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Induction of Potent Neutralizing Antibody Responses by a Designed Protein Nanoparticle Vaccine for Respiratory Syncytial Virus
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SARS-CoV-2 Cell Entry Depends on ACE2 and TMPRSS2 and Is Blocked by a Clinically Proven Protease Inhibitor
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Structure, Function, and Antigenicity of the SARS-CoV-2 Spike Glycoprotein
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Mapping Neutralizing and Immunodominant Sites on the SARS-CoV-2 Spike Receptor-Binding Domain by Structure-Guided High-Resolution Serology
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Elicitation of Potent Neutralizing Antibody Responses by Designed Protein Nanoparticle Vaccines for SARS-CoV-2
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Human neutralizing antibodies against SARS-CoV-2 require intact Fc effector functions for optimal therapeutic protection
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N-terminal domain antigenic mapping reveals a site of vulnerability for SARS-CoV-2
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Neutralizing Antibody and Soluble ACE2 Inhibition of a Replication-Competent VSV-SARS-CoV-2 and a Clinical Isolate of SARS-CoV-2
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Identification of SARS-CoV-2 spike mutations that attenuate monoclonal and serum antibody neutralization
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Comparing infectivity and virulence of emerging SARS-CoV-2 variants in Syrian hamsters
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Cryo-EM structures of MERS-CoV and SARS-CoV spike glycoproteins reveal the dynamic receptor binding domains
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Broadly neutralizing hemagglutinin stalk–specific antibodies require FcγR interactions for protection against influenza virus in vivo
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STAT2 signaling restricts viral dissemination but drives severe pneumonia in SARS-CoV-2 infected hamsters
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A conserved immunogenic and vulnerable site on the coronavirus spike protein delineated by cross-reactive monoclonal antibodies
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Chloroquine does not inhibit infection of human lung cells with SARS-CoV-2
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Fc-optimized antibodies elicit CD8 immunity to viral respiratory infection
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Ultrapotent human antibodies protect against SARS-CoV-2 challenge via multiple mechanisms
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Multiple roles for HIV broadly neutralizing antibodies
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Two Mutations Were Critical for Bat-to-Human Transmission of Middle East Respiratory Syndrome Coronavirus
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