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Ae Nim Pae

Showing results (101-110 of 179) with videos related to

Pageof 18
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Chemical Biology & Drug Design|June 28, 2016
Identification of the first in silico-designed TREK1 antagonists that block channel currents dose dependentlyAmbily Nath Indu Viswanath, Seo Yun Jung, Eun Mi Hwang, et al.
Molecular Pharmacology|August 31, 2016
α-Pinene, a Major Constituent of Pine Tree Oils, Enhances Non-Rapid Eye Movement Sleep in Mice through GABAA-benzodiazepine ReceptorsHyejin Yang, Junsung Woo, Ae Nim Pae, et al.
Pharmacology, Biochemistry, and Behavior|October 12, 2005
KKHA-761, a potent D3 receptor antagonist with high 5-HT1A receptor affinity, exhibits antipsychotic properties in animal models of schizophreniaWoo-Kyu Park, Daeyoung Jeong, Heeyeong Cho, et al.
Progress in Neurobiology|February 28, 2020
Visualization of soluble tau oligomers in TauP301L-BiFC transgenic mice demonstrates the progression of tauopathySeulgi Shin, Dohee Kim, Ji Yeon Song, et al.
ACS Chemical Neuroscience|February 15, 2017
A Potential PET Radiotracer for the 5-HT<sub>2C</sub> Receptor: Synthesis and in Vivo Evaluation of 4-(3-[<sup>18</sup>F]fluorophenethoxy)pyrimidineJuhyeon Kim, Byung Seok Moon, Byung Chul Lee, et al.
Angewandte Chemie (International Ed. in English)|February 11, 2009
Intermolecular double Prins-type cyclization: a facile and efficient synthesis of 1,6-dioxecanesPunna Reddy Ullapu, Sun-Joon Min, Satish N Chavre, et al.
Antioxidants (Basel, Switzerland)|October 23, 2021
Highly Potent, Selective, and Competitive Indole-Based MAO-B Inhibitors Protect PC12 Cells against 6-Hydroxydopamine- and Rotenone-Induced Oxidative StressMohamed H Elsherbeny, Jushin Kim, Noha A Gouda, et al.
Journal of Clinical Medicine|November 6, 2019
Development of Oxadiazole-Based ODZ10117 as a Small-Molecule Inhibitor of STAT3 for Targeted Cancer TherapyByung-Hak Kim, Haeri Lee, Yeonghun Song, et al.
Bioorganic & Medicinal Chemistry Letters|January 22, 2013
Synthesis and biological evaluation of 2-(arylethynyl)quinoline derivatives as mGluR5 antagonists for the treatment of neuropathic painMyung-Hee Son, Ji Young Kim, Eun Jeong Lim, et al.
Pharmacology, Biochemistry, and Behavior|August 4, 2010
KST5468, a new T-type calcium channel antagonist, has an antinociceptive effect on inflammatory and neuropathic pain modelsMin Ju Lee, Teo Jeon Shin, Jie Eun Lee, et al.
Pageof 18

Showing results (101-110 of 179) with videos related to

Sort By:
Pageof 18
Chemical Biology & Drug Design|June 28, 2016
Identification of the first in silico-designed TREK1 antagonists that block channel currents dose dependentlyAmbily Nath Indu Viswanath, Seo Yun Jung, Eun Mi Hwang, et al.
Molecular Pharmacology|August 31, 2016
α-Pinene, a Major Constituent of Pine Tree Oils, Enhances Non-Rapid Eye Movement Sleep in Mice through GABAA-benzodiazepine ReceptorsHyejin Yang, Junsung Woo, Ae Nim Pae, et al.
Pharmacology, Biochemistry, and Behavior|October 12, 2005
KKHA-761, a potent D3 receptor antagonist with high 5-HT1A receptor affinity, exhibits antipsychotic properties in animal models of schizophreniaWoo-Kyu Park, Daeyoung Jeong, Heeyeong Cho, et al.
Progress in Neurobiology|February 28, 2020
Visualization of soluble tau oligomers in TauP301L-BiFC transgenic mice demonstrates the progression of tauopathySeulgi Shin, Dohee Kim, Ji Yeon Song, et al.
ACS Chemical Neuroscience|February 15, 2017
A Potential PET Radiotracer for the 5-HT<sub>2C</sub> Receptor: Synthesis and in Vivo Evaluation of 4-(3-[<sup>18</sup>F]fluorophenethoxy)pyrimidineJuhyeon Kim, Byung Seok Moon, Byung Chul Lee, et al.
Angewandte Chemie (International Ed. in English)|February 11, 2009
Intermolecular double Prins-type cyclization: a facile and efficient synthesis of 1,6-dioxecanesPunna Reddy Ullapu, Sun-Joon Min, Satish N Chavre, et al.
Antioxidants (Basel, Switzerland)|October 23, 2021
Highly Potent, Selective, and Competitive Indole-Based MAO-B Inhibitors Protect PC12 Cells against 6-Hydroxydopamine- and Rotenone-Induced Oxidative StressMohamed H Elsherbeny, Jushin Kim, Noha A Gouda, et al.
Journal of Clinical Medicine|November 6, 2019
Development of Oxadiazole-Based ODZ10117 as a Small-Molecule Inhibitor of STAT3 for Targeted Cancer TherapyByung-Hak Kim, Haeri Lee, Yeonghun Song, et al.
Bioorganic & Medicinal Chemistry Letters|January 22, 2013
Synthesis and biological evaluation of 2-(arylethynyl)quinoline derivatives as mGluR5 antagonists for the treatment of neuropathic painMyung-Hee Son, Ji Young Kim, Eun Jeong Lim, et al.
Pharmacology, Biochemistry, and Behavior|August 4, 2010
KST5468, a new T-type calcium channel antagonist, has an antinociceptive effect on inflammatory and neuropathic pain modelsMin Ju Lee, Teo Jeon Shin, Jie Eun Lee, et al.
Pageof 18