Glaser B - Search Results

1

p57(KIP2) expression in normal islet cells and in hyperinsulinism of infancy.

Kassem SA, Ariel I, Thornton PS, Hussain K, Smith V, Lindley KJ, Aynsley-Green A, Glaser B. Kassem SA, et al. Among authors: glaser b. Diabetes. 2001 Dec;50(12):2763-9. doi: 10.2337/diabetes.50.12.2763. Diabetes. 2001. PMID: 11723059

2

Recombinant mapping of the familial hyperinsulinism gene to an 0.8 cM region on chromosome 11p15.1 and demonstration of a founder effect in Ashkenazi Jews.

Glaser B, Chiu KC, Liu L, Anker R, Nestorowicz A, Cox NJ, Landau H, Kaiser N, Thornton PS, Stanley CA, et al. Glaser B, et al. Hum Mol Genet. 1995 May;4(5):879-86. doi: 10.1093/hmg/4.5.879. Hum Mol Genet. 1995. PMID: 7633448

3

Familial hyperinsulinism maps to chromosome 11p14-15.1, 30 cM centromeric to the insulin gene.

Glaser B, Chiu KC, Anker R, Nestorowicz A, Landau H, Ben-Bassat H, Shlomai Z, Kaiser N, Thornton PS, Stanley CA, et al. Glaser B, et al. Nat Genet. 1994 Jun;7(2):185-8. doi: 10.1038/ng0694-185. Nat Genet. 1994. PMID: 7920639

4

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

5

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

6

Familial hyperinsulinism caused by an activating glucokinase mutation.

Glaser B, Kesavan P, Heyman M, Davis E, Cuesta A, Buchs A, Stanley CA, Thornton PS, Permutt MA, Matschinsky FM, Herold KC. Glaser B, et al. N Engl J Med. 1998 Jan 22;338(4):226-30. doi: 10.1056/NEJM199801223380404. N Engl J Med. 1998. PMID: 9435328 Free article. No abstract available.

7

Familial hyperinsulinism with apparent autosomal dominant inheritance: clinical and genetic differences from the autosomal recessive variant.

Thornton PS, Satin-Smith MS, Herold K, Glaser B, Chiu KC, Nestorowicz A, Permutt MA, Baker L, Stanley CA. Thornton PS, et al. Among authors: glaser b. J Pediatr. 1998 Jan;132(1):9-14. doi: 10.1016/s0022-3476(98)70477-9. J Pediatr. 1998. PMID: 9469993

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

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

10

Clinical and molecular heterogeneity of familial hyperinsulinism.

Glaser B, Thornton PS, Herold K, Stanley CA. Glaser B, et al. J Pediatr. 1998 Dec;133(6):801-2. doi: 10.1016/s0022-3476(98)70160-x. J Pediatr. 1998. PMID: 9843361 No abstract available.

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