(Q44604212)

4 December 2017

title

Genetic study of Saudi diabetes (GSSD): significant association of the KCNJ11 E23K polymorphism with type 2 diabetes (English)

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glutathione synthetase deficiency

4 December 2017

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10

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4 December 2017

Osama Alsmadi

1

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4 December 2017

Khalid Al-Rubeaan

2

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4 December 2017

Salma M Wakil

3

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4 December 2017

Faiqa Imtiaz

4

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4 December 2017

Gamal Mohamed

5

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4 December 2017

Haya Al-Saud

6

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4 December 2017

Nouran Abu Al-Saud

7

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4 December 2017

Nasser Aldaghri

8

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4 December 2017

Shahinaz Mohammad

9

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4 December 2017

language of work or name

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1 February 2008

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Diabetes - Metabolism: Research and Reviews

4 December 2017

published in

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4 December 2017

volume

24

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4 December 2017

issue

2

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4 December 2017

page(s)

137-140

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Electrophysiology of the pancreatic beta-cell

4 December 2017

cites work

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7 January 2021

Reconstitution of IKATP: an inward rectifier subunit plus the sulfonylurea receptor

1 reference

7 January 2021

Cloning and functional expression of the cDNA encoding a novel ATP-sensitive potassium channel subunit expressed in pancreatic beta-cells, brain, heart and skeletal muscle

1 reference

7 January 2021

Cloning of the beta cell high-affinity sulfonylurea receptor: a regulator of insulin secretion

1 reference

7 January 2021

ATP4- mediates closure of pancreatic beta-cell ATP-sensitive potassium channels by interaction with 1 of 4 identical sites

1 reference

7 January 2021

The carboxyl termini of K(ATP) channels bind nucleotides

1 reference

7 January 2021

Identification of residues contributing to the ATP binding site of Kir6.2.

1 reference

7 January 2021

Mutations in the sulfonylurea receptor gene in familial persistent hyperinsulinemic hypoglycemia of infancy

1 reference

7 January 2021

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

1 reference

7 January 2021

Genetic heterogeneity in familial hyperinsulinism.

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7 January 2021

Targeted Overactivity of β Cell KATP Channels Induces Profound Neonatal Diabetes

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7 January 2021

Activating mutations in the gene encoding the ATP-sensitive potassium-channel subunit Kir6.2 and permanent neonatal diabetes

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7 January 2021

Candidate gene association study in type 2 diabetes indicates a role for genes involved in beta-cell function as well as insulin action

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7 January 2021

Association studies of variants in promoter and coding regions of beta-cell ATP-sensitive K-channel genes SUR1 and Kir6.2 with Type 2 diabetes mellitus (UKPDS 53).

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7 January 2021

Large-scale association studies of variants in genes encoding the pancreatic beta-cell KATP channel subunits Kir6.2 (KCNJ11) and SUR1 (ABCC8) confirm that the KCNJ11 E23K variant is associated with type 2 diabetes

1 reference

7 January 2021

Missense mutations in the pancreatic islet beta cell inwardly rectifying K+ channel gene (KIR6.2/BIR): a meta-analysis suggests a role in the polygenic basis of Type II diabetes mellitus in Caucasians

1 reference

7 January 2021

Amino acid polymorphisms in the ATP-regulatable inward rectifier Kir6.2 and their relationships to glucose- and tolbutamide-induced insulin secretion, the insulin sensitivity index, and NIDDM.

1 reference

7 January 2021

Analysis of separate and combined effects of common variation in KCNJ11 and PPARG on risk of type 2 diabetes

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7 January 2021

The E23K variant of Kir6.2 associates with impaired post-OGTT serum insulin response and increased risk of type 2 diabetes

1 reference

7 January 2021

Sequence variations in the human Kir6.2 gene, a subunit of the beta-cell ATP-sensitive K-channel: no association with NIDDM in while Caucasian subjects or evidence of abnormal function when expressed in vitro

1 reference

7 January 2021

Common variants in the ATP-sensitive K+ channel genes KCNJ11 (Kir6.2) and ABCC8 (SUR1) in relation to glucose intolerance: population-based studies and meta-analyses

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7 January 2021

Association studies of variants in the genes involved in pancreatic beta-cell function in type 2 diabetes in Japanese subjects

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7 January 2021

Current status of the E23K Kir6.2 polymorphism: implications for type-2 diabetes

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7 January 2021

Genetic diversity among the Arabs

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7 January 2021

The structure of haplotype blocks in the human genome

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7 January 2021

Identifiers

DOI

10.1002/DMRR.777

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4 December 2017

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