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Kv1.1 and Kv1.2: Similar channels, different seizure models

Epilepsia (Copenhagen), 2012-06, Vol.53 (s1), p.134-141

2012

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The Sound of Silence: Ionic Mechanisms Encoding Sound Termination

Neuron (Cambridge, Mass.), 2011-09, Vol.71 (5), p.911-925

2011

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Hyperexcitability and reduced low threshold potassium currents in auditory neurons of mice lacking the channel subunit Kv1.1

The Journal of physiology, 2003-04, Vol.548 (1), p.1-20

2003

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Mutation of a putative protein degradation gene LITAF/SIMPLE in Charcot-Marie-Tooth disease 1C

Neurology, 2003-01, Vol.60 (1), p.22-26

2003

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Kv1.1-Containing Channels Are Critical for Temporal Precision During Spike Initiation

Journal of neurophysiology, 2006-09, Vol.96 (3), p.1203-1214

2006

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Seizures and Reduced Life Span in Mice Lacking the Potassium Channel Subunit Kv1.2, but Hypoexcitability and Enlarged Kv1 Currents in Auditory Neurons

Journal of neurophysiology, 2007-09, Vol.98 (3), p.1501-1525

2007

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Contribution of Kv1.2 Voltage-gated Potassium Channel to D2 Autoreceptor Regulation of Axonal Dopamine Overflow

The Journal of biological chemistry, 2011-03, Vol.286 (11), p.9360-9372

2011

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The consequences of disrupting cardiac inwardly rectifying K+ current (IK1) as revealed by the targeted deletion of the murine Kir2.1 and Kir2.2 genes

The Journal of physiology, 2001-06, Vol.533 (3), p.697-710

2001

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Activity-dependent regulation of the potassium channel subunits Kv1.1 and Kv3.1

Journal of comparative neurology (1911), 2004-02, Vol.470 (1), p.93-106

2004

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Heteromultimeric K + channels in terminal and juxtaparanodal regions of neurons

Nature (London), 1993-09, Vol.365 (6441), p.75-79

1993

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Structural Consequences of Kcna1 Gene Deletion and Transfer in the Mouse Hippocampus

Epilepsia (Copenhagen), 2007-11, Vol.48 (11), p.2023-2046

2007

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Decreased Temporal Precision of Auditory Signaling in Kcna1-Null Mice: An Electrophysiological Study In Vivo

The Journal of neuroscience, 2003-10, Vol.23 (27), p.9199-9207

2003

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Decreased temporal precision of neuronal signaling as a candidate mechanism of auditory processing disorder

Hearing research, 2015-12, Vol.330 (Pt B), p.213-220

2015

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Low‐voltage activated Kv1.1 subunits are crucial for the processing of sound source location in the lateral superior olive in mice

The Journal of physiology, 2011-03, Vol.589 (5), p.1143-1157

2011

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Changes in Brain Activity During Motor Learning Measured With PET: Effects of Hand of Performance and Practice

Journal of neurophysiology, 1998-10, Vol.80 (4), p.2177-2199

1998

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The value of long-term monitoring of the San Francisco Estuary for Delta Smelt and Longfin Smelt

California fish and wildlife journal, 2021-07, Vol.107 (CESA Special Issue), p.148-171

2021

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Mutations in a plasma membrane Ca2+-ATPase gene cause deafness in deafwaddler mice

Nature genetics, 1998-08, Vol.19 (4), p.390-394

1998

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Anxiety in elite athletes, sex and age characteristics and association with sports

Sportivnai͡a︡ medit͡s︡ina, 2024-05, Vol.13 (4), p.27-35

2024

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Deletion of the K(V)1.1 potassium channel causes epilepsy in mice

Neuron (Cambridge, Mass.), 1998-04, Vol.20 (4), p.809-819

1998

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Mutant β-spectrin 4 causes auditory and motor neuropathies in quivering mice

Nature genetics, 2001-09, Vol.29 (1), p.61-65

2001

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Deafness and retinal degeneration in a novel USH1C knock‐in mouse model

Developmental neurobiology (Hoboken, N.J.), 2010-03, Vol.70 (4), p.253-267

2010

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MPTP induces dystonia and parkinsonism. Clues to the pathophysiology of dystonia

Neurology, 1997-11, Vol.49 (5), p.1432-1438

1997

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Hyperexcitability of CA3 Pyramidal Cells in Mice Lacking the Potassium Channel Subunit Kv1.1

Epilepsia (Copenhagen), 2003-12, Vol.44 (12), p.1506-1512

2003

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Electroconvulsive Thresholds of Inbred Mouse Strains

Genomics (San Diego, Calif.), 2001-06, Vol.74 (3), p.306-312

2001

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Haplo-insufficiency revealed in deafwaddler mice when tested for hearing loss and ataxia

Hearing research, 2004-09, Vol.195 (1), p.90-102

2004

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Kv1.1 and Kv1.2: Similar channels, different seizure models

The Sound of Silence: Ionic Mechanisms Encoding Sound Termination

Hyperexcitability and reduced low threshold potassium currents in auditory neurons of mice lacking the channel subunit Kv1.1

Mutation of a putative protein degradation gene LITAF/SIMPLE in Charcot-Marie-Tooth disease 1C

Kv1.1-Containing Channels Are Critical for Temporal Precision During Spike Initiation

Seizures and Reduced Life Span in Mice Lacking the Potassium Channel Subunit Kv1.2, but Hypoexcitability and Enlarged Kv1 Currents in Auditory Neurons

Contribution of Kv1.2 Voltage-gated Potassium Channel to D2 Autoreceptor Regulation of Axonal Dopamine Overflow

The consequences of disrupting cardiac inwardly rectifying K+ current (IK1) as revealed by the targeted deletion of the murine Kir2.1 and Kir2.2 genes

Activity-dependent regulation of the potassium channel subunits Kv1.1 and Kv3.1

Heteromultimeric K + channels in terminal and juxtaparanodal regions of neurons

Structural Consequences of Kcna1 Gene Deletion and Transfer in the Mouse Hippocampus

Decreased Temporal Precision of Auditory Signaling in Kcna1-Null Mice: An Electrophysiological Study In Vivo

Decreased temporal precision of neuronal signaling as a candidate mechanism of auditory processing disorder

Low‐voltage activated Kv1.1 subunits are crucial for the processing of sound source location in the lateral superior olive in mice

Changes in Brain Activity During Motor Learning Measured With PET: Effects of Hand of Performance and Practice

The value of long-term monitoring of the San Francisco Estuary for Delta Smelt and Longfin Smelt

Mutations in a plasma membrane Ca2+-ATPase gene cause deafness in deafwaddler mice

Anxiety in elite athletes, sex and age characteristics and association with sports

Deletion of the K(V)1.1 potassium channel causes epilepsy in mice

Mutant β-spectrin 4 causes auditory and motor neuropathies in quivering mice

Deafness and retinal degeneration in a novel USH1C knock‐in mouse model

MPTP induces dystonia and parkinsonism. Clues to the pathophysiology of dystonia

Hyperexcitability of CA3 Pyramidal Cells in Mice Lacking the Potassium Channel Subunit Kv1.1

Electroconvulsive Thresholds of Inbred Mouse Strains

Haplo-insufficiency revealed in deafwaddler mice when tested for hearing loss and ataxia

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