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10.1002/stem.1778 http://scihub22266oqcxt.onion/10.1002/stem.1778 C4138266!4138266!24964278     free     free     free Deprecated: Implicit conversion from float 233.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 233.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 233.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 233.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Stem+Cells 2014 ; 32 (9): 2550-6 Nephropedia Template TP {{tp|p=24964278|t=2014. SERPIN SPI2A AS A NOVEL MODULATOR OF HEMATOPOIETIC PROGENITOR CELL FORMATION |pdf=|usr=}}{{24964278}} gab.com Text SERPIN SPI2A AS A NOVEL MODULATOR OF HEMATOPOIETIC PROGENITOR CELL FORMATION JO: Stem Cells http://www.kidney.de/pget.php?&tw=1&pmid=24964278 #FOAvip Prime regulation over hematopoietic progenitor cell (HPC) production is exerted by hematopoietins (HP?s) and their Janus kinase-coupled receptors (HP-R?s). For HP/HP-R studies, one central challenge in determining specific effects involves the delineation of non-redundant signal transduction factors and their lineage restricted actions. Via loss-of-function (LOF) studies, we define roles for an HP-regulated Serpina3g/Spi2A intracellular serpin during granulomyelocytic, B-cell and HSC formation. In granulomyelocytic progenitors, GMCSF strongly induced Serpina3g expression with Stat5-dependency. Spi2A-KO led to 20-fold decreased CFU-GM formation, limited GMCSF-dependent granulocyte formation, and compromised neutrophil survival upon TNF-? exposure. In B-cell progenitors, Serpina3g was an IL7 target. Spi2A-KO elevated CFU-preB >6-fold, and altered B-cell formation in competitive BMT, and CpG challenge experiments. In HSCs, Serpina3g/Spi2A expression was also elevated. Spi2A-KO compromised LT-HSC proliferation (as well as LSK cell lysosomal integrity), and skewed LSK recovery post 5-FU. Spi2A therefore functions to modulate HP-regulated immune cell, and HSC formation post 5-FU challenge. Twit Text FOAVip SERPIN SPI2A AS A NOVEL MODULATOR OF HEMATOPOIETIC PROGENITOR CELL FORMATION ????Stem Cells http://www.kidney.de/pget.php?&tw=1&pmid=24964278 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=24964278 #FOAvip English Wikipedia <ref>{{Cite pmid|24964278}}</ref> SERPIN SPI2A AS A NOVEL MODULATOR OF HEMATOPOIETIC PROGENITOR CELL FORMATION #MMPMID24964278 Li L; Byrne SM; Rainville N; Su S; Jachimowicz E; Aucher A; Davis DM; Ashton-Rickardt PG; Wojchowski DM Stem Cells 2014[Sep]; 32 (9): 2550-6 PMID24964278show ga Prime regulation over hematopoietic progenitor cell (HPC) production is exerted by hematopoietins (HP?s) and their Janus kinase-coupled receptors (HP-R?s). For HP/HP-R studies, one central challenge in determining specific effects involves the delineation of non-redundant signal transduction factors and their lineage restricted actions. Via loss-of-function (LOF) studies, we define roles for an HP-regulated Serpina3g/Spi2A intracellular serpin during granulomyelocytic, B-cell and HSC formation. In granulomyelocytic progenitors, GMCSF strongly induced Serpina3g expression with Stat5-dependency. Spi2A-KO led to 20-fold decreased CFU-GM formation, limited GMCSF-dependent granulocyte formation, and compromised neutrophil survival upon TNF-? exposure. In B-cell progenitors, Serpina3g was an IL7 target. Spi2A-KO elevated CFU-preB >6-fold, and altered B-cell formation in competitive BMT, and CpG challenge experiments. In HSCs, Serpina3g/Spi2A expression was also elevated. Spi2A-KO compromised LT-HSC proliferation (as well as LSK cell lysosomal integrity), and skewed LSK recovery post 5-FU. Spi2A therefore functions to modulate HP-regulated immune cell, and HSC formation post 5-FU challenge. äSERPIN SPI2A AS A NOVEL MODULATOR OF HEMATOPOIETIC PROGENITOR CELL FOR(epmc).pdf DeepDyve Pubget Overpricing