotide repeat instability during colorectal tumour development in Lynch syndrome patients.

Ferreira AM, Westers H, Sousa S, Wu Y, Niessen RC, Olderode-Berends M, van der Sluis T, Reuvekamp PT, Seruca R, Kleibeuker JH, Hollema H, Sijmons RH, Hofstra RM. Ferreira AM, et al. Among authors: niessen rc. J Pathol. 2009 Sep;219(1):96-102. doi: 10.1002/path.2573. J Pathol. 2009. PMID: 19521971

2

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: niessen rc. Hum Mutat. 2007 Nov;28(11):1047-54. doi: 10.1002/humu.20580. Hum Mutat. 2007. PMID: 17594722 Review.

3

A database to support the interpretation of human mismatch repair gene variants.

Ou J, Niessen RC, Vonk J, Westers H, Hofstra RM, Sijmons RH. Ou J, et al. Among authors: niessen rc. Hum Mutat. 2008 Nov;29(11):1337-41. doi: 10.1002/humu.20907. Hum Mutat. 2008. PMID: 18951442

4

PMS2 involvement in patients suspected of Lynch syndrome.

Niessen RC, Kleibeuker JH, Westers H, Jager PO, Rozeveld D, Bos KK, Boersma-van Ek W, Hollema H, Sijmons RH, Hofstra RM. Niessen RC, et al. Genes Chromosomes Cancer. 2009 Apr;48(4):322-9. doi: 10.1002/gcc.20642. Genes Chromosomes Cancer. 2009. PMID: 19132747

5

Biochemical characterization of MLH3 missense mutations does not reveal an apparent role of MLH3 in Lynch syndrome.

Ou J, Rasmussen M, Westers H, Andersen SD, Jager PO, Kooi KA, Niessen RC, Eggen BJ, Nielsen FC, Kleibeuker JH, Sijmons RH, Rasmussen LJ, Hofstra RM. Ou J, et al. Among authors: niessen rc. Genes Chromosomes Cancer. 2009 Apr;48(4):340-50. doi: 10.1002/gcc.20644. Genes Chromosomes Cancer. 2009. PMID: 19156873 Free article.

6

Do microsatellite instability profiles really differ between colorectal and endometrial tumors?

Ferreira AM, Westers H, Wu Y, Niessen RC, Olderode-Berends M, van der Sluis T, van der Zee AG, Hollema H, Kleibeuker JH, Sijmons RH, Hofstra RM. Ferreira AM, et al. Among authors: niessen rc. Genes Chromosomes Cancer. 2009 Jul;48(7):552-7. doi: 10.1002/gcc.20664. Genes Chromosomes Cancer. 2009. PMID: 19373783

7

Germline hypermethylation of MLH1 and EPCAM deletions are a frequent cause of Lynch syndrome.

Niessen RC, Hofstra RM, Westers H, Ligtenberg MJ, Kooi K, Jager PO, de Groote ML, Dijkhuizen T, Olderode-Berends MJ, Hollema H, Kleibeuker JH, Sijmons RH. Niessen RC, et al. Genes Chromosomes Cancer. 2009 Aug;48(8):737-44. doi: 10.1002/gcc.20678. Genes Chromosomes Cancer. 2009. PMID: 19455606

8

Hereditary non-polyposis colorectal cancer: identification of mutation carriers and assessing pathogenicity of mutations.

Niessen RC, Sijmons RH, Berends MJ, Ou J, Hofstra RM, Kleibeuker JH. Niessen RC, et al. Scand J Gastroenterol Suppl. 2004;(241):70-7. doi: 10.1080/00855920410010915. Scand J Gastroenterol Suppl. 2004. PMID: 15696853 Review.

9

Identification of mismatch repair gene mutations in young patients with colorectal cancer and in patients with multiple tumours associated with hereditary non-polyposis colorectal cancer.

Niessen RC, Berends MJ, Wu Y, Sijmons RH, Hollema H, Ligtenberg MJ, de Walle HE, de Vries EG, Karrenbeld A, Buys CH, van der Zee AG, Hofstra RM, Kleibeuker JH. Niessen RC, et al. Gut. 2006 Dec;55(12):1781-8. doi: 10.1136/gut.2005.090159. Epub 2006 Apr 24. Gut. 2006. PMID: 16636019 Free PMC article.

10

BRAF-V600E is not involved in the colorectal tumorigenesis of HNPCC in patients with functional MLH1 and MSH2 genes.

Domingo E, Niessen RC, Oliveira C, Alhopuro P, Moutinho C, Espín E, Armengol M, Sijmons RH, Kleibeuker JH, Seruca R, Aaltonen LA, Imai K, Yamamoto H, Schwartz S Jr, Hofstra RM. Domingo E, et al. Among authors: niessen rc. Oncogene. 2005 Jun 2;24(24):3995-8. doi: 10.1038/sj.onc.1208569. Oncogene. 2005. PMID: 15782118

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