"Chromosome Duplication" 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.
An aberration in which an extra chromosome or a chromosomal segment is made.
| Descriptor ID |
D058674
|
| MeSH Number(s) |
C23.550.210.182 G05.365.590.175.183 G05.558.164
|
| Concept/Terms |
Chromosome Duplication- Chromosome Duplication
- Chromosome Duplications
- Duplications, Chromosome
- Chromosomal Duplication
- Chromosomal Duplications
- Duplications, Chromosomal
- Duplication, Chromosomal
- Duplication, Chromosome
|
Below are MeSH descriptors whose meaning is more general than "Chromosome Duplication".
Below are MeSH descriptors whose meaning is more specific than "Chromosome Duplication".
This graph shows the total number of publications written about "Chromosome Duplication" by people in this website by year, and whether "Chromosome Duplication" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2012 | 0 | 1 | 1 |
| 2014 | 1 | 0 | 1 |
| 2015 | 1 | 0 | 1 |
| 2016 | 1 | 1 | 2 |
| 2017 | 1 | 0 | 1 |
| 2019 | 1 | 0 | 1 |
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Below are the most recent publications written about "Chromosome Duplication" by people in Profiles.
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Duplication 2p16 is associated with perisylvian polymicrogyria. Am J Med Genet A. 2019 12; 179(12):2343-2356.
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Gain of chromosome 1q portends worse prognosis in multiple myeloma despite novel agent-based induction regimens and autologous transplantation. Leuk Lymphoma. 2017 08; 58(8):1823-1831.
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Reversal of dendritic phenotypes in 16p11.2 microduplication mouse model neurons by pharmacological targeting of a network hub. Proc Natl Acad Sci U S A. 2016 07 26; 113(30):8520-5.
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Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders. PLoS Genet. 2016 05; 12(5):e1005993.
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Model mice for 15q11-13 duplication syndrome exhibit late-onset obesity and altered lipid metabolism. Hum Mol Genet. 2015 Aug 15; 24(16):4559-72.
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Increased risk of genetic and epigenetic instability in human embryonic stem cells associated with specific culture conditions. PLoS One. 2015; 10(2):e0118307.
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Classic bladder exstrophy: Frequent 22q11.21 duplications and definition of a 414 kb phenocritical region. Birth Defects Res A Clin Mol Teratol. 2014 Jun; 100(6):512-7.
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Evidence that duplications of 22q11.2 protect against schizophrenia. Mol Psychiatry. 2014 Jan; 19(1):37-40.
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Hypoglycaemia following diabetes remission in patients with 6q24 methylation defects: expanding the clinical phenotype. Diabetologia. 2013 Jan; 56(1):218-21.
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Sequencing papaya X and Yh chromosomes reveals molecular basis of incipient sex chromosome evolution. Proc Natl Acad Sci U S A. 2012 Aug 21; 109(34):13710-5.