"Aneuploidy" 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 chromosomal constitution of cells which deviate from the normal by the addition or subtraction of CHROMOSOMES, chromosome pairs, or chromosome fragments. In a normally diploid cell (DIPLOIDY) the loss of a chromosome pair is termed nullisomy (symbol: 2N-2), the loss of a single chromosome is MONOSOMY (symbol: 2N-1), the addition of a chromosome pair is tetrasomy (symbol: 2N+2), the addition of a single chromosome is TRISOMY (symbol: 2N+1).
| Descriptor ID |
D000782
|
| MeSH Number(s) |
C23.550.210.050 G05.365.590.175.050 G05.700.131
|
| Concept/Terms |
Aneuploidy- Aneuploidy
- Aneuploidies
- Aneuploid
- Aneuploids
Aneuploid Cell- Aneuploid Cell
- Aneuploid Cells
- Cell, Aneuploid
- Cells, Aneuploid
|
Below are MeSH descriptors whose meaning is more general than "Aneuploidy".
Below are MeSH descriptors whose meaning is more specific than "Aneuploidy".
This graph shows the total number of publications written about "Aneuploidy" by people in this website by year, and whether "Aneuploidy" was a major or minor topic of these publications.
To see the data from this visualization as text,
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2007 | 0 | 1 | 1 |
| 2008 | 0 | 1 | 1 |
| 2009 | 0 | 1 | 1 |
| 2013 | 1 | 0 | 1 |
| 2014 | 0 | 1 | 1 |
| 2018 | 0 | 1 | 1 |
| 2022 | 1 | 1 | 2 |
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Below are the most recent publications written about "Aneuploidy" by people in Profiles.
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Hyperdiploidy: the longest known, most prevalent, and most enigmatic form of acute lymphoblastic leukemia in children. Leukemia. 2022 12; 36(12):2769-2783.
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Somatic PMK-1/p38 signaling links environmental stress to germ cell apoptosis and heritable euploidy. Nat Commun. 2022 02 04; 13(1):701.
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Global impacts of chromosomal imbalance on gene expression in Arabidopsis and other taxa. Proc Natl Acad Sci U S A. 2018 11 27; 115(48):E11321-E11330.
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Impact of genomic damage and ageing on stem cell function. Nat Cell Biol. 2014 Mar; 16(3):201-7.
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Exome sequencing identifies recurrent somatic mutations in EIF1AX and SF3B1 in uveal melanoma with disomy 3. Nat Genet. 2013 Aug; 45(8):933-6.
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Outcome of intracytoplasmic sperm injection with and without polar body diagnosis of oocytes. Fertil Steril. 2010 Feb; 93(2):405-15.
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Effects of aneuploidy on genome structure, expression, and interphase organization in Arabidopsis thaliana. PLoS Genet. 2008 Oct; 4(10):e1000226.
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Increased radiosensitivity as an indicator of genes conferring breast cancer susceptibility. Strahlenther Onkol. 2007 Dec; 183(12):655-60.
MeSH information
