Curtis A - Search Results

1

Absence of a genetic association between IL-1RN and IL-1B gene polymorphisms in ulcerative colitis and Crohn disease in multiple populations from northeast England.

Craggs A, West S, Curtis A, Welfare M, Hudson M, Donaldson P, Mansfield J. Craggs A, et al. Among authors: curtis a. Scand J Gastroenterol. 2001 Nov;36(11):1173-8. doi: 10.1080/00365520152584806. Scand J Gastroenterol. 2001. PMID: 11686217

2

Four novel germ-line mutations in the APC gene detected by heteroduplex analysis.

Hamzehloei T, West SP, Chapman PD, Burn J, Curtis A. Hamzehloei T, et al. Among authors: curtis a. Hum Mol Genet. 1994 Jun;3(6):1023-4. doi: 10.1093/hmg/3.6.1023. Hum Mol Genet. 1994. PMID: 7951218 No abstract available.

3

Mutation detection in exons 1-14 of the adenomatous polyposis coli gene: identification of an alternatively spliced transcript.

Hamzehloei T, West SP, Chapman P, Burn J, Curtis A. Hamzehloei T, et al. Among authors: curtis a. Mol Cell Probes. 1996 Oct;10(5):379-85. doi: 10.1006/mcpr.1996.0051. Mol Cell Probes. 1996. PMID: 8910893

4

Familial adenomatous polyposis associated with multiple adrenal adenomas in a patient with a rare 3' APC mutation.

Kartheuser A, Walon C, West S, Breukel C, Detry R, Gribomont AC, Hamzehloei T, Hoang P, Maiter D, Pringot J, Rahier J, Khan PM, Curtis A, Burn J, Fodde R, Verellen-Dumoulin C. Kartheuser A, et al. Among authors: curtis a. J Med Genet. 1999 Jan;36(1):65-7. J Med Genet. 1999. PMID: 9950370 Free PMC article.

5

Detection of mutations in mismatch repair genes in Portuguese families with hereditary non-polyposis colorectal cancer (HNPCC) by a multi-method approach.

Fidalgo P, Almeida MR, West S, Gaspar C, Maia L, Wijnen J, Albuquerque C, Curtis A, Cravo M, Fodde R, Leitao CN, Burn J. Fidalgo P, et al. Among authors: curtis a. Eur J Hum Genet. 2000 Jan;8(1):49-53. doi: 10.1038/sj.ejhg.5200393. Eur J Hum Genet. 2000. PMID: 10713887

6

The genetic background of familial adenomatous polyposis. Linkage analysis, the APC gene identification and mutation screening.

Kartheuser A, West S, Walon C, Curtis A, Hamzehloei T, Lannoy N, Michiels G, Smaers M, Chapman P, Burn J, et al. Kartheuser A, et al. Among authors: curtis a. Acta Gastroenterol Belg. 1995 Sep-Dec;58(5-6):433-51. Acta Gastroenterol Belg. 1995. PMID: 8776001 Review.

7

Dinucleotide repeat polymorphism at the DXS556 locus.

Thiselton DL, Kamakari S, Curtis AR, Coleman MP, Davies KE, Lindsay S, Bhattacharya S. Thiselton DL, et al. Among authors: curtis ar. Hum Mol Genet. 1993 May;2(5):613. doi: 10.1093/hmg/2.5.613. Hum Mol Genet. 1993. PMID: 8518809 No abstract available.

8

The haplotype distribution of the delta F508 mutation in cystic fibrosis families in Scotland.

McIntosh I, Curtis A, Lorenzo ML, Keston M, Gilfillan AJ, Morris G, Brock DJ. McIntosh I, et al. Among authors: curtis a. Hum Genet. 1990 Sep;85(4):419-20. doi: 10.1007/BF02428290. Hum Genet. 1990. PMID: 2210756

9

Isolation and characterization of three microsatellite markers in the proximal long arm of the human X chromosome.

Lindsay S, Curtis AR, Roustan P, Kamakari S, Thiselton DL, Stephenson A, Bhattacharya SS. Lindsay S, et al. Among authors: curtis ar. Genomics. 1993 Jul;17(1):208-10. doi: 10.1006/geno.1993.1303. Genomics. 1993. PMID: 8406451

10

Two dinucleotide repeat polymorphisms at the DXS571 locus.

Curtis AR, Roustan P, Kamakari S, Thiselton D, Lindsay S, Bhattacharya SS. Curtis AR, et al. Hum Mol Genet. 1992 Dec;1(9):776. doi: 10.1093/hmg/1.9.776. Hum Mol Genet. 1992. PMID: 1302618 No abstract available.

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