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10.1016/j.it.2015.09.004 http://scihub22266oqcxt.onion/10.1016/j.it.2015.09.004 C4640954!4640954 !26474675     free     free     free Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Warning: imagejpeg(C:\Inetpub\vhosts\kidney.de\httpdocs\phplern\26474675 .jpg): Failed to open stream: No such file or directory in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 117       Trends+Immunol 2015 ; 36 (11 ): 670-683 Nephropedia Template TP {{tp|p=26474675 |t=2015. Asymmetric Cell Division in T Lymphocyte Fate Diversification |pdf=|usr=}}{{26474675 }} gab.com Text Asymmetric Cell Division in T Lymphocyte Fate Diversification JO: Trends Immunol http://www.kidney.de/pget.php?&tw=1&pmid=26474675 #FOAvip Immunological protection against microbial pathogens is dependent on robust generation of functionally diverse T lymphocyte subsets. Upon microbial infection, naïve CD4(+) or CD8(+) T lymphocytes can give rise to effector- and memory-fated progeny that together mediate a potent immune response. Recent advances in single-cell immunological and genomic profiling technologies have helped elucidate early and late diversification mechanisms that enable the generation of heterogeneity from single T lymphocytes. We discuss these findings here and argue that one such mechanism, asymmetric cell division, creates an early divergence in T lymphocyte fates by giving rise to daughter cells with a propensity towards the terminally differentiated effector or self-renewing memory lineages, with cell-intrinsic and -extrinsic cues from the microenvironment driving the final maturation steps. Twit Text FOAVip Asymmetric Cell Division in T Lymphocyte Fate Diversification ????Trends Immunol http://www.kidney.de/pget.php?&tw=1&pmid=26474675 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=26474675 #FOAvip English Wikipedia <ref>{{Cite pmid|26474675 }}</ref> Asymmetric Cell Division in T Lymphocyte Fate Diversification #MMPMID26474675 Arsenio J ; Metz PJ ; Chang JT Trends Immunol 2015[Nov]; 36 (11 ): 670-683 PMID26474675 show ga Immunological protection against microbial pathogens is dependent on robust generation of functionally diverse T lymphocyte subsets. Upon microbial infection, naïve CD4(+) or CD8(+) T lymphocytes can give rise to effector- and memory-fated progeny that together mediate a potent immune response. Recent advances in single-cell immunological and genomic profiling technologies have helped elucidate early and late diversification mechanisms that enable the generation of heterogeneity from single T lymphocytes. We discuss these findings here and argue that one such mechanism, asymmetric cell division, creates an early divergence in T lymphocyte fates by giving rise to daughter cells with a propensity towards the terminally differentiated effector or self-renewing memory lineages, with cell-intrinsic and -extrinsic cues from the microenvironment driving the final maturation steps. |*Asymmetric Cell Division/immunology [MESH] |Animals [MESH] |Cell Differentiation [MESH] |Cell Lineage [MESH] |Humans [MESH]Asymmetric Cell Division in T Lymphocyte Fate Diversification (epmc).pdf DeepDyve Pubget Overpricing