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Chapter 2 Molecular Biology of Voltage-Gated Chloride Channels
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title
Chapter 2 Molecular Biology of Voltage-Gated Chloride Channels
(English)
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main subject
molecular biology
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voltage
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author name string
Thomas J. Jentsch
series ordinal
1
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publication date
1994
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published in
Current Topics in Membranes
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page(s)
35-57
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cites work
On the repetitive discharge in myotonic muscle fibres
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The protein IsK is a dual activator of K+ and Cl- channels.
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Chloride conductance regulated by cyclic AMP-dependent protein kinase in cardiac myocytes
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Completely functional double-barreled chloride channel expressed from a single Torpedo cDNA
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Selectivity Changes in Site-Directed Mutants of the VDAC Ion Channel: Structural Implications
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Single chloride-selective channels active at resting membrane potentials in cultured rat skeletal muscle
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Muscle chloride channels
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Activators of protein kinase C induce myotonia by lowering chloride conductance in muscle.
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Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member.
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Chloride channel regulation in the skeletal muscle of normal and myotonic goats
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Effects of denervation and colchicine treatment on the chloride conductance of rat skeletal muscle fibers
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Characterization of ion channels on the surface membrane of adult rat skeletal muscle
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The "gamma subunit" of Na,K-ATPase: a small, amphiphilic protein with a unique amino acid sequence.
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Membrane ionic conductances in normal and denervated skeletal muscle of the rat during development
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Cloning and in situ localization of a brain-derived porin that constitutes a large-conductance anion channel in astrocytic plasma membranes.
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Effect of chloride withdrawal on the geometry of the T-tubules in amphibian and mammalian muscle
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Anion channels activated by adrenaline in cardiac myocytes
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Single-channel recordings of chloride currents in cultured human skeletal muscle
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Chloride channels with reduced single-channel conductance in recessive myotonia congenita
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Altered Na+ channel activity and reduced Cl? conductance cause hyperexcitability in recessive generalized myotonia (becker)
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An unstable triplet repeat in a gene related to myotonic muscular dystrophy
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Developmental control of the excitability of muscle: transplantation experiments on a myotonic mouse mutant
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Molecular basis of Thomsen's disease (autosomal dominant myotonia congenita).
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The strychnine-binding subunit of the glycine receptor shows homology with nicotinic acetylcholine receptors
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Regions involved in the opening of CIC-2 chloride channel by voltage and cell volume
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Predicting the orientation of eukaryotic membrane-spanning proteins
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Autonomic regulation of a chloride current in heart
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Optical evidence for a chloride conductance in the T-system of frog skeletal muscle
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Membrane mechanisms in volume and pH regulation in vertebrate cells
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Altered sodium channel behaviour causes myotonia in dominantly inherited myotonia congenita
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Tissue Expression of mRNA of Chloride Channel from MDCK Cells and Its Regulation by Protein Kinases
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Primary structure of a novel 4-acetamido-4'-isothiocyanostilbene-2,2'-disulphonic acid (SITS)-binding membrane protein highly expressed in Torpedo californica electroplax
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Primary structure of Torpedo marmorata chloride channel isolated by expression cloning in Xenopus oocytes
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Reduction of myosin-light-chain phosphorylation and of parvalbumin content in myotonic mouse muscle and its reversal by tocainide
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Two highly homologous members of the ClC chloride channel family in both rat and human kidney
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The skeletal muscle chloride channel in dominant and recessive human myotonia
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Evidence for genetic homogeneity in autosomal recessive generalised myotonia (Becker).
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Hyperpolarization-activated chloride currents in Xenopus oocytes
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Molecular characterization of a swelling-induced chloride conductance regulatory protein, pICln
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Purification and reconstitution of chloride channels from kidney and trachea
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Sodium, Potassium, and Chloride Fluxes in Intercostal Muscle from Normal Goats and Goats with Hereditary Myotonia
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Cable parameters, sodium, potassium, chloride, and water content, and potassium efflux in isolated external intercostal muscle of normal volunteers and patients with myotonia congenita
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Genomic organization of the human muscle chloride channel CIC-1 and analysis of novel mutations leading to Becker-type myotonia.
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cDNA cloning of a serotonin 5-HT1C receptor by electrophysiological assays of mRNA-injected Xenopus oocytes
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The myotonic mouse mutant ADR: electrophysiology of the muscle fiber
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Molecular cloning and immunological characterization of the gamma polypeptide, a small protein associated with the Na,K-ATPase
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Open-state substructure of single chloride channels from Torpedo electroplax
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Molecular distinction between fetal and adult forms of muscle acetylcholine receptor
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The protein kinase A-regulated cardiac Cl- channel resembles the cystic fibrosis transmembrane conductance regulator
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Primary structure of Electrophorus electricus sodium channel deduced from cDNA sequence
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The nucleotide sequence of a voltage-gated chloride channel from the electric organ of Torpedo californica
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Characteristics of the chloride conductance in muscle fibers of the rat diaphragm
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New mammalian chloride channel identified by expression cloning
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Low single channel conductance of the major skeletal muscle chloride channel, ClC-1.
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A ubiquitous 64-kDa protein is a component of a chloride channel of plasma and intracellular membranes
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The myotonic mouse mutant ADR: physiological and histochemical properties of muscle.
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Steady-state coupling of ion-channel conformations to a transmembrane ion gradient
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Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA
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Membrane changes in cells from myotonia patients
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Transient weakness and altered membrane characteristic in recessive generalized myotonia (Becker)
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https://api.crossref.org/works/10.1016%2FS0070-2161%2808%2960817-5
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Sequence and functional expression of the GABA A receptor shows a ligand-gated receptor super-family
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Primary structure and functional expression of a developmentally regulated skeletal muscle chloride channel
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Inactivation of muscle chloride channel by transposon insertion in myotonic mice
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7 January 2021
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Multimeric structure of ClC-1 chloride channel revealed by mutations in dominant myotonia congenita (Thomsen)
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Calcium-binding protein, parvalbumin, is reduced in mutant mammalian muscle with abnormal contractile properties
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Structural parts involved in activation and inactivation of the sodium channel
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Identification of an anion channel protein from electric organ of Narke japonica
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https://api.crossref.org/works/10.1016%2FS0070-2161%2808%2960817-5
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Cloning of a membrane protein that induces a slow voltage-gated potassium current
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A chloride channel widely expressed in epithelial and non-epithelial cells
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Tonische Krämpfe in willkürlich beweglichen Muskeln in Folge von ererbter psychischer Disposition
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Regulation of muscle sodium channel transcripts during development and in response to denervation
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Volume-regulated chloride channels associated with the human multidrug-resistance P-glycoprotein
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Developmental regulation of five subunit specific mRNAs encoding acetylcholine receptor subtypes in rat muscle.
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Whole-cell recordings of chloride currents in cultured human skeletal muscle
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10.1016/S0070-2161(08)60817-5
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