Dronsfield M - Search Results

1

High throughput DNA sequence variant detection by conformation sensitive capillary electrophoresis and automated peak comparison.

Davies H, Dicks E, Stephens P, Cox C, Teague J, Greenman C, Bignell G, O'meara S, Edkins S, Parker A, Stevens C, Menzies A, Blow M, Bottomley B, Dronsfield M, Futreal PA, Stratton MR, Wooster R. Davies H, et al. Among authors: dronsfield m. Genomics. 2006 Mar;87(3):427-32. doi: 10.1016/j.ygeno.2005.11.008. Epub 2006 Jan 9. Genomics. 2006. PMID: 16406726 Free article.

2

The mitochondrial tRNA[Leu(UUR)] A to G 3243 mutation is associated with insulin-dependent and non-insulin-dependent diabetes in a Chinese population.

Smith PR, Dronsfield MJ, Mijovic CH, Hattersley AT, Yeung VT, Cockram C, Chan JC, Barnett AH, Bain SC. Smith PR, et al. Among authors: dronsfield mj. Diabet Med. 1997 Dec;14(12):1026-31. doi: 10.1002/(SICI)1096-9136(199712)14:12<1026::AID-DIA514>3.0.CO;2-M. Diabet Med. 1997. PMID: 9455929

3

Susceptibility to human type 1 diabetes at IDDM2 is determined by tandem repeat variation at the insulin gene minisatellite locus.

Bennett ST, Lucassen AM, Gough SC, Powell EE, Undlien DE, Pritchard LE, Merriman ME, Kawaguchi Y, Dronsfield MJ, Pociot F, et al. Bennett ST, et al. Among authors: dronsfield mj. Nat Genet. 1995 Mar;9(3):284-92. doi: 10.1038/ng0395-284. Nat Genet. 1995. PMID: 7773291

4

Examination of two genetic polymorphisms within the renin-angiotensin system: no evidence for an association with nephropathy in IDDM.

Chowdhury TA, Dronsfield MJ, Kumar S, Gough SL, Gibson SP, Khatoon A, MacDonald F, Rowe BR, Dunger DB, Dean JD, Davies SJ, Webber J, Smith PR, Mackin P, Marshall SM, Adu D, Morris PJ, Todd JA, Barnett AH, Boulton AJ, Bain SC. Chowdhury TA, et al. Among authors: dronsfield mj. Diabetologia. 1996 Sep;39(9):1108-14. doi: 10.1007/BF00400661. Diabetologia. 1996. PMID: 8877296

5

A missense mutation in the hepatocyte nuclear factor 4 alpha gene in a UK pedigree with maturity-onset diabetes of the young.

Bulman MP, Dronsfield MJ, Frayling T, Appleton M, Bain SC, Ellard S, Hattersley AT. Bulman MP, et al. Among authors: dronsfield mj. Diabetologia. 1997 Jul;40(7):859-62. doi: 10.1007/s001250050760. Diabetologia. 1997. PMID: 9243109

6

Allelic drop-out in exon 2 of the hepatocyte nuclear factor-1alpha gene hinders the identification of mutations in three families with maturity-onset diabetes of the young.

Ellard S, Bulman MP, Frayling TM, Allen LI, Dronsfield MJ, Tack CJ, Hattersley AT. Ellard S, et al. Among authors: dronsfield mj. Diabetes. 1999 Apr;48(4):921-3. doi: 10.2337/diabetes.48.4.921. Diabetes. 1999. PMID: 10102714 No abstract available.

7

The 5'-end polymorphism of the aldose reductase gene is not associated with diabetic nephropathy in Caucasian type I diabetic patients.

Dyer PH, Chowdhury TA, Dronsfield MJ, Dunger D, Barnett AH, Bain SC. Dyer PH, et al. Among authors: dronsfield mj. Diabetologia. 1999 Aug;42(8):1030-1. doi: 10.1007/s001250051266. Diabetologia. 1999. PMID: 10491768 No abstract available.

8

Altered insulin secretory responses to glucose in diabetic and nondiabetic subjects with mutations in the diabetes susceptibility gene MODY3 on chromosome 12.

Byrne MM, Sturis J, Menzel S, Yamagata K, Fajans SS, Dronsfield MJ, Bain SC, Hattersley AT, Velho G, Froguel P, Bell GI, Polonsky KS. Byrne MM, et al. Among authors: dronsfield mj. Diabetes. 1996 Nov;45(11):1503-10. doi: 10.2337/diab.45.11.1503. Diabetes. 1996. PMID: 8866553

9

Mutations in the hepatocyte nuclear factor-1alpha gene are a common cause of maturity-onset diabetes of the young in the U.K.

Frayling TM, Bulamn MP, Ellard S, Appleton M, Dronsfield MJ, Mackie AD, Baird JD, Kaisaki PJ, Yamagata K, Bell GI, Bain SC, Hattersley AT. Frayling TM, et al. Among authors: dronsfield mj. Diabetes. 1997 Apr;46(4):720-5. doi: 10.2337/diab.46.4.720. Diabetes. 1997. PMID: 9075818

10

Angiotensin II receptor gene polymorphisms and risk of myocardial infarction.

Choudhury TA, Dronsfield MJ, Jones AF, Bain SC. Choudhury TA, et al. Among authors: dronsfield mj. Lancet. 1994 Nov 26;344(8935):1502-3. doi: 10.1016/s0140-6736(94)90318-2. Lancet. 1994. PMID: 7968135 No abstract available.

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