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http://scihub22266oqcxt.onion/10.1186/s40246-020-00272-6
 32498696!7269898!32498696
free
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Hum+Genomics 2020 ; 14 (1): 20 Nephropedia Template TP
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COVID-19 preclinical models: human angiotensin-converting enzyme 2 transgenic mice #MMPMID32498696Lutz C; Maher L; Lee C; Kang WHum Genomics 2020[Jun]; 14 (1): 20 PMID32498696show ga
Coronavirus disease 2019 (COVID-19) is a declared pandemic that is spreading all over the world at a dreadfully fast rate. Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2), the pathogen of COVID-19, infects the human body using angiotensin-converting enzyme 2 (ACE2) as a receptor identical to the severe acute respiratory syndrome (SARS) pandemic that occurred in 2002-2003. SARS-CoV-2 has a higher binding affinity to human ACE2 than to that of other species. Animal models that mimic the human disease are highly essential to develop therapeutics and vaccines against COVID-19. Here, we review transgenic mice that express human ACE2 in the airway and other epithelia and have shown to develop a rapidly lethal infection after intranasal inoculation with SARS-CoV, the pathogen of SARS. This literature review aims to present the importance of utilizing the human ACE2 transgenic mouse model to better understand the pathogenesis of COVID-19 and develop both therapeutics and vaccines.|Angiotensin-Converting Enzyme 2[MESH]|Animals[MESH]|Betacoronavirus/*metabolism/pathogenicity[MESH]|COVID-19[MESH]|Coronavirus Infections/*pathology[MESH]|Disease Models, Animal[MESH]|Humans[MESH]|Mice[MESH]|Mice, Inbred C57BL[MESH]|Mice, Transgenic[MESH]|Pandemics[MESH]|Peptidyl-Dipeptidase A/*genetics/*metabolism[MESH]|Pneumonia, Viral/*pathology[MESH]|Promoter Regions, Genetic/genetics[MESH]|Protein Binding/physiology[MESH]|Receptors, Virus/genetics/metabolism[MESH]
  
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