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10.1186/s40246-020-00272-6

http://scihub22266oqcxt.onion/10.1186/s40246-020-00272-6
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32498696!7269898!32498696
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suck abstract from ncbi


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pmid32498696      Hum+Genomics 2020 ; 14 (1): 20
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  • COVID-19 preclinical models: human angiotensin-converting enzyme 2 transgenic mice #MMPMID32498696
  • Lutz C; Maher L; Lee C; Kang W
  • Hum 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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