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Query author contributions in Reactome

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Details on Person Oishi, K

Class:IdPerson:199662
_displayNameOishi, K
_timestamp2008-04-18 20:07:44
created[InstanceEdit:199631] D'Eustachio, P, 2007-07-11 18:15:46
firstnameKimihiko
initialK
modified[InstanceEdit:265440] D'Eustachio, P, 2008-04-18 20:07:45
surnameOishi
(author)[LiteratureReference:199655] Mutations in a new gene encoding a thiamine transporter cause thiamine-responsive megaloblastic anaemia syndrome
[LiteratureReference:199880] Akt inhibits the orphan nuclear receptor Nur77 and T-cell apoptosis
[LiteratureReference:265449] Inactivation of NPC1L1 causes multiple lipid transport defects and protects against diet-induced hypercholesterolemia
[LiteratureReference:444324] Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy
[LiteratureReference:517948] The role of {beta}-TrCP1 and {beta}-TrCP2 in circadian rhythm generation by mediating degradation of clock protein PER2
[LiteratureReference:549404] Genome-wide expression analysis of mouse liver reveals CLOCK-regulated circadian output genes
[LiteratureReference:549435] Rhythmic expression of BMAL1 mRNA is altered in Clock mutant mice: differential regulation in the suprachiasmatic nucleus and peripheral tissues
[LiteratureReference:879721] CLOCK is involved in the circadian transactivation of peroxisome-proliferator-activated receptor alpha (PPARalpha) in mice
[LiteratureReference:5626848] Transcription factor Ap2delta associates with Ash2l and ALR, a trithorax family histone methyltransferase, to activate Hoxc8 transcription
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No pathways have been reviewed or authored by Oishi, K (199662)
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