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Neuronal KCNQ potassium channels: physiology and role in disease

Nature reviews. Neuroscience, 2000-10, Vol.1 (1), p.21-30

Jentsch, T J

2000

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A Potassium Channel Mutation in Neonatal Human Epilepsy

Science (American Association for the Advancement of Science), 1998-01, Vol.279 (5349), p.403-406

1998

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Chloride channel diseases resulting from impaired transepithelial transport or vesicular function

The Journal of clinical investigation, 2005-08, Vol.115 (8), p.2039-2046

2005

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ClC-7 expression levels critically regulate bone turnover, but not gastric acid secretion

Bone (New York, N.Y.), 2014-01, Vol.58, p.92-102

2014

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A constitutively open potassium channel formed by KCNQ1 and KCNE3

Nature (London), 2000-01, Vol.403 (6766), p.196-199

2000

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Moderate loss of function of cyclic-AMP-modulated KCNQ2/KCNQ3 K + channels causes epilepsy

Nature (London), 1998-12, Vol.396 (6712), p.687-690

1998

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Mutations in the a3 subunit of the vacuolar H+-ATPase cause infantile malignant osteopetrosis

Human molecular genetics, 2000-08, Vol.9 (13), p.2059-2063

2000

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The CLC chloride channel family

Pflügers Archiv, 1999-05, Vol.437 (6), p.783-795

1999

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Detection and differentiation of sensorineural hearing loss in mice using auditory steady-state responses and transient auditory brainstem responses

Neuroscience, 2007-11, Vol.149 (3), p.673-684

2007

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Myokymia and Neonatal Epilepsy Caused by a Mutation in the Voltage Sensor of the KCNQ2 K+Channel

Proceedings of the National Academy of Sciences - PNAS, 2001-10, Vol.98 (21), p.12272-12277

2001

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Pathophysiological Mechanisms of Dominant and Recessive KvLQT1 K+ Channel Mutations Found in Inherited Cardiac Arrhythmias

Human molecular genetics, 1997-10, Vol.6 (11), p.1943-1949

1997

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Inhibition of KCNQ1-4 potassium channels expressed in mammalian cells via M1 muscarinic acetylcholine receptors

The Journal of physiology, 2000-02, Vol.522 (3), p.349-355

2000

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Two physically distinct pores in the dimeric CIC-0 chloride channel

Nature (London), 1996-09, Vol.383 (6598), p.340-343

1996

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Functional and Structural Analysis of ClC-K Chloride Channels Involved in Renal Disease

The Journal of biological chemistry, 2000-08, Vol.275 (32), p.24527-24533

2000

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Localization and induction by dehydration of ClC-K chloride channels in the rat kidney

American journal of physiology. Renal physiology, 1997-05, Vol.272 (5), p.678-F688

1997

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A common molecular basis for three inherited kidney stone diseases

Nature (London), 1996-02, Vol.379 (6564), p.445-449

1996

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Properties of voltage-gated chloride channels of the ClC gene family

The Journal of physiology, 1995-01, Vol.482 (P), p.19S-25

1995

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Reply from L. P. Cid, T. J. Jentsch and F. V. Sepúlveda: intestinal electrolyte and fluid secretion – a model in trouble?

The Journal of physiology, 2018-06, Vol.596 (12), p.2465-2466

2018

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ClC-1 Chloride Channel Mutations in Myotonia Congenita: Variable Penetrance of Mutations Shifting the Voltage Dependence

Human molecular genetics, 1998-10, Vol.7 (11), p.1753-1760

1998

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ClC-5 Cl - -channel disruption impairs endocytosis in a mouse model for Dent's disease

Nature (London), 2000-11, Vol.408 (6810), p.369-373

2000

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The Skeletal Muscle Chloride Channel in Dominant and Recessive Human Myotonia

Science (American Association for the Advancement of Science), 1992-08, Vol.257 (5071), p.797-800

1992

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Primary structure and functional expression of a developmentally regulated skeletal muscle chloride channel

Nature (London), 1991-11, Vol.354 (6351), p.301-304

1991

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Primary structure of Torpedo marmorata chloride channel isolated by expression cloning in Xenopus oocytes

Nature (London), 1990-12, Vol.348 (6301), p.510-514

1990

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Permeation and block of the skeletal muscle chloride channel, ClC-1, by foreign anions

The Journal of general physiology, 1998-05, Vol.111 (5), p.653-665

1998

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Neuronal KCNQ potassium channels: physiology and role in disease

A Potassium Channel Mutation in Neonatal Human Epilepsy

Chloride channel diseases resulting from impaired transepithelial transport or vesicular function

ClC-7 expression levels critically regulate bone turnover, but not gastric acid secretion

A constitutively open potassium channel formed by KCNQ1 and KCNE3

Moderate loss of function of cyclic-AMP-modulated KCNQ2/KCNQ3 K + channels causes epilepsy

Mutations in the a3 subunit of the vacuolar H+-ATPase cause infantile malignant osteopetrosis

The CLC chloride channel family

Detection and differentiation of sensorineural hearing loss in mice using auditory steady-state responses and transient auditory brainstem responses

Myokymia and Neonatal Epilepsy Caused by a Mutation in the Voltage Sensor of the KCNQ2 K+Channel

Pathophysiological Mechanisms of Dominant and Recessive KvLQT1 K+ Channel Mutations Found in Inherited Cardiac Arrhythmias

Inhibition of KCNQ1-4 potassium channels expressed in mammalian cells via M1 muscarinic acetylcholine receptors

Two physically distinct pores in the dimeric CIC-0 chloride channel

Functional and Structural Analysis of ClC-K Chloride Channels Involved in Renal Disease

Localization and induction by dehydration of ClC-K chloride channels in the rat kidney

A common molecular basis for three inherited kidney stone diseases

De novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and females

Properties of voltage-gated chloride channels of the ClC gene family

Reply from L. P. Cid, T. J. Jentsch and F. V. Sepúlveda: intestinal electrolyte and fluid secretion – a model in trouble?

ClC-1 Chloride Channel Mutations in Myotonia Congenita: Variable Penetrance of Mutations Shifting the Voltage Dependence

ClC-5 Cl - -channel disruption impairs endocytosis in a mouse model for Dent's disease

The Skeletal Muscle Chloride Channel in Dominant and Recessive Human Myotonia

Primary structure and functional expression of a developmentally regulated skeletal muscle chloride channel

Primary structure of Torpedo marmorata chloride channel isolated by expression cloning in Xenopus oocytes

Permeation and block of the skeletal muscle chloride channel, ClC-1, by foreign anions

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