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Bioorganic & Medicinal Chemistry Letters|September 20, 2016
Investigation of the structure activity relationship of flufenamic acid derivatives at the human TRESK channel K<sub>2P</sub>18.1Aymeric Monteillier, Alexandre Loucif, Kiyoyuki Omoto, et al.
Molecular Pharmacology|February 11, 2014
Influence of the N terminus on the biophysical properties and pharmacology of TREK1 potassium channelsEmma L Veale, Ehab Al-Moubarak, Naina Bajaria, et al.
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.
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.
Nature Genetics|June 5, 2019
Publisher Correction: Molecular and functional variation in iPSC-derived sensory neuronsJeremy Schwartzentruber, Stefanie Foskolou, Helena Kilpinen, et al.
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