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Jun-Goo Jee

Showing results (31-40 of 53) with videos related to

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Food and Chemical Toxicology : an International Journal Published for the British Industrial Biological Research Association|July 10, 2013
Selective inhibition of the cytochrome P450 isoform by hyperoside and its potent inhibition of CYP2D6Min Song, Miri Hong, Min Young Lee, et al.
The Journal of Biological Chemistry|October 31, 2003
Structure of the ubiquitin-interacting motif of S5a bound to the ubiquitin-like domain of HR23BKenichiro Fujiwara, Takeshi Tenno, Kaoru Sugasawa, et al.
Molecular Cancer|February 13, 2010
NSC114792, a novel small molecule identified through structure-based computational database screening, selectively inhibits JAK3Byung-Hak Kim, Jun-Goo Jee, Chang-Hong Yin, et al.
Journal of Molecular Biology|April 22, 2006
Crystal structure of SUMO-3-modified thymine-DNA glycosylaseDaichi Baba, Nobuo Maita, Jun-Goo Jee, et al.
Food and Chemical Toxicology : an International Journal Published for the British Industrial Biological Research Association|April 27, 2013
Barrier protective effects of piperlonguminine in LPS-induced inflammation in vitro and in vivoWonhwa Lee, Hayoung Yoo, Jeong Ah Kim, et al.
Bioorganic & Medicinal Chemistry Letters|May 15, 2012
Identification of myricetin and scutellarein as novel chemical inhibitors of the SARS coronavirus helicase, nsP13Mi-Sun Yu, June Lee, Jin Moo Lee, et al.
British Journal of Pharmacology|February 24, 2018
4-Hydroxynonenal-induced GPR109A (HCA<sub>2</sub> receptor) activation elicits bipolar responses, G<sub>αi</sub> -mediated anti-inflammatory effects and G<sub>βγ</sub> -mediated cell deathJaya Gautam, Suhrid Banskota, Sajita Shah, et al.
European Journal of Medicinal Chemistry|July 26, 2014
Synthesis, antitumor activity, and structure-activity relationship study of trihydroxylated 2,4,6-triphenyl pyridines as potent and selective topoisomerase II inhibitorsRadha Karki, Chanmi Park, Kyu-Yeon Jun, et al.
Acta Crystallographica. Section D, Biological Crystallography|December 6, 2014
β-Arm flexibility of HU from Staphylococcus aureus dictates the DNA-binding and recognition mechanismDo Hee Kim, Hookang Im, Jun Goo Jee, et al.
Journal of Cellular and Molecular Medicine|June 20, 2020
Tubulosine selectively inhibits JAK3 signalling by binding to the ATP-binding site of the kinase of JAK3Byung-Hak Kim, Eun Hee Yi, Jun-Goo Jee, et al.
Pageof 6

Showing results (31-40 of 53) with videos related to

Sort By:
Pageof 6
Food and Chemical Toxicology : an International Journal Published for the British Industrial Biological Research Association|July 10, 2013
Selective inhibition of the cytochrome P450 isoform by hyperoside and its potent inhibition of CYP2D6Min Song, Miri Hong, Min Young Lee, et al.
The Journal of Biological Chemistry|October 31, 2003
Structure of the ubiquitin-interacting motif of S5a bound to the ubiquitin-like domain of HR23BKenichiro Fujiwara, Takeshi Tenno, Kaoru Sugasawa, et al.
Molecular Cancer|February 13, 2010
NSC114792, a novel small molecule identified through structure-based computational database screening, selectively inhibits JAK3Byung-Hak Kim, Jun-Goo Jee, Chang-Hong Yin, et al.
Journal of Molecular Biology|April 22, 2006
Crystal structure of SUMO-3-modified thymine-DNA glycosylaseDaichi Baba, Nobuo Maita, Jun-Goo Jee, et al.
Food and Chemical Toxicology : an International Journal Published for the British Industrial Biological Research Association|April 27, 2013
Barrier protective effects of piperlonguminine in LPS-induced inflammation in vitro and in vivoWonhwa Lee, Hayoung Yoo, Jeong Ah Kim, et al.
Bioorganic & Medicinal Chemistry Letters|May 15, 2012
Identification of myricetin and scutellarein as novel chemical inhibitors of the SARS coronavirus helicase, nsP13Mi-Sun Yu, June Lee, Jin Moo Lee, et al.
British Journal of Pharmacology|February 24, 2018
4-Hydroxynonenal-induced GPR109A (HCA<sub>2</sub> receptor) activation elicits bipolar responses, G<sub>αi</sub> -mediated anti-inflammatory effects and G<sub>βγ</sub> -mediated cell deathJaya Gautam, Suhrid Banskota, Sajita Shah, et al.
European Journal of Medicinal Chemistry|July 26, 2014
Synthesis, antitumor activity, and structure-activity relationship study of trihydroxylated 2,4,6-triphenyl pyridines as potent and selective topoisomerase II inhibitorsRadha Karki, Chanmi Park, Kyu-Yeon Jun, et al.
Acta Crystallographica. Section D, Biological Crystallography|December 6, 2014
β-Arm flexibility of HU from Staphylococcus aureus dictates the DNA-binding and recognition mechanismDo Hee Kim, Hookang Im, Jun Goo Jee, et al.
Journal of Cellular and Molecular Medicine|June 20, 2020
Tubulosine selectively inhibits JAK3 signalling by binding to the ATP-binding site of the kinase of JAK3Byung-Hak Kim, Eun Hee Yi, Jun-Goo Jee, et al.
Pageof 6