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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 Roach, Peter J

Class:IdPerson:70201
_displayNameRoach, Peter J
_timestamp2015-10-20 18:16:15
firstnamePeter J
initialPJ
modified[InstanceEdit:6805696] D'Eustachio, Peter, 2015-10-20
surnameRoach
(author)[LiteratureReference:70199] Crystal structure of the autocatalytic initiator of glycogen biosynthesis, glycogenin.
[LiteratureReference:70206] Characterization of human glycogenin-2, a self-glucosylating initiator of liver glycogen metabolism.
[LiteratureReference:70208] Characterization of rabbit skeletal muscle glycogenin. Tyrosine 194 is essential for function.
[LiteratureReference:70212] Glycogenin-2, a novel self-glucosylating protein involved in liver glycogen biosynthesis
[LiteratureReference:3322013] Interaction between glycogenin and glycogen synthase
[LiteratureReference:3322039] Glycogen and its metabolism: some new developments and old themes
[LiteratureReference:3777087] Phosphate incorporation during glycogen synthesis and Lafora disease
[LiteratureReference:5333092] Laforin is a glycogen phosphatase, deficiency of which leads to elevated phosphorylation of glycogen in vivo
[LiteratureReference:5333096] Genetic depletion of the malin E3 ubiquitin ligase in mice leads to lafora bodies and the accumulation of insoluble laforin
[LiteratureReference:5333596] Inhibiting glycogen synthesis prevents lafora disease in a mouse model
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No pathways have been reviewed or authored by Roach, Peter J (70201)