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10.1016/j.vph.2020.106680

http://scihub22266oqcxt.onion/10.1016/j.vph.2020.106680
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suck abstract from ncbi


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pmid32423553      Vascul+Pharmacol 2020 ; 130 (ä): 106680
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  • Angiotensin converting enzyme: A review on expression profile and its association with human disorders with special focus on SARS-CoV-2 infection #MMPMID32423553
  • Ghafouri-Fard S; Noroozi R; Omrani MD; Branicki W; Pospiech E; Sayad A; Pyrc K; Labaj PP; Vafaee R; Taheri M; Sanak M
  • Vascul Pharmacol 2020[Jul]; 130 (ä): 106680 PMID32423553show ga
  • Angiotensin-converting enzyme (ACE) and its homologue, ACE2, have been mostly associated with hypertensive disorder. However, recent pandemia of SARS-CoV-2 has put these proteins at the center of attention, as this virus has been shown to exploit ACE2 protein to enter cells. Clear difference in the response of affected patients to this virus has urged researchers to find the molecular basis and pathophysiology of the cell response to this virus. Different levels of expression and function of ACE proteins, underlying disorders, consumption of certain medications and the existence of certain genomic variants within ACE genes are possible explanations for the observed difference in the response of individuals to the SARS-CoV-2 infection. In the current review, we discuss the putative mechanisms for this observation.
  • |COVID-19[MESH]
  • |Coronavirus Infections/*enzymology/genetics/pathology[MESH]
  • |Humans[MESH]
  • |Pandemics[MESH]
  • |Peptidyl-Dipeptidase A/*biosynthesis/blood/genetics[MESH]


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