Published in Cell Calcium on June 01, 1997
Oxidative stress generated by hemorrhagic shock recruits Toll-like receptor 4 to the plasma membrane in macrophages. J Exp Med (2006) 2.07
Increased calcium entry into dystrophin-deficient muscle fibres of MDX and ADR-MDX mice is reduced by ion channel blockers. J Physiol (1999) 1.47
Calpain mediates calcium-induced activation of the erk1,2 MAPK pathway and cytoskeletal phosphorylation in neurons: relevance to Alzheimer's disease. Am J Pathol (2004) 1.24
Targeting TopBP1 at a convergent point of multiple oncogenic pathways for cancer therapy. Nat Commun (2014) 0.87
N-PEP-12--a novel peptide compound that protects cortical neurons in culture against different age and disease associated lesions. J Neural Transm (Vienna) (2005) 0.85
Calcium transients in isolated amphibian skeletal muscle fibres: detection with aequorin. J Physiol (1978) 6.55
Calcium ion in skeletal muscle: its crucial role for muscle function, plasticity, and disease. Physiol Rev (2000) 3.57
The dynamic chloride component of membrane current in Purkinje fibers. Pflugers Arch Gesamte Physiol Menschen Tiere (1967) 2.90
Interpretation of light diffraction by cross-striated muscle as Bragg reflexion of light by the lattice of contractile proteins. J Physiol (1979) 2.40
Membrane changes in cells from myotonia patients. Physiol Rev (1985) 2.38
CSF filtration is an effective treatment of Guillain-Barré syndrome: a randomized clinical trial. Neurology (2001) 2.16
Excitatory membrane current in heart muscle (Purkinje fibers). Pflugers Arch Gesamte Physiol Menschen Tiere (1966) 2.15
The potassium component of membrane current in Purkinje fibers. Pflugers Arch Gesamte Physiol Menschen Tiere (1967) 2.14
Striated muscle fibers: inactivation of contraction induced by shortening. Science (1970) 2.08
Voltage and time dependence of excitatory sodium current in cooled sheep Purkinje fibres. Pflugers Arch (1970) 1.97
The effect of tetrodotoxin on the membrane current in cardiac muscle (Purkinje fibers). Pflugers Arch Gesamte Physiol Menschen Tiere (1967) 1.95
Adynamia episodica hereditaria with myotonia: a non-inactivating sodium current and the effect of extracellular pH. Muscle Nerve (1987) 1.94
Do laser diffraction studies on striated muscle indicate stepwise sarcomere shortening? Nature (1979) 1.87
An aspartic acid residue important for voltage-dependent gating of human muscle chloride channels. Neuron (1995) 1.79
Calcium transients in amphibian muscle. Fed Proc (1975) 1.61
Mechanism of voltage-dependent gating in skeletal muscle chloride channels. Biophys J (1996) 1.56
An endogenous pentapeptide acting as a sodium channel blocker in inflammatory autoimmune disorders of the central nervous system. Nat Med (2000) 1.50
Striated muscle fibers: facilitation of contraction at short lengths by caffeine. Science (1971) 1.50
Increased calcium entry into dystrophin-deficient muscle fibres of MDX and ADR-MDX mice is reduced by ion channel blockers. J Physiol (1999) 1.47
Hypokalemic periodic paralysis: in vitro investigation of muscle fiber membrane parameters. Muscle Nerve (1984) 1.44
Two cases of adynamia episodica hereditaria: in vitro investigation of muscle cell membrane and contraction parameters. Muscle Nerve (1983) 1.39
A diffractometer using a lateral effect photodiode for the rapid determination of sarcomere length changes in cross-striated muscle. Pflugers Arch (1978) 1.33
Aequorin luminescence during contraction of amphibian skeletal muscle. J Physiol (1973) 1.28
Membrane defects in paramyotonia congenita (Eulenburg). Muscle Nerve (1987) 1.23
The electrogenic sodium pump in guinea-pig ventricular muscle: inhibition of pump current by cardiac glycosides. J Physiol (1982) 1.20
Chloride currents across the membrane of mammalian skeletal muscle fibres. J Physiol (1995) 1.20
Effect of tetrodotoxin on membrane currents in mammalian cardiac fibres. Nature (1967) 1.17
