Acute insulin responses to leucine in children with the hyperinsulinism/hyperammonemia syndrome
about
Expression, purification and characterization of human glutamate dehydrogenase (GDH) allosteric regulatory mutationsMechanisms of amino acid-stimulated insulin secretion in congenital hyperinsulinismClinical characteristics and biochemical mechanisms of congenital hyperinsulinism associated with dominant KATP channel mutations.Mitochondrial regulation of β-cell function: maintaining the momentum for insulin releaseMechanism of hyperinsulinism in short-chain 3-hydroxyacyl-CoA dehydrogenase deficiency involves activation of glutamate dehydrogenaseLeucine metabolism in regulation of insulin secretion from pancreatic beta cells.Mitochondrial GTP insensitivity contributes to hypoglycemia in hyperinsulinemia hyperammonemia by inhibiting glucagon release.Regulation of glutamate metabolism and insulin secretion by glutamate dehydrogenase in hypoglycemic children.Hyperinsulinism in infancy: from basic science to clinical disease.Leucine-sensitive hyperinsulinaemic hypoglycaemia in patients with loss of function mutations in 3-Hydroxyacyl-CoA Dehydrogenase.Perspective on the Genetics and Diagnosis of Congenital Hyperinsulinism DisordersExtremes of clinical and enzymatic phenotypes in children with hyperinsulinism caused by glucokinase activating mutations.Two genetic forms of hyperinsulinemic hypoglycemia caused by dysregulation of glutamate dehydrogenase.Intertissue differences for the role of glutamate dehydrogenase in metabolism.Structural basis for leucine-induced allosteric activation of glutamate dehydrogenase.The glutamine-alpha-ketoglutarate (AKG) metabolism and its nutritional implications.Hyperinsulinemic hypoglycemia: clinical, molecular and therapeutical novelties.Diagnosis and treatment of hyperinsulinaemic hypoglycaemia and its implications for paediatric endocrinology.Congenital Hyperinsulinism: Diagnosis and Treatment Update.A novel mutation in the glutamate dehydrogenase (GLUD1) of a patient with congenital hyperinsulinism-hyperammonemia (HI/HA).Nutrient sensing in pancreatic islets: lessons from congenital hyperinsulinism and monogenic diabetes.Hyperinsulinism/hyperammonemia (HI/HA) syndrome due to a mutation in the glutamate dehydrogenase gene.Hyperinsulinism-hyperammonemia syndrome in an infant with seizures
P2860
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P2860
Acute insulin responses to leucine in children with the hyperinsulinism/hyperammonemia syndrome
description
2001 nî lūn-bûn
@nan
2001 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
Acute insulin responses to leu ...... linism/hyperammonemia syndrome
@ast
Acute insulin responses to leu ...... linism/hyperammonemia syndrome
@en
Acute insulin responses to leu ...... linism/hyperammonemia syndrome
@en-gb
Acute insulin responses to leu ...... linism/hyperammonemia syndrome
@nl
type
label
Acute insulin responses to leu ...... linism/hyperammonemia syndrome
@ast
Acute insulin responses to leu ...... linism/hyperammonemia syndrome
@en
Acute insulin responses to leu ...... linism/hyperammonemia syndrome
@en-gb
Acute insulin responses to leu ...... linism/hyperammonemia syndrome
@nl
prefLabel
Acute insulin responses to leu ...... linism/hyperammonemia syndrome
@ast
Acute insulin responses to leu ...... linism/hyperammonemia syndrome
@en
Acute insulin responses to leu ...... linism/hyperammonemia syndrome
@en-gb
Acute insulin responses to leu ...... linism/hyperammonemia syndrome
@nl
P2093
P2860
P921
P356
P1476
Acute insulin responses to leu ...... linism/hyperammonemia syndrome
@en
P2093
P2860
P304
P356
10.1210/JCEM.86.8.7755
P407
P577
2001-08-01T00:00:00Z