"Chromosome Segregation" 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 orderly segregation of CHROMOSOMES during MEIOSIS or MITOSIS.
| Descriptor ID |
D020090
|
| MeSH Number(s) |
G04.144.220.220.625 G05.113.220.625
|
| Concept/Terms |
Chromosome Segregation- Chromosome Segregation
- Chromosome Segregations
- Segregation, Chromosome
- Segregations, Chromosome
|
Below are MeSH descriptors whose meaning is more general than "Chromosome Segregation".
Below are MeSH descriptors whose meaning is more specific than "Chromosome Segregation".
This graph shows the total number of publications written about "Chromosome Segregation" by people in this website by year, and whether "Chromosome Segregation" 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 |
|---|
| 1998 | 0 | 1 | 1 |
| 1999 | 1 | 0 | 1 |
| 2000 | 1 | 1 | 2 |
| 2001 | 2 | 1 | 3 |
| 2004 | 0 | 1 | 1 |
| 2005 | 2 | 1 | 3 |
| 2009 | 4 | 2 | 6 |
| 2010 | 0 | 1 | 1 |
| 2011 | 2 | 1 | 3 |
| 2012 | 0 | 1 | 1 |
| 2013 | 0 | 2 | 2 |
| 2014 | 0 | 2 | 2 |
| 2015 | 0 | 1 | 1 |
| 2016 | 0 | 1 | 1 |
| 2017 | 1 | 3 | 4 |
| 2018 | 1 | 0 | 1 |
| 2024 | 0 | 1 | 1 |
| 2025 | 1 | 2 | 3 |
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Below are the most recent publications written about "Chromosome Segregation" by people in Profiles.
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Lysine demethylase 4A is a centrosome-associated protein required for centrosome integrity and genomic stability. FEBS J. 2026 01; 293(2):396-417.
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Inferring chromosome segregation error stage and crossover in trisomic disorders with application to Down syndrome. Nat Commun. 2025 Jul 09; 16(1):6316.
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RNA methyltransferase SPOUT1/CENP-32 links mitotic spindle organization with the neurodevelopmental disorder SpADMiSS. Nat Commun. 2025 Feb 17; 16(1):1703.
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Role of chromosomal cohesion and separation in aneuploidy and tumorigenesis. Cell Mol Life Sci. 2024 Feb 22; 81(1):100.
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Global genetic insight contributed by consanguineous Pakistani families segregating hearing loss. Hum Mutat. 2019 01; 40(1):53-72.
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WNT Signaling Perturbations Underlie the Genetic Heterogeneity of Robinow Syndrome. Am J Hum Genet. 2018 01 04; 102(1):27-43.
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Age-Dependent Alterations in Meiotic Recombination Cause Chromosome Segregation Errors in Spermatocytes. Cell. 2017 Oct 19; 171(3):601-614.e13.
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REST Final-Exon-Truncating Mutations Cause Hereditary Gingival Fibromatosis. Am J Hum Genet. 2017 Jul 06; 101(1):149-156.
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Multilocus Imaging of the E. coli Chromosome by Fluorescent In Situ Hybridization. Methods Mol Biol. 2017; 1624:213-226.
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Destabilized SMC5/6 complex leads to chromosome breakage syndrome with severe lung disease. J Clin Invest. 2016 08 01; 126(8):2881-92.