Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Tae-Ho Jang

Showing results (31-40 of 39) with videos related to

Pageof 4
Sort By:
You have reached the last page of results.This site can display upto 39 results.
Acta Crystallographica. Section F, Structural Biology and Crystallization Communications|February 9, 2011
Crystallization and preliminary X-ray crystallographic studies of β-transaminase from Mesorhizobium sp. strain LUKBokyung Kim, Ok Kyeung Park, Ju Young Bae, et al.
Nucleic Acids Research|October 16, 2018
Structural basis of the specific interaction of SMRT corepressor with histone deacetylase 4Suk-Youl Park, Gwang Sik Kim, Hyo-Jeong Hwang, et al.
Plos One|September 6, 2014
Crystal structure of transglutaminase 2 with GTP complex and amino acid sequence evidence of evolution of GTP binding siteTae-Ho Jang, Dong-Sup Lee, Kihang Choi, et al.
Scientific Reports|January 25, 2022
The structure of a novel antibody against the spike protein inhibits Middle East respiratory syndrome coronavirus infectionsTae-Ho Jang, Woo-Jung Park, Hansaem Lee, et al.
Nature Communications|November 20, 2018
Molecular basis of maintaining an oxidizing environment under anaerobiosis by soluble fumarate reductaseSunghwan Kim, Chang Min Kim, Young-Jin Son, et al.
Biochemical Pharmacology|November 8, 2011
Inhibition of genotoxic stress induced apoptosis by novel TAT-fused peptides targeting PIDDosomeTae-Ho Jang, Sung-Jun Lee, Chang-Hoon Woo, et al.
European Journal of Medicinal Chemistry|September 18, 2021
Discovery of highly potent human glutaminyl cyclase (QC) inhibitors as anti-Alzheimer's agents by the combination of pharmacophore-based and structure-based designNguyen Van Manh, Van-Hai Hoang, Van T H Ngo, et al.
Bioorganic & Medicinal Chemistry Letters|December 31, 2018
Identification of BR101549 as a lead candidate of non-TZD PPARγ agonist for the treatment of type 2 diabetes: Proof-of-concept evaluation and SARWonken Choung, Hui Jin Jung, Deokmo Yang, et al.
Bioorganic & Medicinal Chemistry Letters|June 30, 2019
Discovery of BR102375, a new class of non-TZD PPARγ full agonist for the treatment of type 2 diabetesWonken Choung, Deokmo Yang, Hakdo Kim, et al.
Pageof 4

Showing results (31-40 of 39) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 39 results.
Acta Crystallographica. Section F, Structural Biology and Crystallization Communications|February 9, 2011
Crystallization and preliminary X-ray crystallographic studies of β-transaminase from Mesorhizobium sp. strain LUKBokyung Kim, Ok Kyeung Park, Ju Young Bae, et al.
Nucleic Acids Research|October 16, 2018
Structural basis of the specific interaction of SMRT corepressor with histone deacetylase 4Suk-Youl Park, Gwang Sik Kim, Hyo-Jeong Hwang, et al.
Plos One|September 6, 2014
Crystal structure of transglutaminase 2 with GTP complex and amino acid sequence evidence of evolution of GTP binding siteTae-Ho Jang, Dong-Sup Lee, Kihang Choi, et al.
Scientific Reports|January 25, 2022
The structure of a novel antibody against the spike protein inhibits Middle East respiratory syndrome coronavirus infectionsTae-Ho Jang, Woo-Jung Park, Hansaem Lee, et al.
Nature Communications|November 20, 2018
Molecular basis of maintaining an oxidizing environment under anaerobiosis by soluble fumarate reductaseSunghwan Kim, Chang Min Kim, Young-Jin Son, et al.
Biochemical Pharmacology|November 8, 2011
Inhibition of genotoxic stress induced apoptosis by novel TAT-fused peptides targeting PIDDosomeTae-Ho Jang, Sung-Jun Lee, Chang-Hoon Woo, et al.
European Journal of Medicinal Chemistry|September 18, 2021
Discovery of highly potent human glutaminyl cyclase (QC) inhibitors as anti-Alzheimer's agents by the combination of pharmacophore-based and structure-based designNguyen Van Manh, Van-Hai Hoang, Van T H Ngo, et al.
Bioorganic & Medicinal Chemistry Letters|December 31, 2018
Identification of BR101549 as a lead candidate of non-TZD PPARγ agonist for the treatment of type 2 diabetes: Proof-of-concept evaluation and SARWonken Choung, Hui Jin Jung, Deokmo Yang, et al.
Bioorganic & Medicinal Chemistry Letters|June 30, 2019
Discovery of BR102375, a new class of non-TZD PPARγ full agonist for the treatment of type 2 diabetesWonken Choung, Deokmo Yang, Hakdo Kim, et al.
Pageof 4