"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
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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
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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
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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 |
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2005 | 0 | 1 | 1 |
2006 | 0 | 1 | 1 |
2007 | 0 | 1 | 1 |
2009 | 2 | 2 | 4 |
2010 | 1 | 1 | 2 |
2014 | 1 | 0 | 1 |
2015 | 1 | 0 | 1 |
2016 | 0 | 2 | 2 |
2019 | 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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Determining the Likelihood of Variant Pathogenicity Using Amino Acid-level Signal-to-Noise Analysis of Genetic Variation. J Vis Exp. 2019 01 16; (143).
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TGF-?/?2-spectrin/CTCF-regulated tumor suppression in human stem cell disorder Beckwith-Wiedemann syndrome. J Clin Invest. 2016 Feb; 126(2):527-42.
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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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Arrhythmogenic cardiomyopathy in a patient with a rare loss-of-function KCNQ1 mutation. J Am Heart Assoc. 2015 Jan 23; 4(1):e001526.
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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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KCNQ1 autoantibodies: another way to regulate IKs. Cardiovasc Res. 2013 Jun 01; 98(3):329-31.
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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.