相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。Calmodulin regulates the trafficking of KCNQ2 potassium channels
Ainhoa Etxeberria et al.
FASEB JOURNAL (2008)
Neutralization of a negative charge in the S1-S2 region of the KV7.2 (KCNQ2) channel affects voltage-dependent activation in neonatal epilepsy
Thomas V. Wuttke et al.
JOURNAL OF PHYSIOLOGY-LONDON (2008)
Deletions or duplications in KCNQ2 can cause benign familial neonatal seizures
S. E. Heron et al.
JOURNAL OF MEDICAL GENETICS (2007)
Peripheral nerve hyperexcitability due to dominant-negative KCNQ2 mutations
T. V. Wuttke et al.
NEUROLOGY (2007)
Atypical gating of M-type potassium channels conferred by mutations in uncharged residues in the S4 region of KCNQ2 causing benign familial neonatal convulsions
Maria Virginia Soldovieri et al.
JOURNAL OF NEUROSCIENCE (2007)
Self-assembly of the isolated KCNQ2 subunit interaction domain
Christina Wehling et al.
FEBS LETTERS (2007)
Structural Insight into KCNQ (Kv7) Channel Assembly and Channelopathy
Rebecca J. Howard et al.
NEURON (2007)
Benign familial neonatal convulsions: Always benign?
O. K. Steinlein et al.
EPILEPSY RESEARCH (2007)
Novel anticonvulsant drugs targeting voltage-dependent ion channels
Thomas V. Wuttke et al.
EXPERT OPINION ON INVESTIGATIONAL DRUGS (2006)
Subthreshold changes of voltage-dependent activation of the KV7.2 channel in neonatal epilepsy
Jessica Hunter et al.
NEUROBIOLOGY OF DISEASE (2006)
Contribution of persistent Na+ current and M-type K+ current to somatic bursting in CA1 pyramidal cells:: Combined experimental and modeling study
David Golomb et al.
JOURNAL OF NEUROPHYSIOLOGY (2006)
Immunohistochemical analysis of KCNQ3 potassium channels in mouse brain
Julia Geiger et al.
NEUROSCIENCE LETTERS (2006)
Immunohistochemical analysis of KCNQ2 potassium channels in adult and developing mouse brain
YG Weber et al.
BRAIN RESEARCH (2006)
A common ankyrin-G-based mechanism retains KCNQ and NaV channels at electrically active domains of the axon
ZM Pan et al.
JOURNAL OF NEUROSCIENCE (2006)
Decreased subunit stability as a novel mechanism for potassium current impairment by a KCNQ2 C terminus mutation causing benign familial neonatal convulsions
MV Soldovieri et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2006)
Functional analysis of novel KCNQ2 and KCNQ3 gene variants found in a large pedigree with benign familial neonatal convulsions (BFNC)
MT Bassi et al.
NEUROGENETICS (2005)
Pathways modulating neural KCNQ/M (Kv7) potassium channels
P Delmas et al.
NATURE REVIEWS NEUROSCIENCE (2005)
Crystal structure of a mammalian voltage-dependent Shaker family K+ channel
SB Long et al.
SCIENCE (2005)
Neonatal seizures with tonic clonic sequences and poor developmental outcome
B Schmitt et al.
EPILEPSY RESEARCH (2005)
Molecular determinants of KCNQ (KV7) K+ channel sensitivity to the anticonvulsant retigabine
A Schenzer et al.
JOURNAL OF NEUROSCIENCE (2005)
The new anticonvulsant retigabine favors voltage-dependent opening of the Kv7.2 (KCNQ2) channel by binding to its activation gate
TV Wuttke et al.
MOLECULAR PHARMACOLOGY (2005)
Ion channel defects in idiopathic epilepsies
H Lerche et al.
CURRENT PHARMACEUTICAL DESIGN (2005)
Novel mutations in the KCNQ2 gene link epilepsy to a dysfunction of the KCNQ2-calmodulin interaction
MC Richards et al.
JOURNAL OF MEDICAL GENETICS (2004)
A novel mutation in KCNQ2 associated with BFNC, drug resistant epilepsy, and mental retardation
R Borgatti et al.
NEUROLOGY (2004)
A novel KCNQ2 K+ channel mutation in benign neonatal convulsions and centrotemporal spikes
G Coppola et al.
NEUROLOGY (2003)
Neonatal convulsions and epileptic encephalopathy in an Italian family with a missense mutation in the fifth transmembrane region of KCNQ2
K Dedek et al.
EPILEPSY RESEARCH (2003)
Age-dependent modulation of hippocampal excitability by KCNQ-channels
M Okada et al.
EPILEPSY RESEARCH (2003)
KCNQ2 and KCNQ3 potassium channel genes in benign familial neonatal convulsions: expansion of the functional and mutation spectrum
NA Singh et al.
BRAIN (2003)
A carboxy-terminal domain determines the subunit specificity of KCNQ K+ channel assembly
M Schwake et al.
EMBO REPORTS (2003)
Phenotypic variants of autoimmune peripheral nerve hyperexcitability
Ian K. Hart et al.
BRAIN (2002)
The open pore conformation of potassium channels
YX Jiang et al.
NATURE (2002)
Effects of the anticonvulsant retigabine on cultured cortical neurons: Changes in electroresponsive properties and synaptic transmission
JF Otto et al.
MOLECULAR PHARMACOLOGY (2002)
Activation of KCNQ5 channels stably expressed in HEK293 cells by BMS-204352
DS Dupuis et al.
EUROPEAN JOURNAL OF PHARMACOLOGY (2002)
Myokymia and neonatal epilepsy caused by a mutation in the voltage sensor of the KCNQ2 K+ channel
K Dedek et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2001)
Benign familial neonatal convulsions (BFNC) resulting from mutation of the KCNQ2 voltage sensor
EM del Giudice et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2000)
Neuronal KCNQ potassium channels: Physiology and role in disease
TJ Jentsch
NATURE REVIEWS NEUROSCIENCE (2000)
Colocalization and coassembly of two human brain M-type potassium channel subunits that are mutated in epilepsy
EC Cooper et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2000)
Surface expression and single channel properties of KCNQ2/KCNQ3, M-type K+ channels involved in epilepsy
M Schwake et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2000)
The novel anticonvulsant retigabine activates M-currents in Chinese hamster ovary-cells tranfected with human KCNQ2/3 subunits
C Rundfeldt et al.
NEUROSCIENCE LETTERS (2000)
A recessive C-terminal Jervell and Lange-Nielsen mutation of the KCNQ1 channel impairs subunit assembly
N Schmitt et al.
EMBO JOURNAL (2000)