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M A Permutt

Showing results (151-160 of 163) with videos related to

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Diabetes|March 1, 1997
Sequence variants in the pancreatic islet beta-cell inwardly rectifying K+ channel Kir6.2 (Bir) gene: identification and lack of role in Caucasian patients with NIDDMH Inoue, J Ferrer, M Warren-Perry, et al.
Diabetes|March 15, 2001
A genome scan for type 2 diabetes susceptibility loci in a genetically isolated populationM A Permutt, J C Wasson, B K Suarez, et al.
Diabetes|March 29, 2001
Dysregulation of insulin secretion in children with congenital hyperinsulinism due to sulfonylurea receptor mutationsA Grimberg, R J Ferry, A Kelly, et al.
Diabetes|April 1, 1997
Genetic studies of the sulfonylurea receptor gene locus in NIDDM and in morbid obesity among French CaucasiansE H Hani, K Clément, G Velho, et al.
Diabetes|June 1, 1997
Genetics of NIDDM in France: studies with 19 candidate genes in affected sib pairsN Vionnet, E H Hani, S Lesage, et al.
Human Mutation|July 20, 2001
Missense polymorphism in the human carboxypeptidase E gene alters enzymatic activityH Chen, S Jawahar, Y Qian, et al.
Human Molecular Genetics|November 1, 1996
Mutations in the sulonylurea receptor gene are associated with familial hyperinsulinism in Ashkenazi JewsA Nestorowicz, B A Wilson, K P Schoor, et al.
Diabetes|May 6, 1998
Decreased tolbutamide-stimulated insulin secretion in healthy subjects with sequence variants in the high-affinity sulfonylurea receptor geneT Hansen, S M Echwald, L Hansen, et al.
Diabetes|June 1, 1996
Sequence variants in the sulfonylurea receptor (SUR) gene are associated with NIDDM in CaucasiansH Inoue, J Ferrer, C M Welling, et al.
Nature Genetics|October 15, 1998
A gene encoding a transmembrane protein is mutated in patients with diabetes mellitus and optic atrophy (Wolfram syndrome)H Inoue, Y Tanizawa, J Wasson, et al.
Pageof 17

Showing results (151-160 of 163) with videos related to

Sort By:
Pageof 17
Diabetes|March 1, 1997
Sequence variants in the pancreatic islet beta-cell inwardly rectifying K+ channel Kir6.2 (Bir) gene: identification and lack of role in Caucasian patients with NIDDMH Inoue, J Ferrer, M Warren-Perry, et al.
Diabetes|March 15, 2001
A genome scan for type 2 diabetes susceptibility loci in a genetically isolated populationM A Permutt, J C Wasson, B K Suarez, et al.
Diabetes|March 29, 2001
Dysregulation of insulin secretion in children with congenital hyperinsulinism due to sulfonylurea receptor mutationsA Grimberg, R J Ferry, A Kelly, et al.
Diabetes|April 1, 1997
Genetic studies of the sulfonylurea receptor gene locus in NIDDM and in morbid obesity among French CaucasiansE H Hani, K Clément, G Velho, et al.
Diabetes|June 1, 1997
Genetics of NIDDM in France: studies with 19 candidate genes in affected sib pairsN Vionnet, E H Hani, S Lesage, et al.
Human Mutation|July 20, 2001
Missense polymorphism in the human carboxypeptidase E gene alters enzymatic activityH Chen, S Jawahar, Y Qian, et al.
Human Molecular Genetics|November 1, 1996
Mutations in the sulonylurea receptor gene are associated with familial hyperinsulinism in Ashkenazi JewsA Nestorowicz, B A Wilson, K P Schoor, et al.
Diabetes|May 6, 1998
Decreased tolbutamide-stimulated insulin secretion in healthy subjects with sequence variants in the high-affinity sulfonylurea receptor geneT Hansen, S M Echwald, L Hansen, et al.
Diabetes|June 1, 1996
Sequence variants in the sulfonylurea receptor (SUR) gene are associated with NIDDM in CaucasiansH Inoue, J Ferrer, C M Welling, et al.
Nature Genetics|October 15, 1998
A gene encoding a transmembrane protein is mutated in patients with diabetes mellitus and optic atrophy (Wolfram syndrome)H Inoue, Y Tanizawa, J Wasson, et al.
Pageof 17