Pancreatic β-cell KATP channels: Hypoglycaemia and hyperglycaemia. (Q37794032)

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14 February 2020

title

Pancreatic β-cell KATP channels: Hypoglycaemia and hyperglycaemia (English)

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14 February 2020

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14 February 2020

author name string

Kate Bennett

series ordinal

1

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14 February 2020

Khalid Hussain

series ordinal

3

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14 February 2020

publication date

1 September 2010

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Reviews in Endocrine and Metabolic Disorders

14 February 2020

published in

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14 February 2020

volume

11

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14 February 2020

issue

3

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14 February 2020

page(s)

157-163

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K(ATP) channels and insulin secretion disorders

14 February 2020

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS11154-010-9144-2

Unbalanced expression of 11p15 imprinted genes in focal forms of congenital hyperinsulinism: association with a reduction to homozygosity of a mutation in ABCC8 or KCNJ11

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS11154-010-9144-2

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

21 January 2018

1 reference

12 December 2020

Molecular basis for K(ATP) assembly: transmembrane interactions mediate association of a K+ channel with an ABC transporter

1 reference

12 December 2020

Persistent hyperinsulinaemic hypoglycaemia of infancy: a heterogeneous syndrome unrelated to nesidioblastosis

1 reference

12 December 2020

Transmembrane topology of the sulfonylurea receptor SUR1.

1 reference

12 December 2020

Parental genomic imprinting of the human IGF2 gene

1 reference

12 December 2020

Roles of KATP channels as metabolic sensors in acute metabolic changes

1 reference

12 December 2020

Molecular biology of K(ATP) channels and implications for health and disease

1 reference

12 December 2020

Chromosome 11p15 paternal isodisomy in focal forms of neonatal hyperinsulinism

1 reference

12 December 2020

ABC transporters: physiology, structure and mechanism--an overview

1 reference

12 December 2020

Activating mutations in the ABCC8 gene in neonatal diabetes mellitus

1 reference

12 December 2020

Hyperinsulinism of infancy: novel ABCC8 and KCNJ11 mutations and evidence for additional locus heterogeneity

1 reference

12 December 2020

The genetic basis of congenital hyperinsulinism

1 reference

12 December 2020

Targeted Overactivity of β Cell KATP Channels Induces Profound Neonatal Diabetes

1 reference

12 December 2020

Metabolic regulation of the pancreatic beta-cell ATP-sensitive K+ channel: a pas de deux

1 reference

12 December 2020

Nucleotides and phospholipids compete for binding to the C terminus of KATP channels

1 reference

12 December 2020

Monoallelic expression of the human H19 gene

1 reference

12 December 2020

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

1 reference

12 December 2020

Severe congenital hyperinsulinism caused by a mutation in the Kir6.2 subunit of the adenosine triphosphate-sensitive potassium channel impairing trafficking and function

1 reference

12 December 2020

A new ER trafficking signal regulates the subunit stoichiometry of plasma membrane K(ATP) channels

1 reference

12 December 2020

Relapsing diabetes can result from moderately activating mutations in KCNJ11.

1 reference

12 December 2020

Hyperinsulinemic hypoglycemia of infancy (nesidioblastosis) in clinical remission: high incidence of diabetes mellitus and persistent beta-cell dysfunction at long-term follow-up

1 reference

12 December 2020

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

12 December 2020

Structure and mechanism of ABC transporter proteins.

1 reference

12 December 2020

Characteristic interactions with phosphatidylinositol 4,5-bisphosphate determine regulation of kir channels by diverse modulators

1 reference

12 December 2020

Activating mutations in Kir6.2 and neonatal diabetes: new clinical syndromes, new scientific insights, and new therapy

1 reference

12 December 2020

Review. SUR1: a unique ATP-binding cassette protein that functions as an ion channel regulator.

1 reference

12 December 2020

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

1 reference

12 December 2020

A novel glucose-sensing mechanism contributing to glucagon-like peptide-1 secretion from the GLUTag cell line

1 reference

12 December 2020

Permanent neonatal diabetes caused by dominant, recessive, or compound heterozygous SUR1 mutations with opposite functional effects

1 reference

12 December 2020

ATP-regulated K+ channels in cardiac muscle

1 reference

12 December 2020

Octameric stoichiometry of the KATP channel complex

1 reference

12 December 2020

KATP channels as molecular sensors of cellular metabolism

1 reference

12 December 2020

Permanent neonatal diabetes due to mutations in KCNJ11 encoding Kir6.2: patient characteristics and initial response to sulfonylurea therapy

1 reference

12 December 2020

ATP-sensitive K+ channels in pancreatic, cardiac, and vascular smooth muscle cells.

