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10.1016/j.it.2014.09.003 http://scihub22266oqcxt.onion/10.1016/j.it.2014.09.003 C4383740!4383740 !25283967     free     free     free Warning: imagejpeg(C:\Inetpub\vhosts\kidney.de\httpdocs\phplern\25283967 .jpg): Failed to open stream: No such file or directory in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 117       Trends+Immunol 2014 ; 35 (12 ): 613-621 Nephropedia Template TP {{tp|p=25283967 |t=2014. ?? T cell surveillance via CD1 molecules |pdf=|usr=}}{{25283967 }} gab.com Text T cell surveillance via CD1 molecules JO: Trends Immunol http://www.kidney.de/pget.php?&tw=1&pmid=25283967 #FOAvip ?? T cells are a prominent epithelial-resident lymphocyte population, possessing multi-functional capacities in the repair of host tissue, pathogen clearance, and tumor surveillance. Although three decades have now passed since their discovery, the nature of ?? T cell receptor (TCR)-mediated ligand recognition remains poorly defined. Recent studies have provided structural insight into this recognition, demonstrating that ?? T cells survey both CD1 and the presented lipid, and in some cases are exquisitely lipid specific. We review these findings here, examining the molecular basis for and the functional relevance of this interaction. We discuss potential implications on the notion that non-classical major histocompatibility complex (MHC) molecules may function as important restricting elements of ?? TCR specificity, and on our understanding of ?? T cell activation and function. Twit Text FOAVip T cell surveillance via CD1 molecules ????Trends Immunol http://www.kidney.de/pget.php?&tw=1&pmid=25283967 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=25283967 #FOAvip English Wikipedia <ref>{{Cite pmid|25283967 }}</ref> ?? T cell surveillance via CD1 molecules #MMPMID25283967 Luoma AM ; Castro CD ; Adams EJ Trends Immunol 2014[Dec]; 35 (12 ): 613-621 PMID25283967 show ga ?? T cells are a prominent epithelial-resident lymphocyte population, possessing multi-functional capacities in the repair of host tissue, pathogen clearance, and tumor surveillance. Although three decades have now passed since their discovery, the nature of ?? T cell receptor (TCR)-mediated ligand recognition remains poorly defined. Recent studies have provided structural insight into this recognition, demonstrating that ?? T cells survey both CD1 and the presented lipid, and in some cases are exquisitely lipid specific. We review these findings here, examining the molecular basis for and the functional relevance of this interaction. We discuss potential implications on the notion that non-classical major histocompatibility complex (MHC) molecules may function as important restricting elements of ?? TCR specificity, and on our understanding of ?? T cell activation and function. ä?? T cell surveillance via CD1 molecules (epmc).pdf DeepDyve Pubget Overpricing