TY - T1的假定的昼夜的贡献clock and sleep in the context of SARS-CoV-2 infection JF - European Respiratory Journal JO - Eur Respir J DO - 10.1183/13993003.01023-2020 VL - 55 IS - 6 SP - 2001023 AU - Meira e Cruz, Miguel AU - Miyazawa, Masaaki AU - Gozal, David Y1 - 2020/06/01 UR - //www.qdcxjkg.com/content/55/6/2001023.abstract N2 - Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the aetiological agent of the pandemic coronavirus disease 2019 (COVID-19), is a newly found member of the Coronaviridae family, and is closely related to, albeit with important differences from, SARS-CoV [1]. It enters human cells through the binding of surface spike (S) glycoprotein with angiotensin-converting enzyme 2 (ACE2) [2–4]. The distal S1 subunit of the S protein is responsible for receptor binding, while the transmembrane S2 subunit mediates fusion between the viral envelope and the target cell membrane following proteolytic cleavage by specific cellular enzymes such as transmembrane serine protease 2 for S protein priming [5]. As it is likely that expression levels of ACE2 affect the efficiency of virus attachment and entry, as well as disease severity [6], and the interactions between viral S protein and ACE2 may directly cause lung injury [7], ACE2 may be a potential target of therapeutic and preventative interventions [8].Circadian deregulation and poor or insufficient sleep may facilitate COVID-19 infection and severity https://bit.ly/2VUlIIJ ER -