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10.1038/ncomms11689 http://scihub22266oqcxt.onion/10.1038/ncomms11689 C4894968!4894968!27229621     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       Nat+Commun 2016 ; 7 (ä): ä Nephropedia Template TP {{tp|p=27229621|t=2016. A method to rapidly create protein aggregates in living cells |pdf=|usr=}}{{27229621}} gab.com Text A method to rapidly create protein aggregates in living cells JO: Nat Commun http://www.kidney.de/pget.php?&tw=1&pmid=27229621 #FOAvip The accumulation of protein aggregates is a common pathological hallmark of many neurodegenerative diseases. However, we do not fully understand how aggregates are formed or the complex network of chaperones, proteasomes and other regulatory factors involved in their clearance. Here, we report a chemically controllable fluorescent protein that enables us to rapidly produce small aggregates inside living cells on the order of seconds, as well as monitor the movement and coalescence of individual aggregates into larger structures. This method can be applied to diverse experimental systems, including live animals, and may prove valuable for understanding cellular responses and diseases associated with protein aggregates. Twit Text FOAVip A method to rapidly create protein aggregates in living cells ????Nat Commun http://www.kidney.de/pget.php?&tw=1&pmid=27229621 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=27229621 #FOAvip English Wikipedia <ref>{{Cite pmid|27229621}}</ref> A method to rapidly create protein aggregates in living cells #MMPMID27229621 Miyazaki Y; Mizumoto K; Dey G; Kudo T; Perrino J; Chen Lc; Meyer T; Wandless TJ Nat Commun 2016[]; 7 (ä): ä PMID27229621show ga The accumulation of protein aggregates is a common pathological hallmark of many neurodegenerative diseases. However, we do not fully understand how aggregates are formed or the complex network of chaperones, proteasomes and other regulatory factors involved in their clearance. Here, we report a chemically controllable fluorescent protein that enables us to rapidly produce small aggregates inside living cells on the order of seconds, as well as monitor the movement and coalescence of individual aggregates into larger structures. This method can be applied to diverse experimental systems, including live animals, and may prove valuable for understanding cellular responses and diseases associated with protein aggregates. äA method to rapidly create protein aggregates in living cells (epmc).pdf DeepDyve Pubget Overpricing