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dc.contributor.authorGascoigne, Nicholas R. J.
dc.contributor.authorCasas, Javier
dc.contributor.authorBrzostek, Joanna
dc.contributor.authorRybakin, Vasily
dc.date.accessioned2024-01-08T14:25:41Z
dc.date.available2024-01-08T14:25:41Z
dc.date.issued2011
dc.identifier.citationFrontiers Immunol. 2, (2011).es
dc.identifier.urihttps://uvadoc.uva.es/handle/10324/64298
dc.descriptionProducción Científicaes
dc.description.abstractRecent data with CD8+T cells show that the initial phase ofT cell receptor (TCR) binding to MHC–peptide (MHCp) is quickly followed by a second, stronger, binding phase representing the binding of CD8 to the MHCp. This second phase requires signaling by a Src-family kinase such as Lck. These data point out two aspects of the initial stage of TCR signaling that have not yet been clearly resolved. Firstly, how and by which Src-family kinase, is the initial phosphorylation of CD3ζ accomplished, given that the Lck associated with the co-receptors (CD4 or CD8) is not yet available. Secondly, what is the mechanism by which the co-receptor is brought close to the bound TCR before the co-receptor binds to MHCp?es
dc.format.mimetypeapplication/pdfes
dc.language.isoenges
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.titleInitiation of TCR Phosphorylation and Signal Transductiones
dc.typeinfo:eu-repo/semantics/articlees
dc.identifier.doi10.3389/fimmu.2011.00072es
dc.identifier.publicationtitleFrontiers in Immunologyes
dc.identifier.publicationvolume2es
dc.peerreviewedSIes
dc.description.projectSubvenciones NIH GM065230 y AI074074 a Nicholas R. J. Gascoigne. Este es el manuscrito 21444 de The Scripps Research Institute.
dc.identifier.essn1664-3224es
dc.rightsAtribución 4.0 Internacional
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones


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