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John P. Bilello

Harvard University

33

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2003

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Prodrugs of a 1'-CN-4-Aza-7,9-dideazaadenosine C-Nucleoside Leading to the Discovery of Remdesivir (GS-5734) as a Potent Inhibitor of Respiratory Syncytial Virus with Efficacy in the African Green Monkey Model of RSV.

2021 Journal of Medicinal Chemistry
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An atomistic model of the coronavirus replication-transcription complex as a hexamer assembled around nsp15.

2021 Journal of Biological Chemistry
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Author Correction: A nanoluciferase SARS-CoV-2 for rapid neutralization testing and screening of anti-infective drugs for COVID-19

2021 Nature Communications
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Therapeutic efficacy of an oral nucleoside analog of remdesivir against SARS-CoV-2 pathogenesis in mice.

2021 bioRxiv
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Author Correction: Spike mutation D614G alters SARS-CoV-2 fitness

2021 Nature
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An atomistic model of the coronavirus replication-transcription complex as a hexamer assembled around nsp15

2021 bioRxiv
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Oral prodrug of remdesivir parent GS-441524 is efficacious against SARS-CoV-2 in ferrets.

2021 Nature Communications
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A robust SARS-CoV-2 replication model in primary human epithelial cells at the air liquid interface to assess antiviral agents.

2021 Antiviral Research
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Spike mutation D614G alters SARS-CoV-2 fitness and neutralization susceptibility

2020 bioRxiv
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A nanoluciferase SARS-CoV-2 for rapid neutralization testing and screening of anti-infective drugs for COVID-19

2020 bioRxiv
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Citations (18)