"Chromosome Breakpoints" 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 locations in specific DNA sequences where CHROMOSOME BREAKS have occurred.
| Descriptor ID |
D056905
|
| MeSH Number(s) |
G05.200.210.170.500
|
| Concept/Terms |
Chromosome Breakpoints- Chromosome Breakpoints
- Breakpoint, Chromosome
- Chromosome Breakpoint
- Breakpoints, Chromosome
Chromosome Breakpoint Sequence- Chromosome Breakpoint Sequence
- Breakpoint Sequence, Chromosome
- Breakpoint Sequences, Chromosome
- Chromosome Breakpoint Sequences
- Sequence, Chromosome Breakpoint
- Sequences, Chromosome Breakpoint
|
Below are MeSH descriptors whose meaning is more general than "Chromosome Breakpoints".
Below are MeSH descriptors whose meaning is more specific than "Chromosome Breakpoints".
This graph shows the total number of publications written about "Chromosome Breakpoints" by people in this website by year, and whether "Chromosome Breakpoints" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2010 | 0 | 2 | 2 |
| 2014 | 0 | 1 | 1 |
| 2016 | 0 | 1 | 1 |
| 2017 | 0 | 1 | 1 |
| 2018 | 1 | 0 | 1 |
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Below are the most recent publications written about "Chromosome Breakpoints" by people in Profiles.
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Mapping of breakpoints in balanced chromosomal translocations by shallow whole-genome sequencing points to EFNA5, BAHD1 and PPP2R5E as novel candidates for genes causing human Mendelian disorders. J Med Genet. 2019 02; 56(2):104-112.
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Molecular characterization of HDAC8 deletions in individuals with atypical Cornelia de Lange syndrome. J Hum Genet. 2018 Mar; 63(3):349-356.
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Diagnostic evaluation of RNA sequencing for the detection of genetic abnormalities associated with Ph-like acute lymphoblastic leukemia (ALL). Leuk Lymphoma. 2017 04; 58(4):950-958.
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The somatic genomic landscape of chromophobe renal cell carcinoma. Cancer Cell. 2014 Sep 08; 26(3):319-330.
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Both CpG methylation and activation-induced deaminase are required for the fragility of the human bcl-2 major breakpoint region: implications for the timing of the breaks in the t(14;18) translocation. Mol Cell Biol. 2013 Mar; 33(5):947-57.
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Detection of clinically relevant exonic copy-number changes by array CGH. Hum Mutat. 2010 Dec; 31(12):1326-42.
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Searching for large genomic rearrangements of the BRCA1 gene in a Nigerian population. Breast Cancer Res Treat. 2010 Nov; 124(2):573-7.