10077518

Source:http://linkedlifedata.com/resource/pubmed/id/10077518

Download in:

Switch to

Custom View

Named Graph Language Inference

Statements in which the resource exists as a subject.
Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0011071, umls-concept:C0011155, umls-concept:C0019409, umls-concept:C0065170, umls-concept:C0678227, umls-concept:C0878544, umls-concept:C1521725, umls-concept:C1521991
pubmed:issue	10
pubmed:dateCreated	1999-4-15
pubmed:abstractText	Genetic defects are being increasingly recognized in the etiology of primary cardiomyopathy (CM). Very-long-chain acyl-CoA dehydrogenase (VLCAD) catalyzes the first step in the beta-oxidation spiral of fatty acid metabolism, the crucial pathway for cardiac energy production.
pubmed:grant	http://linkedlifedata.com/resource/pubmed/grant/DK33487, http://linkedlifedata.com/resource/pubmed/grant/HL-52350
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0147763
pubmed:citationSubset	AIM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Acyl-CoA Dehydrogenase, Long-Chain, http://linkedlifedata.com/resource/pubmed/chemical/Acyl-CoA Dehydrogenases
pubmed:status	MEDLINE
pubmed:month	Mar
pubmed:issn	0009-7322
pubmed:author	pubmed-author:GibsonBB, pubmed-author:GopalakrishnanDD, pubmed-author:HugGG, pubmed-author:MathurAA, pubmed-author:RinaldoPP, pubmed-author:SimsH FHF, pubmed-author:StraussA WAW, pubmed-author:VockleyJJ
pubmed:issnType	Print
pubmed:day	16
pubmed:volume	99
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1337-43
pubmed:dateRevised	2007-11-14
pubmed:meshHeading	pubmed-meshheading:10077518-Acyl-CoA Dehydrogenase, Long-Chain, pubmed-meshheading:10077518-Acyl-CoA Dehydrogenases, pubmed-meshheading:10077518-Amino Acid Substitution, pubmed-meshheading:10077518-Cardiomyopathies, pubmed-meshheading:10077518-Cell Line, pubmed-meshheading:10077518-Death, Sudden, Cardiac, pubmed-meshheading:10077518-Energy Metabolism, pubmed-meshheading:10077518-Fatty Liver, pubmed-meshheading:10077518-Female, pubmed-meshheading:10077518-Fibroblasts, pubmed-meshheading:10077518-Frameshift Mutation, pubmed-meshheading:10077518-Humans, pubmed-meshheading:10077518-Hypoglycemia, pubmed-meshheading:10077518-Infant, pubmed-meshheading:10077518-Infant, Newborn, pubmed-meshheading:10077518-Male, pubmed-meshheading:10077518-Models, Molecular, pubmed-meshheading:10077518-Mutation, pubmed-meshheading:10077518-Myocardium, pubmed-meshheading:10077518-Polymerase Chain Reaction, pubmed-meshheading:10077518-Polymorphism, Single-Stranded Conformational, pubmed-meshheading:10077518-RNA Splicing, pubmed-meshheading:10077518-Sudden Infant Death
pubmed:year	1999
pubmed:articleTitle	Molecular heterogeneity in very-long-chain acyl-CoA dehydrogenase deficiency causing pediatric cardiomyopathy and sudden death.
pubmed:affiliation	Departments of Pediatrics, Medicine and Molecular Biology and Pharmacology, Washington University School of Medicine, St Louis Children's Hospital, St Louis, MO, USA.
pubmed:publicationType	Journal Article, Research Support, U.S. Gov't, P.H.S.