SARS-CoV-2 before and after Omicron: two different viruses and two different diseases?
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[1] K. Bruxvoort,et al. Effectiveness of mRNA-1273 vaccination against SARS-CoV-2 omicron subvariants BA.1, BA.2, BA.2.12.1, BA.4, and BA.5 , 2023, Nature Communications.
[2] N. Lo,et al. Infectiousness of SARS-CoV-2 breakthrough infections and reinfections during the Omicron wave , 2023, Nature Medicine.
[3] C. Donnelly,et al. Variant-specific symptoms of COVID-19 in a study of 1,542,510 adults in England , 2022, Nature Communications.
[4] E. Callaway. COVID ‘variant soup’ is making winter surges hard to predict , 2022, Nature.
[5] Jue Liu,et al. Incubation Period of COVID-19 Caused by Unique SARS-CoV-2 Strains , 2022, JAMA network open.
[6] Lu Lu,et al. Origin, virological features, immune evasion and intervention of SARS-CoV-2 Omicron sublineages , 2022, Signal Transduction and Targeted Therapy.
[7] William T. Harvey,et al. SARS-CoV-2 Omicron is an immune escape variant with an altered cell entry pathway , 2022, Nature Microbiology.
[8] M. Lipsitch,et al. Clinical outcomes associated with SARS-CoV-2 Omicron (B.1.1.529) variant and BA.1/BA.1.1 or BA.2 subvariant infection in Southern California , 2022, Nature Medicine.
[9] P. Klenerman,et al. Antibody escape of SARS-CoV-2 Omicron BA.4 and BA.5 from vaccine and BA.1 serum , 2022, Cell.
[10] R. Paton,et al. The rapid replacement of the Delta variant by Omicron (B.1.1.529) in England , 2022, Science Translational Medicine.
[11] Shu Wan,et al. SARS-CoV-2 Omicron variant: recent progress and future perspectives , 2022, Signal Transduction and Targeted Therapy.
[12] S. Bhatt,et al. Comparative analysis of the risks of hospitalisation and death associated with SARS-CoV-2 omicron (B.1.1.529) and delta (B.1.617.2) variants in England: a cohort study , 2022, The Lancet.
[13] B. Walker,et al. T cell reactivity to the SARS-CoV-2 Omicron variant is preserved in most but not all individuals , 2022, Cell.
[14] Frances E. Muldoon,et al. Altered TMPRSS2 usage by SARS-CoV-2 Omicron impacts infectivity and fusogenicity , 2022, Nature.
[15] A. Sette,et al. T cell responses to SARS-CoV-2 spike cross-recognize Omicron , 2022, Nature.
[16] S. Mallapaty. Where did Omicron come from? Three key theories , 2022, Nature.
[17] D. Peaper,et al. Rapid emergence of SARS-CoV-2 Omicron variant is associated with an infection advantage over Delta in vaccinated persons , 2022, Med.
[18] M. Kraemer,et al. Rapid epidemic expansion of the SARS-CoV-2 Omicron variant in southern Africa , 2021, Nature.
[19] R. Arbel,et al. Effectiveness of the Bivalent mRNA Vaccine in Preventing Severe COVID-19 Outcomes: An Observational Cohort Study , 2022, SSRN Electronic Journal.
[20] Fei Shao,et al. Omicron escapes the majority of existing SARS-CoV-2 neutralizing antibodies , 2021, bioRxiv.
[21] Xin He,et al. SARS-CoV-2 Omicron strain exhibits potent capabilities for immune evasion and viral entrance , 2021, Signal Transduction and Targeted Therapy.
[22] Y. Kawaoka,et al. Enhanced fusogenicity and pathogenicity of SARS-CoV-2 Delta P681R mutation , 2021, Nature.
[23] D. Wesemann,et al. Membrane fusion and immune evasion by the spike protein of SARS-CoV-2 Delta variant , 2021, Science.
[24] M. Farzan,et al. Mechanisms of SARS-CoV-2 entry into cells , 2021, Nature reviews. Molecular cell biology.
[25] S. Bhatt,et al. SARS-CoV-2 B.1.617.2 Delta variant replication and immune evasion , 2021, Nature.
[26] D. Wesemann,et al. Membrane fusion and immune evasion by the spike protein of SARS-CoV-2 Delta variant , 2021, bioRxiv.
[27] O. Dym,et al. SARS-CoV-2 variant prediction and antiviral drug design are enabled by RBD in vitro evolution , 2021, Nature Microbiology.
[28] Y. Liu,et al. The reproductive number of the Delta variant of SARS-CoV-2 is far higher compared to the ancestral SARS-CoV-2 virus , 2021, Journal of travel medicine.
[29] William T. Harvey,et al. SARS-CoV-2 variants, spike mutations and immune escape , 2021, Nature Reviews Microbiology.
[30] R. Neher,et al. Novel SARS-CoV-2 variants: the pandemics within the pandemic , 2021, Clinical Microbiology and Infection.
[31] M. Giacca,et al. Drugs that inhibit TMEM16 proteins block SARS-CoV-2 spike-induced syncytia , 2021, Nature.
[32] Gene W. Yeo,et al. Emergence and rapid transmission of SARS-CoV-2 B.1.1.7 in the United States , 2021, Cell.
[33] M. Beltramello,et al. N-terminal domain antigenic mapping reveals a site of vulnerability for SARS-CoV-2 , 2021, Cell.
[34] M. Beer,et al. SARS-CoV-2 spike D614G change enhances replication and transmission , 2021, Nature.
[35] M. Hernán,et al. BNT162b2 mRNA Covid-19 Vaccine in a Nationwide Mass Vaccination Setting , 2021, The New England journal of medicine.
[36] W. P. Duprex,et al. Recurrent deletions in the SARS-CoV-2 spike glycoprotein drive antibody escape , 2021, Science.
[37] J. Bloom,et al. Comprehensive mapping of mutations to the SARS-CoV-2 receptor-binding domain that affect recognition by polyclonal human serum antibodies , 2021, bioRxiv.
[38] J. Mascola,et al. Efficacy and Safety of the mRNA-1273 SARS-CoV-2 Vaccine , 2020, The New England journal of medicine.
[39] P. Ball. The lightning-fast quest for COVID vaccines — and what it means for other diseases , 2020, Nature.
[40] P. Dormitzer,et al. Safety and Efficacy of the BNT162b2 mRNA Covid-19 Vaccine , 2020, The New England journal of medicine.
[41] M. Beltramello,et al. Mapping Neutralizing and Immunodominant Sites on the SARS-CoV-2 Spike Receptor-Binding Domain by Structure-Guided High-Resolution Serology , 2020, Cell.
[42] William L. Hamilton,et al. Rapid implementation of SARS-CoV-2 sequencing to investigate cases of health-care associated COVID-19: a prospective genomic surveillance study , 2020, The Lancet Infectious Diseases.
[43] K. Yuen,et al. Structural and Functional Basis of SARS-CoV-2 Entry by Using Human ACE2 , 2020, Cell.
[44] K. Shi,et al. Structural basis of receptor recognition by SARS-CoV-2 , 2020, Nature.
[45] Hilde van der Togt,et al. Publisher's Note , 2003, J. Netw. Comput. Appl..