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http://purl.uniprot.org/citations/16364187http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/16364187http://www.w3.org/2000/01/rdf-schema#comment"T-cell receptor (TCR) engagement initiates intracellular signalling cascades that lead to T-cell proliferation, cytokine production and differentiation into effector cells. These cascades comprise an array of protein-tyrosine kinases, phosphatases, GTP-binding proteins and adaptor proteins that regulate generic and specialised functions. The integration of these signals is essential for the normal development, homeostasis and function of T cells. Defects in a single mediator can produce T cells that are unable to participate fully in an immune response and/or that mount an inappropriate response, which leads to immunodeficiency, autoimmunity or leukaemia/lymphomas. This review highlights some of the key players in T-cell signalling and their involvement in the development of various clinical disease states. Some of these immune-specific signalling proteins are attractive potential targets in the development of therapies to augment T-cell responses to antigen or tumours, and to treat immune cell disorders."xsd:string
http://purl.uniprot.org/citations/16364187http://purl.org/dc/terms/identifier"doi:10.1017/s1462399405010264"xsd:string
http://purl.uniprot.org/citations/16364187http://purl.uniprot.org/core/author"Wilkinson B."xsd:string
http://purl.uniprot.org/citations/16364187http://purl.uniprot.org/core/author"Rudd C.E."xsd:string
http://purl.uniprot.org/citations/16364187http://purl.uniprot.org/core/author"Downey J.S."xsd:string
http://purl.uniprot.org/citations/16364187http://purl.uniprot.org/core/date"2005"xsd:gYear
http://purl.uniprot.org/citations/16364187http://purl.uniprot.org/core/name"Expert Rev Mol Med"xsd:string
http://purl.uniprot.org/citations/16364187http://purl.uniprot.org/core/pages"1-29"xsd:string
http://purl.uniprot.org/citations/16364187http://purl.uniprot.org/core/title"T-cell signalling and immune system disorders."xsd:string
http://purl.uniprot.org/citations/16364187http://purl.uniprot.org/core/volume"7"xsd:string
http://purl.uniprot.org/citations/16364187http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/16364187
http://purl.uniprot.org/citations/16364187http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/16364187
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http://purl.uniprot.org/uniprot/#_P13762-mappedCitation-16364187http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/16364187
http://purl.uniprot.org/uniprot/#_P20036-mappedCitation-16364187http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/16364187
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http://purl.uniprot.org/uniprot/#_P06239-mappedCitation-16364187http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/16364187
http://purl.uniprot.org/uniprot/#_P01730-mappedCitation-16364187http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/16364187
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http://purl.uniprot.org/uniprot/#_P01850-mappedCitation-16364187http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/16364187
http://purl.uniprot.org/uniprot/#_Q30154-mappedCitation-16364187http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/16364187