"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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click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2009 | 1 | 0 | 1 |
| 2011 | 1 | 0 | 1 |
| 2016 | 1 | 0 | 1 |
| 2017 | 0 | 1 | 1 |
| 2018 | 4 | 0 | 4 |
| 2019 | 1 | 0 | 1 |
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Below are the most recent publications written about "KCNQ1 Potassium Channel" by people in Profiles.
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Generation of the human induced pluripotent stem cell (hiPSC) line PSMi007-A from a Long QT Syndrome type 1 patient carrier of two common variants in the NOS1AP gene. Stem Cell Res. 2019 04; 36:101416.
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Postmortem Analysis of 4 Mutation Hotspots of KCNQ1, KCNH2, and SCN5A Genes in Sudden Unexplained Death in Southwest of China. Am J Forensic Med Pathol. 2018 Sep; 39(3):218-222.
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Functionally Aberrant Mutant KCNQ1 With Intermediate Heterozygous and Homozygous Phenotypes. Can J Cardiol. 2018 09; 34(9):1174-1184.
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Generation of the human induced pluripotent stem cell (hiPSC) line PSMi002-A from a patient affected by the Jervell and Lange-Nielsen syndrome and carrier of two compound heterozygous mutations on the KCNQ1 gene. Stem Cell Res. 2018 05; 29:157-161.
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Application of Multigene Panel Sequencing in Patients with Prolonged Rate-corrected QT Interval and No Pathogenic Variants Detected in KCNQ1, KCNH2, and SCN5A. Ann Lab Med. 2018 Jan; 38(1):54-58.
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Loss of type 9 adenylyl cyclase triggers reduced phosphorylation of Hsp20 and diastolic dysfunction. Sci Rep. 2017 07 17; 7(1):5522.
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Gene-Targeted Analysis of Clinically Diagnosed Long QT Russian Families. Int Heart J. 2017 Feb 07; 58(1):81-87.
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Variants in KCNQ1 increase type II diabetes susceptibility in South Asians: a study of 3,310 subjects from India and the US. BMC Med Genet. 2011 Jan 24; 12:18.
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Expression of a common LQT1 mutation in five apparently unrelated families in a regional inherited arrhythmia clinic. J Cardiovasc Electrophysiol. 2010 Mar; 21(3):296-300.