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10.3389/fmolb.2020.00204 http://scihub22266oqcxt.onion/10.3389/fmolb.2020.00204 33195397!7477106!33195397     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=33195397&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       Front+Mol+Biosci 2020 ; 7 (?): 204 Nephropedia Template TP {{tp|p=33195397|t=2020. Drug Weaponry to Fight Against SARS-CoV-2 |pdf=|usr=}}{{33195397}} gab.com Text Drug Weaponry to Fight Against SARS-CoV-2 JO: Front Mol Biosci http://www.kidney.de/pget.php?&tw=1&pmid=33195397 #FOAvip The current outbreak of SARS-CoV-2 virus has caused a large increase in mortality and morbidity associated with respiratory diseases. Huge efforts are currently ongoing to develop a vaccine against this virus. However, alternative approaches could be considered in the fight against this disease. Among other strategies, structural-based drug design could be an effective approach to generate specific molecules against SARS-CoV-2, thus reducing viral burden in infected patients. Here, in addition to this structural approach, we also revise several therapeutic strategies to fight against this viral threat. Furthermore, we report ACE-2 genetic polymorphic variants affecting residues involved in close contacts with SARS-CoV-2 that might be associated to different infection risks. These analyses could provide valuable information to predict the course of the disease. Twit Text FOAVip Drug Weaponry to Fight Against SARS-CoV-2 ????Front Mol Biosci http://www.kidney.de/pget.php?&tw=1&pmid=33195397 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=33195397 #FOAvip English Wikipedia <ref>{{Cite pmid|33195397}}</ref> Drug Weaponry to Fight Against SARS-CoV-2 #MMPMID33195397 Cabezon E; Arechaga I Front Mol Biosci 2020[]; 7 (?): 204 PMID33195397show ga The current outbreak of SARS-CoV-2 virus has caused a large increase in mortality and morbidity associated with respiratory diseases. Huge efforts are currently ongoing to develop a vaccine against this virus. However, alternative approaches could be considered in the fight against this disease. Among other strategies, structural-based drug design could be an effective approach to generate specific molecules against SARS-CoV-2, thus reducing viral burden in infected patients. Here, in addition to this structural approach, we also revise several therapeutic strategies to fight against this viral threat. Furthermore, we report ACE-2 genetic polymorphic variants affecting residues involved in close contacts with SARS-CoV-2 that might be associated to different infection risks. These analyses could provide valuable information to predict the course of the disease. ?Drug Weaponry to Fight Against SARS-CoV-2 (epmc).pdf DeepDyve Pubget Overpricing