"KCNQ1 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 voltage-gated potassium channel that is expressed primarily in the HEART.
| Descriptor ID |
D051657
|
| MeSH Number(s) |
D12.776.157.530.400.600.900.124.249.500 D12.776.543.550.450.750.900.124.249.500 D12.776.543.585.400.750.900.124.249.500
|
| Concept/Terms |
KCNQ1 Potassium Channel- KCNQ1 Potassium Channel
- Potassium Channel, KCNQ1
- Voltage-Gated K+ Channel KCNQ1
- Voltage Gated K+ Channel KCNQ1
- Kv7.1 Potassium Channel
- Potassium Channel, Kv7.1
- KVLQT1 Protein
- KCNQ1 Protein
|
Below are MeSH descriptors whose meaning is more general than "KCNQ1 Potassium Channel".
Below are MeSH descriptors whose meaning is more specific than "KCNQ1 Potassium Channel".
This graph shows the total number of publications written about "KCNQ1 Potassium Channel" by people in this website by year, and whether "KCNQ1 Potassium Channel" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2006 | 0 | 1 | 1 |
| 2007 | 0 | 1 | 1 |
| 2009 | 2 | 2 | 4 |
| 2010 | 1 | 1 | 2 |
| 2011 | 0 | 1 | 1 |
| 2014 | 1 | 0 | 1 |
| 2016 | 0 | 1 | 1 |
| 2022 | 0 | 1 | 1 |
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Below are the most recent publications written about "KCNQ1 Potassium Channel" by people in Profiles.
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Long QT and Hearing Loss in High-Risk Infants Prospective Study Registry. Pediatr Cardiol. 2022 Dec; 43(8):1898-1902.
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Sudden unexpected death in epilepsy genetics: Molecular diagnostics and prevention. Epilepsia. 2016 Jan; 57 Suppl 1:17-25.
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Meta-analysis of genome-wide association studies in African Americans provides insights into the genetic architecture of type 2 diabetes. PLoS Genet. 2014 Aug; 10(8):e1004517.
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Genotype- and mutation site-specific QT adaptation during exercise, recovery, and postural changes in children with long-QT syndrome. Circ Arrhythm Electrophysiol. 2011 Dec; 4(6):867-73.
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Hypothyroidism of gene-targeted mice lacking Kcnq1. Pflugers Arch. 2011 Jan; 461(1):45-52.
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Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. Nat Genet. 2010 Jul; 42(7):579-89.
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Arrhythmia in heart and brain: KCNQ1 mutations link epilepsy and sudden unexplained death. Sci Transl Med. 2009 Oct 14; 1(2):2ra6.
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Enhanced insulin sensitivity of gene-targeted mice lacking functional KCNQ1. Am J Physiol Regul Integr Comp Physiol. 2009 Jun; 296(6):R1695-701.
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Common variants at ten loci modulate the QT interval duration in the QTSCD Study. Nat Genet. 2009 Apr; 41(4):407-14.
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APC sensitive gastric acid secretion. Cell Physiol Biochem. 2009; 23(1-3):133-42.