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Overview Leadership Blog JoVE Help Center

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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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D C Benton

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The Journal of Physiology|September 5, 2001

SK3 is an important component of K(+) channels mediating the afterhyperpolarization in cultured rat SCG neuronesR Hosseini, D C Benton, P M Dunn, et al.

British Journal of Pharmacology|March 2, 1999

Differences in the actions of some blockers of the calcium-activated potassium permeability in mammalian red cellsD C Benton, C J Roxburgh, C R Ganellin, et al.

British Journal of Pharmacology|January 1, 1996

Discrimination between subtypes of apamin-sensitive Ca(2+)-activated K+ channels by gallamine and a novel bis-quaternary quinolinium cyclophane, UCL 1530P M Dunn, D C Benton, J Campos Rosa, et al.

International Nursing Review|January 28, 2015

Analysis of a global random stratified sample of nurse legislationD C Benton, M P Fernández-Fernández, M A González-Jurado, et al.

The Journal of Pharmacy and Pharmacology|August 1, 1996

The synthesis and some pharmacological actions of the enantiomers of the K(+)-channel blocker cetiedilC J Roxburgh, C R Ganellin, M A Shiner, et al.

Journal of Medicinal Chemistry|September 21, 2001

Synthesis and structure-activity relationships of cetiedil analogues as blockers of the Ca(2+)-activated K+ permeability of erythrocytesC J Roxburgh, C R Ganellin, S Athmani, et al.

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Search research articles

Showing results (21-30 of 26) with videos related to

Sort By:

Pageof 3

You have reached the last page of results.This site can display upto 26 results.

The Journal of Physiology|September 5, 2001

SK3 is an important component of K(+) channels mediating the afterhyperpolarization in cultured rat SCG neuronesR Hosseini, D C Benton, P M Dunn, et al.

British Journal of Pharmacology|March 2, 1999

Differences in the actions of some blockers of the calcium-activated potassium permeability in mammalian red cellsD C Benton, C J Roxburgh, C R Ganellin, et al.

British Journal of Pharmacology|January 1, 1996

Discrimination between subtypes of apamin-sensitive Ca(2+)-activated K+ channels by gallamine and a novel bis-quaternary quinolinium cyclophane, UCL 1530P M Dunn, D C Benton, J Campos Rosa, et al.

International Nursing Review|January 28, 2015

Analysis of a global random stratified sample of nurse legislationD C Benton, M P Fernández-Fernández, M A González-Jurado, et al.

The Journal of Pharmacy and Pharmacology|August 1, 1996

The synthesis and some pharmacological actions of the enantiomers of the K(+)-channel blocker cetiedilC J Roxburgh, C R Ganellin, M A Shiner, et al.

Journal of Medicinal Chemistry|September 21, 2001

Synthesis and structure-activity relationships of cetiedil analogues as blockers of the Ca(2+)-activated K+ permeability of erythrocytesC J Roxburgh, C R Ganellin, S Athmani, et al.

Pageof 3