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The Roles of N- and C-terminal Determinants in the Activation of the Kv2.1 Potassium Channel

The Journal of biological chemistry, 2003-04, Vol.278 (15), p.12769-12778

2003

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Roles of Molecular Regions in Determining Differences between Voltage Dependence of Activation of CaV3.1 and CaV1.2 Calcium Channels

The Journal of biological chemistry, 2004-06, Vol.279 (26), p.26858-26867

2004

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Molecular Rearrangements of the Kv2.1 Potassium Channel Termini Associated with Voltage Gating

The Journal of biological chemistry, 2006-07, Vol.281 (28), p.19233-19240

2006

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Structural Determinants of Drugs Acting on the Nav1.8 Channel

The Journal of biological chemistry, 2009-04, Vol.284 (16), p.10523-10536

2009

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Structure and function of ion channels

European biophysics journal, 2009-03, Vol.38 (3), p.271-272

Wray, Dennis

2009

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Role of intracellular domains in the function of the herg potassium channel

European biophysics journal, 2009-06, Vol.38 (5), p.569-576

2009

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Roles of surface residues of intracellular domains of heag potassium channels

European biophysics journal, 2009-04, Vol.38 (4), p.523-532

2009

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Functional properties of Kch, a prokaryotic homologue of eukaryotic potassium channels

Biochemical and biophysical research communications, 2002-09, Vol.297 (1), p.10-16

2002

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Passive transfer of seronegative myasthenia gravis to mice

Muscle & nerve, 1994-12, Vol.17 (12), p.1393-1400

1994

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Molecular regions responsible for differences in activation between heag channels

Biochemical and biophysical research communications, 2006-04, Vol.342 (4), p.1088-1097

2006

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Functional and pharmacological properties of human and rat NaV1.8 channels

Neuropharmacology, 2009-04, Vol.56 (5), p.905-914

2009

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Functional and pharmacological properties of human and rat Na V1.8 channels

Neuropharmacology, 2009, Vol.56 (5), p.905-914

2009

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Tubulin as a Binding Partner of the Heag2 Voltage-Gated Potassium Channel

The Journal of membrane biology, 2008-04, Vol.222 (3), p.115-125

2008

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Functional and Molecular Aspects of Voltage-Gated K+ Channel β Subunits

Annals of the New York Academy of Sciences, 1999-04, Vol.868 (1), p.344-355

1999

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Measurement of the movement of the S4 segment during the activation of a voltage-gated potassium channel

Pflügers Archiv, 1996-11, Vol.433 (1-2), p.91-97

1996

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Coupling of Voltage-dependent Potassium Channel Inactivation and Oxidoreductase Active Site of Kvβ Subunits

The Journal of biological chemistry, 2001-06, Vol.276 (25), p.22923-22929

2001

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Molecular regions underlying the activation of low- and high-voltage activating calcium channels

European biophysics journal, 2005-11, Vol.34 (8), p.1017-1029

2005

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Evidence for multiple Src binding sites on the alpha1c L-type Ca2+ channel and their roles in activity regulation

Cardiovascular research, 2006-02, Vol.69 (2), p.391-401

2006

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Evidence for multiple Src binding sites on the α1c L-type Ca2+ channel and their roles in activity regulation

Cardiovascular research, 2006-02, Vol.69 (2), p.391-401

2006

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Motor Nerve Terminal Calcium Channels in Lambert-Eaton Myasthenic Syndrome

Annals of the New York Academy of Sciences, 1989-06, Vol.560 (1), p.278-290

1989

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Hard pions, current and field commutators, and low energy pion nucleon scattering

Annals of physics, 1969, Vol.51 (1), p.162-186

Wray, Dennis A

1969

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Coupling of Voltage-dependent Potassium Channel Inactivation and Oxidoreductase Active Site of KvÎ² Subunits

The Journal of biological chemistry, 2001-06, Vol.276 (25), p.22923

2001

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AUTOIMMUNE AETIOLOGY FOR MYASTHENIC (EATON-LAMBERT) SYNDROME

The Lancet (British edition), 1981-08, Vol.318 (8240), p.224-226

1981

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Changes in activation gating of IsK potassium currents brought about by mutations in the transmembrane sequence

FEBS letters, 1994-10, Vol.353 (3), p.251-254

1994

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Changes in activation gating of I sK potassium currents brought about by mutations in the transmembrane sequence

FEBS letters, 1994-10, Vol.353 (3), p.251-254

1994

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The Roles of N- and C-terminal Determinants in the Activation of the Kv2.1 Potassium Channel

Roles of Molecular Regions in Determining Differences between Voltage Dependence of Activation of CaV3.1 and CaV1.2 Calcium Channels

Molecular Rearrangements of the Kv2.1 Potassium Channel Termini Associated with Voltage Gating

Structural Determinants of Drugs Acting on the Nav1.8 Channel

Structure and function of ion channels

Role of intracellular domains in the function of the herg potassium channel

Roles of surface residues of intracellular domains of heag potassium channels

Functional properties of Kch, a prokaryotic homologue of eukaryotic potassium channels

Passive transfer of seronegative myasthenia gravis to mice

Molecular regions responsible for differences in activation between heag channels

Functional and pharmacological properties of human and rat NaV1.8 channels

Functional and pharmacological properties of human and rat Na V1.8 channels

Tubulin as a Binding Partner of the Heag2 Voltage-Gated Potassium Channel

Functional and Molecular Aspects of Voltage-Gated K+ Channel β Subunits

Measurement of the movement of the S4 segment during the activation of a voltage-gated potassium channel

Coupling of Voltage-dependent Potassium Channel Inactivation and Oxidoreductase Active Site of Kvβ Subunits

Molecular regions underlying the activation of low- and high-voltage activating calcium channels

Evidence for multiple Src binding sites on the alpha1c L-type Ca2+ channel and their roles in activity regulation

Evidence for multiple Src binding sites on the α1c L-type Ca2+ channel and their roles in activity regulation

Motor Nerve Terminal Calcium Channels in Lambert-Eaton Myasthenic Syndrome

Hard pions, current and field commutators, and low energy pion nucleon scattering

Coupling of Voltage-dependent Potassium Channel Inactivation and Oxidoreductase Active Site of KvÎ² Subunits

AUTOIMMUNE AETIOLOGY FOR MYASTHENIC (EATON-LAMBERT) SYNDROME

Changes in activation gating of IsK potassium currents brought about by mutations in the transmembrane sequence

Changes in activation gating of I sK potassium currents brought about by mutations in the transmembrane sequence

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