 Aneuploidy
"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
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| MeSH Number(s) |
C23.550.210.050 G05.365.590.175.050 G05.700.131
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| Concept/Terms |
Aneuploidy- Aneuploidy
- Aneuploidies
- Aneuploid
- Aneuploids
Aneuploid Cell- Aneuploid Cell
- Aneuploid Cells
- Cell, Aneuploid
- Cells, Aneuploid
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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 UAMS Profiles by year, and whether "Aneuploidy" 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 |
|---|
| 2022 | 1 | 0 | 1 | | 2020 | 0 | 2 | 2 | | 2016 | 0 | 1 | 1 | | 2015 | 0 | 1 | 1 | | 2011 | 1 | 0 | 1 | | 2010 | 0 | 1 | 1 | | 2004 | 1 | 1 | 2 | | 2000 | 0 | 1 | 1 | | 1999 | 1 | 2 | 3 | | 1995 | 0 | 1 | 1 | | 1990 | 0 | 1 | 1 |
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Below are the most recent publications written about "Aneuploidy" by people in Profiles over the past ten years.
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Moutos CP, Ly P, Moutos DM, Clark SM. Pregnancy After 40: Recommendations for Counseling, Evaluation, and Management From Preconception to Delivery. Obstet Gynecol Surv. 2022 Feb; 77(2):111-121.
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Choudhury SR, Ashby C, Tytarenko R, Bauer M, Wang Y, Deshpande S, Den J, Schinke C, Zangari M, Thanendrarajan S, Davies FE, van Rhee F, Morgan GJ, Walker BA. The functional epigenetic landscape of aberrant gene expression in molecular subgroups of newly diagnosed multiple myeloma. J Hematol Oncol. 2020 08 06; 13(1):108.
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Maura F, Rustad EH, Boyle EM, Morgan GJ. Reconstructing the evolutionary history of multiple myeloma. Best Pract Res Clin Haematol. 2020 03; 33(1):101145.
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V?tsveen TK, B?rset M, Dikic A, Tian E, Micci F, Lid AH, Meza-Zepeda LA, Coward E, Waage A, Sundan A, Kuehl WM, Holien T. VOLIN and KJON-Two novel hyperdiploid myeloma cell lines. Genes Chromosomes Cancer. 2016 11; 55(11):890-901.
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Zarate YA, Bosanko KA, Bhoj E, Ganetzky R, Starr LJ, Zackai EH, Schaefer GB. Phenotypic modifications of patients with full chromosome aneuploidies and concurrent suspected or confirmed second diagnoses. Am J Med Genet A. 2015 Sep; 167A(9):2168-75.
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