Distinctive pharmacology and kinetics of cloned neuronal Ca2+ channels and their possible counterparts in mammalian CNS neurons

Author:

Zhang J.-F.,Randall A.D.,Ellinor P.T.,Horne W.A.,Sather W.A.,Tanabe T.,Schwarz T.L.,Tsien R.W.

Publisher

Elsevier BV

Subject

Cellular and Molecular Neuroscience,Pharmacology

Reference41 articles.

1. ω-Conotoxin GVIA blocks a Ca2+ current in bovine chromaffin cells that is not of the “classic” N type;Artalejo;Neuron,1992

2. Classes of calcium channels in vertebrate cells;Bean;A. Rev. Physiol.,1989

3. Receptor sites for Ca2+ channel antagonists;Catterall;Trends Pharmac. Sci.,1992

4. Multiple modes of N-type calcium channel activity distinguished by differences in gating kinetics;Delcour;J. Neurosci.,1993

5. Molecular cloning of the α 1 subunit of an ω-conotoxin-sensitive calcium channel;Dubel,1992

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