Validation of an Atomic Absorption Rubidium Ion Efflux Assay for KCNQ/M-Channels Using the Ion Channel Reader 8000
Author:
Affiliation:
1. Discovery Neuroscience, Wyeth Research, CN-8000, Princeton, NJ.
Publisher
Mary Ann Liebert Inc
Subject
Drug Discovery,Molecular Medicine
Link
http://www.liebertpub.com/doi/pdf/10.1089/adt.2004.2.525
Reference21 articles.
1. KCNQ2 and KCNQ3 Potassium Channel Subunits: Molecular Correlates of the M-Channel
2. A Potassium Channel Mutation in Neonatal Human Epilepsy
3. Benign Familial Neonatal Convulsions Caused by Altered Gating of KCNQ2/KCNQ3 Potassium Channels
4. A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family
5. Disruption of the Epilepsy KCNQ2 Gene Results in Neural Hyperexcitability
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