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10.1016/j.imlet.2020.05.008 http://scihub22266oqcxt.onion/10.1016/j.imlet.2020.05.008 32534867!7289111!32534867     free     free     free Deprecated: Implicit conversion from float 215.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 215.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 215.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 215.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 215.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Immunol+Lett 2020 ; 224 (ä): 38-39 Nephropedia Template TP {{tp|p=32534867|t=2020. Sequence homology between human PARP14 and the SARS-CoV-2 ADP ribose 1 -phosphatase |pdf=|usr=}}{{32534867}} gab.com Text Sequence homology between human PARP14 and the SARS-CoV-2 ADP ribose 1 -phosphatase JO: Immunol Lett http://www.kidney.de/pget.php?&tw=1&pmid=32534867 #FOAvip * There is amino acid sequence homology between the ADP-ribose binding sites of human PARP14 and SARS-CoV-2 ADRP. * This homology is even more pronounced in bat species. * The model proposed highlights the potential of the PARP axis to yield druggable targets for the treatment of COVID-19. Twit Text FOAVip Sequence homology between human PARP14 and the SARS-CoV-2 ADP ribose 1 -phosphatase ????Immunol Lett http://www.kidney.de/pget.php?&tw=1&pmid=32534867 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=32534867 #FOAvip English Wikipedia <ref>{{Cite pmid|32534867}}</ref> Sequence homology between human PARP14 and the SARS-CoV-2 ADP ribose 1 -phosphatase #MMPMID32534867 Webb TE; Saad R Immunol Lett 2020[Aug]; 224 (ä): 38-39 PMID32534867show ga * There is amino acid sequence homology between the ADP-ribose binding sites of human PARP14 and SARS-CoV-2 ADRP. * This homology is even more pronounced in bat species. * The model proposed highlights the potential of the PARP axis to yield druggable targets for the treatment of COVID-19. |Amino Acid Sequence[MESH] |Animals[MESH] |Betacoronavirus/*enzymology/genetics[MESH] |COVID-19[MESH] |Coronavirus Infections/enzymology/immunology/*virology[MESH] |Host-Pathogen Interactions[MESH] |Humans[MESH] |Macrophage Activation[MESH] |Macrophages/enzymology/immunology/virology[MESH] |Pandemics[MESH] |Pneumonia, Viral/enzymology/immunology/*virology[MESH] |Poly(ADP-ribose) Polymerases/chemistry/genetics/*metabolism[MESH] |Pyrophosphatases/chemistry/genetics/*metabolism[MESH] |SARS-CoV-2[MESH] |Sequence Homology[MESH] |T-Lymphocytes, Helper-Inducer/enzymology/immunology/virology[MESH] |Th1-Th2 Balance[MESH]Sequence homology between human PARP14 and the SARS-CoV-2 ADP ribose (epmc).pdf DeepDyve Pubget Overpricing