Buys CH - Search Results

1

DNA mismatch repair gene mutations in 55 kindreds with verified or putative hereditary non-polyposis colorectal cancer.

Nyström-Lahti M, Wu Y, Moisio AL, Hofstra RM, Osinga J, Mecklin JP, Järvinen HJ, Leisti J, Buys CH, de la Chapelle A, Peltomäki P. Nyström-Lahti M, et al. Among authors: buys ch. Hum Mol Genet. 1996 Jun;5(6):763-9. doi: 10.1093/hmg/5.6.763. Hum Mol Genet. 1996. PMID: 8776590

2

MSH2 and MLH1 mutations in sporadic replication error-positive colorectal carcinoma as assessed by two-dimensional DNA electrophoresis.

Wu Y, Nyström-Lahti M, Osinga J, Looman MW, Peltomäki P, Aaltonen LA, de la Chapelle A, Hofstra RM, Buys CH. Wu Y, et al. Among authors: buys ch. Genes Chromosomes Cancer. 1997 Apr;18(4):269-78. Genes Chromosomes Cancer. 1997. PMID: 9087566

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: buys ch. 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

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: buys ch. Nat Genet. 2001 Oct;29(2):137-8. doi: 10.1038/ng1001-137. Nat Genet. 2001. PMID: 11586295

5

MUTYH and the mismatch repair system: partners in crime?

Niessen RC, Sijmons RH, Ou J, Olthof SG, Osinga J, Ligtenberg MJ, Hogervorst FB, Weiss MM, Tops CM, Hes FJ, de Bock GH, Buys CH, Kleibeuker JH, Hofstra RM. Niessen RC, et al. Among authors: buys ch. Hum Genet. 2006 Mar;119(1-2):206-11. doi: 10.1007/s00439-005-0118-5. Epub 2006 Jan 12. Hum Genet. 2006. PMID: 16408224

6

Comprehensive and accurate mutation scanning of the CFTR gene by two-dimensional DNA electrophoresis.

Wu Y, Hofstra RM, Scheffer H, Uitterlinden AG, Mullaart E, Buys CH, Vijg J. Wu Y, et al. Among authors: buys ch. Hum Mutat. 1996;8(2):160-7. doi: 10.1002/(SICI)1098-1004(1996)8:2<160::AID-HUMU8>3.0.CO;2-F. Hum Mutat. 1996. PMID: 8844214

7

Mutation analysis of the RET receptor tyrosine kinase in Hirschsprung disease.

Angrist M, Bolk S, Thiel B, Puffenberger EG, Hofstra RM, Buys CH, Cass DT, Chakravarti A. Angrist M, et al. Among authors: buys ch. Hum Mol Genet. 1995 May;4(5):821-30. doi: 10.1093/hmg/4.5.821. Hum Mol Genet. 1995. PMID: 7633441

8

A sublocus of the multicopy microsatellite marker CMS1 maps proximal to spinal muscular atrophy (SMA) as shown by recombinant analysis.

van der Steege G, Cobben JM, Osinga J, Scheffer H, van Ommen GJ, Buys CH. van der Steege G, et al. Among authors: buys ch. Hum Genet. 1995 Nov;96(5):589-91. doi: 10.1007/BF00197416. Hum Genet. 1995. PMID: 8530008

9

Mutation analysis of the RET proto-oncogene in Dutch families with MEN 2A, MEN 2B and FMTC: two novel mutations and one de novo mutation for MEN 2A.

Landsvater RM, Jansen RP, Hofstra RM, Buys CH, Lips CJ, Ploos van Amstel HK. Landsvater RM, et al. Among authors: buys ch. Hum Genet. 1996 Jan;97(1):11-4. doi: 10.1007/BF00218825. Hum Genet. 1996. PMID: 8557249

10

No mutations found by RET mutation scanning in sporadic and hereditary neuroblastoma.

Hofstra RM, Cheng NC, Hansen C, Stulp RP, Stelwagen T, Clausen N, Tommerup N, Caron H, Westerveld A, Versteeg R, Buys CH. Hofstra RM, et al. Among authors: buys ch. Hum Genet. 1996 Mar;97(3):362-4. doi: 10.1007/BF02185773. Hum Genet. 1996. PMID: 8786083

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