Overexcited or inactive: ion channels in muscle disease. Cell (1995) 1.15
Drug-induced myotonia in human intercostal muscle. Muscle Nerve (1988) 1.13
The myotonic mouse mutant ADR: electrophysiology of the muscle fiber. Muscle Nerve (1988) 1.13
Intracellular Ca2+ concentrations are not elevated in resting cultured muscle from Duchenne (DMD) patients and in MDX mouse muscle fibres. Pflugers Arch (1994) 1.11
The resting membrane parameters of human intercostal muscle at low, normal, and high extracellular potassium. Muscle Nerve (1984) 1.10
Regulation of the human skeletal muscle chloride channel hClC-1 by protein kinase C. J Physiol (1999) 1.10
Mammalian skeletal muscle: reduced chloride conductance in drug-induced myotonia and induction of myotonia by low-chloride solution. Naunyn Schmiedebergs Arch Pharmacol (1972) 1.10
Efficiency of light diffraction by cross-striated muscle fibers under stretch and during isometric contraction. Biophys J (1980) 1.08
Altered sodium channel behaviour causes myotonia in dominantly inherited myotonia congenita. Neuromuscul Disord (1991) 1.08
Adynamia episodica hereditaria: what causes the weakness? Muscle Nerve (1989) 1.05
Membrane defects in paramyotonia congenita with and without myotonia in a warm environment. Muscle Nerve (1981) 1.05
Probing the major skeletal muscle chloride channel with Zn2+ and other sulfhydryl-reactive compounds. Pflugers Arch (1997) 1.05
Giga-seal formation alters properties of sodium channels of human myoballs. Pflugers Arch (1992) 1.03
Molecular pathophysiology of voltage-gated ion channels. Rev Physiol Biochem Pharmacol (1996) 1.03
Intensity behaviour of light diffracted by single frog muscle fibres from narrow laser beams [proceedings]. J Physiol (1977) 1.02
Hereditary nondystrophic myotonias and periodic paralyses. Curr Opin Neurol (1995) 1.02
Improved therapy of myotonia with the lidocaine derivative tocainide. J Neurol (1980) 0.99
Proof of a non-functional muscle chloride channel in recessive myotonia congenita (Becker) by detection of a 4 base pair deletion. Hum Mol Genet (1994) 0.98
The influence of stimulus parameters on contractions of isolated frog muscle fibres. J Physiol (1969) 0.98
Characterization of the sodium currents in isolated human cardiocytes. Pflugers Arch (1994) 0.97
A common mutation (epsilon1267delG) in congenital myasthenic patients of Gypsy ethnic origin. Neurology (1999) 0.97
Electrical myotonia in heterozygous carriers of recessive myotonia congenita. Muscle Nerve (1999) 0.94
Linkage data suggesting allelic heterogeneity for paramyotonia congenita and hyperkalemic periodic paralysis on chromosome 17. Hum Genet (1991) 0.93
Hodgkin-Huxley parameters of the sodium channels in human myoballs. Pflugers Arch (1988) 0.91
Non-dystrophic myotonias and periodic paralyses. A European Neuromuscular Center Workshop held 4-6 October 1992, Ulm, Germany. Neuromuscul Disord (1993) 0.89
Confirmation of linkage of hyperkalaemic periodic paralysis to chromosome 17. J Med Genet (1991) 0.89
Correlation between the light diffraction pattern and the structure of a muscle fibre realized with Ewald's construction. J Muscle Res Cell Motil (1986) 0.89
Myotonic ADR-MDX mutant mice show less severe muscular dystrophy than MDX mice. Neuromuscul Disord (1998) 0.89
Anti-GM1 antibodies can block neuronal voltage-gated sodium channels. Muscle Nerve (2000) 0.88
Development of electrical myotonia in the ADR mouse: role of chloride conductance in myotubes and neonatal animals. Neuromuscul Disord (1993) 0.88
Chloride channels with reduced single-channel conductance in recessive myotonia congenita. Neuron (1993) 0.88
Mutant channels contribute <50% to Na+ current in paramyotonia congenita muscle. Brain (1999) 0.88
Influence of divalent cations on potassium contracture duration in frog muscle fibres. Pflugers Arch (1983) 0.88
Transient weakness and compound muscle action potential decrement in myotonia congenita. Muscle Nerve (1998) 0.87
