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Edward B Stevens

Showing results (41-50 of 53) with videos related to

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The Journal of Biological Chemistry|September 14, 2011
The chimeric approach reveals that differences in the TRPV1 pore domain determine species-specific sensitivity to block of heat activationMarianthi Papakosta, Carine Dalle, Alison Haythornthwaite, et al.
British Journal of Pharmacology|October 13, 2021
A small molecule CFTR potentiator restores ATP-dependent channel gating to the cystic fibrosis mutant G551D-CFTRJia Liu, Allison P Berg, Yiting Wang, et al.
Aging Cell|June 27, 2018
Differential aging-related changes in neurophysiology and gene expression in IB4-positive and IB4-negative nociceptive neuronsMalgorzata A Mis, Mark F Rogers, Aaron R Jeffries, et al.
Journal of Medicinal Chemistry|November 6, 2012
Ion channels as therapeutic targets: a drug discovery perspectiveSharan K Bagal, Alan D Brown, Peter J Cox, et al.
British Journal of Pharmacology|November 19, 2017
GI-530159, a novel, selective, mechanosensitive two-pore-domain potassium (K<sub>2P</sub> ) channel opener, reduces rat dorsal root ganglion neuron excitabilityAlexandre J C Loucif, Pierre-Philippe Saintot, Jia Liu, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|May 17, 2014
Characterizing human stem cell-derived sensory neurons at the single-cell level reveals their ion channel expression and utility in pain researchGareth T Young, Alex Gutteridge, Heather DE Fox, et al.
Structure (London, England : 1993)|March 27, 2018
An Intracellular Allosteric Modulator Binding Pocket in SK2 Ion Channels Is Shared by Multiple ChemotypesLily T-Y Cho, Aristos J Alexandrou, Rubben Torella, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|September 6, 2018
CACHD1 is an α2δ-Like Protein That Modulates Ca<sub>V</sub>3 Voltage-Gated Calcium Channel ActivityGraeme S Cottrell, Camille H Soubrane, James A Hounshell, et al.
Science Translational Medicine|April 22, 2016
Pharmacological reversal of a pain phenotype in iPSC-derived sensory neurons and patients with inherited erythromelalgiaLishuang Cao, Aoibhinn McDonnell, Anja Nitzsche, et al.
Bioorganic & Medicinal Chemistry|December 13, 2018
The discovery and optimization of benzimidazoles as selective Na<sub>V</sub>1.8 blockers for the treatment of painAlan D Brown, Sharan K Bagal, Paul Blackwell, et al.
Pageof 6

Showing results (41-50 of 53) with videos related to

Sort By:
Pageof 6
The Journal of Biological Chemistry|September 14, 2011
The chimeric approach reveals that differences in the TRPV1 pore domain determine species-specific sensitivity to block of heat activationMarianthi Papakosta, Carine Dalle, Alison Haythornthwaite, et al.
British Journal of Pharmacology|October 13, 2021
A small molecule CFTR potentiator restores ATP-dependent channel gating to the cystic fibrosis mutant G551D-CFTRJia Liu, Allison P Berg, Yiting Wang, et al.
Aging Cell|June 27, 2018
Differential aging-related changes in neurophysiology and gene expression in IB4-positive and IB4-negative nociceptive neuronsMalgorzata A Mis, Mark F Rogers, Aaron R Jeffries, et al.
Journal of Medicinal Chemistry|November 6, 2012
Ion channels as therapeutic targets: a drug discovery perspectiveSharan K Bagal, Alan D Brown, Peter J Cox, et al.
British Journal of Pharmacology|November 19, 2017
GI-530159, a novel, selective, mechanosensitive two-pore-domain potassium (K<sub>2P</sub> ) channel opener, reduces rat dorsal root ganglion neuron excitabilityAlexandre J C Loucif, Pierre-Philippe Saintot, Jia Liu, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|May 17, 2014
Characterizing human stem cell-derived sensory neurons at the single-cell level reveals their ion channel expression and utility in pain researchGareth T Young, Alex Gutteridge, Heather DE Fox, et al.
Structure (London, England : 1993)|March 27, 2018
An Intracellular Allosteric Modulator Binding Pocket in SK2 Ion Channels Is Shared by Multiple ChemotypesLily T-Y Cho, Aristos J Alexandrou, Rubben Torella, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|September 6, 2018
CACHD1 is an α2δ-Like Protein That Modulates Ca<sub>V</sub>3 Voltage-Gated Calcium Channel ActivityGraeme S Cottrell, Camille H Soubrane, James A Hounshell, et al.
Science Translational Medicine|April 22, 2016
Pharmacological reversal of a pain phenotype in iPSC-derived sensory neurons and patients with inherited erythromelalgiaLishuang Cao, Aoibhinn McDonnell, Anja Nitzsche, et al.
Bioorganic & Medicinal Chemistry|December 13, 2018
The discovery and optimization of benzimidazoles as selective Na<sub>V</sub>1.8 blockers for the treatment of painAlan D Brown, Sharan K Bagal, Paul Blackwell, et al.
Pageof 6