"DNA End-Joining Repair" 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.
The repair of DOUBLE-STRAND DNA BREAKS by rejoining the broken ends of DNA to each other directly.
| Descriptor ID |
D059766
|
| MeSH Number(s) |
G02.111.222.200 G05.219.200
|
| Concept/Terms |
DNA End-Joining Repair- DNA End-Joining Repair
- DNA End Joining Repair
- End-Joining Repair, DNA
- Repair, DNA End-Joining
- End-Joining DNA Repair
- DNA Repair, End-Joining
- End Joining DNA Repair
- Repair, End-Joining DNA
Non-Homologous DNA End-Joining- Non-Homologous DNA End-Joining
- DNA End-Joining, Non-Homologous
- End-Joining, Non-Homologous DNA
- Non Homologous DNA End Joining
- Nonhomologous DNA End-Joining
- DNA End-Joining, Nonhomologous
- Nonhomologous DNA End Joining
- NHEJ DNA Repair
- DNA Repair, NHEJ
- Repair, NHEJ DNA
|
Below are MeSH descriptors whose meaning is more general than "DNA End-Joining Repair".
Below are MeSH descriptors whose meaning is more specific than "DNA End-Joining Repair".
This graph shows the total number of publications written about "DNA End-Joining Repair" by people in this website by year, and whether "DNA End-Joining Repair" 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 |
|---|
| 2015 | 0 | 1 | 1 |
| 2016 | 1 | 0 | 1 |
| 2017 | 0 | 1 | 1 |
| 2018 | 1 | 0 | 1 |
To return to the timeline, click here.
Below are the most recent publications written about "DNA End-Joining Repair" by people in Profiles.
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Dna2 nuclease deficiency results in large and complex DNA insertions at chromosomal breaks. Nature. 2018 12; 564(7735):287-290.
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PGBD5 promotes site-specific oncogenic mutations in human tumors. Nat Genet. 2017 Jul; 49(7):1005-1014.
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PREVENTING THE CHROMOSOMAL TRANSLOCATIONS THAT CAUSE CANCER. Trans Am Clin Climatol Assoc. 2016; 127:176-195.
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PRKDC mutations associated with immunodeficiency, granuloma, and autoimmune regulator-dependent autoimmunity. J Allergy Clin Immunol. 2015 Jun; 135(6):1578-88.e5.