ATP-Binding Cassette Transporters
"ATP-Binding Cassette Transporters" 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 family of MEMBRANE TRANSPORT PROTEINS that require ATP hydrolysis for the transport of substrates across membranes. The protein family derives its name from the ATP-binding domain found on the protein.
| Descriptor ID |
D018528
|
| MeSH Number(s) |
D12.776.157.530.100 D12.776.395.550.020 D12.776.543.550.192 D12.776.543.585.100
|
| Concept/Terms |
ATP-Binding Cassette Transporters- ATP-Binding Cassette Transporters
- ATP Binding Cassette Transporters
- Transporters, ATP-Binding Cassette
- ABC Transporters
- Transporters, ABC
|
Below are MeSH descriptors whose meaning is more general than "ATP-Binding Cassette Transporters".
Below are MeSH descriptors whose meaning is more specific than "ATP-Binding Cassette Transporters".
This graph shows the total number of publications written about "ATP-Binding Cassette Transporters" by people in this website by year, and whether "ATP-Binding Cassette Transporters" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2009 | 0 | 1 | 1 |
| 2015 | 1 | 0 | 1 |
| 2020 | 0 | 1 | 1 |
| 2021 | 1 | 0 | 1 |
| 2022 | 2 | 1 | 3 |
| 2023 | 0 | 2 | 2 |
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Below are the most recent publications written about "ATP-Binding Cassette Transporters" by people in Profiles.
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Natural History of Visual Dysfunction in ABCA4 Retinopathy and Its Genetic Correlates. Am J Ophthalmol. 2023 09; 253:224-232.
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Genotype-Phenotype Association in ABCA4-Associated Retinopathy. Adv Exp Med Biol. 2023; 1415:289-295.
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ABCA4 c.859-25A>G, a Frequent Palestinian Founder Mutation Affecting the Intron 7 Branchpoint, Is Associated With Early-Onset Stargardt Disease. Invest Ophthalmol Vis Sci. 2022 04 01; 63(4):20.
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Rare and common variants in ROM1 and PRPH2 genes trans-modify Stargardt/ABCA4 disease. PLoS Genet. 2022 03; 18(3):e1010129.
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Photoreceptor degeneration in ABCA4-associated retinopathy and its genetic correlates. JCI Insight. 2022 01 25; 7(2).
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The common ABCA3E292V variant disrupts AT2 cell quality control and increases susceptibility to lung injury and aberrant remodeling. Am J Physiol Lung Cell Mol Physiol. 2021 08 01; 321(2):L291-L307.
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Genetic testing for inherited eye conditions in over 6,000 individuals through the eyeGENE network. Am J Med Genet C Semin Med Genet. 2020 09; 184(3):828-837.
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Two novel loci, COBL and SLC10A2, for Alzheimer's disease in African Americans. Alzheimers Dement. 2017 02; 13(2):119-129.
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Role of ABCA7 loss-of-function variant in Alzheimer's disease: a replication study in European-Americans. Alzheimers Res Ther. 2015 Dec 10; 7(1):73.
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Global and local ancestry in African-Americans: Implications for Alzheimer's disease risk. Alzheimers Dement. 2016 Mar; 12(3):233-43.