Pages that link to "Q22008501"
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The following pages link to KCNQ2 and KCNQ3 potassium channel subunits: molecular correlates of the M-channel (Q22008501):
Displaying 50 items.
- Potassium voltage-gated channel subfamily Q member 2 (Q6449561) (← links)
- Ion channel clustering at the axon initial segment and node of Ranvier evolved sequentially in early chordates (Q21145023) (← links)
- The orthosteric agonist 2-chloro-5-hydroxyphenylglycine activates mGluR5 and mGluR1 with similar efficacy and potency (Q21262024) (← links)
- KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness (Q22008780) (← links)
- Molecular cloning and functional expression of KCNQ5, a potassium channel subunit that may contribute to neuronal M-current diversity (Q22254006) (← links)
- A common ankyrin-G-based mechanism retains KCNQ and NaV channels at electrically active domains of the axon (Q24307090) (← links)
- A carboxy-terminal domain determines the subunit specificity of KCNQ K+ channel assembly (Q24534565) (← links)
- Polarized axonal surface expression of neuronal KCNQ channels is mediated by multiple signals in the KCNQ2 and KCNQ3 C-terminal domains (Q24545908) (← links)
- Myokymia and neonatal epilepsy caused by a mutation in the voltage sensor of the KCNQ2 K+ channel (Q24555140) (← links)
- Structural insight into KCNQ (Kv7) channel assembly and channelopathy (Q24619681) (← links)
- Neural KCNQ (Kv7) channels (Q24644947) (← links)
- Inhibition of KCNQ1-4 potassium channels expressed in mammalian cells via M1 muscarinic acetylcholine receptors (Q24651211) (← links)
- New molecular targets for antiepileptic drugs: alpha(2)delta, SV2A, and K(v)7/KCNQ/M potassium channels (Q24654230) (← links)
- Characterization of KCNQ5/Q3 potassium channels expressed in mammalian cells (Q24674102) (← links)
- Colocalization and coassembly of two human brain M-type potassium channel subunits that are mutated in epilepsy (Q24675995) (← links)
- Inactivation as a new regulatory mechanism for neuronal Kv7 channels (Q24676507) (← links)
- Kv2 subunits underlie slowly inactivating potassium current in rat neocortical pyramidal neurons (Q24679678) (← links)
- Comparison of K+-channel genes within the genomes of Anopheles gambiae and Drosophila melanogaster (Q24797176) (← links)
- Pulmonary vasoconstrictor action of KCNQ potassium channel blockers. (Q25257466) (← links)
- Electrical resonance with voltage-gated ion channels: perspectives from biophysical mechanisms and neural electrophysiology (Q26771354) (← links)
- KCNQ potassium channels in sensory system and neural circuits (Q26774667) (← links)
- Genetic neurological channelopathies: molecular genetics and clinical phenotypes (Q26777559) (← links)
- Molecular pathophysiology and pharmacology of the voltage-sensing module of neuronal ion channels (Q26800090) (← links)
- Channelopathy pathogenesis in autism spectrum disorders (Q26864726) (← links)
- Driving with no brakes: molecular pathophysiology of Kv7 potassium channels (Q27023978) (← links)
- Redistribution of Kv1 and Kv7 enhances neuronal excitability during structural axon initial segment plasticity (Q27318598) (← links)
- M-current preservation contributes to anticonvulsant effects of valproic acid. (Q27332374) (← links)
- Structure of a Ca2+/CaM:Kv7.4 (KCNQ4) B-Helix Complex Provides Insight into M Current Modulation (Q27675217) (← links)
- Molecular underpinnings of ventral surface chemoreceptor function: focus on KCNQ channels (Q28081514) (← links)
- The novel anticonvulsant retigabine activates M-currents in Chinese hamster ovary-cells tranfected with human KCNQ2/3 subunits (Q28138343) (← links)
- M-type KCNQ2-KCNQ3 potassium channels are modulated by the KCNE2 subunit (Q28141346) (← links)
- Differential expression of kcnq2 splice variants: implications to m current function during neuronal development (Q28143016) (← links)
- Two types of K(+) channel subunit, Erg1 and KCNQ2/3, contribute to the M-like current in a mammalian neuronal cell (Q28144004) (← links)
- A reduced K+ current due to a novel mutation in KCNQ2 causes neonatal convulsions (Q28144219) (← links)
- KCNQ5, a novel potassium channel broadly expressed in brain, mediates M-type currents (Q28144661) (← links)
- Reconstitution of muscarinic modulation of the KCNQ2/KCNQ3 K(+) channels that underlie the neuronal M current (Q28145290) (← links)
- Ion channels and epilepsy (Q28189601) (← links)
- Localization of KCNQ5 in the normal and epileptic human temporal neocortex and hippocampal formation (Q28190825) (← links)
- Potassium leak channels and the KCNK family of two-P-domain subunits (Q28205333) (← links)
- Functional significance of K+ channel β-subunit KCNE3 in auditory neurons (Q28238047) (← links)
- A novel splicing mutation in KCNQ2 in a multigenerational family with BFNC followed for 25 years (Q28239316) (← links)
- KCNE1 and KCNE3 stabilize and/or slow voltage sensing S4 segment of KCNQ1 channel (Q28240701) (← links)
- A comparative analysis of integrating visual information in local neuronal ensembles (Q28263879) (← links)
- Functional analysis of novel KCNQ2 and KCNQ3 gene variants found in a large pedigree with benign familial neonatal convulsions (BFNC) (Q28277873) (← links)
- Regulation of the voltage-gated potassium channel KCNQ4 in the auditory pathway (Q28303262) (← links)
- Differential tetraethylammonium sensitivity of KCNQ1-4 potassium channels (Q28344000) (← links)
- The acrylamide (S)-2 as a positive and negative modulator of Kv7 channels expressed in Xenopus laevis oocytes (Q28472214) (← links)
- Kv3 voltage-gated potassium channels regulate neurotransmitter release from mouse motor nerve terminals (Q28508160) (← links)
- Calmodulin is an auxiliary subunit of KCNQ2/3 potassium channels (Q28511803) (← links)
- From pan-reactive KV7 channel opener to subtype selective opener/inhibitor by addition of a methyl group (Q28539924) (← links)