Results 11 to 20 of about 2,282 (189)

In Silico Methods for the Discovery of Kv7.2/7.3 Channels Modulators: A Comprehensive Review [PDF]

open access: yesMolecules
The growing interest in Kv7.2/7.3 agonists originates from the involvement of these channels in several brain hyperexcitability disorders. In particular, Kv7.2/7.3 mutants have been clearly associated with epileptic encephalopathies (DEEs) as well as ...
Claudio Stagno   +6 more
doaj   +5 more sources

Pivoting between calmodulin lobes triggered by calcium in the Kv7.2/calmodulin complex. [PDF]

open access: yesPLoS ONE, 2014
Kv7.2 (KCNQ2) is the principal molecular component of the slow voltage gated M-channel, which strongly influences neuronal excitability. Calmodulin (CaM) binds to two intracellular C-terminal segments of Kv7.2 channels, helices A and B, and it is ...
Alessandro Alaimo   +8 more
doaj   +9 more sources

The Role of Kv7.2 in Neurodevelopment: Insights and Gaps in Our Understanding [PDF]

open access: yesFrontiers in Physiology, 2020
Kv7.2 subunits encoded by the KCNQ2 gene constitute a critical molecular component of the M-current, a subthreshold voltage-gated potassium current controlling neuronal excitability by dampening repetitive action potential firing.
Nina Dirkx   +5 more
doaj   +6 more sources

Differential Regulation of PI(4,5)P2 Sensitivity of Kv7.2 and Kv7.3 Channels by Calmodulin [PDF]

open access: yesFrontiers in Molecular Neuroscience, 2017
HIGHLIGHTS- Calmodulin-dependent Kv7.2 current density without the need of binding calcium.- Kv7.2 current density increase is accompanied with resistance to PI(4,5)P2 depletion.- Kv7.3 current density is insensitive to calmodulin elevation.- Kv7.3 is ...
Alvaro Villarroel   +7 more
doaj   +8 more sources

Calmodulin: A Multitasking Protein in Kv7.2 Potassium Channel Functions [PDF]

open access: yesBiomolecules, 2018
The ubiquitous calcium transducer calmodulin (CaM) plays a pivotal role in many cellular processes, regulating a myriad of structurally different target proteins.
Alessandro Alaimo, Alvaro Villarroel
doaj   +6 more sources

Tamoxifen inhibition of kv7.2/kv7.3 channels. [PDF]

open access: yesPLoS ONE, 2013
KCNQ genes encode five Kv7 K(+) channel subunits (Kv7.1-Kv7.5). Four of these (Kv7.2-Kv7.5) are expressed in the nervous system. Kv7.2 and Kv7.3 are the principal molecular components of the slow voltage-gated M-channel, which regulates neuronal ...
Tania Ferrer   +4 more
doaj   +5 more sources

Ethanol inhibits Kv7.2/7.3 channel open probability by reducing the PI(4,5)P2 sensitivity of Kv7.2 subunit

open access: yesBMB Reports, 2021
Ethanol often causes critical health problems by altering the neuronal activities of the central and peripheral nerve systems. One of the cellular targets of ethanol is the plasma membrane proteins including ion channels and receptors. Recently, we reported that ethanol elevates membrane excitability in sympathetic neurons by inhibiting Kv7.2/7.3 ...
Kim, Kwon Woo, Suh, Byung-Chang
openaire   +5 more sources

Accumulation of Kv7.2 channels in putative ectopic transduction zones of mice nerve-end neuromas [PDF]

open access: yesMolecular Pain, 2011
Background Modulation of M-type currents has been proposed as a new strategy for the treatment of neuropathic pain due to their role in regulating neuronal excitability.
Lopez-García Jose A   +2 more
doaj   +5 more sources

The Kv7.2/Kv7.3 Heterotetramer Assembles with a Random Subunit Arrangement [PDF]

open access: yesJournal of Biological Chemistry, 2012
Voltage-gated K(+) channels composed of Kv7.2 and Kv7.3 are the predominant contributors to the M-current, which plays a key role in controlling neuronal activity. Various lines of evidence have indicated that Kv7.2 and Kv7.3 form a heteromeric channel. However, the subunit stoichiometry and arrangement within this putative heteromer are so far unknown.
Andrew P, Stewart   +6 more
openaire   +3 more sources

Cannabidiol counters the effects of a dominant-negative pathogenic Kv7.2 variant

open access: yesiScience, 2022
Summary: Epilepsy and neurodevelopmental disorders can arise from pathogenic variants of KCNQ (Kv7) channels. A patient with developmental and epileptic encephalopathy exhibited an in-frame deletion of histidine 260 on Kv7.2. Coexpression of Kv7.2 mutant
Xiaoqin Zhan   +7 more
doaj   +3 more sources

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