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Author Details
Full Name
Kris M White
Affiliation
Quantitative Biosciences Institute (QBI) Coronavirus Research Group (QCRG)
ORCID
Career Start Year
2010
Papers
45
H Index
23
Expertise
CM4AI Collaborator
Trey Ideker (CM4AI)
PMID
Paper Title
Journal Title
Published Year
36894709
Pharmacological disruption of mSWI/SNF complex activity restricts SARS-CoV-2 infection.
Nat Genet
2023
37758692
Proteomic and genetic analyses of influenza A viruses identify pan-viral host targets.
Nat Commun
2023
37523415
Structures of SARS-CoV-2 N7-methyltransferase with DOT1L and PRMT7 inhibitors provide a platform for new antivirals.
PLoS Pathog
2023
37738970
SARS-CoV-2 variants evolve convergent strategies to remodel the host response.
Cell
2023
37354015
Large library docking for novel SARS-CoV-2 main protease non-covalent and covalent inhibitors.
Protein Sci
2023
37294077
Structure-Based Discovery of Inhibitors of the SARS-CoV-2 Nsp14 N7-Methyltransferase.
J Med Chem
2023
34669512
Functional Effects of Cardiomyocyte Injury in COVID-19.
J Virol
2022
35766385
Sec61 Inhibitor Apratoxin S4 Potently Inhibits SARS-CoV-2 and Exhibits Broad-Spectrum Antiviral Activity.
ACS Infect Dis
2022
36558898
SARS-CoV-2 Inhibitors Identified by Phenotypic Analysis of a Collection of Viral RNA-Binding Molecules.
Pharmaceuticals (Basel)
2022
36197970
Common and species-specific molecular signatures, networks, and regulators of influenza virus infection in mice, ferrets, and humans.
Sci Adv
2022
35012962
Preclinical and randomized phase I studies of plitidepsin in adults hospitalized with COVID-19.
Life Sci Alliance
2022
34942634
Evolution of enhanced innate immune evasion by SARS-CoV-2.
Nature
2022
35332335
Publisher Correction: Evolution of enhanced innate immune evasion by SARS-CoV-2.
Nature
2022
35169796
The oral drug nitazoxanide restricts SARS-CoV-2 infection and attenuates disease pathogenesis in Syrian hamsters.
bioRxiv
2022
34112877
Transcriptomics-based drug repositioning pipeline identifies therapeutic candidates for COVID-19.
Sci Rep
2021
33495306
Plitidepsin has potent preclinical efficacy against SARS-CoV-2 by targeting the host protein eEF1A.
Science
2021
33791693
Phospholipidosis is a shared mechanism underlying the in vitro antiviral activity of many repurposed drugs against SARS-CoV-2.
bioRxiv
2021
33821262
Transcriptomics-based drug repositioning pipeline identifies therapeutic candidates for COVID-19.
Res Sq
2021
33836156
TOP1 inhibition therapy protects against SARS-CoV-2-induced lethal inflammation.
Cell
2021
34663813
Preclinical characterization of an intravenous coronavirus 3CL protease inhibitor for the potential treatment of COVID19.
Nat Commun
2021
34326236
Drug-induced phospholipidosis confounds drug repurposing for SARS-CoV-2.
Science
2021
34075384
Plitidepsin has a positive therapeutic index in adult patients with COVID-19 requiring hospitalization.
medRxiv
2021
33984267
Hepatitis C virus drugs that inhibit SARS-CoV-2 papain-like protease synergize with remdesivir to suppress viral replication in cell culture.
Cell Rep
2021
34260245
Aryl Sulfonamide Inhibits Entry and Replication of Diverse Influenza Viruses via the Hemagglutinin Protein.
J Med Chem
2021
32511357
A Large-scale Drug Repositioning Survey for SARS-CoV-2 Antivirals.
bioRxiv
2020
33200140
Physiology of cardiomyocyte injury in COVID-19.
medRxiv
2020
33060197
Comparative host-coronavirus protein interaction networks reveal pan-viral disease mechanisms.
Science
2020
33299999
Topoisomerase 1 inhibition therapy protects against SARS-CoV-2-induced inflammation and death in animal models.
bioRxiv
2020
33154106
An ultrapotent synthetic nanobody neutralizes SARS-CoV-2 by stabilizing inactive Spike.
Science
2020
33097660
SARS-CoV-2 Orf6 hijacks Nup98 to block STAT nuclear import and antagonize interferon signaling.
Proc Natl Acad Sci U S A
2020
32707573
Discovery of SARS-CoV-2 antiviral drugs through large-scale compound repurposing.
Nature
2020
32817938
An ultra-potent synthetic nanobody neutralizes SARS-CoV-2 by locking Spike into an inactive conformation.
bioRxiv
2020
32645325
The Global Phosphorylation Landscape of SARS-CoV-2 Infection.
Cell
2020
32585083
An In Vitro Microneutralization Assay for SARS-CoV-2 Serology and Drug Screening.
Curr Protoc Microbiol
2020
32240278
Chemical intervention of influenza virus mRNA nuclear export.
PLoS Pathog
2020
32353859
A SARS-CoV-2 protein interaction map reveals targets for drug repurposing.
Nature
2020
32268088
Passenger Mutations Confound Phenotypes of SARM1-Deficient Mice.
Cell Rep
2020
29268608
Broad Spectrum Inhibitor of Influenza A and B Viruses Targeting the Viral Nucleoprotein.
ACS Infect Dis
2018
30146161
Transcription Elongation Can Affect Genome 3D Structure.
Cell
2018
29395518
Influenza B virus reverse genetic backbones with improved growth properties in the EB66® cell line as basis for vaccine seed virus generation.
Vaccine
2018
28953980
Influenza virus differentially activates mTORC1 and mTORC2 signaling to maximize late stage replication.
PLoS Pathog
2017
25984567
A Potent Anti-influenza Compound Blocks Fusion through Stabilization of the Prefusion Conformation of the Hemagglutinin Protein.
ACS Infect Dis
2015
23933115
New-generation screening assays for the detection of anti-influenza compounds targeting viral and host functions.
Antiviral Res
2013
20130051
Role of the IE62 consensus binding site in transactivation by the varicella-zoster virus IE62 protein.
J Virol
2010
20631144
Varicella-zoster virus immediate-early protein 62 blocks interferon regulatory factor 3 (IRF3) phosphorylation at key serine residues: a novel mechanism of IRF3 inhibition among herpesviruses.
J Virol
2010
1 - 45 of 45
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