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10.1002/jbm.a.32545 http://scihub22266oqcxt.onion/10.1002/jbm.a.32545 C4396830!4396830!19569212     free     free     free Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 245.2 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       J+Biomed+Mater+Res+A 2010 ; 93 (2): 419-28 Nephropedia Template TP {{tp|p=19569212|t=2010. A Role for Decorin in Controlling Proliferation, Adhesion, and Migration of Murine Embryonic Fibroblasts |pdf=|usr=}}{{19569212}} gab.com Text A Role for Decorin in Controlling Proliferation, Adhesion, and Migration of Murine Embryonic Fibroblasts JO: J Biomed Mater Res A http://www.kidney.de/pget.php?&tw=1&pmid=19569212 #FOAvip The proteoglycan decorin putatively inhibits cell adhesion and cell migration on various extracellular matrix substrates through interactions with ?1 integrins. This study therefore examined the adhesive, migration, and proliferative characteristics of decorin knockout (Dcn?/?) murine embryonic fibroblasts compared to wild-type controls on collagen-coated, fibronectin-coated, and uncoated tissue culture plates. The Dcn?/? cells showed significantly greater proliferation than wild-type controls on all substrates. The Dcn?/? cells also showed significantly greater adhesion to both collagen and fibronectin; both cell types showed greater adhesion to collagen. The addition of exogenous decorin had a differential effect on adhesion to collagen between cell types, but not on fibronectin. For collagen, blocking either ?2 or ?1 integrin subunits significantly reduced adhesion for Dcn?/? cells; whereas for fibronectin, blocking either the ?5 or ?1 integrin subunits reduced adhesion for both cell types. Decorin and the ?5?1 integrin may have lesser roles in adhesion to fibronectin than previously presumed. Finally, compared to wild-type cells, Dcn?/? cells showed greater migration on both uncoated and collagen substrates. This study demonstrates that decorin affects the biology of various integrins that participate in cell proliferation, adhesion, and migration on various substrates. Twit Text FOAVip A Role for Decorin in Controlling Proliferation, Adhesion, and Migration of Murine Embryonic Fibroblasts ????J Biomed Mater Res A http://www.kidney.de/pget.php?&tw=1&pmid=19569212 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=19569212 #FOAvip English Wikipedia <ref>{{Cite pmid|19569212}}</ref> A Role for Decorin in Controlling Proliferation, Adhesion, and Migration of Murine Embryonic Fibroblasts #MMPMID19569212 Ferdous Z; Peterson S; Tseng H; Anderson D; Iozzo R; Grande-Allen K J Biomed Mater Res A 2010[May]; 93 (2): 419-28 PMID19569212show ga The proteoglycan decorin putatively inhibits cell adhesion and cell migration on various extracellular matrix substrates through interactions with ?1 integrins. This study therefore examined the adhesive, migration, and proliferative characteristics of decorin knockout (Dcn?/?) murine embryonic fibroblasts compared to wild-type controls on collagen-coated, fibronectin-coated, and uncoated tissue culture plates. The Dcn?/? cells showed significantly greater proliferation than wild-type controls on all substrates. The Dcn?/? cells also showed significantly greater adhesion to both collagen and fibronectin; both cell types showed greater adhesion to collagen. The addition of exogenous decorin had a differential effect on adhesion to collagen between cell types, but not on fibronectin. For collagen, blocking either ?2 or ?1 integrin subunits significantly reduced adhesion for Dcn?/? cells; whereas for fibronectin, blocking either the ?5 or ?1 integrin subunits reduced adhesion for both cell types. Decorin and the ?5?1 integrin may have lesser roles in adhesion to fibronectin than previously presumed. Finally, compared to wild-type cells, Dcn?/? cells showed greater migration on both uncoated and collagen substrates. This study demonstrates that decorin affects the biology of various integrins that participate in cell proliferation, adhesion, and migration on various substrates. äA Role for Decorin in Controlling Proliferation, Adhesion, and Migrati(epmc).pdf DeepDyve Pubget Overpricing