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Kohei Tsuji

Showing results (41-50 of 66) with videos related to

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Biochemical and Biophysical Research Communications|September 5, 2021
A linear five-ring pyrrole-imidazole polyamide-triphenylphosphonium conjugate targeting a mitochondrial DNA mutation efficiently induces apoptosis of HeLa cybrid cells carrying the mutationNobuko Koshikawa, Yuki Kida, Nanami Yasui, et al.
Virology|December 29, 2022
Sensitivity to a CD4 mimic of a consensus clone of monkey-adapted CCR5-tropic SHIV-MK38CKanako Matsuura, Mizuki Yamaura, Hiromi Sakawaki, et al.
Chemmedchem|February 12, 2026
CD4 Mimic-Neutralizing Antibody Conjugates Synthesized by Site-Specific Modification Methods as HIV-1 Entry InhibitorsKohei Tsuji, Yutaro Miura, Takeo Kuwata, et al.
RSC Medicinal Chemistry|October 20, 2023
Development of anti-HBV agents targeting HBV capsid proteinsTakuya Kobayakawa, Masayuki Amano, Miyuki Nakayama, et al.
The Journal of Biological Chemistry|July 16, 2015
Amyloidogenic Mutation Promotes Fibril Formation of the N-terminal Apolipoprotein A-I on Lipid MembranesChiharu Mizuguchi, Fuka Ogata, Shiho Mikawa, et al.
Bioorganic & Medicinal Chemistry|December 14, 2020
Potent leads based on CA-19L, an anti-HIV active HIV-1 capsid fragmentKohei Tsuji, Rongyi Wang, Takuya Kobayakawa, et al.
FEBS Letters|December 10, 2013
The extreme N-terminal region of human apolipoprotein A-I has a strong propensity to form amyloid fibrilsEmi Adachi, Asako Kosaka, Kohei Tsuji, et al.
Chemistryopen|October 20, 2015
Development of a Chemical Methodology for the Preparation of Peptide Thioesters Applicable to Naturally Occurring Peptides Using a Sequential Quadruple Acyl Transfer SystemYusuke Tsuda, Akira Shigenaga, Kohei Tsuji, et al.
Bioorganic & Medicinal Chemistry|April 20, 2020
Exploratory studies on CA-15L, an anti-HIV active HIV-1 capsid fragmentKohei Tsuji, Kofi Baffour-Awuah Owusu, Takuya Kobayakawa, et al.
ACS Omega|September 22, 2025
SARS-CoV‑2 Main Protease Inhibitors Containing 5‑Substituted Benzothiazole-2-carbonyl Moieties at the P1' Site and Their DerivativesKohei Tsuji, Takuya Kobayakawa, Nobuyo Higashi-Kuwata, et al.
Pageof 7

Showing results (41-50 of 66) with videos related to

Sort By:
Pageof 7
Biochemical and Biophysical Research Communications|September 5, 2021
A linear five-ring pyrrole-imidazole polyamide-triphenylphosphonium conjugate targeting a mitochondrial DNA mutation efficiently induces apoptosis of HeLa cybrid cells carrying the mutationNobuko Koshikawa, Yuki Kida, Nanami Yasui, et al.
Virology|December 29, 2022
Sensitivity to a CD4 mimic of a consensus clone of monkey-adapted CCR5-tropic SHIV-MK38CKanako Matsuura, Mizuki Yamaura, Hiromi Sakawaki, et al.
Chemmedchem|February 12, 2026
CD4 Mimic-Neutralizing Antibody Conjugates Synthesized by Site-Specific Modification Methods as HIV-1 Entry InhibitorsKohei Tsuji, Yutaro Miura, Takeo Kuwata, et al.
RSC Medicinal Chemistry|October 20, 2023
Development of anti-HBV agents targeting HBV capsid proteinsTakuya Kobayakawa, Masayuki Amano, Miyuki Nakayama, et al.
The Journal of Biological Chemistry|July 16, 2015
Amyloidogenic Mutation Promotes Fibril Formation of the N-terminal Apolipoprotein A-I on Lipid MembranesChiharu Mizuguchi, Fuka Ogata, Shiho Mikawa, et al.
Bioorganic & Medicinal Chemistry|December 14, 2020
Potent leads based on CA-19L, an anti-HIV active HIV-1 capsid fragmentKohei Tsuji, Rongyi Wang, Takuya Kobayakawa, et al.
FEBS Letters|December 10, 2013
The extreme N-terminal region of human apolipoprotein A-I has a strong propensity to form amyloid fibrilsEmi Adachi, Asako Kosaka, Kohei Tsuji, et al.
Chemistryopen|October 20, 2015
Development of a Chemical Methodology for the Preparation of Peptide Thioesters Applicable to Naturally Occurring Peptides Using a Sequential Quadruple Acyl Transfer SystemYusuke Tsuda, Akira Shigenaga, Kohei Tsuji, et al.
Bioorganic & Medicinal Chemistry|April 20, 2020
Exploratory studies on CA-15L, an anti-HIV active HIV-1 capsid fragmentKohei Tsuji, Kofi Baffour-Awuah Owusu, Takuya Kobayakawa, et al.
ACS Omega|September 22, 2025
SARS-CoV‑2 Main Protease Inhibitors Containing 5‑Substituted Benzothiazole-2-carbonyl Moieties at the P1' Site and Their DerivativesKohei Tsuji, Takuya Kobayakawa, Nobuyo Higashi-Kuwata, et al.
Pageof 7