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dc.contributor.authorPalou, Eduard
dc.contributor.authorFuente García, Miguel Ángel de la 
dc.contributor.authorNicolás, Josep Maria
dc.contributor.authorVilardell, Carme
dc.contributor.authorVives, Jordi
dc.contributor.authorGayá, Antoni
dc.date.accessioned2015-04-10T11:29:46Z
dc.date.available2015-04-10T11:29:46Z
dc.date.issued1997
dc.identifier.citationImmunology Letters, 1997, 57(1-3):101-103es
dc.identifier.issn0165-2478es
dc.identifier.urihttp://uvadoc.uva.es/handle/10324/10380
dc.descriptionProducción Científicaes
dc.description.abstractCD148 is a new cluster of differentiation defined in the VI International Workshop on Leucocyte Differentiation Antigens. It has been identified as the hematopoietic form of a formerly described membrane protein tyrosine phosphatase called HPTP eta/ DEP-1. Previous data have demonstrated that this molecule is able to give rise to [Ca2+]i increase. In the present work we show its capability to induce protein tyrosine phosphorylation in human lymphocytes in spite of its intrinsic protein tyrosine phosphatase activity. The induction of kinase activity suggests the involvement of some protein tyrosine kinase based signaling pathway. The activation of this postulated kinase could be carried out through a direct association or via an adapter molecule.es
dc.format.mimetypeapplication/pdfes
dc.language.isoenges
dc.publisherElsevieres
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectCélulas hematopoyéticases
dc.subjectHematología
dc.titleCD148, a membrane protein tyrosine phosphatase, is able to induce tyrosine phosphorylation on human lymphocyteses
dc.typeinfo:eu-repo/semantics/articlees
dc.identifier.doi10.1016/S0165-2478(97)00069-2es
dc.identifier.publicationfirstpage101es
dc.identifier.publicationissue1-3es
dc.identifier.publicationlastpage103es
dc.identifier.publicationtitleImmunology Letteres
dc.identifier.publicationvolume57es
dc.peerreviewedSIes
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International


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