Fanconi Anemia Complementation Group Proteins
"Fanconi Anemia Complementation Group Proteins" 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 diverse group of proteins whose genetic MUTATIONS have been associated with the chromosomal instability syndrome FANCONI ANEMIA. Many of these proteins play important roles in protecting CELLS against OXIDATIVE STRESS.
| Descriptor ID |
D051856
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| MeSH Number(s) |
D12.776.313
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| Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Fanconi Anemia Complementation Group Proteins".
Below are MeSH descriptors whose meaning is more specific than "Fanconi Anemia Complementation Group Proteins".
This graph shows the total number of publications written about "Fanconi Anemia Complementation Group Proteins" by people in this website by year, and whether "Fanconi Anemia Complementation Group Proteins" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2000 | 0 | 1 | 1 |
| 2010 | 1 | 0 | 1 |
| 2014 | 1 | 0 | 1 |
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Below are the most recent publications written about "Fanconi Anemia Complementation Group Proteins" by people in Profiles.
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Characterization of docosahexaenoic acid (DHA)-induced heme oxygenase-1 (HO-1) expression in human cancer cells: the importance of enhanced BTB and CNC homology 1 (Bach1) degradation. J Nutr Biochem. 2014 May; 25(5):515-25.
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Bivariate genetic association of KIAA1797 with heart rate in American Indians: the Strong Heart Family Study. Hum Mol Genet. 2010 Sep 15; 19(18):3662-71.
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Interferon-gamma-induced apoptotic responses of Fanconi anemia group C hematopoietic progenitor cells involve caspase 8-dependent activation of caspase 3 family members. Blood. 2000 Dec 15; 96(13):4204-11.