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10.4103/ijmr.IJMR_3215_20

http://scihub22266oqcxt.onion/10.4103/ijmr.IJMR_3215_20
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33818465!8184076!33818465
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suck abstract from ncbi


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pmid33818465      Indian+J+Med+Res 2021 ; 153 (1 & 2): 17-25
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  • An overview of preclinical animal models for SARS-CoV-2 pathogenicity #MMPMID33818465
  • Munshi I; Khandvilkar A; Chavan SM; Sachdeva G; Mahale SD; Chaudhari UK
  • Indian J Med Res 2021[Jan]; 153 (1 & 2): 17-25 PMID33818465show ga
  • Severe acute respiratory syndrome coronavirus (SARS-CoV)-2 has caused millions of fatalities globally since its origin in November 2019. The SARS-CoV-2 shares 79 and 50 per cent genome similarity with its predecessors, severe SARS-CoV and Middle East respiratory syndrome (MERS) coronavirus, all belonging to the same genus, Betacoronavirus. This relatively new virus has stymied the effective control of COVID-19 pandemic and caused huge social and economic impact worldwide. The FDA-approved drugs were re-purposed to reduce the number of fatalities caused by SARS-CoV-2. However, controversy surrounds about the efficacy of these re-purposed antiviral drugs against SARS-CoV-2.This necessitates the identification of new drug targets for SARS-CoV-2. Hence, the development of pre-clinical animal model is warranted. Such animal models may help us gain better understanding of the pathophysiology of SARS-CoV-2 infection and will be effective tools for the evaluation and licensure of therapeutic strategies against SARS-CoV-2. This review provides a summary of the attempts made till to develop a suitable animal model to understand pathophysiology and effectiveness of therapeutic agents against SARS-CoV-2.
  • |*Disease Models, Animal[MESH]
  • |Animals[MESH]
  • |COVID-19/*physiopathology[MESH]
  • |Humans[MESH]
  • |SARS-CoV-2/*pathogenicity[MESH]


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