"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 |
|---|
| 2006 | 1 | 0 | 1 |
| 2010 | 2 | 1 | 3 |
| 2012 | 1 | 0 | 1 |
| 2013 | 3 | 0 | 3 |
| 2015 | 1 | 0 | 1 |
| 2016 | 1 | 1 | 2 |
| 2019 | 0 | 1 | 1 |
| 2023 | 0 | 1 | 1 |
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Below are the most recent publications written about "ATP-Binding Cassette Transporters" by people in Profiles.
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Mutational Spectrum of the ABCA12 Gene and Genotype-Phenotype Correlation in a Cohort of 64 Patients with Autosomal Recessive Congenital Ichthyosis. Genes (Basel). 2023 03 15; 14(3).
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Membrane Cholesterol Efflux Drives Tumor-Associated Macrophage Reprogramming and Tumor Progression. Cell Metab. 2019 06 04; 29(6):1376-1389.e4.
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Intrahepatic cholestasis of pregnancy (ICP): case report and review of the literature. Z Gastroenterol. 2016 Dec; 54(12):1327-1333.
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Association between DNA Methylation in Whole Blood and Measures of Glucose Metabolism: KORA F4 Study. PLoS One. 2016; 11(3):e0152314.
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DNA methylation of lipid-related genes affects blood lipid levels. Circ Cardiovasc Genet. 2015 Apr; 8(2):334-42.
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No evidence for an involvement of copy number variation in ABCA13 in schizophrenia, bipolar disorder, or major depressive disorder. Psychiatr Genet. 2013 Feb; 23(1):45-6.
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Genetic and functional identification of the likely causative variant for cholesterol gallstone disease at the ABCG5/8 lithogenic locus. Hepatology. 2013 Jun; 57(6):2407-17.
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Wide clinical variability in conditions with coarse facial features and hypertrichosis caused by mutations in ABCC9. Am J Med Genet A. 2013 Feb; 161A(2):295-300.
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Mutations in ABCD4 cause a new inborn error of vitamin B12 metabolism. Nat Genet. 2012 Oct; 44(10):1152-5.
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Loci from a genome-wide analysis of bilirubin levels are associated with gallstone risk and composition. Gastroenterology. 2010 Dec; 139(6):1942-1951.e2.
MeSH information
