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Heike Wulff

Showing results (111-120 of 222) with videos related to

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Molecular Pharmacology|April 22, 2017
Rapid Throughput Analysis of GABA<sub>A</sub> Receptor Subtype Modulators and Blockers Using DiSBAC<sub>1</sub>(3) Membrane Potential Red DyeAtefeh Mousavi Nik, Brandon Pressly, Vikrant Singh, et al.
Frontiers in Pharmacology|September 5, 2022
Editorial: Venoms, animal and microbial toxins, volume IIZhijian Cao, Delavar Shahbazzadeh, Hervé Kovacic, et al.
Plos One|July 5, 2013
K(Ca)3.1 channel-blockade attenuates airway pathophysiology in a sheep model of chronic asthmaJoanne Van Der Velden, Grace Sum, Donna Barker, et al.
Frontiers in Pharmacology|June 14, 2021
Editorial: Venoms, Animal and Microbial ToxinsZhijian Cao, Jing-Lin Wang, Patrick Michael McNutt, et al.
Structure (London, England : 1993)|May 15, 2026
Structural basis for the subtype-selective activation of K<sub>Ca</sub>3.1 channelsAlena Ramanishka, Joshua A Nasburg, Yang Xu, et al.
Neurotoxicology|December 8, 2019
Susceptibility of larval zebrafish to the seizurogenic activity of GABA type A receptor antagonistsSuren B Bandara, Dennis R Carty, Vikrant Singh, et al.
The Biochemical Journal|December 14, 2004
K+ channel types targeted by synthetic OSK1, a toxin from Orthochirus scrobiculosus scorpion venomStéphanie Mouhat, Violeta Visan, S Ananthakrishnan, et al.
Research Square|June 5, 2025
Structural basis for the subtype-selectivity of K<sub>Ca</sub>2.2 channel activatorsMiao Zhang, Young-Woo Nam, Alena Ramanishka, et al.
The Biochemical Journal|September 10, 2003
The 'functional' dyad of scorpion toxin Pi1 is not itself a prerequisite for toxin binding to the voltage-gated Kv1.2 potassium channelsStéphanie Mouhat, Amor Mosbah, Violeta Visan, et al.
The Journal of Organic Chemistry|February 6, 2016
Chasing the Elusive Benzofuran Impurity of the THR Antagonist NH-3: Synthesis, Isotope Labeling, and Biological ActivityLatika Singh, Brandon Pressly, Brenda J Mengeling, et al.
Pageof 23

Showing results (111-120 of 222) with videos related to

Sort By:
Pageof 23
Molecular Pharmacology|April 22, 2017
Rapid Throughput Analysis of GABA<sub>A</sub> Receptor Subtype Modulators and Blockers Using DiSBAC<sub>1</sub>(3) Membrane Potential Red DyeAtefeh Mousavi Nik, Brandon Pressly, Vikrant Singh, et al.
Frontiers in Pharmacology|September 5, 2022
Editorial: Venoms, animal and microbial toxins, volume IIZhijian Cao, Delavar Shahbazzadeh, Hervé Kovacic, et al.
Plos One|July 5, 2013
K(Ca)3.1 channel-blockade attenuates airway pathophysiology in a sheep model of chronic asthmaJoanne Van Der Velden, Grace Sum, Donna Barker, et al.
Frontiers in Pharmacology|June 14, 2021
Editorial: Venoms, Animal and Microbial ToxinsZhijian Cao, Jing-Lin Wang, Patrick Michael McNutt, et al.
Structure (London, England : 1993)|May 15, 2026
Structural basis for the subtype-selective activation of K<sub>Ca</sub>3.1 channelsAlena Ramanishka, Joshua A Nasburg, Yang Xu, et al.
Neurotoxicology|December 8, 2019
Susceptibility of larval zebrafish to the seizurogenic activity of GABA type A receptor antagonistsSuren B Bandara, Dennis R Carty, Vikrant Singh, et al.
The Biochemical Journal|December 14, 2004
K+ channel types targeted by synthetic OSK1, a toxin from Orthochirus scrobiculosus scorpion venomStéphanie Mouhat, Violeta Visan, S Ananthakrishnan, et al.
Research Square|June 5, 2025
Structural basis for the subtype-selectivity of K<sub>Ca</sub>2.2 channel activatorsMiao Zhang, Young-Woo Nam, Alena Ramanishka, et al.
The Biochemical Journal|September 10, 2003
The 'functional' dyad of scorpion toxin Pi1 is not itself a prerequisite for toxin binding to the voltage-gated Kv1.2 potassium channelsStéphanie Mouhat, Amor Mosbah, Violeta Visan, et al.
The Journal of Organic Chemistry|February 6, 2016
Chasing the Elusive Benzofuran Impurity of the THR Antagonist NH-3: Synthesis, Isotope Labeling, and Biological ActivityLatika Singh, Brandon Pressly, Brenda J Mengeling, et al.
Pageof 23