Query author contributions in Reactome

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Details on Person IJlst, L

Class:Id	Person:77165
_displayName	IJlst, L
_timestamp	2003-10-17 02:05:19
firstname	Lodewijk
initial	L
surname	IJlst
(author)	[LiteratureReference:70776] 3-Methylglutaconic aciduria type I is caused by mutations in AUH. [LiteratureReference:201067] Cloning of the human carnitine-acylcarnitine carrier cDNA and identification of the molecular defect in a patient [LiteratureReference:213268] Ether lipid biosynthesis: alkyl-dihydroxyacetonephosphate synthase protein deficiency leads to reduced dihydroxyacetonephosphate acyltransferase activities [LiteratureReference:389890] Subcellular localization and physiological role of alpha-methylacyl-CoA racemase [LiteratureReference:390239] Clinical, biochemical, and mutational spectrum of peroxisomal acyl-coenzyme A oxidase deficiency [LiteratureReference:390279] Molecular cloning and expression of human carnitine octanoyltransferase: evidence for its role in the peroxisomal beta-oxidation of branched-chain fatty acids [LiteratureReference:390350] First identification of a 2-ketoglutarate/isocitrate transport system in mammalian peroxisomes and its characterization [LiteratureReference:390395] The human peroxisomal ABC half transporter ALDP functions as a homodimer and accepts acyl-CoA esters [LiteratureReference:452919] Molecular cloning and expression of human L-pipecolate oxidase [LiteratureReference:549206] Molecular basis of hepatic carnitine palmitoyltransferase I deficiency List all 13 refering instances
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No pathways have been reviewed or authored by IJlst, L (77165)