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Han-Shen Tae

Showing results (31-40 of 58) with videos related to

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Journal of Medicinal Chemistry|January 13, 2024
Dual Antagonism of α9α10 nAChR and GABA<sub>B</sub> Receptor-Coupled Ca<sub>V</sub>2.2 Channels by an Analgesic αO-Conotoxin AnalogueXiao Li, Han-Shen Tae, Shen Chen, et al.
Neuropharmacology|September 18, 2017
In vivo and in vitro testing of native α-conotoxins from the injected venom of Conus purpurascensMickelene F Hoggard, Alena M Rodriguez, Herminsul Cano, et al.
The International Journal of Biochemistry & Cell Biology|September 2, 2008
A dihydropyridine receptor alpha1s loop region critical for skeletal muscle contraction is intrinsically unstructured and binds to a SPRY domain of the type 1 ryanodine receptorYanfang Cui, Han-Shen Tae, Nicole C Norris, et al.
Marine Drugs|August 25, 2022
Single-Disulfide Conopeptide Czon1107, an Allosteric Antagonist of the Human α3β4 Nicotinic Acetylcholine ReceptorYuan Ma, Qiushi Cao, Mengke Yang, et al.
Journal of Medicinal Chemistry|December 8, 2025
Dual Agonist/Antagonist Modulation of α9-Containing Nicotinic Acetylcholine Receptors by 2-Ammoniumethyl Ethers of Stilbenol and Stilbenol AnaloguesAlessandro Giraudo, Han-Shen Tae, Andrew Hung, et al.
Journal of Neurochemistry|May 19, 2021
α-Conotoxin Bt1.8 from Conus betulinus selectively inhibits α6/α3β2β3 and α3β2 nicotinic acetylcholine receptor subtypesHuying Ning, Biling Huang, Han-Shen Tae, et al.
Journal of Medicinal Chemistry|December 3, 2025
Dual-Action Tetrapeptide Analogue of Psychrophilic Fungal Origin: Potent Inhibitor of Human Nicotinic Acetylcholine Receptors with Antinociceptive and Muscle-Relaxant ActivityLu Lu, Han-Shen Tae, Cheng Ge, et al.
The Journal of Biological Chemistry|August 31, 2017
Backbone cyclization of analgesic conotoxin GeXIVA facilitates direct folding of the ribbon isomerXiaosa Wu, Yen-Hua Huang, Quentin Kaas, et al.
Neurological Research|July 20, 2021
(E)-3-furan-2-yl-N-phenylacrylamide (PAM-4) decreases nociception and emotional manifestations of neuropathic pain in mice by α7 nicotinic acetylcholine receptor potentiationDeniz Bagdas, Gulce Sevdar, Zulfiye Gul, et al.
Journal of Medicinal Chemistry|October 24, 2024
Development of an Intravenously Stable Disulfide-Rich Peptide for the Treatment of Chemotherapy-Induced Neuropathic PainTianmiao Li, Han-Shen Tae, Shen Chen, et al.
Pageof 6

Showing results (31-40 of 58) with videos related to

Sort By:
Pageof 6
Journal of Medicinal Chemistry|January 13, 2024
Dual Antagonism of α9α10 nAChR and GABA<sub>B</sub> Receptor-Coupled Ca<sub>V</sub>2.2 Channels by an Analgesic αO-Conotoxin AnalogueXiao Li, Han-Shen Tae, Shen Chen, et al.
Neuropharmacology|September 18, 2017
In vivo and in vitro testing of native α-conotoxins from the injected venom of Conus purpurascensMickelene F Hoggard, Alena M Rodriguez, Herminsul Cano, et al.
The International Journal of Biochemistry & Cell Biology|September 2, 2008
A dihydropyridine receptor alpha1s loop region critical for skeletal muscle contraction is intrinsically unstructured and binds to a SPRY domain of the type 1 ryanodine receptorYanfang Cui, Han-Shen Tae, Nicole C Norris, et al.
Marine Drugs|August 25, 2022
Single-Disulfide Conopeptide Czon1107, an Allosteric Antagonist of the Human α3β4 Nicotinic Acetylcholine ReceptorYuan Ma, Qiushi Cao, Mengke Yang, et al.
Journal of Medicinal Chemistry|December 8, 2025
Dual Agonist/Antagonist Modulation of α9-Containing Nicotinic Acetylcholine Receptors by 2-Ammoniumethyl Ethers of Stilbenol and Stilbenol AnaloguesAlessandro Giraudo, Han-Shen Tae, Andrew Hung, et al.
Journal of Neurochemistry|May 19, 2021
α-Conotoxin Bt1.8 from Conus betulinus selectively inhibits α6/α3β2β3 and α3β2 nicotinic acetylcholine receptor subtypesHuying Ning, Biling Huang, Han-Shen Tae, et al.
Journal of Medicinal Chemistry|December 3, 2025
Dual-Action Tetrapeptide Analogue of Psychrophilic Fungal Origin: Potent Inhibitor of Human Nicotinic Acetylcholine Receptors with Antinociceptive and Muscle-Relaxant ActivityLu Lu, Han-Shen Tae, Cheng Ge, et al.
The Journal of Biological Chemistry|August 31, 2017
Backbone cyclization of analgesic conotoxin GeXIVA facilitates direct folding of the ribbon isomerXiaosa Wu, Yen-Hua Huang, Quentin Kaas, et al.
Neurological Research|July 20, 2021
(E)-3-furan-2-yl-N-phenylacrylamide (PAM-4) decreases nociception and emotional manifestations of neuropathic pain in mice by α7 nicotinic acetylcholine receptor potentiationDeniz Bagdas, Gulce Sevdar, Zulfiye Gul, et al.
Journal of Medicinal Chemistry|October 24, 2024
Development of an Intravenously Stable Disulfide-Rich Peptide for the Treatment of Chemotherapy-Induced Neuropathic PainTianmiao Li, Han-Shen Tae, Shen Chen, et al.
Pageof 6