NAV1.3 Voltage-Gated Sodium Channel
"NAV1.3 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 found in neuronal tissue that mediates the sodium ion PERMEABILITY of excitable membranes.
| Descriptor ID |
D062552
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| MeSH Number(s) |
D12.776.157.530.400.875.750.300 D12.776.543.550.450.875.750.300 D12.776.543.585.400.875.750.300 D12.776.631.960.300
|
| Concept/Terms |
NAV1.3 Voltage-Gated Sodium Channel- NAV1.3 Voltage-Gated Sodium Channel
- NAV1.3 Voltage Gated Sodium Channel
- Type 3 Voltage-Gated Sodium Channel
- Type 3 Voltage Gated Sodium Channel
- Voltage-Gated Sodium Channel Type 3
- Voltage Gated Sodium Channel Type 3
Voltage-Gated Sodium Channel Type 3 Subunit alpha- Voltage-Gated Sodium Channel Type 3 Subunit alpha
- Voltage Gated Sodium Channel Type 3 Subunit alpha
- Voltage-Gated Sodium Channel Type 3 alpha Subunit
- Voltage Gated Sodium Channel Type 3 alpha Subunit
- SCN3A Sodium Channel alpha Subunit
- NAV1.3 alpha Subunit
- alpha Subunit, NAV1.3
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Below are MeSH descriptors whose meaning is more general than "NAV1.3 Voltage-Gated Sodium Channel".
Below are MeSH descriptors whose meaning is more specific than "NAV1.3 Voltage-Gated Sodium Channel".
This graph shows the total number of publications written about "NAV1.3 Voltage-Gated Sodium Channel" by people in this website by year, and whether "NAV1.3 Voltage-Gated Sodium Channel" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2010 | 0 | 1 | 1 |
| 2012 | 0 | 1 | 1 |
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Below are the most recent publications written about "NAV1.3 Voltage-Gated Sodium Channel" by people in Profiles.
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Translocations disrupting PHF21A in the Potocki-Shaffer-syndrome region are associated with intellectual disability and craniofacial anomalies. Am J Hum Genet. 2012 Jul 13; 91(1):56-72.
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Disruption of the SCN2A and SCN3A genes in a patient with mental retardation, neurobehavioral and psychiatric abnormalities, and a history of infantile seizures. Clin Genet. 2011 Aug; 80(2):191-5.