Dunlop MG - Search Results

1

The MSH2 c.388_389del mutation shows a founder effect in Portuguese Lynch syndrome families.

Pinheiro M, Pinto C, Peixoto A, Veiga I, Mesquita B, Henrique R, Lopes P, Sousa O, Fragoso M, Dias LM, Baptista M, Marinho C, Mangold E, Vaccaro C, Evans DG, Farrington S, Dunlop MG, Teixeira MR. Pinheiro M, et al. Among authors: dunlop mg. Clin Genet. 2013 Sep;84(3):244-50. doi: 10.1111/cge.12062. Epub 2012 Dec 27. Clin Genet. 2013. PMID: 23170986

2

Suggested screening guidelines for familial colorectal cancer.

Hodgson SV, Bishop DT, Dunlop MG, Evans DG, Northover JM. Hodgson SV, et al. Among authors: dunlop mg. J Med Screen. 1995;2(1):45-51. doi: 10.1177/096914139500200112. J Med Screen. 1995. PMID: 7497146

3

Genetic instability occurs in the majority of young patients with colorectal cancer.

Liu B, Farrington SM, Petersen GM, Hamilton SR, Parsons R, Papadopoulos N, Fujiwara T, Jen J, Kinzler KW, Wyllie AH, Vogelstein B, Dunlop MG, et al. Liu B, et al. Among authors: dunlop mg. Nat Med. 1995 Apr;1(4):348-52. doi: 10.1038/nm0495-348. Nat Med. 1995. PMID: 7585065

4

Detailed physical and deletion mapping of 8p with isolation of YAC clones from tumour suppressor loci involved in colorectal cancer.

Farrington SM, Cunningham C, Boyle SM, Wyllie AH, Dunlop MG. Farrington SM, et al. Among authors: dunlop mg. Oncogene. 1996 Apr 18;12(8):1803-8. Oncogene. 1996. PMID: 8622901

5

Cancer risk associated with germline DNA mismatch repair gene mutations.

Dunlop MG, Farrington SM, Carothers AD, Wyllie AH, Sharp L, Burn J, Liu B, Kinzler KW, Vogelstein B. Dunlop MG, et al. Hum Mol Genet. 1997 Jan;6(1):105-10. doi: 10.1093/hmg/6.1.105. Hum Mol Genet. 1997. PMID: 9002677

6

Systematic analysis of hMSH2 and hMLH1 in young colon cancer patients and controls.

Farrington SM, Lin-Goerke J, Ling J, Wang Y, Burczak JD, Robbins DJ, Dunlop MG. Farrington SM, et al. Among authors: dunlop mg. Am J Hum Genet. 1998 Sep;63(3):749-59. doi: 10.1086/301996. Am J Hum Genet. 1998. PMID: 9718327 Free PMC article.

7

Mosaicism and sporadic familial adenomatous polyposis.

Farrington SM, Dunlop MG. Farrington SM, et al. Among authors: dunlop mg. Am J Hum Genet. 1999 Feb;64(2):653-8. doi: 10.1086/302236. Am J Hum Genet. 1999. PMID: 9973305 Free PMC article. No abstract available.

8

Sequence interruptions confer differential stability at microsatellite alleles in mismatch repair-deficient cells.

Bacon AL, Farrington SM, Dunlop MG. Bacon AL, et al. Among authors: dunlop mg. Hum Mol Genet. 2000 Nov 1;9(18):2707-13. doi: 10.1093/hmg/9.18.2707. Hum Mol Genet. 2000. PMID: 11063729

9

Population carrier frequency of hMSH2 and hMLH1 mutations.

Dunlop MG, Farrington SM, Nicholl I, Aaltonen L, Petersen G, Porteous M, Carothers A. Dunlop MG, et al. Br J Cancer. 2000 Dec;83(12):1643-5. doi: 10.1054/bjoc.2000.1520. Br J Cancer. 2000. PMID: 11104559 Free PMC article.

10

Hypermutability at a poly(A/T) tract in the human germline.

Bacon AL, Dunlop MG, Farrington SM. Bacon AL, et al. Among authors: dunlop mg. Nucleic Acids Res. 2001 Nov 1;29(21):4405-13. doi: 10.1093/nar/29.21.4405. Nucleic Acids Res. 2001. PMID: 11691928 Free PMC article.

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