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.

Details on Person Yoshida, K

Class:Id	Person:114013
_displayName	Yoshida, K
_timestamp	2004-06-24 03:49:15
firstname	K
initial	K
surname	Yoshida
(author)	[LiteratureReference:111948] Synergistic action of diacylglycerol and unsaturated fatty acid for protein kinase C activation: its possible implications. [LiteratureReference:113627] Regulation of Geminin and Cdt1 expression by E2F transcription factors [LiteratureReference:208214] A novel mechanism of JNK1 activation. Nuclear translocation and activation of JNK1 during ischemia and reperfusion. [LiteratureReference:212510] Caspase-3-mediated cleavage of protein kinase C theta in induction of apoptosis [LiteratureReference:373474] Identification of CD72 as a lymphocyte receptor for the class IV semaphorin CD100: a novel mechanism for regulating B cell signaling [LiteratureReference:913311] The mouse RecA-like gene Dmc1 is required for homologous chromosome synapsis during meiosis [LiteratureReference:1112505] Activation of JAK2 kinase mediated by the interleukin 6 signal transducer gp130 [LiteratureReference:1112553] Molecular cloning of APRF, a novel IFN-stimulated gene factor 3 p91-related transcription factor involved in the gp130-mediated signaling pathway [LiteratureReference:1181362] A histone H3 methyltransferase controls epigenetic events required for meiotic prophase [LiteratureReference:1605704] Human beta-galactosidase gene mutations in GM1-gangliosidosis: a common mutation among Japanese adult/chronic cases List all 16 refering instances
[Change default viewing format]

No pathways have been reviewed or authored by Yoshida, K (114013)