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Atypical gating of M-type potassium channels conferred by mutations in uncharged residues in the S4 region of KCNQ2 causing benign familial neonatal convulsions
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Self-assembly of the isolated KCNQ2 subunit interaction domain
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Benign familial neonatal convulsions: Always benign?
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Novel anticonvulsant drugs targeting voltage-dependent ion channels
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Subthreshold changes of voltage-dependent activation of the KV7.2 channel in neonatal epilepsy
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Contribution of persistent Na+ current and M-type K+ current to somatic bursting in CA1 pyramidal cells:: Combined experimental and modeling study
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Immunohistochemical analysis of KCNQ3 potassium channels in mouse brain
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Immunohistochemical analysis of KCNQ2 potassium channels in adult and developing mouse brain
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A common ankyrin-G-based mechanism retains KCNQ and NaV channels at electrically active domains of the axon
ZM Pan et al.
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Decreased subunit stability as a novel mechanism for potassium current impairment by a KCNQ2 C terminus mutation causing benign familial neonatal convulsions
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Functional analysis of novel KCNQ2 and KCNQ3 gene variants found in a large pedigree with benign familial neonatal convulsions (BFNC)
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Pathways modulating neural KCNQ/M (Kv7) potassium channels
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Crystal structure of a mammalian voltage-dependent Shaker family K+ channel
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Neonatal seizures with tonic clonic sequences and poor developmental outcome
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Molecular determinants of KCNQ (KV7) K+ channel sensitivity to the anticonvulsant retigabine
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Ion channel defects in idiopathic epilepsies
H Lerche et al.
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Novel mutations in the KCNQ2 gene link epilepsy to a dysfunction of the KCNQ2-calmodulin interaction
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A novel mutation in KCNQ2 associated with BFNC, drug resistant epilepsy, and mental retardation
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A novel KCNQ2 K+ channel mutation in benign neonatal convulsions and centrotemporal spikes
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Neonatal convulsions and epileptic encephalopathy in an Italian family with a missense mutation in the fifth transmembrane region of KCNQ2
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Age-dependent modulation of hippocampal excitability by KCNQ-channels
M Okada et al.
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KCNQ2 and KCNQ3 potassium channel genes in benign familial neonatal convulsions: expansion of the functional and mutation spectrum
NA Singh et al.
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A carboxy-terminal domain determines the subunit specificity of KCNQ K+ channel assembly
M Schwake et al.
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Phenotypic variants of autoimmune peripheral nerve hyperexcitability
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Activation of KCNQ5 channels stably expressed in HEK293 cells by BMS-204352
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Myokymia and neonatal epilepsy caused by a mutation in the voltage sensor of the KCNQ2 K+ channel
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Benign familial neonatal convulsions (BFNC) resulting from mutation of the KCNQ2 voltage sensor
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Neuronal KCNQ potassium channels: Physiology and role in disease
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Colocalization and coassembly of two human brain M-type potassium channel subunits that are mutated in epilepsy
EC Cooper et al.
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Surface expression and single channel properties of KCNQ2/KCNQ3, M-type K+ channels involved in epilepsy
M Schwake et al.
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The novel anticonvulsant retigabine activates M-currents in Chinese hamster ovary-cells tranfected with human KCNQ2/3 subunits
C Rundfeldt et al.
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A recessive C-terminal Jervell and Lange-Nielsen mutation of the KCNQ1 channel impairs subunit assembly
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