1 reference

12 December 2020

Crystal structure of the potassium channel KirBac1.1 in the closed state

1 reference

12 December 2020

Regulation of cardiac Na+,Ca2+ exchange and KATP potassium channels by PIP2.

1 reference

12 December 2020

Analysis of endoplasmic reticulum trafficking signals by combinatorial screening in mammalian cells

1 reference

12 December 2020

Functional analysis of a structural model of the ATP-binding site of the KATP channel Kir6.2 subunit.

1 reference

12 December 2020

Kir6.2 mutations causing neonatal diabetes prevent endocytosis of ATP-sensitive potassium channels

1 reference

12 December 2020

The common single nucleotide polymorphism E23K in K(IR)6.2 sensitizes pancreatic beta-cell ATP-sensitive potassium channels toward activation through nucleoside diphosphates

1 reference

12 December 2020

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

1 reference

12 December 2020

ATP-sensitive potassium channels in health and disease

1 reference

12 December 2020

Domain reorientation and rotation of an intracellular assembly regulate conduction in Kir potassium channels

1 reference

12 December 2020

Origin of de novo KCNJ11 mutations and risk of neonatal diabetes for subsequent siblings

1 reference

12 December 2020

Molecular determinants of KATP channel inhibition by ATP.

1 reference

12 December 2020

Paternal mutation of the sulfonylurea receptor (SUR1) gene and maternal loss of 11p15 imprinted genes lead to persistent hyperinsulinism in focal adenomatous hyperplasia

1 reference

12 December 2020

Update of mutations in the genes encoding the pancreatic beta-cell K(ATP) channel subunits Kir6.2 (KCNJ11) and sulfonylurea receptor 1 (ABCC8) in diabetes mellitus and hyperinsulinism

1 reference

12 December 2020

An ABCC8 gene mutation and mosaic uniparental isodisomy resulting in atypical diffuse congenital hyperinsulinism

1 reference

12 December 2020

The C terminus of SUR1 is required for trafficking of KATP channels

1 reference

12 December 2020

Noninvasive diagnosis of focal hyperinsulinism of infancy with [18F]-DOPA positron emission tomography.

1 reference

12 December 2020

The Structure of the Potassium Channel: Molecular Basis of K+ Conduction and Selectivity

1 reference

12 December 2020

A novel mutation causing DEND syndrome: a treatable channelopathy of pancreas and brain.

1 reference

12 December 2020

A multidisciplinary approach to the focal form of congenital hyperinsulinism leads to successful treatment by partial pancreatectomy

1 reference

12 December 2020

Prenatal Diagnosis and Postnatal Management of Diffuse Congenital Hyperinsulinism: A Case Report

1 reference

12 December 2020

Kir6.2 mutations are a common cause of permanent neonatal diabetes in a large cohort of French patients

1 reference

12 December 2020

Identification of a familial hyperinsulinism-causing mutation in the sulfonylurea receptor 1 that prevents normal trafficking and function of KATP channels

1 reference

12 December 2020

Assembly, maturation, and turnover of K(ATP) channel subunits

1 reference

12 December 2020

Characterization of hyperinsulinism in infancy assessed with PET and 18F-fluoro-L-DOPA.

1 reference

12 December 2020

Mutations in the K+ channel signature sequence

1 reference

12 December 2020

Mechanism of rectification in inward-rectifier K+ channels

1 reference

12 December 2020

Molecular basis of Kir6.2 mutations associated with neonatal diabetes or neonatal diabetes plus neurological features

1 reference

12 December 2020

Mapping the architecture of the ATP-binding site of the KATP channel subunit Kir6.2.

1 reference

12 December 2020

Clinical characteristics and biochemical mechanisms of congenital hyperinsulinism associated with dominant KATP channel mutations

1 reference

12 December 2020

Genomic imprinting of human p57KIP2 and its reduced expression in Wilms' tumors

1 reference

12 December 2020

Truncation of Kir6.2 produces ATP-sensitive K+ channels in the absence of the sulphonylurea receptor

1 reference

12 December 2020

Adenosine 5'-triphosphate-sensitive potassium channels

1 reference

12 December 2020