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dc.contributor.authorSeagal, J.es
dc.contributor.authorMelamed, D.es
dc.date.accessioned2011-06-08T09:03:01Z-
dc.date.available2011-06-08T09:03:01Z-
dc.date.issued2003-
dc.identifier.issn0213-3911es
dc.identifier.urihttp://hdl.handle.net/10201/21433-
dc.description.abstractHomeostasis in the B cell compartment (as well as in T cells) is controlled by tightly regulated selection events. Throughout their life span, B cells are subjected to selection signals determining not only developmental progression, but also maturation and survival. It is now clear that most of these signals require the expression of B cell antigen receptor (or preB receptor) with functional signaling capacity. The administration of numerous mutations into the mouse germline enabled us to identify several checkpoints along the B cell developmental pathway, and provided us with powerful experimental tools to probe for selection events regulating developmental progression. In here, we will discuss recent studies in this field.es
dc.formatapplication/pdfes
dc.format.extent9es
dc.languageenges
dc.publisherMurcia : F. Hernándezes
dc.relation.ispartofHistology and histopathologyes
dc.rightsinfo:eu-repo/semantics/openAccesses
dc.subjectPositive selectiones
dc.subjectNegative selectiones
dc.subject.otherCDU::6 - Ciencias aplicadas::61 - Medicinaes
dc.titleSelection events in directing B cell developmentes
dc.typeinfo:eu-repo/semantics/articlees
Aparece en las colecciones:Vol.18, nº 2 (2003)

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