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The use of common laboratory strains of mice for this end is hindered by considerable divergence for the angiotensin-converting enzyme 2 (ACE2), that will be the receptor required for entry of SARS-CoV-2. In the present research, we designed and utilized an mRNA-based transfection system to induce phrase for the hACE2 receptor in order to confer entry of SARS-CoV-2 in otherwise non-permissive cells. By employing this expression system in an in vivo environment, we had been able to interro
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