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The SARS-CoV-2 monoclonal antibody combination, AZD7442, is protective in nonhuman primates and has an extended half-life in humans.
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- Science Translational Medicine, 2022, v. 14, n. 635, p. 1, doi. 10.1126/scitranslmed.abl8124
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- Article
Unveiling viral enablers.
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- Nature Biotechnology, 2008, v. 26, n. 10, p. 1093, doi. 10.1038/nbt1008-1093
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- Article
The majority of human replication protein A remains complexed throughout the cell cycle.
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- Nucleic Acids Research, 2000, v. 28, n. 17, p. 3354, doi. 10.1093/nar/28.17.3354
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- Article
AZD3152 neutralizes SARS-CoV-2 historical and contemporary variants and is protective in hamsters and well tolerated in adults.
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- Science Translational Medicine, 2024, v. 16, n. 753, p. 1, doi. 10.1126/scitranslmed.ado2817
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- Article
A bivalent SARS-CoV-2 monoclonal antibody combination does not affect the immunogenicity of a vector-based COVID-19 vaccine in macaques.
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- Science Translational Medicine, 2022, v. 14, n. 665, p. 1, doi. 10.1126/scitranslmed.abo6160
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- Article
IRF5 regulates unique subset of genes in dendritic cells during West Nile virus infection.
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- Journal of Leukocyte Biology, 2019, v. 105, n. 2, p. 411, doi. 10.1002/JLB.MA0318-136RRR
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- Article
Convergent Evolution of Escape from Hepaciviral Antagonism in Primates.
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- PLoS Biology, 2012, v. 10, n. 3, p. 1, doi. 10.1371/journal.pbio.1001282
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- Article
Convergent Evolution of Escape from Hepaciviral Antagonism in Primates.
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- PLoS Biology, 2012, v. 10, n. 1, p. 1
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- Article