Glaser B - Search Results

1

Mapping of the human insulin receptor substrate-2 gene, identification of a linked polymorphic marker and linkage analysis in families with Type II diabetes: no evidence for a major susceptibility role.

Kalidas K, Wasson J, Glaser B, Meyer JM, Duprat LJ, White MF, Permutt MA. Kalidas K, et al. Among authors: glaser b. Diabetologia. 1998 Nov;41(11):1389-91. doi: 10.1007/s001250051081. Diabetologia. 1998. PMID: 9833949

2

Searching for type 2 diabetes genes on chromosome 20.

Permutt MA, Wasson J, Love-Gregory L, Ma J, Skolnick G, Suarez B, Lin J, Glaser B. Permutt MA, et al. Among authors: glaser b. Diabetes. 2002 Dec;51 Suppl 3:S308-15. doi: 10.2337/diabetes.51.2007.s308. Diabetes. 2002. PMID: 12475768

3

A common polymorphism in the upstream promoter region of the hepatocyte nuclear factor-4 alpha gene on chromosome 20q is associated with type 2 diabetes and appears to contribute to the evidence for linkage in an ashkenazi jewish population.

Love-Gregory LD, Wasson J, Ma J, Jin CH, Glaser B, Suarez BK, Permutt MA. Love-Gregory LD, et al. Among authors: glaser b. Diabetes. 2004 Apr;53(4):1134-40. doi: 10.2337/diabetes.53.4.1134. Diabetes. 2004. PMID: 15047632

4

A genome scan for type 2 diabetes susceptibility loci in a genetically isolated population.

Permutt MA, Wasson JC, Suarez BK, Lin J, Thomas J, Meyer J, Lewitzky S, Rennich JS, Parker A, DuPrat L, Maruti S, Chayen S, Glaser B. Permutt MA, et al. Among authors: glaser b. Diabetes. 2001 Mar;50(3):681-5. doi: 10.2337/diabetes.50.3.681. Diabetes. 2001. PMID: 11246891

5

Isolation and characterization of the human AKT1 gene, identification of 13 single nucleotide polymorphisms (SNPs), and their lack of association with Type II diabetes.

Matsubara A, Wasson JC, Donelan SS, Welling CM, Glaser B, Permutt MA. Matsubara A, et al. Among authors: glaser b. Diabetologia. 2001 Jul;44(7):910-3. doi: 10.1007/s001250100577. Diabetologia. 2001. PMID: 11508278

6

Dinucleotide repeat polymorphism at the human CCKBR locus.

Glaser B, Anker R, Chiu KC, Donis-Keller H, Permutt MA. Glaser B, et al. Hum Mol Genet. 1994 Nov;3(11):2081. Hum Mol Genet. 1994. PMID: 7874137 No abstract available.

7

A nonsense mutation in the inward rectifier potassium channel gene, Kir6.2, is associated with familial hyperinsulinism.

Nestorowicz A, Inagaki N, Gonoi T, Schoor KP, Wilson BA, Glaser B, Landau H, Stanley CA, Thornton PS, Seino S, Permutt MA. Nestorowicz A, et al. Among authors: glaser b. Diabetes. 1997 Nov;46(11):1743-8. doi: 10.2337/diab.46.11.1743. Diabetes. 1997. PMID: 9356020

8

Hepatocyte nuclear factor 1alpha coding mutations are an uncommon contributor to early-onset type 2 diabetes in Ashkenazi Jews.

Behn PS, Wasson J, Chayen S, Smolovitch I, Thomas J, Glaser B, Permutt MA. Behn PS, et al. Among authors: glaser b. Diabetes. 1998 Jun;47(6):967-9. doi: 10.2337/diabetes.47.6.967. Diabetes. 1998. PMID: 9604876 No abstract available.

9

Isolation and characterization of the human PAX4 gene.

Tao T, Wasson J, Bernal-Mizrachi E, Behn PS, Chayen S, Duprat L, Meyer J, Glaser B, Permutt MA. Tao T, et al. Among authors: glaser b. Diabetes. 1998 Oct;47(10):1650-3. doi: 10.2337/diabetes.47.10.1650. Diabetes. 1998. PMID: 9753306 No abstract available.

10

Genetics of type II diabetes.

Permutt MA, Chiu K, Ferrer J, Glaser B, Inoue H, Nestorowicz A, Stanley CA, Tanizawa Y. Permutt MA, et al. Among authors: glaser b. Recent Prog Horm Res. 1998;53:201-16. Recent Prog Horm Res. 1998. PMID: 9769709 Review.

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