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1.
Introduction of two prolines and removal of the polybasic cleavage site leads to optimal efficacy of a recombinant spike based SARS-CoV-2 vaccine in the mouse model
Preprint
en Inglés
| PREPRINT-BIORXIV | ID: ppbiorxiv-300970
2.
Vaccination with B.1.1.7, B.1.351 and P.1 variants protects mice from challenge with wild type SARS-CoV-2
Preprint
en Inglés
| PREPRINT-BIORXIV | ID: ppbiorxiv-455212
3.
Murine monoclonal antibodies against RBD of SARS-CoV-2 neutralize authentic wild type SARS-CoV-2 as well as B.1.1.7 and B.1.351 viruses and protect in vivo in a mouse model in a neutralization dependent manner
Preprint
en Inglés
| PREPRINT-BIORXIV | ID: ppbiorxiv-438547
4.
Comparison of Transgenic and Adenovirus hACE2 Mouse Models for SARS-CoV-2 Infection
Preprint
en Inglés
| PREPRINT-BIORXIV | ID: ppbiorxiv-190066
5.
Immunity to seasonal coronavirus spike proteins does not protect from SARS-CoV-2 challenge in a mouse model but has no detrimental effect on protection mediated by COVID-19 mRNA vaccination
Preprint
en Inglés
| PREPRINT-BIORXIV | ID: ppbiorxiv-513804
6.
SARS-CoV-2 infection induces robust, neutralizing antibody responses that are stable for at least three months
Preprint
en Inglés
| PREPRINT-MEDRXIV | ID: ppmedrxiv-20151126
7.
Long-lasting neutralizing antibody responses in SARS-CoV-2 seropositive individuals are robustly boosted by immunization with the CoronaVac and BNT162b2 vaccines
Preprint
en Inglés
| PREPRINT-MEDRXIV | ID: ppmedrxiv-21257197
8.
Sterilizing Immunity against SARS-CoV-2 Infection in Mice by a Single-Shot and Modified Imidazoquinoline TLR7/8 Agonist-Adjuvanted Recombinant Spike Protein Vaccine
Preprint
en Inglés
| PREPRINT-BIORXIV | ID: ppbiorxiv-344085
9.
The plasmablast response to SARS-CoV-2 mRNA vaccination is dominated by non-neutralizing antibodies that target both the NTD and the RBD
Preprint
en Inglés
| PREPRINT-MEDRXIV | ID: ppmedrxiv-21253098
10.
A serological assay to detect SARS-CoV-2 seroconversion in humans
Preprint
en Inglés
| PREPRINT-MEDRXIV | ID: ppmedrxiv-20037713
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