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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.

If you have an ORCID ID that is not listed on this page, please forward this information to us and we will update your Reactome pathway records.

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Details on Person Suzuki, Y

Class:IdPerson:2285500
_displayNameSuzuki, Y
_timestamp2012-05-28 12:15:54
created[InstanceEdit:2285516] Jassal, B, 2012-05-28
firstnameY
initialY
surnameSuzuki
(author)[LiteratureReference:2285513] Clinical and molecular analysis of a Japanese boy with Morquio B disease
[LiteratureReference:2457668] Mucopolysaccharidosis type IVA (Morquio A disease): clinical review and current treatment
[LiteratureReference:2458253] Cloning, sequencing, and expression of cDNA for human beta-galactosidase
[LiteratureReference:2458281] Mucopolysaccharidosis IV A: molecular cloning of the human N-acetylgalactosamine-6-sulfatase gene (GALNS) and analysis of the 5'-flanking region
[LiteratureReference:2744353] Human and mouse homologues of the Drosophila melanogaster tweety (tty) gene: a novel gene family encoding predicted transmembrane proteins
[LiteratureReference:2993864] Relationship between kinetic properties of mutant enzyme and biochemical and clinical responsiveness to biotin in holocarboxylase synthetase deficiency
[LiteratureReference:3323129] Identification of holocarboxylase synthetase (HCS) proteins in human placenta
[LiteratureReference:3325445] Haplotype analysis suggests that the two predominant mutations in Japanese patients with holocarboxylase synthetase deficiency are founder mutations
[LiteratureReference:3325489] Structure of human holocarboxylase synthetase gene and mutation spectrum of holocarboxylase synthetase deficiency
[LiteratureReference:3325498] Identification and characterization of mutations in patients with holocarboxylase synthetase deficiency
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No pathways have been reviewed or authored by Suzuki, Y (2285500)