Mensink RG - Search Results

1

MBD4 mutations are rare in gastric carcinomas with microsatellite instability.

Pinto M, Wu Y, Suriano G, Mensink RG, Duval A, Oliveira C, Carvalho B, Hamelin R, Seruca R, Hofstra RM. Pinto M, et al. Among authors: mensink rg. Cancer Genet Cytogenet. 2003 Sep;145(2):103-7. doi: 10.1016/s0165-4608(03)00062-1. Cancer Genet Cytogenet. 2003. PMID: 12935920

2

Somatic mutations in mismatch repair genes in sporadic gastric carcinomas are not a cause but a consequence of the mutator phenotype.

Pinto M, Wu Y, Mensink RG, Cirnes L, Seruca R, Hofstra RM. Pinto M, et al. Among authors: mensink rg. Cancer Genet Cytogenet. 2008 Jan 15;180(2):110-4. doi: 10.1016/j.cancergencyto.2007.09.022. Cancer Genet Cytogenet. 2008. PMID: 18206535

3

Association of hereditary nonpolyposis colorectal cancer-related tumors displaying low microsatellite instability with MSH6 germline mutations.

Wu Y, Berends MJ, Mensink RG, Kempinga C, Sijmons RH, van Der Zee AG, Hollema H, Kleibeuker JH, Buys CH, Hofstra RM. Wu Y, et al. Among authors: mensink rg. Am J Hum Genet. 1999 Nov;65(5):1291-8. doi: 10.1086/302612. Am J Hum Genet. 1999. PMID: 10521294 Free PMC article.

4

Molecular and clinical characteristics of MSH6 variants: an analysis of 25 index carriers of a germline variant.

Berends MJ, Wu Y, Sijmons RH, Mensink RG, van der Sluis T, Hordijk-Hos JM, de Vries EG, Hollema H, Karrenbeld A, Buys CH, van der Zee AG, Hofstra RM, Kleibeuker JH. Berends MJ, et al. Among authors: mensink rg. Am J Hum Genet. 2002 Jan;70(1):26-37. doi: 10.1086/337944. Am J Hum Genet. 2002. PMID: 11709755 Free PMC article.

5

MLH1 and MSH2 protein expression as a pre-screening marker in hereditary and non-hereditary endometrial hyperplasia and cancer.

Berends MJ, Hollema H, Wu Y, van Der Sluis T, Mensink RG, ten Hoor KA, Sijmons RH, de Vries EG, Pras E, Mourits MJ, Hofstra RM, Buys CH, Kleibeuker JH, van Der Zee AG. Berends MJ, et al. Among authors: mensink rg. Int J Cancer. 2001 May 1;92(3):398-403. doi: 10.1002/ijc.1206. Int J Cancer. 2001. PMID: 11291077

6

Germline mutations of EXO1 gene in patients with hereditary nonpolyposis colorectal cancer (HNPCC) and atypical HNPCC forms.

Wu Y, Berends MJ, Post JG, Mensink RG, Verlind E, Van Der Sluis T, Kempinga C, Sijmons RH, van der Zee AG, Hollema H, Kleibeuker JH, Buys CH, Hofstra RM. Wu Y, et al. Among authors: mensink rg. Gastroenterology. 2001 Jun;120(7):1580-7. doi: 10.1053/gast.2001.25117. Gastroenterology. 2001. PMID: 11375940

7

A role for MLH3 in hereditary nonpolyposis colorectal cancer.

Wu Y, Berends MJ, Sijmons RH, Mensink RG, Verlind E, Kooi KA, van der Sluis T, Kempinga C, van dDer Zee AG, Hollema H, Buys CH, Kleibeuker JH, Hofstra RM. Wu Y, et al. Among authors: mensink rg. Nat Genet. 2001 Oct;29(2):137-8. doi: 10.1038/ng1001-137. Nat Genet. 2001. PMID: 11586295

8

Adrenocortical adenocarcinoma in an MSH2 carrier: coincidence or causal relation?

Berends MJ, Cats A, Hollema H, Karrenbeld A, Beentjes JA, Sijmons RH, Mensink RG, Hofstra RM, Verschueren RC, Kleibeuker JH. Berends MJ, et al. Among authors: mensink rg. Hum Pathol. 2000 Dec;31(12):1522-7. doi: 10.1053/hupa.2000.20409. Hum Pathol. 2000. PMID: 11150379

9

Inclusion of malignant fibrous histiocytoma in the tumour spectrum associated with hereditary non-polyposis colorectal cancer.

Sijmons R, Hofstra R, Hollema H, Mensink R, van der Hout A, Hoekstra H, Kleibeuker J, Molenaar W, Wijnen J, Fodde R, Vasen H, Buys C. Sijmons R, et al. Genes Chromosomes Cancer. 2000 Dec;29(4):353-5. doi: 10.1002/1098-2264(2000)9999:9999<::aid-gcc1042>3.0.co;2-t. Genes Chromosomes Cancer. 2000. PMID: 11066081

10

Refinement by linkage analysis in two large families of the candidate region of the third locus (SCA3) for autosomal dominant cerebellar ataxia type I.

Verschuuren-Bemelmans CC, Brunt ER, Burton M, Mensink RG, van der Meulen MA, Smit NH, Stolte-Dijkstra I, Buys CH, Scheffer H. Verschuuren-Bemelmans CC, et al. Among authors: mensink rg. Hum Genet. 1995 Dec;96(6):691-4. doi: 10.1007/BF00210301. Hum Genet. 1995. PMID: 8522329

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