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 Ackerman, Michael J

Class:IdPerson:5577045
_displayNameAckerman, Michael J
_timestamp2014-05-29 15:58:12
created[InstanceEdit:5577230] Jassal, Bijay, 2014-05-29
firstnameMichael J
initialMJ
surnameAckerman
(author)[LiteratureReference:444324] Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy
[LiteratureReference:1482588] GPD1L links redox state to cardiac excitability by PKC-dependent phosphorylation of the sodium channel SCN5A
[LiteratureReference:5577145] A ubiquitous splice variant and a common polymorphism affect heterologous expression of recombinant human SCN5A heart sodium channels
[LiteratureReference:5634746] Mutation of an A-kinase-anchoring protein causes long-QT syndrome
[LiteratureReference:9660390] Elucidation of MRAS-mediated Noonan syndrome with cardiac hypertrophy
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No pathways have been reviewed or authored by Ackerman, Michael J (5577045)