(Q80149655)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16924481%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

title

Hyperinsulinism in mice with heterozygous loss of K(ATP) channels (English)

1 reference

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29 December 2019

1 reference

M S Remedi

1

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29 December 2019

J V Rocheleau

2

1 reference

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29 December 2019

A Tong

3

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29 December 2019

B L Patton

4

1 reference

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29 December 2019

M L McDaniel

5

1 reference

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29 December 2019

D W Piston

6

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29 December 2019

J C Koster

7

1 reference

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29 December 2019

C G Nichols

8

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29 December 2019

publication date

19 August 2006

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29 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16924481%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

volume

49

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29 December 2019

page(s)

2368-2378

1 reference

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29 December 2019

issue

10

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https://scigraph.springernature.com/pub.10.1007/s00125-006-0367-4

29 December 2019

exact match

0 references

cites work

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

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12 December 2020

Both triggering and amplifying pathways contribute to fuel-induced insulin secretion in the absence of sulfonylurea receptor-1 in pancreatic beta-cells

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12 December 2020

K(ATP) channels and insulin secretion disorders

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12 December 2020

Functional analyses of novel mutations in the sulfonylurea receptor 1 associated with persistent hyperinsulinemic hypoglycemia of infancy.

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12 December 2020

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

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12 December 2020

Mutation of the pancreatic islet inward rectifier Kir6.2 also leads to familial persistent hyperinsulinemic hypoglycemia of infancy

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12 December 2020

Association and stoichiometry of K(ATP) channel subunits

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12 December 2020

Subunit stoichiometry of the pancreatic β-cell ATP-sensitive K+ channel

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12 December 2020

A point mutation inactivating the sulfonylurea receptor causes the severe form of persistent hyperinsulinemic hypoglycemia of infancy in Finland.

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12 December 2020

Targeted Overactivity of β Cell KATP Channels Induces Profound Neonatal Diabetes

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12 December 2020

Carriers of an inactivating beta-cell ATP-sensitive K(+) channel mutation have normal glucose tolerance and insulin sensitivity and appropriate insulin secretion

1 reference

12 December 2020

Familial persistent hyperinsulinemic hypoglycemia of infancy and mutations in the sulfonylurea receptor

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12 December 2020

ATP-sensitive potassium channels participate in glucose uptake in skeletal muscle and adipose tissue

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12 December 2020

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

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12 December 2020

Adenosine diphosphate as an intracellular regulator of insulin secretion.

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12 December 2020

Hypothalamic K(ATP) channels control hepatic glucose production

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12 December 2020

Disruption of Sur2-containing K(ATP) channels enhances insulin-stimulated glucose uptake in skeletal muscle

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12 December 2020

Dysregulation of insulin secretion in children with congenital hyperinsulinism due to sulfonylurea receptor mutations

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12 December 2020

Oscillations of membrane potential and cytosolic Ca(2+) concentration in SUR1(-/-) beta cells

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12 December 2020

Fabrication of microfluidic systems in poly(dimethylsiloxane).

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12 December 2020

Critical role of gap junction coupled KATP channel activity for regulated insulin secretion

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12 December 2020

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

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12 December 2020

Microfluidic glucose stimulation reveals limited coordination of intracellular Ca2+ activity oscillations in pancreatic islets

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12 December 2020

SUR1 regulates PKA-independent cAMP-induced granule priming in mouse pancreatic B-cells

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12 December 2020

Loss of functional KATP channels in pancreatic beta-cells causes persistent hyperinsulinemic hypoglycemia of infancy

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12 December 2020

Octameric stoichiometry of the KATP channel complex

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12 December 2020

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

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12 December 2020

Nesidioblastosis of the pancreas in infancy

1 reference

12 December 2020

Defective trafficking and function of KATP channels caused by a sulfonylurea receptor 1 mutation associated with persistent hyperinsulinemic hypoglycemia of infancy

1 reference

12 December 2020

Functional roles of cardiac and vascular ATP-sensitive potassium channels clarified by Kir6.2-knockout mice

1 reference

12 December 2020

Heterogeneity of persistent hyperinsulinaemic hypoglycaemia. A series of 175 cases

1 reference

12 December 2020

Nutritionally induced insulin resistance and receptor defect leading to beta-cell failure in animal models

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12 December 2020

Diet-induced glucose intolerance in mice with decreased beta-cell ATP-sensitive K+ channels

1 reference

12 December 2020

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

1 reference

12 December 2020

Homozygosity mapping, to chromosome 11p, of the gene for familial persistent hyperinsulinemic hypoglycemia of infancy

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12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Sulfonylurea receptor type 1 knock-out mice have intact feeding-stimulated insulin secretion despite marked impairment in their response to glucose

1 reference

12 December 2020

Genotype-phenotype correlations in children with congenital hyperinsulinism due to recessive mutations of the adenosine triphosphate-sensitive potassium channel genes

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12 December 2020

Hyperinsulinism induced by targeted suppression of beta cell KATP channels

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12 December 2020

A signaling role of glutamine in insulin secretion

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12 December 2020

Restitution of defective glucose-stimulated insulin release of sulfonylurea type 1 receptor knockout mice by acetylcholine

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12 December 2020

Mutations in the sulonylurea receptor gene are associated with familial hyperinsulinism in Ashkenazi Jews.

1 reference

12 December 2020

ATP and sulfonylurea sensitivity of mutant ATP-sensitive K+ channels in neonatal diabetes: implications for pharmacogenomic therapy

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

Defective insulin secretion and enhanced insulin action in KATP channel-deficient mice.

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

Genetic heterogeneity in familial hyperinsulinism.

1 reference

12 December 2020