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10.3390/antib9030033 http://scihub22266oqcxt.onion/10.3390/antib9030033 32708525!7551747!32708525     free     free     free Deprecated: Implicit conversion from float 217.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 217.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 217.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 217.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Antibodies+(Basel) 2020 ; 9 (3): ä Nephropedia Template TP {{tp|p=32708525|t=2020. From Anti-SARS-CoV-2 Immune Responses to COVID-19 via Molecular Mimicry |pdf=|usr=}}{{32708525}} gab.com Text From Anti-SARS-CoV-2 Immune Responses to COVID-19 via Molecular Mimicry JO: Antibodies (Basel) http://www.kidney.de/pget.php?&tw=1&pmid=32708525 #FOAvip AIM: To define the autoimmune potential of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) infection. METHODS: Experimentally validated epitopes cataloged at the Immune Epitope DataBase (IEDB) and present in SARS-CoV-2 were analyzed for peptide sharing with the human proteome. RESULTS: Immunoreactive epitopes present in SARS-CoV-2 were mostly composed of peptide sequences present in human proteins that-when altered, mutated, deficient or, however, improperly functioning-may associate with a wide range of disorders, from respiratory distress to multiple organ failure. CONCLUSIONS: This study represents a starting point or hint for future scientific-clinical investigations and suggests a range of possible protein targets of autoimmunity in SARS-CoV-2 infection. From an experimental perspective, the results warrant the testing of patients' sera for autoantibodies against these protein targets. Clinically, the results warrant a stringent surveillance on the future pathologic sequelae of the current SARS-CoV-2 pandemic. Twit Text FOAVip From Anti-SARS-CoV-2 Immune Responses to COVID-19 via Molecular Mimicry ????Antibodies (Basel) http://www.kidney.de/pget.php?&tw=1&pmid=32708525 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=32708525 #FOAvip English Wikipedia <ref>{{Cite pmid|32708525}}</ref> From Anti-SARS-CoV-2 Immune Responses to COVID-19 via Molecular Mimicry #MMPMID32708525 Kanduc D Antibodies (Basel) 2020[Jul]; 9 (3): ä PMID32708525show ga AIM: To define the autoimmune potential of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) infection. METHODS: Experimentally validated epitopes cataloged at the Immune Epitope DataBase (IEDB) and present in SARS-CoV-2 were analyzed for peptide sharing with the human proteome. RESULTS: Immunoreactive epitopes present in SARS-CoV-2 were mostly composed of peptide sequences present in human proteins that-when altered, mutated, deficient or, however, improperly functioning-may associate with a wide range of disorders, from respiratory distress to multiple organ failure. CONCLUSIONS: This study represents a starting point or hint for future scientific-clinical investigations and suggests a range of possible protein targets of autoimmunity in SARS-CoV-2 infection. From an experimental perspective, the results warrant the testing of patients' sera for autoantibodies against these protein targets. Clinically, the results warrant a stringent surveillance on the future pathologic sequelae of the current SARS-CoV-2 pandemic. äFrom Anti-SARS-CoV-2 Immune Responses to COVID-19 via Molecular Mimicr(epmc).pdf DeepDyve Pubget Overpricing