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Vincent P Santarelli

Showing results (1-10 of 13) with videos related to

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Biophysical Journal|June 5, 2007
Calcium block of single sodium channels: role of a pore-lining aromatic residueVincent P Santarelli, Amy L Eastwood, Dennis A Dougherty, et al.
The Journal of Biological Chemistry|January 24, 2007
A cation-pi interaction discriminates among sodium channels that are either sensitive or resistant to tetrodotoxin blockVincent P Santarelli, Amy L Eastwood, Dennis A Dougherty, et al.
Assay and Drug Development Technologies|April 20, 2004
Generation and characterization of a cell line with inducible expression of Ca(v)3.2 (T-type) channelsMenghang Xia, John P Imredy, Vincent P Santarelli, et al.
Hypertension (Dallas, Tex. : 1979)|June 21, 2017
Functional TASK-3-Like Channels in Mitochondria of Aldosterone-Producing Zona Glomerulosa CellsJunlan Yao, David McHedlishvili, William E McIntire, et al.
ACS Medicinal Chemistry Letters|June 19, 2024
2-Aminopyridines as Potent and Selective Na<sub>v</sub>1.8 Inhibitors Exhibiting Efficacy in a Nonhuman Primate Pain ModelMichael J Breslin, Jeffrey W Schubert, Deping Wang, et al.
Neuroreport|February 13, 2009
T-type calcium channels regulate cortical plasticity in-vivo. [corrected]Victor N Uebele, Cindy E Nuss, Vincent P Santarelli, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 9, 2023
Identification, structural, and biophysical characterization of a positive modulator of human Kv3.1 channelsYun-Ting Chen, Mee Ra Hong, Xin-Jun Zhang, et al.
Neurobiology of Pain (Cambridge, Mass.)|April 11, 2025
Humanized Na<sub>V</sub>1.8 rats overcome cross-species potency shifts in developing novel Na<sub>V</sub>1.8 inhibitorsDillon S McDevitt, Joshua D Vardigan, Xiaoping Zhou, et al.
Brain Research|September 3, 2011
TASK-3 as a potential antidepressant targetAnthony L Gotter, Vincent P Santarelli, Scott M Doran, et al.
Chemmedchem|September 15, 2011
Discovery of a pharmacologically active antagonist of the two-pore-domain potassium channel K2P9.1 (TASK-3)Craig A Coburn, Yunfu Luo, Mingxiang Cui, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Biophysical Journal|June 5, 2007
Calcium block of single sodium channels: role of a pore-lining aromatic residueVincent P Santarelli, Amy L Eastwood, Dennis A Dougherty, et al.
The Journal of Biological Chemistry|January 24, 2007
A cation-pi interaction discriminates among sodium channels that are either sensitive or resistant to tetrodotoxin blockVincent P Santarelli, Amy L Eastwood, Dennis A Dougherty, et al.
Assay and Drug Development Technologies|April 20, 2004
Generation and characterization of a cell line with inducible expression of Ca(v)3.2 (T-type) channelsMenghang Xia, John P Imredy, Vincent P Santarelli, et al.
Hypertension (Dallas, Tex. : 1979)|June 21, 2017
Functional TASK-3-Like Channels in Mitochondria of Aldosterone-Producing Zona Glomerulosa CellsJunlan Yao, David McHedlishvili, William E McIntire, et al.
ACS Medicinal Chemistry Letters|June 19, 2024
2-Aminopyridines as Potent and Selective Na<sub>v</sub>1.8 Inhibitors Exhibiting Efficacy in a Nonhuman Primate Pain ModelMichael J Breslin, Jeffrey W Schubert, Deping Wang, et al.
Neuroreport|February 13, 2009
T-type calcium channels regulate cortical plasticity in-vivo. [corrected]Victor N Uebele, Cindy E Nuss, Vincent P Santarelli, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 9, 2023
Identification, structural, and biophysical characterization of a positive modulator of human Kv3.1 channelsYun-Ting Chen, Mee Ra Hong, Xin-Jun Zhang, et al.
Neurobiology of Pain (Cambridge, Mass.)|April 11, 2025
Humanized Na<sub>V</sub>1.8 rats overcome cross-species potency shifts in developing novel Na<sub>V</sub>1.8 inhibitorsDillon S McDevitt, Joshua D Vardigan, Xiaoping Zhou, et al.
Brain Research|September 3, 2011
TASK-3 as a potential antidepressant targetAnthony L Gotter, Vincent P Santarelli, Scott M Doran, et al.
Chemmedchem|September 15, 2011
Discovery of a pharmacologically active antagonist of the two-pore-domain potassium channel K2P9.1 (TASK-3)Craig A Coburn, Yunfu Luo, Mingxiang Cui, et al.
Pageof 2