Microbiology
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mRNA-1273 and Ad26.COV2.S vaccines protect against the B.1.621 variant of SARS-CoV-2
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Expanded ACE2 dependencies of diverse SARS-like coronavirus receptor binding domains
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Super-immunity by broadly protective nanobodies to sarbecoviruses
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Improved binding affinity of the Omicron’s spike protein with hACE2 receptor is the key factor behind its increased virulence
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SARS-CoV-2 diverges from other betacoronaviruses in only partially activating the IRE1α/XBP1 ER stress pathway in human lung-derived cells
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Reduced infectivity but increased immune escape of the new SARS-CoV-2 variant of concern Omicron
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The omicron (B.1.1.529) SARS-CoV-2 variant of concern does not readily infect Syrian hamsters
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Rapid selection of P323L in the SARS-CoV-2 polymerase (NSP12) in humans and non-human primate models and confers a large plaque phenotype
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A subset of Memory B-derived antibody repertoire from 3-dose vaccinees is ultrapotent against diverse and highly transmissible SARS-CoV-2 variants, including Omicron
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Homologous or Heterologous Booster of Inactivated Vaccine Reduces SARS-CoV-2 Omicron Variant Escape from Neutralizing Antibodies
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