 KCNQ2 Potassium Channel
"KCNQ2 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 very slow opening and closing voltage-gated potassium channel that is expressed in NEURONS and is commonly mutated in BENIGN FAMILIAL NEONATAL CONVULSIONS.
| Descriptor ID |
D051658
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| MeSH Number(s) |
D12.776.157.530.400.600.900.124.249.750 D12.776.543.550.450.750.900.124.249.750 D12.776.543.585.400.750.900.124.249.750
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| Concept/Terms |
KCNQ2 Potassium Channel- KCNQ2 Potassium Channel
- Potassium Channel, KCNQ2
- Kv7.2 Potassium Channel
- Potassium Channel, Kv7.2
- Voltage-Gated K+ Channel KCNQ2
- Voltage Gated K+ Channel KCNQ2
- KCNQ2 Protein
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Below are MeSH descriptors whose meaning is more general than "KCNQ2 Potassium Channel".
Below are MeSH descriptors whose meaning is more specific than "KCNQ2 Potassium Channel".
This graph shows the total number of publications written about "KCNQ2 Potassium Channel" by people in this website by year, and whether "KCNQ2 Potassium Channel" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2003 | 0 | 1 | 1 | | 2010 | 0 | 1 | 1 | | 2020 | 1 | 0 | 1 |
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Below are the most recent publications written about "KCNQ2 Potassium Channel" by people in Profiles.
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Berg AT, Gaebler-Spira D, Wilkening G, Zelko F, Knupp K, Dixon-Salazar T, Villas N, Meskis MA, Harwell V, Thompson T, Sims S, Nesbitt G. Nonseizure consequences of Dravet syndrome, KCNQ2-DEE, KCNB1-DEE, Lennox-Gastaut syndrome, ESES: A functional framework. Epilepsy Behav. 2020 10; 111:107287.
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Prince JT, Ahn NG. The case of the disappearing drug target. Mol Cell. 2010 Feb 26; 37(4):455-6.
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Ford CP, Stemkowski PL, Light PE, Smith PA. Experiments to test the role of phosphatidylinositol 4,5-bisphosphate in neurotransmitter-induced M-channel closure in bullfrog sympathetic neurons. J Neurosci. 2003 Jun 15; 23(12):4931-41.
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Cooper EC, Aldape KD, Abosch A, Barbaro NM, Berger MS, Peacock WS, Jan YN, Jan LY. Colocalization and coassembly of two human brain M-type potassium channel subunits that are mutated in epilepsy. Proc Natl Acad Sci U S A. 2000 Apr 25; 97(9):4914-9.
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