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10.1016/j.meegid.2020.104428 http://scihub22266oqcxt.onion/10.1016/j.meegid.2020.104428 32565362!7301787!32565362     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=32565362&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       Infect+Genet+Evol 2020 ; 85 (?): 104428 Nephropedia Template TP {{tp|p=32565362|t=2020. Comparative analysis of SARS-CoV-2 receptor ACE2 expression in multiple solid tumors and matched non-diseased tissues |pdf=|usr=}}{{32565362}} gab.com Text Comparative analysis of SARS-CoV-2 receptor ACE2 expression in multiple solid tumors and matched non-diseased tissues JO: Infect Genet Evol http://www.kidney.de/pget.php?&tw=1&pmid=32565362 #FOAvip The emerging severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) poses a global public health emergency. SARS-CoV-2 employs the host cell receptor ACE2 for cellular entry. Nonetheless, the differences in ACE2 expression pattern in lung versus other normal and solid tumor tissues remain incompletely characterized. Here, we analyze a large data set comprising ACE2 mRNA expression for 7592 tissue samples across 22 types of primary solid tumor and 4461 samples across matched 18 non-diseased tissues. Our results unravel eight normal tissues and 10 primary solid tumors, which might be at high risk of SARS-CoV-2 infection. These findings may provide additional insight into the prevention and treatment of SARS-CoV-2 infection, in particular for patients with these 10 vulnerable cancer types. Twit Text FOAVip Comparative analysis of SARS-CoV-2 receptor ACE2 expression in multiple solid tumors and matched non-diseased tissues ????Infect Genet Evol http://www.kidney.de/pget.php?&tw=1&pmid=32565362 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=32565362 #FOAvip English Wikipedia <ref>{{Cite pmid|32565362}}</ref> Comparative analysis of SARS-CoV-2 receptor ACE2 expression in multiple solid tumors and matched non-diseased tissues #MMPMID32565362 Zhang L; Han X; Shi Y Infect Genet Evol 2020[Nov]; 85 (?): 104428 PMID32565362show ga The emerging severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) poses a global public health emergency. SARS-CoV-2 employs the host cell receptor ACE2 for cellular entry. Nonetheless, the differences in ACE2 expression pattern in lung versus other normal and solid tumor tissues remain incompletely characterized. Here, we analyze a large data set comprising ACE2 mRNA expression for 7592 tissue samples across 22 types of primary solid tumor and 4461 samples across matched 18 non-diseased tissues. Our results unravel eight normal tissues and 10 primary solid tumors, which might be at high risk of SARS-CoV-2 infection. These findings may provide additional insight into the prevention and treatment of SARS-CoV-2 infection, in particular for patients with these 10 vulnerable cancer types. |Angiotensin-Converting Enzyme 2/*genetics[MESH] |COVID-19/*genetics[MESH] |Case-Control Studies[MESH] |Gene Expression Profiling[MESH] |Gene Expression Regulation[MESH] |Humans[MESH] |Lung/chemistry/pathology[MESH]Comparative analysis of SARS-CoV-2 receptor ACE2 expression in multipl(epmc).pdf DeepDyve Pubget Overpricing