Chien-Te K. Tseng
Affiliations: | University of Texas Medical Branch, Galveston, TX |
Area:
Virology Biology, Microbiology BiologyGoogle:
"Chien-Te Tseng"
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Publications
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| Song IW, Washington M, Leynes C, et al. (2024) Generation of a humanized mAce2 and a conditional hACE2 mouse models permissive to SARS-COV-2 infection. Mammalian Genome : Official Journal of the International Mammalian Genome Society |
| Fisher T, Gluck A, Narayanan K, et al. (2022) Parsing the role of NSP1 in SARS-CoV-2 infection. Cell Reports. 110954 |
| Fisher T, Gluck A, Narayanan K, et al. (2022) Parsing the role of NSP1 in SARS-CoV-2 infection. Biorxiv : the Preprint Server For Biology |
| Chan CEZ, Seah SGK, Chye H, et al. (2021) 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. 16: e0253487 |
| Vatansever EC, Yang KS, Drelich AK, et al. (2021) Bepridil is potent against SARS-CoV-2 in vitro. Proceedings of the National Academy of Sciences of the United States of America. 118 |
| Curreli F, Victor SMB, Ahmed S, et al. (2020) Stapled Peptides Based on Human Angiotensin-Converting Enzyme 2 (ACE2) Potently Inhibit SARS-CoV-2 Infection . Mbio. 11 |
| Li W, Chen C, Drelich A, et al. (2020) Rapid identification of a human antibody with high prophylactic and therapeutic efficacy in three animal models of SARS-CoV-2 infection. Proceedings of the National Academy of Sciences of the United States of America |
| Chen WH, Tao X, Agrawal AS, et al. (2020) Yeast-expressed SARS-CoV recombinant receptor-binding domain (RBD219-N1) formulated with aluminum hydroxide induces protective immunity and reduces immune enhancement. Vaccine |
| Chen WH, Tao X, Agrawal A, et al. (2020) Yeast-Expressed SARS-CoV Recombinant Receptor-Binding Domain (RBD219-N1) Formulated with Alum Induces Protective Immunity and Reduces Immune Enhancement. Biorxiv : the Preprint Server For Biology |
| Xing J, Shankar R, Drelich A, et al. (2020) Reversal of Infected Host Gene Expression Identifies Repurposed Drug Candidates for COVID-19. Biorxiv : the Preprint Server For Biology |