KCNQ3 Potassium Channel
"KCNQ3 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 closely related to KCNQ2 POTASSIUM CHANNEL. It is commonly mutated in BENIGN FAMILIAL NEONATAL CONVULSIONS.
Descriptor ID |
D051659
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MeSH Number(s) |
D12.776.157.530.400.600.900.124.249.875 D12.776.543.550.425.750.900.124.249.875 D12.776.543.585.400.750.900.124.249.875
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Concept/Terms |
KCNQ3 Potassium Channel- KCNQ3 Potassium Channel
- Potassium Channel, KCNQ3
- Voltage-Gated K+ Channel KCNQ3
- Voltage Gated K+ Channel KCNQ3
- KCNQ3 Protein
- Kv7.3 Potassium Channel
- Potassium Channel, Kv7.3
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Below are MeSH descriptors whose meaning is more general than "KCNQ3 Potassium Channel".
Below are MeSH descriptors whose meaning is more specific than "KCNQ3 Potassium Channel".
This graph shows the total number of publications written about "KCNQ3 Potassium Channel" by people in UAMS Profiles by year, and whether "KCNQ3 Potassium Channel" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2022 | 1 | 0 | 1 | 2021 | 1 | 0 | 1 | 2014 | 0 | 1 | 1 |
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Below are the most recent publications written about "KCNQ3 Potassium Channel" by people in Profiles over the past ten years.
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Sheng ZF, Zhang H, Zheng P, Chen S, Gu Z, Zhou JJ, Phaup JG, Chang HM, Yeh ETH, Pan HL, Li DP. Impaired Kv7 channel activity in the central amygdala contributes to elevated sympathetic outflow in hypertension. Cardiovasc Res. 2022 01 29; 118(2):585-596.
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Chen X, Zhang Y, Ren X, Su Q, Liu Y, Dang X, Qin Y, Yang X, Xing Z, Shen Y, Wang Y, Bai Z, Yeh ETH, Wu H, Qi Y. The SUMO-specific protease SENP2 plays an essential role in the regulation of Kv7.2 and Kv7.3 potassium channels. J Biol Chem. 2021 10; 297(4):101183.
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Sands TT, Miceli F, Lesca G, Beck AE, Sadleir LG, Arrington DK, Sch?newolf-Greulich B, Moutton S, Lauritano A, Nappi P, Soldovieri MV, Scheffer IE, Mefford HC, Stong N, Heinzen EL, Goldstein DB, Perez AG, Kossoff EH, Stocco A, Sullivan JA, Shashi V, Gerard B, Francannet C, Bisgaard AM, T?mer Z, Willems M, Rivier F, Vitobello A, Thakkar K, Rajan DS, Barkovich AJ, Weckhuysen S, Cooper EC, Taglialatela M, Cilio MR. Autism and developmental disability caused by KCNQ3 gain-of-function variants. Ann Neurol. 2019 08; 86(2):181-192.
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