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Nomenclature of voltage-gated sodium channels

Neuron (Cambridge, Mass.), 2000-11, Vol.28 (2), p.365-368

2000

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Primary Structure and Functional Expression of the Human Cardiac Tetrodotoxin-Insensitive Voltage-Dependent Sodium Channel

Proceedings of the National Academy of Sciences - PNAS, 1992-01, Vol.89 (2), p.554-558

1992

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Loss of electrical excitability in an animal model of acute quadriplegic myopathy

Annals of neurology, 1998-02, Vol.43 (2), p.171-179

1998

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Sodium Channel Mutations in Paramyotonia Congenita Exhibit Similar Biophysical Phenotypes In vitro

Proceedings of the National Academy of Sciences - PNAS, 1994-12, Vol.91 (26), p.12785-12789

1994

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Mutations in an S4 segment of the adult skeletal muscle sodium channel cause paramyotonia congenita

Neuron (Cambridge, Mass.), 1992-05, Vol.8 (5), p.891-897

1992

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Primary structure of the adult human skeletal muscle voltage-dependent sodium channel

Annals of neurology, 1992-02, Vol.31 (2), p.131-137

1992

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Paramyotonia congenita and hyperkalemic periodic paralysis are linked to the adult muscle sodium channel gene

Annals of neurology, 1991-12, Vol.30 (6), p.810-816

1991

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Chimeric study of sodium channels from rat skeletal and cardiac muscle

FEBS letters, 1992-09, Vol.309 (3), p.253-257

1992

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SkM2, a Na+ channel cDNA clone from denervated skeletal muscle, encodes a tetrodotoxin-insensitive Na+ channel

Molecular pharmacology, 1991-05, Vol.39 (5), p.604-608

1991

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Sodium channel mutations in paramyotonia congenita and hyperkalemic periodic paralysis

Annals of neurology, 1993-03, Vol.33 (3), p.300-307

1993

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Phenotype and genotype in the myotonic disorders

Muscle & nerve, 1998-09, Vol.21 (9), p.1119-1121

Barchi, Robert L.

1998

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Ion channel mutations and diseases of skeletal muscle

Neurobiology of disease, 1997, Vol.4 (3-4), p.254-264

Barchi, R L

1997

Volltextzugriff (PDF)

Sodium channel mutations in paramyotonia congenita uncouple inactivation from activation

Neuron (Cambridge, Mass.), 1994-02, Vol.12 (2), p.281-294

1994

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The voltage-sensitive sodium channel from rabbit skeletal muscle. Chemical characterization of subunits

The Journal of biological chemistry, 1987-02, Vol.262 (5), p.2298-2303

1987

Volltextzugriff (PDF)

Lidocaine block of human heart sodium channels expressed in Xenopus oocytes

Journal of molecular and cellular cardiology, 1992-11, Vol.24 (11), p.1231-1236

1992

Volltextzugriff (PDF)

Identification of a mutation in the gene causing hyperkalemic periodic paralysis

Cell, 1991-11, Vol.67 (5), p.1021-1027

1991

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Genomic Organization of the Human Skeletal Muscle Sodium Channel Gene

Genomics (San Diego, Calif.), 1993-03, Vol.15 (3), p.598-606

1993

Volltextzugriff (PDF)

Pharmacological modulation of human cardiac Na + channels

European journal of pharmacology, 1994-02, Vol.266 (3), p.245-254

1994

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Scholarship in the Medical Faculty from the University Perspective: Retaining Academic Values

Academic medicine, 2000-09, Vol.75 (9), p.899-905

2000

Volltextzugriff (PDF)

Localization of sodium channel subtypes in adult rat skeletal muscle using channel-specific monoclonal antibodies

The Journal of neuroscience, 1987-09, Vol.7 (9), p.2957-2966

1987

Volltextzugriff (PDF)

Probing the molecular structure of the voltage-dependent sodium channel

Annual review of neuroscience, 1988, Vol.11 (1), p.455-495

Barchi, R L

1988

Volltextzugriff (PDF)

Ion channel mutations affecting muscle and brain

Current opinion in neurology, 1998-10, Vol.11 (5), p.461-468

Barchi, R L

1998

Volltextzugriff (PDF)

Purification and functional reconstitution of the voltage-sensitive sodium channel from rabbit T-tubular membranes

The Journal of biological chemistry, 1985-05, Vol.260 (10), p.6341-6347

1985

Volltextzugriff (PDF)

Analysis of Local Structure in the D2/S1–S2 Region of the Rat Skeletal Muscle Type 1 Sodium Channel Using Insertional Mutagenesis

Journal of neurochemistry, 1998-04, Vol.70 (4), p.1628-1635

1998

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Altered Gene Expression in Steroid-Treated Denervated Muscle

Neurobiology of disease, 1999-12, Vol.6 (6), p.515-522

1999

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Nomenclature of voltage-gated sodium channels

Primary Structure and Functional Expression of the Human Cardiac Tetrodotoxin-Insensitive Voltage-Dependent Sodium Channel

Loss of electrical excitability in an animal model of acute quadriplegic myopathy

Sodium Channel Mutations in Paramyotonia Congenita Exhibit Similar Biophysical Phenotypes In vitro

Mutations in an S4 segment of the adult skeletal muscle sodium channel cause paramyotonia congenita

Primary structure of the adult human skeletal muscle voltage-dependent sodium channel

Paramyotonia congenita and hyperkalemic periodic paralysis are linked to the adult muscle sodium channel gene

Chimeric study of sodium channels from rat skeletal and cardiac muscle

SkM2, a Na+ channel cDNA clone from denervated skeletal muscle, encodes a tetrodotoxin-insensitive Na+ channel

Sodium channel mutations in paramyotonia congenita and hyperkalemic periodic paralysis

Phenotype and genotype in the myotonic disorders

Ion channel mutations and diseases of skeletal muscle

Sodium channel mutations in paramyotonia congenita uncouple inactivation from activation

The voltage-sensitive sodium channel from rabbit skeletal muscle. Chemical characterization of subunits

Lidocaine block of human heart sodium channels expressed in Xenopus oocytes

Identification of a mutation in the gene causing hyperkalemic periodic paralysis

Genomic Organization of the Human Skeletal Muscle Sodium Channel Gene

Pharmacological modulation of human cardiac Na + channels

Scholarship in the Medical Faculty from the University Perspective: Retaining Academic Values

Localization of sodium channel subtypes in adult rat skeletal muscle using channel-specific monoclonal antibodies

Probing the molecular structure of the voltage-dependent sodium channel

Ion channel mutations affecting muscle and brain

Purification and functional reconstitution of the voltage-sensitive sodium channel from rabbit T-tubular membranes

Analysis of Local Structure in the D2/S1–S2 Region of the Rat Skeletal Muscle Type 1 Sodium Channel Using Insertional Mutagenesis

Altered Gene Expression in Steroid-Treated Denervated Muscle

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