Kv7 (KCNQ) potassium channels that are mutated in human diseases
Author:
Publisher
Wiley
Subject
Physiology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1113/jphysiol.2008.153007/fullpdf
Reference35 articles.
1. KvLQT1 and IsK (minK) proteins associate to form the IKS cardiac potassium current
2. A Potassium Channel Mutation in Neonatal Human Epilepsy
3. Muscarinic suppression of a novel voltage-sensitive K+ current in a vertebrate neurone
4. Vasopressin stimulates action potential firing by protein kinase C-dependent inhibition of KCNQ5 in A7r5 rat aortic smooth muscle cells
5. A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family
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1. Overlooked KCNQ4 variants augment the risk of hearing loss;Experimental & Molecular Medicine;2023-04-03
2. A novel KCNQ4 gene variant (c.857A>G; p.Tyr286Cys) in an extended family with non‑syndromic deafness 2A;Molecular Medicine Reports;2021-04-01
3. Chemical modulation of Kv7 potassium channels;RSC Medicinal Chemistry;2021
4. Muscarinic M1 Receptors Modulate Working Memory Performance and Activity via KCNQ Potassium Channels in the Primate Prefrontal Cortex;Neuron;2020-05
5. A recurrent mutation in KCNQ4 in Korean families with nonsyndromic hearing loss and rescue of the channel activity by KCNQ activators;Human Mutation;2018-12-17
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