A C Hargreaves - JoVE Visualize

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Molecular Pharmacology|December 1, 1994

Ca2+ permeability of cloned and native 5-hydroxytryptamine type 3 receptorsA C Hargreaves, S C Lummis, C W Taylor

Molecular Pharmacology|November 1, 1996

Direct inhibition of 5-hydroxytryptamine3 receptors by antagonists of L-type Ca2+ channelsA C Hargreaves, M J Gunthorpe, C W Taylor, et al.

Biochemical and Biophysical Research Communications|April 15, 1992

BQ-123, cyclo(-D-Trp-D-Asp-Pro-D-Val-Leu), is a non-competitive antagonist of the actions of endothelin-1 in SK-N-MC human neuroblastoma cellsC R Hiley, D J Cowley, J T Pelton, et al.

The Biochemical Journal|July 25, 1998

Stimulation of neuropeptide Y gene expression by brain-derived neurotrophic factor requires both the phospholipase Cgamma and Shc binding sites on its receptor, TrkBA G Williams, A C Hargreaves, F J Gunn-Moore, et al.

Journal of Pharmacological and Toxicological Methods|March 28, 2006

Optimisation and validation of a medium-throughput electrophysiology-based hERG assay using IonWorks HTM H Bridgland-Taylor, A C Hargreaves, A Easter, et al.

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Showing results (1-10 of 5) with videos related to

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Pageof 1

Molecular Pharmacology|December 1, 1994

Ca2+ permeability of cloned and native 5-hydroxytryptamine type 3 receptorsA C Hargreaves, S C Lummis, C W Taylor

Molecular Pharmacology|November 1, 1996

Direct inhibition of 5-hydroxytryptamine3 receptors by antagonists of L-type Ca2+ channelsA C Hargreaves, M J Gunthorpe, C W Taylor, et al.

Biochemical and Biophysical Research Communications|April 15, 1992

BQ-123, cyclo(-D-Trp-D-Asp-Pro-D-Val-Leu), is a non-competitive antagonist of the actions of endothelin-1 in SK-N-MC human neuroblastoma cellsC R Hiley, D J Cowley, J T Pelton, et al.

The Biochemical Journal|July 25, 1998

Stimulation of neuropeptide Y gene expression by brain-derived neurotrophic factor requires both the phospholipase Cgamma and Shc binding sites on its receptor, TrkBA G Williams, A C Hargreaves, F J Gunn-Moore, et al.

Journal of Pharmacological and Toxicological Methods|March 28, 2006

Optimisation and validation of a medium-throughput electrophysiology-based hERG assay using IonWorks HTM H Bridgland-Taylor, A C Hargreaves, A Easter, et al.

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