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Query author contributions in Reactome

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Details on Person Gould, Stephen J

Class:IdPerson:70933
_displayNameGould, Stephen J
_timestamp2015-06-18 21:54:27
firstnameStephen J
initialSJ
modified[InstanceEdit:6784221] D'Eustachio, Peter, 2015-06-18
surnameGould
(author)[LiteratureReference:70929] Identification of the alpha-aminoadipic semialdehyde synthase gene, which is defective in familial hyperlysinemia
[LiteratureReference:193495] Identification of peroxisomal acyl-CoA thioesterases in yeast and humans
[LiteratureReference:199205] Identification of the alpha-aminoadipic semialdehyde dehydrogenase-phosphopantetheinyl transferase gene, the human ortholog of the yeast LYS5 gene
[LiteratureReference:382605] PEX19 binds multiple peroxisomal membrane proteins, is predominantly cytoplasmic, and is required for peroxisome membrane synthesis
[LiteratureReference:382607] PEX3 functions as a PEX19 docking factor in the import of class I peroxisomal membrane proteins
[LiteratureReference:389560] The human PICD gene encodes a cytoplasmic and peroxisomal NADP(+)-dependent isocitrate dehydrogenase
[LiteratureReference:389880] Identification and characterization of HAOX1, HAOX2, and HAOX3, three human peroxisomal 2-hydroxy acid oxidases
[LiteratureReference:452488] L-Pipecolic acid oxidase, a human enzyme essential for the degradation of L-pipecolic acid, is most similar to the monomeric sarcosine oxidases
[LiteratureReference:480263] PEX13 is mutated in complementation group 13 of the peroxisome-biogenesis disorders
[LiteratureReference:977322] MCD encodes peroxisomal and cytoplasmic forms of malonyl-CoA decarboxylase and is mutated in malonyl-CoA decarboxylase deficiency
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No pathways have been reviewed or authored by Gould, Stephen J (70933)
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