A new subtype of autosomal dominant diabetes attributable to a mutation in the gene for sulfonylurea receptor 1. (Q44297979)

1 December 2017

A new subtype of autosomal dominant diabetes attributable to a mutation in the gene for sulfonylurea receptor 1. (English)

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1 December 2017

Frank Reimann

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Markku Laakso

6

object named as

Markku Laakso

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1 December 2017

Hanna Huopio

1

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1 December 2017

Timo Otonkoski

2

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1 December 2017

Ilkka Vauhkonen

3

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1 December 2017

Frances M Ashcroft

5

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1 December 2017

language of work or name

English

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publication date

1 January 2003

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1 December 2017

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1 December 2017

361

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1 December 2017

301-307

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1 December 2017

9354

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Pathogenesis of NIDDM. A balanced overview

1 December 2017

1 reference

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Nesidioblastosis of the pancreas: definition of the syndrome and the management of the severe neonatal hyperinsulinaemic hypoglycaemia

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Roles of ATP-sensitive K+ channels in cell survival and differentiation in the endocrine pancreas

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Beta-cell proliferation and apoptosis in the developing normal human pancreas and in hyperinsulinism of infancy

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Dominantly inherited hyperinsulinism caused by a mutation in the sulfonylurea receptor type 1.

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Characterization of the MODY3 phenotype. Early-onset diabetes caused by an insulin secretion defect

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Defects in insulin secretion and insulin action in non-insulin-dependent diabetes mellitus are inherited. Metabolic studies on offspring of diabetic probands

1 reference

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Definition, diagnosis and classification of diabetes mellitus and its complications. Part 1: diagnosis and classification of diabetes mellitus provisional report of a WHO consultation

1 reference

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7 January 2021

Hyperinsulinism caused by paternal-specific inheritance of a recessive mutation in the sulfonylurea-receptor gene.

1 reference

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7 January 2021

Glucose and tolbutamide induce apoptosis in pancreatic beta-cells. A process dependent on intracellular Ca2+ concentration

1 reference

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7 January 2021

Abnormalities of pancreatic islets by targeted expression of a dominant-negative KATP channel

1 reference

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7 January 2021

High frequency of mutations in MODY and mitochondrial genes in Scandinavian patients with familial early-onset diabetes

1 reference

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7 January 2021

Sequence variants in the sulfonylurea receptor (SUR) gene are associated with NIDDM in Caucasians

1 reference

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7 January 2021

Decreased tolbutamide-stimulated insulin secretion in healthy subjects with sequence variants in the high-affinity sulfonylurea receptor gene

1 reference

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7 January 2021

Variant in sulfonylurea receptor-1 gene is associated with high insulin concentrations in non-diabetic Mexican Americans: SUR-1 gene variant and hyperinsulinemia.

1 reference

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7 January 2021

Variants in the sulphonylurea receptor gene: association of the exon 16-3t variant with Type II diabetes mellitus in Dutch Caucasians

1 reference

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7 January 2021

Clinical characterization of polymorphisms in the sulphonylurea receptor 1 gene in Japanese subjects with Type 2 diabetes mellitus

1 reference

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7 January 2021

Decreased fasting and oral glucose stimulated C-peptide in nondiabetic subjects with sequence variants in the sulfonylurea receptor 1 gene

1 reference

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7 January 2021

Sur1 knockout mice. A model for K(ATP) channel-independent regulation of insulin secretion

1 reference

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Diverse roles of K(ATP) channels learned from Kir6.2 genetically engineered mice

1 reference

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7 January 2021

Glucose intolerance but normal satiety in mice with a null mutation in the glucagon-like peptide 1 receptor gene.

1 reference

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7 January 2021

Glucose intolerance caused by a defect in the entero-insular axis: a study in gastric inhibitory polypeptide receptor knockout mice

1 reference

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7 January 2021

Series introduction: the molecular and physiological basis of insulin resistance: emerging implications for metabolic and cardiovascular diseases

1 reference

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7 January 2021

10.1016/S0140-6736(03)12325-2

Identifiers

DOI

1 reference

1 December 2017

1 reference