 Nondisjunction, Genetic
"Nondisjunction, Genetic" 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 failure of homologous CHROMOSOMES or CHROMATIDS to segregate during MITOSIS or MEIOSIS with the result that one daughter cell has both of a pair of parental chromosomes or chromatids and the other has none.
| Descriptor ID |
D009630
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| MeSH Number(s) |
C23.550.210.645 G05.355.105.220.625.620 G05.355.600.620
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| Concept/Terms |
Nondisjunction, Genetic- Nondisjunction, Genetic
- Genetic Nondisjunctions
- Nondisjunctions, Genetic
- Genetic Nondisjunction
- Genetic Non-Disjunction
- Genetic Non Disjunction
- Genetic Non-Disjunctions
- Non-Disjunctions, Genetic
- Non-Disjunction, Genetic
- Non Disjunction, Genetic
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Below are MeSH descriptors whose meaning is more general than "Nondisjunction, Genetic".
Below are MeSH descriptors whose meaning is more specific than "Nondisjunction, Genetic".
This graph shows the total number of publications written about "Nondisjunction, Genetic" by people in this website by year, and whether "Nondisjunction, Genetic" 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 |
|---|
| 1991 | 0 | 1 | 1 |
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Below are the most recent publications written about "Nondisjunction, Genetic" by people in Profiles.
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Sakaguchi A, Sarkies P, Simon M, Doebley AL, Goldstein LD, Hedges A, Ikegami K, Alvares SM, Yang L, LaRocque JR, Hall J, Miska EA, Ahmed S. Caenorhabditis elegans RSD-2 and RSD-6 promote germ cell immortality by maintaining small interfering RNA populations. Proc Natl Acad Sci U S A. 2014 Oct 14; 111(41):E4323-31.
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Hanna CW, Blair JD, Stephenson MD, Robinson WP. Absence of SYCP3 mutations in women with recurrent miscarriage with at least one trisomic miscarriage. Reprod Biomed Online. 2012 Feb; 24(2):251-3.
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Rudd MK, Mays RW, Schwartz S, Willard HF. Human artificial chromosomes with alpha satellite-based de novo centromeres show increased frequency of nondisjunction and anaphase lag. Mol Cell Biol. 2003 Nov; 23(21):7689-97.
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Lorber BJ, Grantham M, Peters J, Willard HF, Hassold TJ. Nondisjunction of chromosome 21: comparisons of cytogenetic and molecular studies of the meiotic stage and parent of origin. Am J Hum Genet. 1992 Dec; 51(6):1265-76.
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Coyne JA, Aulard S, Berry A. Lack of underdominance in a naturally occurring pericentric inversion in Drosophila melanogaster and its implications for chromosome evolution. Genetics. 1991 Nov; 129(3):791-802.
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Willard HF. Alpha and beta satellite sequences on chromosome 21: the possible role of centromere and chromosome structure in nondisjunction. Prog Clin Biol Res. 1990; 360:39-52.
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Spence JE, Perciaccante RG, Greig GM, Willard HF, Ledbetter DH, Hejtmancik JF, Pollack MS, O'Brien WE, Beaudet AL. Uniparental disomy as a mechanism for human genetic disease. Am J Hum Genet. 1988 Feb; 42(2):217-26.
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