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 Ramsden, DA

Class:IdPerson:76728
_displayNameRamsden, DA
_timestamp2003-10-15 13:47:12
firstnameDale A
initialDA
surnameRamsden
(author)[LiteratureReference:76278] Werner protein is a target of DNA-dependent protein kinase in vivo and in vitro, and its catalytic activities are regulated by phosphorylation.
[LiteratureReference:76280] Ku heterodimer binds to both ends of the Werner protein and functional interaction occurs at the Werner N-terminus.
[LiteratureReference:76305] Autophosphorylation of the catalytic subunit of the DNA-dependent protein kinase is required for efficient end processing during DNA double-strand break repair.
[LiteratureReference:5687387] Tyrosyl-DNA phosphodiesterase and the repair of 3'-phosphoglycolate-terminated DNA double-strand breaks
[LiteratureReference:5687406] End-bridging is required for pol mu to efficiently promote repair of noncomplementary ends by nonhomologous end joining
[LiteratureReference:5687410] Association of DNA polymerase mu (pol mu) with Ku and ligase IV: role for pol mu in end-joining double-strand break repair
[LiteratureReference:5687422] A gradient of template dependence defines distinct biological roles for family X polymerases in nonhomologous end joining
[LiteratureReference:9764603] Mechanism, cellular functions and cancer roles of polymerase-theta-mediated DNA end joining
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No pathways have been reviewed or authored by Ramsden, DA (76728)