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10.1074/jbc.R114.550707 http://scihub22266oqcxt.onion/10.1074/jbc.R114.550707 C4106304!4106304!24860095     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 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       J+Biol+Chem 2014 ; 289 (29): 19841-9 Nephropedia Template TP {{tp|p=24860095|t=2014. Mouse Models for Studying the Formation and Propagation of Prions* |pdf=|usr=}}{{24860095}} gab.com Text Mouse Models for Studying the Formation and Propagation of Prions* JO: J Biol Chem http://www.kidney.de/pget.php?&tw=1&pmid=24860095 #FOAvip Prions are self-propagating protein conformers that cause a variety of neurodegenerative disorders in humans and animals. Mouse models have played key roles in deciphering the biology of prions and in assessing candidate therapeutics. The development of transgenic mice that form prions spontaneously in the brain has advanced our understanding of sporadic and genetic prion diseases. Furthermore, the realization that many proteins can become prions has necessitated the development of mouse models for assessing the potential transmissibility of common neurodegenerative diseases. As the universe of prion diseases continues to expand, mouse models will remain crucial for interrogating these devastating illnesses. Twit Text FOAVip Mouse Models for Studying the Formation and Propagation of Prions* ????J Biol Chem http://www.kidney.de/pget.php?&tw=1&pmid=24860095 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=24860095 #FOAvip English Wikipedia <ref>{{Cite pmid|24860095}}</ref> Mouse Models for Studying the Formation and Propagation of Prions* #MMPMID24860095 Watts JC; Prusiner SB J Biol Chem 2014[Jul]; 289 (29): 19841-9 PMID24860095show ga Prions are self-propagating protein conformers that cause a variety of neurodegenerative disorders in humans and animals. Mouse models have played key roles in deciphering the biology of prions and in assessing candidate therapeutics. The development of transgenic mice that form prions spontaneously in the brain has advanced our understanding of sporadic and genetic prion diseases. Furthermore, the realization that many proteins can become prions has necessitated the development of mouse models for assessing the potential transmissibility of common neurodegenerative diseases. As the universe of prion diseases continues to expand, mouse models will remain crucial for interrogating these devastating illnesses. äMouse Models for Studying the Formation and Propagation of Prions* (epmc).pdf DeepDyve Pubget Overpricing