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10.1186/s40824-016-0074-2 http://scihub22266oqcxt.onion/10.1186/s40824-016-0074-2 C5006370!5006370!27583168     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       Biomater+Res 2016 ; 20 (1): ä Nephropedia Template TP {{tp|p=27583168|t=2016. Solid organ fabrication: comparison of decellularization to 3D bioprinting |pdf=|usr=}}{{27583168}} gab.com Text Solid organ fabrication: comparison of decellularization to 3D bioprinting JO: Biomater Res http://www.kidney.de/pget.php?&tw=1&pmid=27583168 #FOAvip Solid organ fabrication is an ultimate goal of Regenerative Medicine. Since the introduction of Tissue Engineering in 1993, functional biomaterials, stem cells, tunable microenvironments, and high-resolution imaging technologies have significantly advanced efforts to regenerate in vitro culture or tissue platforms. Relatively simple flat or tubular organs are already in (pre)clinical trials and a few commercial products are in market. The road to more complex, high demand, solid organs including heart, kidney and lung will require substantive technical advancement. Here, we consider two emerging technologies for solid organ fabrication. One is decellularization of cadaveric organs followed by repopulation with terminally differentiated or progenitor cells. The other is 3D bioprinting to deposit cell-laden bio-inks to attain complex tissue architecture. We reviewed the development and evolution of the two technologies and evaluated relative strengths needed to produce solid organs, with special emphasis on the heart and other tissues of the cardiovascular system. Twit Text FOAVip Solid organ fabrication: comparison of decellularization to 3D bioprinting ????Biomater Res http://www.kidney.de/pget.php?&tw=1&pmid=27583168 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=27583168 #FOAvip English Wikipedia <ref>{{Cite pmid|27583168}}</ref> Solid organ fabrication: comparison of decellularization to 3D bioprinting #MMPMID27583168 Jung JP; Bhuiyan DB; Ogle BM Biomater Res 2016[]; 20 (1): ä PMID27583168show ga Solid organ fabrication is an ultimate goal of Regenerative Medicine. Since the introduction of Tissue Engineering in 1993, functional biomaterials, stem cells, tunable microenvironments, and high-resolution imaging technologies have significantly advanced efforts to regenerate in vitro culture or tissue platforms. Relatively simple flat or tubular organs are already in (pre)clinical trials and a few commercial products are in market. The road to more complex, high demand, solid organs including heart, kidney and lung will require substantive technical advancement. Here, we consider two emerging technologies for solid organ fabrication. One is decellularization of cadaveric organs followed by repopulation with terminally differentiated or progenitor cells. The other is 3D bioprinting to deposit cell-laden bio-inks to attain complex tissue architecture. We reviewed the development and evolution of the two technologies and evaluated relative strengths needed to produce solid organs, with special emphasis on the heart and other tissues of the cardiovascular system. äSolid organ fabrication: comparison of decellularization to 3D bioprin(epmc).pdf DeepDyve Pubget Overpricing