"Sodium Channels" 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.
Ion channels that specifically allow the passage of SODIUM ions. A variety of specific sodium channel subtypes are involved in serving specialized functions such as neuronal signaling, CARDIAC MUSCLE contraction, and KIDNEY function.
| Descriptor ID |
D015222
|
| MeSH Number(s) |
D12.776.157.530.400.875 D12.776.543.550.450.875 D12.776.543.585.400.875
|
| Concept/Terms |
Sodium Channels- Sodium Channels
- Channels, Sodium
- Sodium Ion Channels
- Channels, Sodium Ion
- Sodium Channel
- Channel, Sodium
- Ion Channel, Sodium
- Channel, Sodium Ion
- Sodium Ion Channel
- Ion Channels, Sodium
|
Below are MeSH descriptors whose meaning is more general than "Sodium Channels".
Below are MeSH descriptors whose meaning is more specific than "Sodium Channels".
This graph shows the total number of publications written about "Sodium Channels" by people in this website by year, and whether "Sodium Channels" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2007 | 1 | 0 | 1 |
| 2011 | 1 | 0 | 1 |
| 2012 | 0 | 1 | 1 |
| 2018 | 1 | 0 | 1 |
| 2019 | 1 | 0 | 1 |
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Below are the most recent publications written about "Sodium Channels" by people in Profiles.
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[Neuropathic pain syndromes and channelopathies]. Internist (Berl). 2019 Jan; 60(1):90-97.
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Genetic variants in components of the NALCN-UNC80-UNC79 ion channel complex cause a broad clinical phenotype (NALCN channelopathies). Hum Genet. 2018 Sep; 137(9):753-768.
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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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Severe case and literature review of primary erythromelalgia: novel SCN9A gene mutation. Vasc Med. 2012 Feb; 17(1):44-9.
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Brain MRI findings in severe myoclonic epilepsy in infancy and genotype-phenotype correlations. Epilepsia. 2007 Jun; 48(6):1092-6.
MeSH information
