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10.1016/j.etap.2020.103436 http://scihub22266oqcxt.onion/10.1016/j.etap.2020.103436 32562764!7833001!32562764     free     free     free Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Environ+Toxicol+Pharmacol 2020 ; 79 (ä): 103436 Nephropedia Template TP {{tp|p=32562764|t=2020. Dual function of sialic acid in gastrointestinal SARS-CoV-2 infection |pdf=|usr=}}{{32562764}} gab.com Text Dual function of sialic acid in gastrointestinal SARS-CoV-2 infection JO: Environ Toxicol Pharmacol http://www.kidney.de/pget.php?&tw=1&pmid=32562764 #FOAvip Recent analysis concerning the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)- angiotensin converting enzyme (ACE) receptor interaction in enterocytes, the definition of gut-lung axis, as well as the molecular basis of sialic acid-related dual recognition concept in gastrointestinal SARS-CoV-2 infection, have brought a new perspective to potential therapeutic targets. In this review evolving research and clinical data on gastrointestinal SARS-CoV-2 infection are discussed in the context of viral fusion and entry mechanisms, focusing on the different triggers used by coronaviruses. Furthermore, it is emphasized that the viral spike protein is prevented from binding gangliosides, which are composed of a glycosphingolipid with one or more sialic acids, in the presence of chloroquine or hydroxychloroquine. In gastrointestinal SARS-CoV-2 infection the efficiency of these repositioned drugs is debated. Twit Text FOAVip Dual function of sialic acid in gastrointestinal SARS-CoV-2 infection ????Environ Toxicol Pharmacol http://www.kidney.de/pget.php?&tw=1&pmid=32562764 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=32562764 #FOAvip English Wikipedia <ref>{{Cite pmid|32562764}}</ref> Dual function of sialic acid in gastrointestinal SARS-CoV-2 infection #MMPMID32562764 Engin AB; Engin ED; Engin A Environ Toxicol Pharmacol 2020[Oct]; 79 (ä): 103436 PMID32562764show ga Recent analysis concerning the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)- angiotensin converting enzyme (ACE) receptor interaction in enterocytes, the definition of gut-lung axis, as well as the molecular basis of sialic acid-related dual recognition concept in gastrointestinal SARS-CoV-2 infection, have brought a new perspective to potential therapeutic targets. In this review evolving research and clinical data on gastrointestinal SARS-CoV-2 infection are discussed in the context of viral fusion and entry mechanisms, focusing on the different triggers used by coronaviruses. Furthermore, it is emphasized that the viral spike protein is prevented from binding gangliosides, which are composed of a glycosphingolipid with one or more sialic acids, in the presence of chloroquine or hydroxychloroquine. In gastrointestinal SARS-CoV-2 infection the efficiency of these repositioned drugs is debated. |*Betacoronavirus[MESH] |Antiviral Agents/pharmacology[MESH] |COVID-19[MESH] |Coronavirus Infections/drug therapy/*metabolism[MESH] |Gastrointestinal Diseases/*metabolism/*virology[MESH] |Humans[MESH] |N-Acetylneuraminic Acid/*metabolism[MESH] |Pandemics[MESH] |Pneumonia, Viral/drug therapy/*metabolism[MESH] |SARS-CoV-2[MESH]Dual function of sialic acid in gastrointestinal SARS-CoV-2 infection (epmc).pdf DeepDyve Pubget Overpricing