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10.1371/journal.ppat.1005099 http://scihub22266oqcxt.onion/10.1371/journal.ppat.1005099 C4574736!4574736!26379246     free     free     free Warning: imagejpeg(C:\Inetpub\vhosts\kidney.de\httpdocs\phplern\26379246.jpg): Failed to open stream: No such file or directory in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 117       PLoS+Pathog 2015 ; 11 (9): ä Nephropedia Template TP {{tp|p=26379246|t=2015. Microbial Regulation of p53 Tumor Suppressor |pdf=|usr=}}{{26379246}} gab.com Text Microbial Regulation of p53 Tumor Suppressor JO: PLoS Pathog http://www.kidney.de/pget.php?&tw=1&pmid=26379246 #FOAvip p53 tumor suppressor has been identified as a protein interacting with the large T antigen produced by simian vacuolating virus 40 (SV40). Subsequent research on p53 inhibition by SV40 and other tumor viruses has not only helped to gain a better understanding of viral biology, but also shaped our knowledge of human tumorigenesis. Recent studies have found, however, that inhibition of p53 is not strictly in the realm of viruses. Some bacterial pathogens also actively inhibit p53 protein and induce its degradation, resulting in alteration of cellular stress responses. This phenomenon was initially characterized in gastric epithelial cells infected with Helicobacter pylori, a bacterial pathogen that commonly infects the human stomach and is strongly linked to gastric cancer. Besides H. pylori, a number of other bacterial species were recently discovered to inhibit p53. These findings provide novel insights into host?bacteria interactions and tumorigenesis associated with bacterial infections. Twit Text FOAVip Microbial Regulation of p53 Tumor Suppressor ????PLoS Pathog http://www.kidney.de/pget.php?&tw=1&pmid=26379246 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=26379246 #FOAvip English Wikipedia <ref>{{Cite pmid|26379246}}</ref> Microbial Regulation of p53 Tumor Suppressor #MMPMID26379246 Zaika AI; Wei J; Noto JM; Peek RM PLoS Pathog 2015[Sep]; 11 (9): ä PMID26379246show ga p53 tumor suppressor has been identified as a protein interacting with the large T antigen produced by simian vacuolating virus 40 (SV40). Subsequent research on p53 inhibition by SV40 and other tumor viruses has not only helped to gain a better understanding of viral biology, but also shaped our knowledge of human tumorigenesis. Recent studies have found, however, that inhibition of p53 is not strictly in the realm of viruses. Some bacterial pathogens also actively inhibit p53 protein and induce its degradation, resulting in alteration of cellular stress responses. This phenomenon was initially characterized in gastric epithelial cells infected with Helicobacter pylori, a bacterial pathogen that commonly infects the human stomach and is strongly linked to gastric cancer. Besides H. pylori, a number of other bacterial species were recently discovered to inhibit p53. These findings provide novel insights into host?bacteria interactions and tumorigenesis associated with bacterial infections. äMicrobial Regulation of p53 Tumor Suppressor (epmc).pdf DeepDyve Pubget Overpricing