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10.1016/j.celrep.2020.01.021 http://scihub22266oqcxt.onion/10.1016/j.celrep.2020.01.021 C7039342!7039342!32049003     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       Cell+Rep 2020 ; 30 (6): 1690-1701.e4 Nephropedia Template TP {{tp|p=32049003|t=2020. A Requirement for Argonaute 4 in Mammalian Antiviral Defense |pdf=|usr=}}{{32049003}} gab.com Text A Requirement for Argonaute 4 in Mammalian Antiviral Defense JO: Cell Rep http://www.kidney.de/pget.php?&tw=1&pmid=32049003 #FOAvip While interferon (IFN) responses are critical for mammalian antiviral defense, induction of antiviral RNA interference (RNAi) is evident. To date, individual functions of the mammalian RNAi and micro RNA (miRNA) effector proteins Argonautes 1?4 (AGO1?AGO4) during virus infection remain undetermined. AGO2 was recently implicated in mammalian antiviral defense, so we examined antiviral activity of AGO1, AGO3, or AGO4 in IFN-competent immune cells. Only AGO4-deficient cells are hyper-susceptible to virus infection. AGO4 antiviral function is both IFN dependent and IFN independent, since AGO4 promotes IFN but also maintains antiviral capacity following prevention of IFN signaling or production. We identified AGO-loaded virus-derived short interfering RNAs (vsiRNAs), a molecular marker of antiviral RNAi, in macrophages infected with influenza or influenza lacking the IFN and RNAi suppressor NS1, which are uniquely diminished without AGO4. Importantly, AGO4-deficient influenza-infected mice have significantly higher burden and viral titers in vivo. Together, our data assign an essential role for AGO4 in mammalian antiviral defense. Twit Text FOAVip A Requirement for Argonaute 4 in Mammalian Antiviral Defense ????Cell Rep http://www.kidney.de/pget.php?&tw=1&pmid=32049003 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=32049003 #FOAvip English Wikipedia <ref>{{Cite pmid|32049003}}</ref> A Requirement for Argonaute 4 in Mammalian Antiviral Defense #MMPMID32049003 Adiliaghdam F; Basavappa M; Saunders TL; Harjanto D; Prior JT; Cronkite DA; Papavasiliou N; Jeffrey KL Cell Rep 2020[Feb]; 30 (6): 1690-1701.e4 PMID32049003show ga While interferon (IFN) responses are critical for mammalian antiviral defense, induction of antiviral RNA interference (RNAi) is evident. To date, individual functions of the mammalian RNAi and micro RNA (miRNA) effector proteins Argonautes 1?4 (AGO1?AGO4) during virus infection remain undetermined. AGO2 was recently implicated in mammalian antiviral defense, so we examined antiviral activity of AGO1, AGO3, or AGO4 in IFN-competent immune cells. Only AGO4-deficient cells are hyper-susceptible to virus infection. AGO4 antiviral function is both IFN dependent and IFN independent, since AGO4 promotes IFN but also maintains antiviral capacity following prevention of IFN signaling or production. We identified AGO-loaded virus-derived short interfering RNAs (vsiRNAs), a molecular marker of antiviral RNAi, in macrophages infected with influenza or influenza lacking the IFN and RNAi suppressor NS1, which are uniquely diminished without AGO4. Importantly, AGO4-deficient influenza-infected mice have significantly higher burden and viral titers in vivo. Together, our data assign an essential role for AGO4 in mammalian antiviral defense. äA Requirement for Argonaute 4 in Mammalian Antiviral Defense (epmc).pdf DeepDyve Pubget Overpricing