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Author Details
Full Name
Chien-Te K Tseng
Affiliation
The University of Texas Medical Branch
ORCID
Career Start Year
1991
Papers
91
H Index
48
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36969239
A pan-variant mRNA-LNP T cell vaccine protects HLA transgenic mice from mortality after infection with SARS-CoV-2 Beta.
Front Immunol
2023
37441066
Circulating Reelin promotes inflammation and modulates disease activity in acute and long COVID-19 cases.
Front Immunol
2023
34730959
Potent Anti-SARS-CoV-2 Activity by the Natural Product Gallinamide A and Analogues via Inhibition of Cathepsin L.
J Med Chem
2022
35665009
The DNA glycosylase NEIL2 plays a vital role in combating SARS-CoV-2 infection.
Res Sq
2022
35860632
Self-Masked Aldehyde Inhibitors of Human Cathepsin L Are Potent Anti-CoV-2 Agents.
Front Chem
2022
36469521
Correction: A Truncated Receptor-Binding Domain of MERS-CoV Spike Protein Potently Inhibits MERS-CoV Infection and Induces Strong Neutralizing Antibody Responses: Implication for Developing Therapeutics and Vaccines.
PLoS One
2022
36001674
Comparison of replicating and nonreplicating vaccines against SARS-CoV-2.
Sci Adv
2022
35900097
A Bacteriophage-Based, Highly Efficacious, Needle- and Adjuvant-Free, Mucosal COVID-19 Vaccine.
mBio
2022
35982307
Programmable antivirals targeting critical conserved viral RNA secondary structures from influenza A virus and SARS-CoV-2.
Nat Med
2022
35313595
Parsing the role of NSP1 in SARS-CoV-2 infection.
bioRxiv
2022
35086724
Efficacy and self-similarity of SARS-CoV-2 thermal decontamination.
J Hazard Mater
2022
35169121
Broad ultra-potent neutralization of SARS-CoV-2 variants by monoclonal antibodies specific to the tip of RBD.
Cell Discov
2022
33283984
A Quick Route to Multiple Highly Potent SARS-CoV-2 Main Protease Inhibitors*.
ChemMedChem
2021
33597253
Bepridil is potent against SARS-CoV-2 in vitro.
Proc Natl Acad Sci U S A
2021
33787221
A Clinical-Stage Cysteine Protease Inhibitor blocks SARS-CoV-2 Infection of Human and Monkey Cells.
ACS Chem Biol
2021
33501450
A Universal Bacteriophage T4 Nanoparticle Platform to Design Multiplex SARS-CoV-2 Vaccine Candidates by CRISPR Engineering.
bioRxiv
2021
35062273
Discovery of Highly Potent Fusion Inhibitors with Potential Pan-Coronavirus Activity That Effectively Inhibit Major COVID-19 Variants of Concern (VOCs) in Pseudovirus-Based Assays.
Viruses
2021
34492082
Novel virus-like nanoparticle vaccine effectively protects animal model from SARS-CoV-2 infection.
PLoS Pathog
2021
34516878
A universal bacteriophage T4 nanoparticle platform to design multiplex SARS-CoV-2 vaccine candidates by CRISPR engineering.
Sci Adv
2021
34161386
The Fc-mediated effector functions of a potent SARS-CoV-2 neutralizing antibody, SC31, isolated from an early convalescent COVID-19 patient, are essential for the optimal therapeutic efficacy of the antibody.
PLoS One
2021
34155200
Author Correction: A nanoluciferase SARS-CoV-2 for rapid neutralization testing and screening of anti-infective drugs for COVID-19.
Nat Commun
2021
34288674
Self-Masked Aldehyde Inhibitors: A Novel Strategy for Inhibiting Cysteine Proteases.
J Med Chem
2021
32511385
Yeast-Expressed SARS-CoV Recombinant Receptor-Binding Domain (RBD219-N1) Formulated with Aluminum Hydroxide Induces Protective Immunity and Reduces Immune Enhancement.
bioRxiv
2020
31883090
Quantification of the Middle East Respiratory Syndrome-Coronavirus RNA in Tissues by Quantitative Real-Time RT-PCR.
Methods Mol Biol
2020
33060595
A nanoluciferase SARS-CoV-2 for rapid neutralization testing and screening of anti-infective drugs for COVID-19.