Identification of three cysteines as targets for the Zn2+ blockade of the human skeletal muscle chloride channel. J Biol Chem (1999) 0.87
Voltage-dependent K+ channels in the sarcolemma of mouse skeletal muscle. Pflugers Arch (1991) 0.87
Single-channel recordings of chloride currents in cultured human skeletal muscle. Pflugers Arch (1992) 0.86
Thyrotoxic periodic paralysis and the sodium/potassium pump. Muscle Nerve (1989) 0.85
Experimental myotonia in mammalian skeletal muscle: changes in membrane properties. Pflugers Arch (1972) 0.85
Role of the cytoskeleton in the regulation of Cl- channels in human embryonic skeletal muscle cells. Pflugers Arch (1994) 0.84
Interleukin-2 inhibits sodium currents in human muscle cells. Pflugers Arch (1992) 0.84
Successuful treatment of paramyotonia congenita (Eulenburg): muscle stiffness and weakness prevented by tocainide. J Neurol Neurosurg Psychiatry (1980) 0.84
Bragg-reflexion of light by cross-striated frog muscle [proceedings]. J Physiol (1978) 0.84
Inactivation of TTX-sensitive and TTX-insensitive sodium channels of rat myoballs. Neurosci Lett (1987) 0.83
The acute paralysis in Guillain-Barré syndrome is related to a Na+ channel blocking factor in the cerebrospinal fluid. Pflugers Arch (1992) 0.83
A transient and a persistent calcium release are induced by chlorocresol in cultivated mouse myotubes. Pflugers Arch (1999) 0.83
Human nicotinic acetylcholine receptor: the influence of second messengers on activation and desensitization. Pflugers Arch (1990) 0.83
Effects of tocainide on normal and myotonic mammalian skeletal muscle. Arzneimittelforschung (1979) 0.83
Specific modifications of the membrane fatty acid composition of human myotubes and their effects on the muscular sodium channels. Biochim Biophys Acta (1993) 0.82
The different use dependences of tocainide and benzocaine are correlated with different effects on sodium channel inactivation. Naunyn Schmiedebergs Arch Pharmacol (1991) 0.82
Experimental myotonia in mammalian skeletal muscle: changes in contractile properties. Pflugers Arch (1972) 0.82
Factors in the cerebrospinal fluid of multiple sclerosis patients interfering with voltage-dependent sodium channels. Neurosci Lett (1993) 0.82
Chloride channels in cultured human skeletal muscle are regulated by G proteins. Pflugers Arch (1992) 0.82
The dominant chloride channel mutant G200R causing fluctuating myotonia: clinical findings, electrophysiology, and channel pathology. Muscle Nerve (1998) 0.82
Altered calcium currents in human hypokalemic periodic paralysis myotubes expressing mutant L-type calcium channels. Soc Gen Physiol Ser (1995) 0.82
Absence of acetylcholine-induced current in epithelial cells from thymus glands and thymomas of myasthenia gravis patients. Neurology (1991) 0.82
Culture conditions for the production of porcine myotubes and myoballs. J Anim Sci (1993) 0.81
Effects of potassium depletion and insulin on resting and stimulated skeletal rat muscle. J Neurol Neurosurg Psychiatry (1979) 0.81
Diagnostics and therapy of muscle channelopathies--Guidelines of the Ulm Muscle Centre. Acta Myol (2008) 0.81
Muscle stiffness and electrical activity in paramyotonia congenita. Muscle Nerve (1986) 0.81
Cardiac glycoside binding to the Na/K-ATPase in the intact myocardial cell: electrophysiological measurement of chemical kinetics. J Mol Cell Cardiol (1981) 0.81
Effects of quinidine, procaine amide, and N-propyl-ajmaline on skeletal muscle. Naunyn Schmiedebergs Arch Pharmacol (1973) 0.80
A simple method for controlling the fluid level in a small experimental chamber during slow and rapid fluid exchange. Pflugers Arch (1983) 0.80
Corticosteroids and neuromuscular transmission: electrophysiological investigation of the effects of prednisolone on normal and anticholinesterase-treated neuromuscular junction. Pflugers Arch (1979) 0.80
Topology of the human skeletal muscle chloride channel hClC-1 probed with hydrophilic epitope insertion. Pflugers Arch (2001) 0.80