"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 | 0 | 1 |
| 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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Generation of An Endogenous FGFR2-BICC1 Gene Fusion/58 Megabase Inversion Using Single-Plasmid CRISPR/Cas9 Editing in Biliary Cells. Int J Mol Sci. 2020 Apr 02; 21(7).
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Genotype-phenotype correlation of unusual BCR-ABL1 transcripts in Philadelphia chromosome-positive leukaemia. Br J Haematol. 2020 06; 189(5):e207-e211.
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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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Genomic heterogeneity of ALK fusion breakpoints in non-small-cell lung cancer. Mod Pathol. 2018 05; 31(5):791-808.
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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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An Organismal CNV Mutator Phenotype Restricted to Early Human Development. Cell. 2017 02 23; 168(5):830-842.e7.