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Items: 8

1.

Common variants in WFS1 confer risk of type 2 diabetes.

Sandhu MS, Weedon MN, Fawcett KA, Wasson J, Debenham SL, Daly A, Lango H, Frayling TM, Neumann RJ, Sherva R, Blech I, Pharoah PD, Palmer CN, Kimber C, Tavendale R, Morris AD, McCarthy MI, Walker M, Hitman G, Glaser B, Permutt MA, Hattersley AT, Wareham NJ, Barroso I.

Nat Genet. 2007 Aug;39(8):951-3. Epub 2007 Jul 1.

2.

WFS1/wolframin mutations, Wolfram syndrome, and associated diseases.

Khanim F, Kirk J, Latif F, Barrett TG.

Hum Mutat. 2001 May;17(5):357-67. Review.

PMID:
11317350
3.

Genes of type 2 diabetes in beta cells.

Trajkovski M, Mziaut H, Schwarz PE, Solimena M.

Endocrinol Metab Clin North Am. 2006 Jun;35(2):357-69, x. Review.

PMID:
16632098
4.

Mutational spectrum of the WFS1 gene in Wolfram syndrome, nonsyndromic hearing impairment, diabetes mellitus, and psychiatric disease.

Cryns K, Sivakumaran TA, Van den Ouweland JM, Pennings RJ, Cremers CW, Flothmann K, Young TL, Smith RJ, Lesperance MM, Van Camp G.

Hum Mutat. 2003 Oct;22(4):275-87. Review.

PMID:
12955714
5.

[From gene to disease; mutations in the WFS1-gene as the cause of juvenile type I diabetes mellitus with optic atrophy (Wolfram syndrome)].

Pennings RJ, Dikkeschei LD, Cremers CW, van den Ouweland JM.

Ned Tijdschr Geneeskd. 2002 May 25;146(21):985-7. Review. Dutch.

PMID:
12058630
6.

New gene variants alter type 2 diabetes risk predominantly through reduced beta-cell function.

Perry JR, Frayling TM.

Curr Opin Clin Nutr Metab Care. 2008 Jul;11(4):371-7. doi: 10.1097/MCO.0b013e32830349a1. Review.

PMID:
18541994
7.

Wolfram syndrome 1 and Wolfram syndrome 2.

Rigoli L, Di Bella C.

Curr Opin Pediatr. 2012 Aug;24(4):512-7. doi: 10.1097/MOP.0b013e328354ccdf. Review.

PMID:
22790102
8.

Genetics: how the UKPDS contributed to determining the genetic landscape of Type 2 diabetes.

Gloyn AL, McCarthy MI.

Diabet Med. 2008 Aug;25 Suppl 2:35-40. doi: 10.1111/j.1464-5491.2008.02500.x. Review.

PMID:
18717977

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