Minton JA - Search Results

1

Syndromic obesity and diabetes: changes in body composition with age and mutation analysis of ALMS1 in 12 United Kingdom kindreds with Alstrom syndrome.

Minton JA, Owen KR, Ricketts CJ, Crabtree N, Shaikh G, Ehtisham S, Porter JR, Carey C, Hodge D, Paisey R, Walker M, Barrett TG. Minton JA, et al. J Clin Endocrinol Metab. 2006 Aug;91(8):3110-6. doi: 10.1210/jc.2005-2633. Epub 2006 May 23. J Clin Endocrinol Metab. 2006. PMID: 16720663

2

Common variations in the ALMS1 gene do not contribute to susceptibility to type 2 diabetes in a large white UK population.

Patel S, Minton JA, Weedon MN, Frayling TM, Ricketts C, Hitman GA, McCarthy MI, Hattersley AT, Walker M, Barrett TG. Patel S, et al. Among authors: minton ja. Diabetologia. 2006 Jun;49(6):1209-13. doi: 10.1007/s00125-006-0227-2. Epub 2006 Apr 7. Diabetologia. 2006. PMID: 16601972

3

Thiamine-responsive megaloblastic anaemia syndrome: long-term follow-up and mutation analysis of seven families.

Ricketts CJ, Minton JA, Samuel J, Ariyawansa I, Wales JK, Lo IF, Barrett TG. Ricketts CJ, et al. Among authors: minton ja. Acta Paediatr. 2006 Jan;95(1):99-104. doi: 10.1080/08035250500323715. Acta Paediatr. 2006. PMID: 16373304

4

Association studies of genetic variation in the WFS1 gene and type 2 diabetes in U.K. populations.

Minton JA, Hattersley AT, Owen K, McCarthy MI, Walker M, Latif F, Barrett T, Frayling TM. Minton JA, et al. Diabetes. 2002 Apr;51(4):1287-90. doi: 10.2337/diabetes.51.4.1287. Diabetes. 2002. PMID: 11916957

5

Wolfram syndrome.

Minton JA, Rainbow LA, Ricketts C, Barrett TG. Minton JA, et al. Rev Endocr Metab Disord. 2003 Mar;4(1):53-9. doi: 10.1023/a:1021875403463. Rev Endocr Metab Disord. 2003. PMID: 12618560 Review. No abstract available.

6

Sodium-potassium ATPase 1 subunit is a molecular partner of Wolframin, an endoplasmic reticulum protein involved in ER stress.

Zatyka M, Ricketts C, da Silva Xavier G, Minton J, Fenton S, Hofmann-Thiel S, Rutter GA, Barrett TG. Zatyka M, et al. Hum Mol Genet. 2008 Jan 15;17(2):190-200. doi: 10.1093/hmg/ddm296. Epub 2007 Oct 18. Hum Mol Genet. 2008. PMID: 17947299 Free PMC article.

7

Wolcott-Rallison syndrome is the most common genetic cause of permanent neonatal diabetes in consanguineous families.

Rubio-Cabezas O, Patch AM, Minton JA, Flanagan SE, Edghill EL, Hussain K, Balafrej A, Deeb A, Buchanan CR, Jefferson IG, Mutair A; Neonatal Diabetes International Collaborative Group; Hattersley AT, Ellard S. Rubio-Cabezas O, et al. Among authors: minton ja. J Clin Endocrinol Metab. 2009 Nov;94(11):4162-70. doi: 10.1210/jc.2009-1137. Epub 2009 Oct 16. J Clin Endocrinol Metab. 2009. PMID: 19837917 Free PMC article.

8

Sequencing of candidate genes selected by beta cell experts in monogenic diabetes of unknown aetiology.

Edghill EL, Minton JA, Groves CJ, Flanagan SE, Patch AM, Rubio-Cabezas O, Shepherd M, Lenzen S, McCarthy MI, Ellard S, Hattersley AT. Edghill EL, et al. Among authors: minton ja. JOP. 2010 Jan 8;11(1):14-7. JOP. 2010. PMID: 20065546

9

Association analysis of 6,736 U.K. subjects provides replication and confirms TCF7L2 as a type 2 diabetes susceptibility gene with a substantial effect on individual risk.

Groves CJ, Zeggini E, Minton J, Frayling TM, Weedon MN, Rayner NW, Hitman GA, Walker M, Wiltshire S, Hattersley AT, McCarthy MI. Groves CJ, et al. Diabetes. 2006 Sep;55(9):2640-4. doi: 10.2337/db06-0355. Diabetes. 2006. PMID: 16936215

10

Mutation surveyor: software for DNA sequence analysis.

Minton JA, Flanagan SE, Ellard S. Minton JA, et al. Methods Mol Biol. 2011;688:143-53. doi: 10.1007/978-1-60761-947-5_10. Methods Mol Biol. 2011. PMID: 20938837

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