Reactome: A Curated Pathway Database
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Query author contributions in Reactome

Reactome depends on collaboration between our curation team and outside experts to assemble and peer-review its pathway modules. The integration of ORCID within Reactome enables us to meet a key challenge with authoring, curating and reviewing biological information by incentivizing and crediting the external experts that contribute their expertise and time to the Reactome curation process. More information is available at ORCID and Reactome.

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Details on Person Holzinger, A

Class:IdPerson:70750
_displayNameHolzinger, A
_timestamp0000-00-00 00:00:00
firstnameAndreas
initialA
surnameHolzinger
(author)[LiteratureReference:70749] Cloning of the human MCCA and MCCB genes and mutations therein reveal the molecular cause of 3-methylcrotonyl-CoA: carboxylase deficiency
[LiteratureReference:382588] Human adrenoleukodystrophy protein and related peroxisomal ABC transporters interact with the peroxisomal assembly protein PEX19p
[LiteratureReference:382598] Characterization and functional analysis of the nucleotide binding fold in human peroxisomal ATP binding cassette transporters
[LiteratureReference:1112677] Mitochondrial targeting signals and mature peptides of 3-methylcrotonyl-CoA carboxylase
[LiteratureReference:1456461] cDNA cloning and mRNA expression of the human adrenoleukodystrophy related protein (ALDRP), a peroxisomal ABC transporter
[LiteratureReference:8985870] Mutations in the proenteropeptidase gene are the molecular cause of congenital enteropeptidase deficiency
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No pathways have been reviewed or authored by Holzinger, A (70750)