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10.3389/fcell.2022.807149 http://scihub22266oqcxt.onion/10.3389/fcell.2022.807149 35223838!8873527!35223838     free     free     free Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Front+Cell+Dev+Biol 2022 ; 10 (ä): 807149 Nephropedia Template TP {{tp|p=35223838|t=2022. Protein Posttranslational Signatures Identified in COVID-19 Patient Plasma |pdf=|usr=}}{{35223838}} gab.com Text Protein Posttranslational Signatures Identified in COVID-19 Patient Plasma JO: Front Cell Dev Biol http://www.kidney.de/pget.php?&tw=1&pmid=35223838 #FOAvip Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) is a highly contagious virus of the coronavirus family that causes coronavirus disease-19 (COVID-19) in humans and a number of animal species. COVID-19 has rapidly propagated in the world in the past 2 years, causing a global pandemic. Here, we performed proteomic analysis of plasma samples from COVID-19 patients compared to healthy control donors in an exploratory study to gain insights into protein-level changes in the patients caused by SARS-CoV-2 infection and to identify potential proteomic and posttranslational signatures of this disease. Our results suggest a global change in protein processing and regulation that occurs in response to SARS-CoV-2, and the existence of a posttranslational COVID-19 signature that includes an elevation in threonine phosphorylation, a change in glycosylation, and a decrease in arginylation, an emerging posttranslational modification not previously implicated in infectious disease. This study provides a resource for COVID-19 researchers and, longer term, and will inform our understanding of this disease and its treatment. Twit Text FOAVip Protein Posttranslational Signatures Identified in COVID-19 Patient Plasma ????Front Cell Dev Biol http://www.kidney.de/pget.php?&tw=1&pmid=35223838 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=35223838 #FOAvip English Wikipedia <ref>{{Cite pmid|35223838}}</ref> Protein Posttranslational Signatures Identified in COVID-19 Patient Plasma #MMPMID35223838 Vedula P; Tang HY; Speicher DW; Kashina A Front Cell Dev Biol 2022[]; 10 (ä): 807149 PMID35223838show ga Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) is a highly contagious virus of the coronavirus family that causes coronavirus disease-19 (COVID-19) in humans and a number of animal species. COVID-19 has rapidly propagated in the world in the past 2 years, causing a global pandemic. Here, we performed proteomic analysis of plasma samples from COVID-19 patients compared to healthy control donors in an exploratory study to gain insights into protein-level changes in the patients caused by SARS-CoV-2 infection and to identify potential proteomic and posttranslational signatures of this disease. Our results suggest a global change in protein processing and regulation that occurs in response to SARS-CoV-2, and the existence of a posttranslational COVID-19 signature that includes an elevation in threonine phosphorylation, a change in glycosylation, and a decrease in arginylation, an emerging posttranslational modification not previously implicated in infectious disease. This study provides a resource for COVID-19 researchers and, longer term, and will inform our understanding of this disease and its treatment. äProtein Posttranslational Signatures Identified in COVID-19 Patient Pl(epmc).pdf DeepDyve Pubget Overpricing