"Chloride Channels" 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.
Cell membrane glycoproteins that form channels to selectively pass chloride ions. Nonselective blockers include FENAMATES; ETHACRYNIC ACID; and TAMOXIFEN.
| Descriptor ID |
D018118
|
| MeSH Number(s) |
D12.776.157.530.400.175 D12.776.543.550.450.175 D12.776.543.585.400.175
|
| Concept/Terms |
Chloride Channels- Chloride Channels
- Channels, Chloride
- Chlorine Channels
- Channels, Chlorine
- Ion Channel, Chloride
- Channel, Chloride Ion
- Chloride Ion Channel
- Ion Channels, Chloride
- Chloride Channel
- Channel, Chloride
- Chloride Ion Channels
- Channels, Chloride Ion
Calcium-Activated Chloride Channels- Calcium-Activated Chloride Channels
- Calcium Activated Chloride Channels
- Channels, Calcium-Activated Chloride
- Chloride Channels, Calcium-Activated
- CaCCs
|
Below are MeSH descriptors whose meaning is more general than "Chloride Channels".
Below are MeSH descriptors whose meaning is more specific than "Chloride Channels".
This graph shows the total number of publications written about "Chloride Channels" by people in this website by year, and whether "Chloride Channels" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1996 | 0 | 1 | 1 |
| 1998 | 0 | 1 | 1 |
| 2000 | 1 | 0 | 1 |
| 2002 | 1 | 0 | 1 |
| 2003 | 0 | 1 | 1 |
| 2005 | 2 | 0 | 2 |
| 2006 | 2 | 0 | 2 |
| 2007 | 1 | 0 | 1 |
| 2008 | 0 | 1 | 1 |
| 2010 | 1 | 1 | 2 |
| 2011 | 1 | 0 | 1 |
| 2012 | 1 | 0 | 1 |
| 2013 | 0 | 1 | 1 |
| 2014 | 0 | 1 | 1 |
| 2015 | 1 | 1 | 2 |
| 2020 | 0 | 1 | 1 |
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Below are the most recent publications written about "Chloride Channels" by people in Profiles.
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Pathobiologic Mechanisms of Neurodegeneration in Osteopetrosis Derived From Structural and Functional Analysis of 14 ClC-7 Mutants. J Bone Miner Res. 2021 03; 36(3):531-545.
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PKCa regulates TMEM16A-mediated Cl? secretion in human biliary cells. Am J Physiol Gastrointest Liver Physiol. 2016 Jan 01; 310(1):G34-42.
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Efficacy and safety of ivacaftor in patients with cystic fibrosis who have an Arg117His-CFTR mutation: a double-blind, randomised controlled trial. Lancet Respir Med. 2015 Jul; 3(7):524-33.
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Expanding the phenotype of proteinuria in Dent disease. A case series. Pediatr Nephrol. 2014 Oct; 29(10):2051-4.
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A rational free energy-based approach to understanding and targeting disease-causing missense mutations. J Am Med Inform Assoc. 2013 Jul-Aug; 20(4):643-51.
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An X-linked channelopathy with cardiomegaly due to a CLIC2 mutation enhancing ryanodine receptor channel activity. Hum Mol Genet. 2012 Oct 15; 21(20):4497-507.
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A missense mutation in CLIC2 associated with intellectual disability is predicted by in silico modeling to affect protein stability and dynamics. Proteins. 2011 Aug; 79(8):2444-54.
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Identification and functional characterization of TMEM16A, a Ca2+-activated Cl- channel activated by extracellular nucleotides, in biliary epithelium. J Biol Chem. 2011 Jan 07; 286(1):766-76.
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Novel CLCN1 mutation in carbamazepine-responsive myotonia congenita. Pediatr Neurol. 2010 May; 42(5):365-8.
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Interleukin-17A induces bicarbonate secretion in normal human bronchial epithelial cells. Am J Physiol Lung Cell Mol Physiol. 2009 Feb; 296(2):L257-66.