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Details on Person Molecular characterization of the human peroxisomal branched-chain acyl-CoA oxidase: cDNA cloning, chromosomal assignment, tissue distribution, and evidence for the absence of the protein in Zellweger syndrome

Class:IdLiteratureReference:192346
_displayNameMolecular characterization of the human peroxisomal branched-chain acyl-CoA oxidase: cDNA cloning, chromosomal assignment, tissue distribution, and evidence for the absence of the protein in Zellweger syndrome
_timestamp2007-01-31 12:01:00
author[Person:192355] Baumgart, E
[Person:192326] Vanhooren, JC
[Person:192337] Fransen, M
[Person:192317] Marynen, P
[Person:192347] Puype, M
[Person:192334] Vandekerckhove, J
[Person:192343] Leunissen, JA
[Person:192338] Fahimi, HD
[Person:192353] Mannaerts, Guy P
[Person:192116] Van Veldhoven, Paul P
created[InstanceEdit:192352] Jassal, B, 2007-01-31 11:59:37
journalProc Natl Acad Sci U S A
pages13748-53
pubMedIdentifier8943006
titleMolecular characterization of the human peroxisomal branched-chain acyl-CoA oxidase: cDNA cloning, chromosomal assignment, tissue distribution, and evidence for the absence of the protein in Zellweger syndrome
volume93
year1996
(literatureReference)[Reaction:192335] 25(S) THCA-CoA is dehydrogenated to 3alpha,7alpha,12alpha-trihydroxy-5beta-cholest-24-enoyl-CoA (THCA-CoA) [Homo sapiens]
[Reaction:193369] 25(S) DHCA-CoA is dehydrogenated to 25(S) 3alpha,7alpha-dihydroxy-5beta-cholest-24-enoyl-CoA [Homo sapiens]
[Reaction:389889] ACOX2:FAD, ACOXL:FAD oxidise (2S)-pristanoyl-CoA to trans-2,3-dehydropristanoyl-CoA [Homo sapiens]
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No pathways have been reviewed or authored by Molecular characterization of the human peroxisomal branched-chain acyl-CoA oxidase: cDNA cloning, chromosomal assignment, tissue distribution, and evidence for the absence of the protein in Zellweger syndrome (192346)