Modulation of Kv7 channels and excitability in the brain

DL Greene, N Hoshi - Cellular and Molecular Life Sciences, 2017 - Springer
Neuronal Kv7 channels underlie a voltage-gated non-inactivating potassium current known
as the M-current. Due to its particular characteristics, Kv7 channels show pronounced …

Therapeutic approaches to genetic ion channelopathies and perspectives in drug discovery

P Imbrici, A Liantonio, GM Camerino… - Frontiers in …, 2016 - frontiersin.org
In the human genome more than 400 genes encode ion channels, which are
transmembrane proteins mediating ion fluxes across membranes. Being expressed in all …

Molecular basis for ligand activation of the human KCNQ2 channel

X Li, Q Zhang, P Guo, J Fu, L Mei, D Lv, J Wang, D Lai… - Cell research, 2021 - nature.com
The voltage-gated potassium channel KCNQ2 is responsible for M-current in neurons and is
an important drug target to treat epilepsy, pain and several other diseases related to …

KCNQ2 encephalopathy: Features, mutational hot spots, and ezogabine treatment of 11 patients

JJ Millichap, KL Park, T Tsuchida, B Ben-Zeev… - Neurology …, 2016 - AAN Enterprises
Objective: To advance the understanding of KCNQ2 encephalopathy genotype–phenotype
relationships and to begin to assess the potential of selective KCNQ channel openers as …

Epileptic channelopathies caused by neuronal Kv7 (KCNQ) channel dysfunction

P Nappi, F Miceli, MV Soldovieri, P Ambrosino… - … -European Journal of …, 2020 - Springer
Seizures are the most common neurological manifestation in the newborn period, with an
estimated incidence of 1.8–3.5 per 1000 live births. Prolonged or intractable seizures have a …

Genotype–phenotype correlations in neonatal epilepsies caused by mutations in the voltage sensor of Kv7.2 potassium channel subunits

F Miceli, MV Soldovieri, P Ambrosino… - Proceedings of the …, 2013 - National Acad Sciences
Mutations in the KV7. 2 gene encoding for voltage-dependent K+ channel subunits cause
neonatal epilepsies with wide phenotypic heterogeneity. Two mutations affecting the same …

Mitochondrial dysfunction in cardiovascular disease: Current status of translational research/clinical and therapeutic implications

AS Manolis, AA Manolis, TA Manolis… - Medicinal Research …, 2021 - Wiley Online Library
Mitochondria provide energy to the cell during aerobic respiration by supplying~ 95% of the
adenosine triphosphate (ATP) molecules via oxidative phosphorylation. These organelles …

KCNQ-encoded potassium channels as therapeutic targets

V Barrese, JB Stott, IA Greenwood - Annual review of …, 2018 - annualreviews.org
Kv7 channels are voltage-gated potassium channels encoded by KCNQ genes that have a
considerable physiological impact in many cell types. This reliance upon Kv7 channels for …

KCNQ2 R144 variants cause neurodevelopmental disability with language impairment and autistic features without neonatal seizures through a gain-of-function …

F Miceli, C Millevert, MV Soldovieri, I Mosca… - …, 2022 - thelancet.com
Background Prior studies have revealed remarkable phenotypic heterogeneity in KCNQ2-
related disorders, correlated with effects on biophysical features of heterologously …

Effects of natural and synthetic isothiocyanate-based H2S-releasers against chemotherapy-induced neuropathic pain: Role of Kv7 potassium channels

LDC Mannelli, E Lucarini, L Micheli, I Mosca… - …, 2017 - Elsevier
Hydrogen sulfide (H 2 S) is a crucial signaling molecule involved in several physiological
and pathological processes. Nonetheless, the role of this gasotransmitter in the …