Serveur d'exploration sur la COVID en France

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[SARS-CoV-2 protease: an excellent target to develop drugs against COVID-19].

Identifieur interne : 000019 ( Main/Exploration ); précédent : 000018; suivant : 000020

[SARS-CoV-2 protease: an excellent target to develop drugs against COVID-19].

Auteurs : Annie Ladoux [France] ; Stéphane Azoulay [France] ; Christian Dani [France]

Source :

RBID : pubmed:32558640

Descripteurs français

English descriptors


DOI: 10.1051/medsci/2020106
PubMed: 32558640


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

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<Citation>Lee EYP, Ng MY, Khong PL. COVID-19 pneumonia: what has CT taught us? Lancet Infect Dis 2020; 20 : 384–5.</Citation>
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<Reference>
<Citation>Jager S, Cimermancic P, Gulbahce N, et al. Global landscape of HIV-human protein complexes. Nature 2011 ; 481 : 365–370.</Citation>
</Reference>
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<Citation>Ravaud C, Pare M, Azoulay S, et al. Impairment of the activin A autocrine loop by lopinavir reduces self-renewal of distinct human adipose progenitors. Sci Rep 2017 ; 7 : 2986.</Citation>
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<Citation>Ravaud C, Paré M, Yao X, et al. Resveratrol and HIV-protease inhibitors control UCP1 expression through opposite effects on p38 MAPK phosphorylation in human adipocytes. J Cell Physiol 2019 ; 235 : 1184–1196.</Citation>
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<Citation>Vernochet C, Azoulay S, Duval D, et al. Human immunodeficiency virus protease inhibitors accumulate into cultured human adipocytes and alter expression of adipocytokines. J Biol Chem 2005 ; 280 : 2238–2243.</Citation>
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