Spinocerebellar ataxia type 19/22 mutations alter heterocomplex Kv4.3 channel function and gating in a dominant manner

The Stoichiometry and Biophysical Properties of the Kv4 Potassium Channel Complex with K+Channel-interacting Protein (KChIP) Subunits Are Variable, Depending on the Relative Expression Level

(2014) Masahiro Kitazawa et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Kv3.3 channels harbouring a mutation of spinocerebellar ataxia type 13 alter excitability and induce cell death in cultured cerebellar Purkinje cells

(2013) Tomohiko Irie et al.   JOURNAL OF PHYSIOLOGY-LONDON

The L450P mutation in KCND3 brings spinocerebellar ataxia and Brugada syndrome closer together

(2013) Anna Duarri et al.   NEUROGENETICS

Climbing Fiber Input Shapes Reciprocity of Purkinje Cell Firing

(2013) Aleksandra Badura et al.   NEURON

Mutation in the Kv3.3 Voltage-Gated Potassium Channel Causing Spinocerebellar Ataxia 13 Disrupts Sound-Localization Mechanisms

(2013) John C. Middlebrooks et al.   PLoS One

Mutations in potassium channelkcnd3cause spinocerebellar ataxia type 19

(2012) Anna Duarri et al.   ANNALS OF NEUROLOGY

Mutations inKCND3cause spinocerebellar ataxia type 22

(2012) Yi-Chung Lee et al.   ANNALS OF NEUROLOGY

Changes in Purkinje cell firing and gene expression precede behavioral pathology in a mouse model of SCA2

(2012) S. T. Hansen et al.   HUMAN MOLECULAR GENETICS

Low Temperature and Chemical Rescue Affect Molecular Proximity of ΔF508-Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) and Epithelial Sodium Channel (ENaC)

(2012) Yawar J. Qadri et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Altered Kv3.3 channel gating in early-onset spinocerebellar ataxia type 13

(2012) Natali A. Minassian et al.   JOURNAL OF PHYSIOLOGY-LONDON

Changes in Channel Trafficking and Protein Stability Caused by LQT2 Mutations in the PAS Domain of the HERG Channel

(2012) Carol A. Harley et al.   PLoS One

The influence of synaptic activity on neuronal health

(2011) Karen FS Bell et al.   CURRENT OPINION IN NEUROBIOLOGY

Early Changes in Cerebellar Physiology Accompany Motor Dysfunction in the Polyglutamine Disease Spinocerebellar Ataxia Type 3

(2011) V. G. Shakkottai et al.   JOURNAL OF NEUROSCIENCE

Voltage-gated K+ channel modulators as neuroprotective agents

(2010) Yuk-Man Leung   LIFE SCIENCES

KChIP1 modulation of Kv4.3-mediated A-type K+ currents and repetitive firing in hippocampal interneurons

(2010) M.L. Bourdeau et al.   NEUROSCIENCE

KChIP1: a potential modulator to GABAergic system

(2009) H. Xiong et al.   ACTA BIOCHIMICA ET BIOPHYSICA SINICA

KCNC3: phenotype, mutations, channel biophysics-a study of 260 familial ataxia patients

(2009) Karla P. Figueroa et al.   HUMAN MUTATION

Low temperature restoring effect on F508del-CFTR misprocessing: A proteomic approach

(2009) Patricia Gomes-Alves et al.   Journal of Proteomics

FGF14 regulates the intrinsic excitability of cerebellar Purkinje neurons

(2008) Vikram G. Shakkottai et al.   NEUROBIOLOGY OF DISEASE

The G604S-hERG mutation alters the biophysical properties and exerts a dominant-negative effect on expression of hERG channels in HEK293 cells

(2008) Jianhua Huo et al.   PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY