"Kv1.1 Potassium 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 delayed rectifier subtype of shaker potassium channels that is commonly mutated in human episodic ATAXIA and MYOKYMIA.
| Descriptor ID |
D051662
|
| MeSH Number(s) |
D12.776.157.530.400.600.900.500.124 D12.776.543.550.450.750.900.124.311 D12.776.543.550.450.750.900.500.124 D12.776.543.585.400.750.900.624.124
|
| Concept/Terms |
Kv1.1 Potassium Channel- Kv1.1 Potassium Channel
- Potassium Channel, Kv1.1
- KCNA1 Potassium Channel
- Potassium Channel, KCNA1
|
Below are MeSH descriptors whose meaning is more general than "Kv1.1 Potassium Channel".
Below are MeSH descriptors whose meaning is more specific than "Kv1.1 Potassium Channel".
This graph shows the total number of publications written about "Kv1.1 Potassium Channel" by people in this website by year, and whether "Kv1.1 Potassium Channel" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1995 | 0 | 1 | 1 |
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Below are the most recent publications written about "Kv1.1 Potassium Channel" by people in Profiles.
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Familial periodic cerebellar ataxia without myokymia maps to a 19-cM region on 19p13. Am J Hum Genet. 1995 Jun; 56(6):1443-9.
MeSH information