Nat Commun
2020
33310780
Stapled Peptides Based on Human Angiotensin-Converting Enzyme 2 (ACE2) Potently Inhibit SARS-CoV-2 Infection <i>In Vitro</i>.
mBio
2020
33140046
A cysteine protease inhibitor blocks SARS-CoV-2 infection of human and monkey cells.
bioRxiv
2020
33139569
Rapid identification of a human antibody with high prophylactic and therapeutic efficacy in three animal models of SARS-CoV-2 infection.
Proc Natl Acad Sci U S A
2020
33398273
Potent <i>in vitro</i> anti-SARS-CoV-2 activity by gallinamide A and analogues via inhibition of cathepsin L.
bioRxiv
2020
33236012
The Development of a Novel Nanobody Therapeutic for SARS-CoV-2.
bioRxiv
2020
33039209
Yeast-expressed SARS-CoV recombinant receptor-binding domain (RBD219-N1) formulated with aluminum hydroxide induces protective immunity and reduces immune enhancement.
Vaccine
2020
32607511
A nanoluciferase SARS-CoV-2 for rapid neutralization testing and screening of anti-infective drugs for COVID-19.
bioRxiv
2020
32941803
High Potency of a Bivalent Human V<sub>H</sub> Domain in SARS-CoV-2 Animal Models.
Cell
2020
32766582
A Speedy Route to Multiple Highly Potent SARS-CoV-2 Main Protease Inhibitors.
bioRxiv
2020
32706609
Inducible Epithelial Resistance against Coronavirus Pneumonia in Mice.
Am J Respir Cell Mol Biol
2020
32759966
A novel receptor-binding domain (RBD)-based mRNA vaccine against SARS-CoV-2.
Cell Res
2020
33010978
Enhanced elicitation of potent neutralizing antibodies by the SARS-CoV-2 spike receptor binding domain Fc fusion protein in mice.
Vaccine
2020
32544372
Potent neutralization of SARS-CoV-2 by human antibody heavy-chain variable domains isolated from a large library with a new stable scaffold.
MAbs
2020
30911758
A Highly Immunogenic, Protective, and Safe Adenovirus-Based Vaccine Expressing Middle East Respiratory Syndrome Coronavirus S1-CD40L Fusion Protein in a Transgenic Human Dipeptidyl Peptidase 4 Mouse Model.
J Infect Dis
2019
32313544
Viromimetic STING Agonist-Loaded Hollow Polymeric Nanoparticles for Safe and Effective Vaccination against Middle East Respiratory Syndrome Coronavirus.
Adv Funct Mater
2019
30256968
Elevated Human Dipeptidyl Peptidase 4 Expression Reduces the Susceptibility of hDPP4 Transgenic Mice to Middle East Respiratory Syndrome Coronavirus Infection and Disease.
J Infect Dis
2019
30989115
A pan-coronavirus fusion inhibitor targeting the HR1 domain of human coronavirus spike.
Sci Adv
2019
29496347
Engineering a stable CHO cell line for the expression of a MERS-coronavirus vaccine antigen.
Vaccine
2018
28277821
Receptor-binding domain of MERS-CoV with optimal immunogen dosage and immunization interval protects human transgenic mice from MERS-CoV infection.
Hum Vaccin Immunother
2017
25640653
Identification of an ideal adjuvant for receptor-binding domain-based subunit vaccines against Middle East respiratory syndrome coronavirus.
Cell Mol Immunol
2016
27874853
Introduction of neutralizing immunogenicity index to the rational design of MERS coronavirus subunit vaccines.
Nat Commun
2016
27750111
A recombinant receptor-binding domain of MERS-CoV in trimeric form protects human dipeptidyl peptidase 4 (hDPP4) transgenic mice from MERS-CoV infection.
Virology
2016
27538452
Passive Transfer of A Germline-like Neutralizing Human Monoclonal Antibody Protects Transgenic Mice Against Lethal Middle East Respiratory Syndrome Coronavirus Infection.
Sci Rep
2016
27269431
Immunization with inactivated Middle East Respiratory Syndrome coronavirus vaccine leads to lung immunopathology on challenge with live virus.
Hum Vaccin Immunother
2016
25589660
Generation of a transgenic mouse model of Middle East respiratory syndrome coronavirus infection and disease.
J Virol
2015
1 - 50 of 91
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