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10.1002/wrna.1372 http://scihub22266oqcxt.onion/10.1002/wrna.1372 C5607777!5607777 !27307117     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=27307117 &cmd=llinks): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 215 Warning: imagejpeg(C:\Inetpub\vhosts\kidney.de\httpdocs\phplern\27307117 .jpg): Failed to open stream: No such file or directory in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 117       Wiley+Interdiscip+Rev+RNA 2017 ; 8 (1 ): ä Nephropedia Template TP {{tp|p=27307117 |t=2017. Posttranslational control of HuR function |pdf=|usr=}}{{27307117 }} gab.com Text Posttranslational control of HuR function JO: Wiley Interdiscip Rev RNA http://www.kidney.de/pget.php?&tw=1&pmid=27307117 #FOAvip The RNA-binding protein HuR (human antigen R) associates with numerous transcripts, coding and noncoding, and controls their splicing, localization, stability, and translation. Through its regulation of target transcripts, HuR has been implicated in cellular events including proliferation, senescence, differentiation, apoptosis, and the stress and immune responses. In turn, HuR influences processes such as cancer and inflammation. HuR function is primarily regulated through posttranslational modifications that alter its subcellular localization and its ability to bind target RNAs; such modifications include phosphorylation, methylation, ubiquitination, NEDDylation, and proteolytic cleavage. In this review, we describe the modifications that impact upon HuR function on gene expression programs and disease states. WIREs RNA 2017, 8:e1372. doi: 10.1002/wrna.1372 For further resources related to this article, please visit the WIREs website. Twit Text FOAVip Posttranslational control of HuR function ????Wiley Interdiscip Rev RNA http://www.kidney.de/pget.php?&tw=1&pmid=27307117 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=27307117 #FOAvip English Wikipedia <ref>{{Cite pmid|27307117 }}</ref> Posttranslational control of HuR function #MMPMID27307117 Grammatikakis I ; Abdelmohsen K ; Gorospe M Wiley Interdiscip Rev RNA 2017[Jan]; 8 (1 ): ä PMID27307117 show ga The RNA-binding protein HuR (human antigen R) associates with numerous transcripts, coding and noncoding, and controls their splicing, localization, stability, and translation. Through its regulation of target transcripts, HuR has been implicated in cellular events including proliferation, senescence, differentiation, apoptosis, and the stress and immune responses. In turn, HuR influences processes such as cancer and inflammation. HuR function is primarily regulated through posttranslational modifications that alter its subcellular localization and its ability to bind target RNAs; such modifications include phosphorylation, methylation, ubiquitination, NEDDylation, and proteolytic cleavage. In this review, we describe the modifications that impact upon HuR function on gene expression programs and disease states. WIREs RNA 2017, 8:e1372. doi: 10.1002/wrna.1372 For further resources related to this article, please visit the WIREs website. |*Gene Expression Regulation [MESH] |Animals [MESH] |ELAV-Like Protein 1/*genetics/*metabolism [MESH] |Humans [MESH] |Protein Processing, Post-Translational/*genetics [MESH]Posttranslational control of HuR function (epmc).pdf DeepDyve Pubget Overpricing