Functional genomics of the beta-cell: short-chain 3-hydroxyacyl-coenzyme A dehydrogenase regulates insulin secretion independent of K+ currents.
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Specificity in beta cell expression of L-3-hydroxyacyl-CoA dehydrogenase, short chain, and potential role in down-regulating insulin releaseProtein markers for insulin-producing beta cells with higher glucose sensitivityMolecular mechanisms of protein induced hyperinsulinaemic hypoglycaemia.Foxa1 and Foxa2 maintain the metabolic and secretory features of the mature beta-cellShort-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: the clinical relevance of an early diagnosis and report of four new cases.Mechanism of hyperinsulinism in short-chain 3-hydroxyacyl-CoA dehydrogenase deficiency involves activation of glutamate dehydrogenaseShort-chain 3-hydroxyacyl-coenzyme A dehydrogenase associates with a protein super-complex integrating multiple metabolic pathwaysGenome-wide homozygosity analysis reveals HADH mutations as a common cause of diazoxide-responsive hyperinsulinemic-hypoglycemia in consanguineous pedigreesLeucine-sensitive hyperinsulinaemic hypoglycaemia in patients with loss of function mutations in 3-Hydroxyacyl-CoA Dehydrogenase.Overexpression of hepatocyte nuclear factor-4α initiates cell cycle entry, but is not sufficient to promote β-cell expansion in human isletsThe molecular mechanisms, diagnosis and management of congenital hyperinsulinismMetabolic profiling of PPARalpha-/- mice reveals defects in carnitine and amino acid homeostasis that are partially reversed by oral carnitine supplementationCell-type, allelic, and genetic signatures in the human pancreatic beta cell transcriptomeEffects of high-fat diet feeding on Znt8-null mice: differences between β-cell and global knockout of Znt8Transcriptomes of the major human pancreatic cell types.Current understanding of K ATP channels in neonatal diseases: focus on insulin secretion disorders.Hyperinsulinaemic hypoglycaemia: genetic mechanisms, diagnosis and management.Hyperinsulinaemic hypoglycaemia:genetic mechanisms, diagnosis and management.Lessons in human biology from a monogenic pancreatic β cell disease.3-hydroxyacyl-coenzyme a dehydrogenase deficiency: identification of a new mutation causing hyperinsulinemic hypoketotic hypoglycemia, altered organic acids and acylcarnitines concentrations.Hyperinsulinemic hypoglycemia of infancy due to novel HADH mutation in two siblings
P2860
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P2860
Functional genomics of the beta-cell: short-chain 3-hydroxyacyl-coenzyme A dehydrogenase regulates insulin secretion independent of K+ currents.
description
2006 nî lūn-bûn
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2006年の論文
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2006年学术文章
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2006年学术文章
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2006年学术文章
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2006年学术文章
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2006年学术文章
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name
Functional genomics of the bet ...... on independent of K+ currents.
@en
Functional genomics of the bet ...... on independent of K+ currents.
@nl
type
label
Functional genomics of the bet ...... on independent of K+ currents.
@en
Functional genomics of the bet ...... on independent of K+ currents.
@nl
prefLabel
Functional genomics of the bet ...... on independent of K+ currents.
@en
Functional genomics of the bet ...... on independent of K+ currents.
@nl
P2093
P356
P1476
Functional genomics of the bet ...... ion independent of K+ currents
@en
P2093
Christian J Stoeckert
Christopher B Newgard
Franz M Matschinsky
Hans E Hohmeier
Klaus H Kaestner
Nicolai M Doliba
Olga T Hardy
Rana K Gupta
Thomas C Becker
P304
P356
10.1210/ME.2006-0411
P577
2006-12-21T00:00:00Z