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Ion channel clustering at the axon initial segment and node of Ranvier evolved sequentially in early chordatesCerebellar ataxia and Purkinje cell dysfunction caused by Ca2+-activated K+ channel deficiencyTherapeutic Approaches to Genetic Ion Channelopathies and Perspectives in Drug DiscoveryNew insights into the pathogenesis and therapeutics of episodic ataxia type 1Control of human potassium channel inactivation by editing of a small mRNA hairpinAn essential function for NBS1 in the prevention of ataxia and cerebellar defectsRad50 is dispensable for the maintenance and viability of postmitotic tissuesA defined heteromeric KV1 channel stabilizes the intrinsic pacemaking and regulates the output of deep cerebellar nuclear neurons to thalamic targetsUnderstanding protein non-folding.Auditory deficits of Kcna1 deletion are similar to those of a monaural hearing impairment.Subcellular localization of K+ channels in mammalian brain neurons: remarkable precision in the midst of extraordinary complexity.K(+) channelepsy: progress in the neurobiology of potassium channels and epilepsy.Clinical, genetic, neurophysiological and functional study of new mutations in episodic ataxia type 1.Mutations underlying Episodic Ataxia type-1 antagonize Kv1.1 RNA editingOsteopenia due to enhanced cathepsin K release by BK channel ablation in osteoclasts.Editing of neurotransmitter receptor and ion channel RNAs in the nervous systemA new Kv1.2 channelopathy underlying cerebellar ataxia.Kv1.1 knock-in ataxic mice exhibit spontaneous myokymic activity exacerbated by fatigue, ischemia and low temperatureVoltage-gated potassium channels at the crossroads of neuronal function, ischemic tolerance, and neurodegeneration.Made for "anchorin": Kv7.2/7.3 (KCNQ2/KCNQ3) channels and the modulation of neuronal excitability in vertebrate axons.Novel phenotype associated with a mutation in the KCNA1(Kv1.1) geneSex difference in sensitivity to allopregnanolone neuroprotection in mice correlates with effect on spontaneous inhibitory post synaptic currents.First genome-wide association study in an Australian aboriginal population provides insights into genetic risk factors for body mass index and type 2 diabetesThe role of interneurons in shaping Purkinje cell responses in the cerebellar cortexSelective Loss of Presynaptic Potassium Channel Clusters at the Cerebellar Basket Cell Terminal Pinceau in Adam11 Mutants Reveals Their Role in Ephaptic Control of Purkinje Cell Firing.Human ataxias: a genetic dissection of inositol triphosphate receptor (ITPR1)-dependent signaling.The episodic ataxia type 1 mutation I262T alters voltage-dependent gating and disrupts protein biosynthesis of human Kv1.1 potassium channels.Presynaptic GluN2D receptors detect glutamate spillover and regulate cerebellar GABA release.Episodic ataxia type 1: a neuronal potassium channelopathy.Action potential broadening in a presynaptic channelopathy.Physiologic alterations in ataxia: channeling changes into novel therapies.Consensus paper: pathological mechanisms underlying neurodegeneration in spinocerebellar ataxias.Voltage-gated potassium channels and the diversity of electrical signalling.Derivation and application of pluripotent stem cells for regenerative medicine.Long-term depression in Purkinje neurons is persistently impaired following cardiac arrest and cardiopulmonary resuscitation in mice.Kv1.1 channelopathy abolishes presynaptic spike width modulation by subthreshold somatic depolarization.Episodic ataxia type 1 mutations differentially affect neuronal excitability and transmitter release.Alteration of Neuronal Excitability and Short-Term Synaptic Plasticity in the Prefrontal Cortex of a Mouse Model of Mental Illness.Genotypic differences in ethanol sensitivity in two tests of motor incoordination.Seizures and reduced life span in mice lacking the potassium channel subunit Kv1.2, but hypoexcitability and enlarged Kv1 currents in auditory neurons.
P2860
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P2860
description
2003 nî lūn-bûn
@nan
2003 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
A mouse model of episodic ataxia type-1
@ast
A mouse model of episodic ataxia type-1
@en
A mouse model of episodic ataxia type-1
@nl
type
label
A mouse model of episodic ataxia type-1
@ast
A mouse model of episodic ataxia type-1
@en
A mouse model of episodic ataxia type-1
@nl
prefLabel
A mouse model of episodic ataxia type-1
@ast
A mouse model of episodic ataxia type-1
@en
A mouse model of episodic ataxia type-1
@nl
P2093
P2860
P3181
P356
P1433
P1476
A mouse model of episodic ataxia type-1
@en
P2093
Chris T Bond
James Maylie
John C Crabbe
John P Adelman
Michael Virk
Nathan R Rustay
Paco S Herson
P2860
P2888
P304
P3181
P356
10.1038/NN1025
P407
P577
2003-04-01T00:00:00Z