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Details on Person Wanders, Ronald J A
| Class:Id | Person:201079 |
| _displayName | Wanders, Ronald J A |
| _timestamp | 2022-08-16 22:37:26 |
| created | [InstanceEdit:201070] Gopinathrao, G, 2007-07-30 14:54:02 |
| firstname | Ronald J A |
| initial | RJA |
| modified | [InstanceEdit:538689] D'Eustachio, P, 2010-03-08 [InstanceEdit:6809257] D'Eustachio, Peter, 2015-11-09 [InstanceEdit:9815308] D'Eustachio, Peter, 2022-08-16 |
| surname | Wanders |
| (author) | [LiteratureReference:191291] Phosphomevalonate kinase is a cytosolic protein in humans [LiteratureReference:191379] Mevalonate kinase is a cytosolic enzyme in humans [LiteratureReference:193392] Peroxisomal fatty acid oxidation disorders and 58 kDa sterol carrier protein X (SCPx). Activity measurements in liver and fibroblasts using a newly developed method. [LiteratureReference:193409] The CoA esters of 2-methyl-branched chain fatty acids and of the bile acid intermediates di- and trihydroxycoprostanic acids are oxidized by one single peroxisomal branched chain acyl-CoA oxidase in human liver and kidney [LiteratureReference:193432] Participation of two members of the very long-chain acyl-CoA synthetase family in bile acid synthesis and recycling [LiteratureReference:193502] Mutations in the gene encoding peroxisomal alpha-methylacyl-CoA racemase cause adult-onset sensory motor neuropathy [LiteratureReference:200031] Alkyl-dihydroxyacetone phosphate synthase and dihydroxyacetone phosphate acyltransferase form a protein complex in peroxisomes [LiteratureReference:201067] Cloning of the human carnitine-acylcarnitine carrier cDNA and identification of the molecular defect in a patient [LiteratureReference:389602] Phytanic acid alpha-oxidation, new insights into an old problem: a review [LiteratureReference:389645] Identification of human PMP34 as a peroxisomal ATP transporter |
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No pathways have been reviewed or authored by Wanders, Ronald J A (201079)