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10.3390/v7092865 http://scihub22266oqcxt.onion/10.3390/v7092865 C4584309!4584309 !26404354     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=26404354 &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\26404354 .jpg): Failed to open stream: No such file or directory in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 117       Viruses 2015 ; 7 (9 ): 5145-54 Nephropedia Template TP {{tp|p=26404354 |t=2015. Tight Junctions Go Viral! |pdf=|usr=}}{{26404354 }} gab.com Text Tight Junctions Go Viral! JO: Viruses http://www.kidney.de/pget.php?&tw=1&pmid=26404354 #FOAvip Tight junctions (TJs) are highly specialized membrane domains involved in many important cellular processes such as the regulation of the passage of ions and macromolecules across the paracellular space and the establishment of cell polarity in epithelial cells. Over the past few years there has been increasing evidence that different components of the TJs can be hijacked by viruses in order to complete their infectious cycle. Viruses from at least nine different families of DNA and RNA viruses have been reported to use TJ proteins in their benefit. For example, TJ proteins such as JAM-A or some members of the claudin family of proteins are used by members of the Reoviridae family and hepatitis C virus as receptors or co-receptors during their entry into their host cells. Reovirus, in addition, takes advantage of the TJ protein Junction Adhesion Molecule-A (JAM-A) to achieve its hematogenous dissemination. Some other viruses are capable of regulating the expression or the localization of TJ proteins to induce cell transformation or to improve the efficiency of their exit process. This review encompasses the importance of TJs for viral entry, replication, dissemination, and egress, and makes a clear statement of the importance of studying these proteins to gain a better understanding of the replication strategies used by viruses that infect epithelial and/or endothelial cells. Twit Text FOAVip Tight Junctions Go Viral! ????Viruses http://www.kidney.de/pget.php?&tw=1&pmid=26404354 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=26404354 #FOAvip English Wikipedia <ref>{{Cite pmid|26404354 }}</ref> Tight Junctions Go Viral! #MMPMID26404354 Torres-Flores JM ; Arias CF Viruses 2015[Sep]; 7 (9 ): 5145-54 PMID26404354 show ga Tight junctions (TJs) are highly specialized membrane domains involved in many important cellular processes such as the regulation of the passage of ions and macromolecules across the paracellular space and the establishment of cell polarity in epithelial cells. Over the past few years there has been increasing evidence that different components of the TJs can be hijacked by viruses in order to complete their infectious cycle. Viruses from at least nine different families of DNA and RNA viruses have been reported to use TJ proteins in their benefit. For example, TJ proteins such as JAM-A or some members of the claudin family of proteins are used by members of the Reoviridae family and hepatitis C virus as receptors or co-receptors during their entry into their host cells. Reovirus, in addition, takes advantage of the TJ protein Junction Adhesion Molecule-A (JAM-A) to achieve its hematogenous dissemination. Some other viruses are capable of regulating the expression or the localization of TJ proteins to induce cell transformation or to improve the efficiency of their exit process. This review encompasses the importance of TJs for viral entry, replication, dissemination, and egress, and makes a clear statement of the importance of studying these proteins to gain a better understanding of the replication strategies used by viruses that infect epithelial and/or endothelial cells. |*Virus Internalization [MESH] |*Virus Release [MESH] |*Virus Replication [MESH] |Animals [MESH] |DNA Viruses/*physiology [MESH] |Humans [MESH] |RNA Viruses/*physiology [MESH] |Receptors, Virus/metabolism [MESH] |Tight Junction Proteins/metabolism [MESH]Tight Junctions Go Viral! (epmc).pdf DeepDyve Pubget Overpricing