HCN channelopathies: pathophysiology in genetic epilepsy and therapeutic implications
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Title
HCN channelopathies: pathophysiology in genetic epilepsy and therapeutic implications
Authors
Keywords
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Journal
BRITISH JOURNAL OF PHARMACOLOGY
Volume 165, Issue 1, Pages 49-56
Publisher
Wiley
Online
2011-05-26
DOI
10.1111/j.1476-5381.2011.01507.x
References
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- New therapeutic opportunities in epilepsy: A genetic perspective
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- Proteolytic Processing of HCN2 and Co-assembly with HCN4 in the Generation of Cardiac Pacemaker Channels
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- HCN1 Channel Subunits Are a Molecular Substrate for Hypnotic Actions of Ketamine
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- Loss of Dendritic HCN1 Subunits Enhances Cortical Excitability and Epileptogenesis
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- Alternatively Spliced Isoforms of TRIP8b Differentially Control h Channel Trafficking and Function
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