about
Evidence for physical association of mitochondrial fatty acid oxidation and oxidative phosphorylation complexesCharacterization of new ACADSB gene sequence mutations and clinical implications in patients with 2-methylbutyrylglycinuria identified by newborn screeningNovel high throughput pooled shRNA screening identifies NQO1 as a potential drug target for host directed therapy for tuberculosisCLOCK is suggested to associate with comorbid alcohol use and depressive disorders.Metabolic autopsy with next generation sequencing in sudden unexpected death in infancy: Postmortem diagnosis of fatty acid oxidation disordersClinical aspects of short-chain acyl-CoA dehydrogenase deficiency.Ethylene glycol monomethyl ether-induced toxicity is mediated through the inhibition of flavoprotein dehydrogenase enzyme familySerum glycine is associated with regional body fat and insulin resistance in functionally-limited older adultsDelineating 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.Clinical and biochemical characterization of four patients with mutations in ECHS1.Quantitative proteomics analysis reveals glutamine deprivation activates fatty acid β-oxidation pathway in HepG2 cells.Compound heterozygous mutations of ACADS gene in newborn with short chain acyl-CoA dehydrogenase deficiency: case report and literatures review.Treatment strategies for acute metabolic disorders in neonates.ECHS1 mutations cause combined respiratory chain deficiency resulting in Leigh syndrome.Short-chain acyl-CoA dehydrogenase deficiency: from gene to cell pathology and possible disease mechanisms.Histone deacetylase inhibition results in a common metabolic profile associated with HT29 differentiation.A case report of short-chain acyl-CoA dehydrogenase deficiency (SCADD).Clinical and genetic characteristics of patients with fatty acid oxidation disorders identified by newborn screening.Precision medicine screening using whole-genome sequencing and advanced imaging to identify disease risk in adults.
P2860
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P2860
description
2008 nî lūn-bûn
@nan
2008 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
Short-chain acyl-coenzyme A dehydrogenase deficiency
@ast
Short-chain acyl-coenzyme A dehydrogenase deficiency
@en
Short-chain acyl-coenzyme A dehydrogenase deficiency
@nl
type
label
Short-chain acyl-coenzyme A dehydrogenase deficiency
@ast
Short-chain acyl-coenzyme A dehydrogenase deficiency
@en
Short-chain acyl-coenzyme A dehydrogenase deficiency
@nl
prefLabel
Short-chain acyl-coenzyme A dehydrogenase deficiency
@ast
Short-chain acyl-coenzyme A dehydrogenase deficiency
@en
Short-chain acyl-coenzyme A dehydrogenase deficiency
@nl
P2860
P3181
P1476
Short-chain acyl-coenzyme A dehydrogenase deficiency
@en
P2093
Michael J Bennett
Reena Jethva
P2860
P304
P3181
P356
10.1016/J.YMGME.2008.09.007
P407
P577
2008-11-05T00:00:00Z