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dc.contributor.author이수영*
dc.date.accessioned2016-08-28T12:08:44Z-
dc.date.available2016-08-28T12:08:44Z-
dc.date.issued2007*
dc.identifier.isbn9780387706290*
dc.identifier.issn0065-2598*
dc.identifier.otherOAK-4120*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/219876-
dc.description.abstractTumor necrosis factor (TNF) receptor-associated factor (TRAF)1 was originally identified based on its ability to interact with the cytosolic domain of TNF receptor type 2 (TNFR2). TRAF1 is unique among TRAF proteins in that it lacks RING domain found in the N-terminal regions of other TRAFs. TRAF1 can associate with multiple TNFR family members and can also bind several protein kinases and adaptor proteins suggesting that this protein likely possesses multiple functions in cytokine signaling networks. Although our understanding of TRAF1 functions and the underlying mechanisms at molecular and cellular levels has been advanced in recent years, much still needs to be learned before we have a full grasp of TRAF1 biology. © 2007 Landes Bioscience and Springer Science+Business Media, LLC.*
dc.languageEnglish*
dc.titleTRAF1 and its biological functions*
dc.typeReview*
dc.relation.volume597*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage25*
dc.relation.lastpage31*
dc.relation.journaltitleAdvances in Experimental Medicine and Biology*
dc.identifier.doi10.1007/978-0-387-70630-6-2*
dc.identifier.wosidWOS:000247960100002*
dc.identifier.scopusid2-s2.0-34547785607*
dc.author.googleLee S.Y.*
dc.author.googleChoi Y.*
dc.contributor.scopusid이수영(53980218900;7409697278)*
dc.date.modifydate20240415140424*
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자연과학대학 > 생명과학전공 > Journal papers
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