Glaser B - Search Results

1

Functional analyses of novel mutations in the sulfonylurea receptor 1 associated with persistent hyperinsulinemic hypoglycemia of infancy.

Shyng SL, Ferrigni T, Shepard JB, Nestorowicz A, Glaser B, Permutt MA, Nichols CG. Shyng SL, et al. Among authors: glaser b. Diabetes. 1998 Jul;47(7):1145-51. doi: 10.2337/diabetes.47.7.1145. Diabetes. 1998. PMID: 9648840

2

Adenosine diphosphate as an intracellular regulator of insulin secretion.

Nichols CG, Shyng SL, Nestorowicz A, Glaser B, Clement JP 4th, Gonzalez G, Aguilar-Bryan L, Permutt MA, Bryan J. Nichols CG, et al. Among authors: glaser b. Science. 1996 Jun 21;272(5269):1785-7. doi: 10.1126/science.272.5269.1785. Science. 1996. PMID: 8650576

3

Mutations in the sulonylurea receptor gene are associated with familial hyperinsulinism in Ashkenazi Jews.

Nestorowicz A, Wilson BA, Schoor KP, Inoue H, Glaser B, Landau H, Stanley CA, Thornton PS, Clement JP 4th, Bryan J, Aguilar-Bryan L, Permutt MA. Nestorowicz A, et al. Among authors: glaser b. Hum Mol Genet. 1996 Nov;5(11):1813-22. doi: 10.1093/hmg/5.11.1813. Hum Mol Genet. 1996. PMID: 8923011

4

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

5

Genetic heterogeneity in familial hyperinsulinism.

Nestorowicz A, Glaser B, Wilson BA, Shyng SL, Nichols CG, Stanley CA, Thornton PS, Permutt MA. Nestorowicz A, et al. Among authors: glaser b. Hum Mol Genet. 1998 Jul;7(7):1119-28. doi: 10.1093/hmg/7.7.1119. Hum Mol Genet. 1998. PMID: 9618169

6

Dysregulation of insulin secretion in children with congenital hyperinsulinism due to sulfonylurea receptor mutations.

Grimberg A, Ferry RJ Jr, Kelly A, Koo-McCoy S, Polonsky K, Glaser B, Permutt MA, Aguilar-Bryan L, Stafford D, Thornton PS, Baker L, Stanley CA. Grimberg A, et al. Among authors: glaser b. Diabetes. 2001 Feb;50(2):322-8. doi: 10.2337/diabetes.50.2.322. Diabetes. 2001. PMID: 11272143 Free PMC article.

7

Novel de novo mutation in sulfonylurea receptor 1 presenting as hyperinsulinism in infancy followed by overt diabetes in early adolescence.

Abdulhadi-Atwan M, Bushman J, Tornovsky-Babaey S, Perry A, Abu-Libdeh A, Glaser B, Shyng SL, Zangen DH. Abdulhadi-Atwan M, et al. Among authors: glaser b. Diabetes. 2008 Jul;57(7):1935-40. doi: 10.2337/db08-0159. Epub 2008 Apr 4. Diabetes. 2008. PMID: 18390792 Free PMC article.

8

Relative expression of a dominant mutated ABCC8 allele determines the clinical manifestation of congenital hyperinsulinism.

Shemer R, Avnon Ziv C, Laiba E, Zhou Q, Gay J, Tunovsky-Babaey S, Shyng SL, Glaser B, Zangen DH. Shemer R, et al. Among authors: glaser b. Diabetes. 2012 Jan;61(1):258-63. doi: 10.2337/db11-0984. Epub 2011 Nov 21. Diabetes. 2012. PMID: 22106158 Free PMC article.

9

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

10

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.

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