ArticleBiophysical journal1994
Slow Na+ channel inactivation must be disrupted to evoke prolonged depolarization-induced paralysis.
Article in Biophysical journal, 1994. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
23 citing papers in PubMed.
- Novel compound heterozygous mutations inHeliyon · 2024Article
- Article
- Substitutions of the S4DIV R2 residue (R1451) in NaScientific reports · 2018Article
- Sodium Channelopathies of Skeletal Muscle.Handbook of experimental pharmacology · 2018Review
- A recessive Nav1.4 mutation underlies congenital myasthenic syndrome with periodic paralysis.Neurology · 2016Article
- Channelopathies of skeletal muscle excitability.Comprehensive Physiology · 2015Review
- Enhanced slow inactivation of the human skeletal muscle sodium channel causing normokalemic periodic paralysis.Cellular and molecular neurobiology · 2014Article
- Keeping hyperactive voltage-gated sodium channels in silent mode.The Journal of physiology · 2012Article
- Cold-induced disruption of Na+ channel slow inactivation underlies paralysis in highly thermosensitive paramyotonia.The Journal of physiology · 2009Article
- Genotype-phenotype correlation and therapeutic rationale in hyperkalemic periodic paralysis.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2007Review
- Inherited disorders of voltage-gated sodium channels.The Journal of clinical investigation · 2005Review
- Electrophysiological properties of mutant Nav1.7 sodium channels in a painful inherited neuropathy.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2004Article
- The human skeletal muscle Na channel mutation R669H associated with hypokalemic periodic paralysis enhances slow inactivation.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2000Article
- A double mutation in families with periodic paralysis defines new aspects of sodium channel slow inactivation.The Journal of clinical investigation · 2000Article
- Activation and inactivation of the voltage-gated sodium channel: role of segment S5 revealed by a novel hyperkalaemic periodic paralysis mutation.The Journal of neuroscience : the official journal of the Society for Neuroscience · 1999Article
- Enhanced slow inactivation by V445M: a sodium channel mutation associated with myotonia.Biophysical journal · 1999Article
- Functional expression of the Ile693Thr Na+ channel mutation associated with paramyotonia congenita in a human cell line.The Journal of physiology · 1998Article
- Effect of alkali metal cations on slow inactivation of cardiac Na+ channels.The Journal of general physiology · 1997Article
- Human Na+ channel fast and slow inactivation in paramyotonia congenita mutants expressed in Xenopus laevis oocytes.The Journal of physiology · 1997Article
- Alterations of Na+ channel gating in myotonia.The Journal of physiology · 1997Article
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Abstract
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Registered trials
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