"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.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2010 | 1 | 1 | 2 |
| 2011 | 1 | 1 | 2 |
| 2012 | 0 | 1 | 1 |
| 2013 | 0 | 5 | 5 |
| 2014 | 0 | 5 | 5 |
| 2015 | 0 | 4 | 4 |
| 2016 | 0 | 1 | 1 |
| 2017 | 0 | 1 | 1 |
| 2018 | 1 | 1 | 2 |
| 2019 | 0 | 3 | 3 |
| 2020 | 0 | 1 | 1 |
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Below are the most recent publications written about "Chromosome Breakpoints" by people in Profiles.
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Validating Gene Fusion as the Source of Chimeric RNAs. Methods Mol Biol. 2020; 2079:187-207.
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Distinct patterns of complex rearrangements and a mutational signature of microhomeology are frequently observed in PLP1 copy number gain structural variants. Genome Med. 2019 12 09; 11(1):80.
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Xq22 deletions and correlation with distinct neurological disease traits in females: Further evidence for a contiguous gene syndrome. Hum Mutat. 2020 01; 41(1):150-168.
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Megabase Length Hypermutation Accompanies Human Structural Variation at 17p11.2. Cell. 2019 03 07; 176(6):1310-1324.e10.
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Phenotypic association of 15q11.2 CNVs of the region of breakpoints 1-2 (BP1-BP2) in a large cohort of samples referred for genetic diagnosis. J Hum Genet. 2019 Mar; 64(3):253-255.
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Distinct Mechanisms of Nuclease-Directed DNA-Structure-Induced Genetic Instability in Cancer Genomes. Cell Rep. 2018 01 30; 22(5):1200-1210.
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An Organismal CNV Mutator Phenotype Restricted to Early Human Development. Cell. 2017 02 23; 168(5):830-842.e7.
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Copy-Number Variation Contributes to the Mutational Load of Bardet-Biedl Syndrome. Am J Hum Genet. 2016 08 04; 99(2):318-36.
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Novel MYBL1 Gene Rearrangements with Recurrent MYBL1-NFIB Fusions in Salivary Adenoid Cystic Carcinomas Lacking t(6;9) Translocations. Clin Cancer Res. 2016 Feb 01; 22(3):725-33.
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Complex genomic rearrangements at the PLP1 locus include triplication and quadruplication. PLoS Genet. 2015 Mar; 11(3):e1005050.