"Chromothripsis" 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.
Massive number of chromosomal rearrangements and shattering that occurs in cancer cells. The breakpoints are located within one chromosome or chromosome arm.
Descriptor ID |
D000072837
|
MeSH Number(s) |
C23.550.210.310 G05.365.590.175.310
|
Concept/Terms |
Chromothripsis- Chromothripsis
- Chromothripses
- Chromosome Shattering
- Chromosome Shatterings
- Shattering, Chromosome
|
Below are MeSH descriptors whose meaning is more general than "Chromothripsis".
Below are MeSH descriptors whose meaning is more specific than "Chromothripsis".
This graph shows the total number of publications written about "Chromothripsis" by people in this website by year, and whether "Chromothripsis" 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 |
---|
2017 | 0 | 2 | 2 |
2019 | 0 | 1 | 1 |
2020 | 0 | 1 | 1 |
To return to the timeline,
click here.
Below are the most recent publications written about "Chromothripsis" by people in Profiles.
-
Somatic structural variant formation is guided by and influences genome architecture. Genome Res. 2022 04; 32(4):643-655.
-
A user guide for the online exploration and visualization of PCAWG data. Nat Commun. 2020 07 07; 11(1):3400.
-
An enhanced genetic model of colorectal cancer progression history. Genome Biol. 2019 08 15; 20(1):168.
-
Chromosomal Instability in Tumor Initiation and Development. Cancer Res. 2019 08 15; 79(16):3995-4002.
-
Recurrent Genomic Alterations in Soft Tissue Perineuriomas. Am J Surg Pathol. 2018 12; 42(12):1708-1714.
-
Identification of Small and Non-Small Cell Lung Cancer Markers in Peripheral Blood Using Cytokinesis-Blocked Micronucleus and Spectral Karyotyping Assays. Cytogenet Genome Res. 2017; 152(3):122-131.
-
Genome-wide copy number aberrations and HER2 and FGFR1 alterations in primary breast cancer by molecular inversion probe microarray. Oncotarget. 2017 02 14; 8(7):10845-10857.