NAV1.4 Voltage-Gated Sodium Channel
"NAV1.4 Voltage-Gated Sodium Channel" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A voltage-gated sodium channel subtype that mediates the sodium ion PERMEABILITY of SKELETAL MYOCYTES. Defects in the SCN4A gene, which codes for the alpha subunit of this sodium channel, are associated with several MYOTONIC DISORDERS.
Descriptor ID |
D062553
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MeSH Number(s) |
D12.776.157.530.400.875.750.400 D12.776.210.500.675 D12.776.543.550.450.875.750.400 D12.776.543.585.400.875.750.400
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Concept/Terms |
NAV1.4 Voltage-Gated Sodium Channel- NAV1.4 Voltage-Gated Sodium Channel
- NAV1.4 Voltage Gated Sodium Channel
- Voltage-Gated Sodium Channel Type 4
- Voltage Gated Sodium Channel Type 4
- Type 4 Voltage-Gated Sodium Channel
- Type 4 Voltage Gated Sodium Channel
Voltage-Gated Sodium Channel Type 4 Subunit alpha- Voltage-Gated Sodium Channel Type 4 Subunit alpha
- Voltage Gated Sodium Channel Type 4 Subunit alpha
- SCN4A Sodium Channel alpha Subunit
- Sodium Channel, Voltage-Gated, Type IV, alpha 1 Subunit
- NAV1.4 alpha Subunit
- Subunit, NAV1.4 alpha
- alpha Subunit, NAV1.4
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Below are MeSH descriptors whose meaning is more general than "NAV1.4 Voltage-Gated Sodium Channel".
Below are MeSH descriptors whose meaning is more specific than "NAV1.4 Voltage-Gated Sodium Channel".
This graph shows the total number of publications written about "NAV1.4 Voltage-Gated Sodium Channel" by people in this website by year, and whether "NAV1.4 Voltage-Gated Sodium Channel" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2016 | 0 | 1 | 1 |
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Below are the most recent publications written about "NAV1.4 Voltage-Gated Sodium Channel" by people in Profiles.
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Elucidation of the Covalent and Tertiary Structures of Biologically Active Ts3 Toxin. Angew Chem Int Ed Engl. 2016 07 18; 55(30):8639-42.
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A sodium channel myotonia due to a novel SCN4A mutation accompanied by acquired autoimmune myasthenia gravis. Neurosci Lett. 2012 Jun 21; 519(1):67-72.
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A novel mutation in SCN4A causes severe myotonia and school-age-onset paralytic episodes. J Neurol Sci. 2012 Apr 15; 315(1-2):15-9.
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A mutation in a rare type of intron in a sodium-channel gene results in aberrant splicing and causes myotonia. Hum Mutat. 2011 Jul; 32(7):773-82.
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New mutation of the Na channel in the severe form of potassium-aggravated myotonia. Muscle Nerve. 2009 May; 39(5):666-73.