"Anoctamin-1" 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.
An anoctamin chloride channel expressed at high levels in the liver, skeletal muscle, and gastrointestinal muscles that functions in transepithelial anion transport and smooth muscle contraction. It is essential for the function of the INTERSTITIAL CELLS OF CAJAL and plays a major role in chloride conduction by airway epithelial cells and in tracheal cartilage development.
| Descriptor ID |
D000075369
|
| MeSH Number(s) |
D12.776.157.530.400.175.032.500 D12.776.543.550.450.175.032.500 D12.776.543.585.400.175.032.500
|
| Concept/Terms |
Anoctamin-1- Anoctamin-1
- Anoctamin 1
- Transmembrane Protein 16A
- TMEM16A Protein
|
Below are MeSH descriptors whose meaning is more general than "Anoctamin-1".
Below are MeSH descriptors whose meaning is more specific than "Anoctamin-1".
This graph shows the total number of publications written about "Anoctamin-1" by people in this website by year, and whether "Anoctamin-1" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2017 | 0 | 2 | 2 |
| 2018 | 1 | 0 | 1 |
| 2019 | 1 | 0 | 1 |
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Below are the most recent publications written about "Anoctamin-1" by people in Profiles.
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Genome-wide copy number variation analysis identified ANO1 as a novel oncogene and prognostic biomarker in esophageal squamous cell cancer. Carcinogenesis. 2019 10 16; 40(10):1198-1208.
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Expression and function of Anoctamin 1/TMEM16A calcium-activated chloride channels in airways of in vivo mouse models for cystic fibrosis research. Pflugers Arch. 2018 09; 470(9):1335-1348.
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Bypassing CFTR dysfunction in cystic fibrosis with alternative pathways for anion transport. Curr Opin Pharmacol. 2017 06; 34:91-97.
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A Duodenal SDH-Deficient Gastrointestinal Stromal Tumor in a Patient With a Germline SDHB Mutation. J Clin Endocrinol Metab. 2017 05 01; 102(5):1447-1450.