about
Sodium taurocholate cotransporting polypeptide is a functional receptor for human hepatitis B and D virusTIM-family proteins promote infection of multiple enveloped viruses through virion-associated phosphatidylserineInfluenza A virus neuraminidase limits viral superinfectionNTCP and beyond: opening the door to unveil hepatitis B virus entryStructural basis for activation and inhibition of the secreted chlamydia protease CPAFAngiotensin-converting enzyme 2 is a functional receptor for the SARS coronavirusA 193-amino acid fragment of the SARS coronavirus S protein efficiently binds angiotensin-converting enzyme 2DNA Polymerase κ Is a Key Cellular Factor for the Formation of Covalently Closed Circular DNA of Hepatitis B VirusNonmuscle myosin heavy chain IIA is a critical factor contributing to the efficiency of early infection of severe fever with thrombocytopenia syndrome virus.Evaluation of human monoclonal antibody 80R for immunoprophylaxis of severe acute respiratory syndrome by an animal study, epitope mapping, and analysis of spike variants.Structure of SARS coronavirus spike receptor-binding domain complexed with receptor.Entry of hepatitis B and hepatitis D virus into hepatocytes: Basic insights and clinical implications.Conformational states of the severe acute respiratory syndrome coronavirus spike protein ectodomain.Development and evaluation of a pseudovirus-luciferase assay for rapid and quantitative detection of neutralizing antibodies against enterovirus 71.Alpha-interferon suppresses hepadnavirus transcription by altering epigenetic modification of cccDNA minichromosomesTransferrin receptor 1 is a cellular receptor for New World haemorrhagic fever arenaviruses.Hepatitis D Virus Infection of Mice Expressing Human Sodium Taurocholate Co-transporting PolypeptideHuman Coronavirus HKU1 Spike Protein Uses O-Acetylated Sialic Acid as an Attachment Receptor Determinant and Employs Hemagglutinin-Esterase Protein as a Receptor-Destroying EnzymeMolecular determinants of enterovirus 71 viral entry: cleft around GLN-172 on VP1 protein interacts with variable region on scavenge receptor B 2.Angiotensin-converting enzyme 2: a functional receptor for SARS coronavirus.Animal origins of the severe acute respiratory syndrome coronavirus: insight from ACE2-S-protein interactions.Potent neutralization of severe acute respiratory syndrome (SARS) coronavirus by a human mAb to S1 protein that blocks receptor association.Insights from the association of SARS-CoV S-protein with its receptor, ACE2.Sodium taurocholate cotransporting polypeptide mediates woolly monkey hepatitis B virus infection of Tupaia hepatocytes.Molecular determinants of hepatitis B and D virus entry restriction in mouse sodium taurocholate cotransporting polypeptideRetroviruses pseudotyped with the severe acute respiratory syndrome coronavirus spike protein efficiently infect cells expressing angiotensin-converting enzyme 2.Viral entry of hepatitis B and D viruses and bile salts transportation share common molecular determinants on sodium taurocholate cotransporting polypeptide.NTCP opens the door for hepatitis B virus infection.The hepatitis B virus receptor.Woodchuck sodium taurocholate cotransporting polypeptide supports low-level hepatitis B and D virus entry.NTCP-Reconstituted In Vitro HBV Infection System.Sodium taurocholate cotransporting polypeptide acts as a receptor for hepatitis B and D virus.A research agenda for curing chronic hepatitis B virus infection.The S proteins of human coronavirus NL63 and severe acute respiratory syndrome coronavirus bind overlapping regions of ACE2.Efficient replication of severe acute respiratory syndrome coronavirus in mouse cells is limited by murine angiotensin-converting enzyme 2.Recombinant vaccinia vector-based vaccine (Tiantan) boosting a novel HBV subunit vaccine induced more robust and lasting immunity in rhesus macaques.SARS-CoV, but not HCoV-NL63, utilizes cathepsins to infect cells: viral entry.Interactions between SARS coronavirus and its receptor.Conserved receptor-binding domains of Lake Victoria marburgvirus and Zaire ebolavirus bind a common receptor.SARS coronavirus, but not human coronavirus NL63, utilizes cathepsin L to infect ACE2-expressing cells.
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description
researcher
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wetenschapper
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հետազոտող
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Wenhui Li
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Wenhui Li
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Wenhui Li
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Wenhui Li
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Wenhui Li
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Wenhui Li
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Wenhui Li
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Wenhui Li
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Wenhui Li
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Wenhui Li
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Wenhui Li
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Wenhui Li
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Wenhui Li
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Wenhui Li
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Wenhui Li
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Wenhui Li
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P106
P1153
55718630900
P31
P496
0000-0003-1305-7404