New genetic defects in mitochondrial fatty acid oxidation and carnitine deficiency.
about
Peroxisome proliferator-activated receptor alpha mediates the adaptive response to fastingMedium chain acyl-CoA dehydrogenase deficiencyCloning of the human carnitine-acylcarnitine carrier cDNA and identification of the molecular defect in a patientDilated cardiomyopathy due to type II X-linked 3-methylglutaconic aciduria: successful treatment with pantothenic acidProgressive adaptation of hepatic ketogenesis in mice fed a high-fat diet.Plasma and hepatic carnitine and coenzyme A pools in a patient with fatal, valproate induced hepatotoxicity.Carnitine biosynthesis in mammals.Diminished hepatic gluconeogenesis via defects in tricarboxylic acid cycle flux in peroxisome proliferator-activated receptor gamma coactivator-1alpha (PGC-1alpha)-deficient mice.Delineating the role of alterations in lipid metabolism to the pathogenesis of inherited skeletal and cardiac muscle disorders: Thematic Review Series: Genetics of Human Lipid Diseases.Partial resistance to peroxisome proliferator-activated receptor-alpha agonists in ZDF rats is associated with defective hepatic mitochondrial metabolism.Fatal Nonhepatic Hyperammonemia in ICU Setting: A Rare but Serious Complication following Bariatric Surgery.Altered carnitine homeostasis is associated with decreased mitochondrial function and altered nitric oxide signaling in lambs with pulmonary hypertension.Two genetic forms of hyperinsulinemic hypoglycemia caused by dysregulation of glutamate dehydrogenase.Diagnosis and management of inborn errors of metabolismPhase I clinical studies of S-1108: safety and pharmacokinetics in a multiple-administration study with special emphasis on the influence on carnitine body stores.Mammalian mitochondrial beta-oxidation.Serum hepatocyte growth factor as an index of extensive catabolism of patients awaiting liver transplantation.Fat and cardiotoxicity in hereditary pulmonary hypertension.An unusually high frequency of SCAD deficiency caused by two pathogenic variants in the ACADS gene and its relationship to the ethnic structure in Slovakia.
P2860
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P2860
New genetic defects in mitochondrial fatty acid oxidation and carnitine deficiency.
description
1987 nî lūn-bûn
@nan
1987年の論文
@ja
1987年論文
@yue
1987年論文
@zh-hant
1987年論文
@zh-hk
1987年論文
@zh-mo
1987年論文
@zh-tw
1987年论文
@wuu
1987年论文
@zh
1987年论文
@zh-cn
name
New genetic defects in mitochondrial fatty acid oxidation and carnitine deficiency.
@en
New genetic defects in mitochondrial fatty acid oxidation and carnitine deficiency.
@nl
type
label
New genetic defects in mitochondrial fatty acid oxidation and carnitine deficiency.
@en
New genetic defects in mitochondrial fatty acid oxidation and carnitine deficiency.
@nl
prefLabel
New genetic defects in mitochondrial fatty acid oxidation and carnitine deficiency.
@en
New genetic defects in mitochondrial fatty acid oxidation and carnitine deficiency.
@nl
P1476
New genetic defects in mitochondrial fatty acid oxidation and carnitine deficiency.
@en
P2093
Stanley CA
P577
1987-01-01T00:00:00Z