Chromosomes, Human, Pair 10
"Chromosomes, Human, Pair 10" 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.
A specific pair of GROUP C CHROMOSOMES of the human chromosome classification.
| Descriptor ID |
D002879
|
| MeSH Number(s) |
A11.284.187.520.300.325.350 G05.360.162.520.300.325.350
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Chromosomes, Human, Pair 10".
- Anatomy [A]
- Cells [A11]
- Cellular Structures [A11.284]
- Chromosomes [A11.284.187]
- Chromosomes, Mammalian [A11.284.187.520]
- Chromosomes, Human [A11.284.187.520.300]
- Chromosomes, Human, 6-12 and X [A11.284.187.520.300.325]
- Chromosomes, Human, Pair 10 [A11.284.187.520.300.325.350]
- Biological Sciences [G]
- Genetic Phenomena [G05]
- Genetic Structures [G05.360]
- Chromosomes [G05.360.162]
- Chromosomes, Mammalian [G05.360.162.520]
- Chromosomes, Human [G05.360.162.520.300]
- Chromosomes, Human, 6-12 and X [G05.360.162.520.300.325]
- Chromosomes, Human, Pair 10 [G05.360.162.520.300.325.350]
Below are MeSH descriptors whose meaning is more specific than "Chromosomes, Human, Pair 10".
This graph shows the total number of publications written about "Chromosomes, Human, Pair 10" by people in this website by year, and whether "Chromosomes, Human, Pair 10" was a major or minor topic of these publications.
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click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1996 | 1 | 0 | 1 |
| 2005 | 0 | 1 | 1 |
| 2008 | 0 | 1 | 1 |
| 2009 | 1 | 0 | 1 |
| 2010 | 0 | 1 | 1 |
| 2017 | 1 | 0 | 1 |
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Below are the most recent publications written about "Chromosomes, Human, Pair 10" by people in Profiles.
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Hasbrook M, Yonekawa Y, Van Laere L, Shah AR, Capone A. Bilateral persistent fetal vasculature and a chromosome 10 mutation including COX15. Can J Ophthalmol. 2017 12; 52(6):e203-e205.
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Elco CP, Mariño-Enríquez A, Abraham JA, Dal Cin P, Hornick JL. Hybrid myxoinflammatory fibroblastic sarcoma/hemosiderotic fibrolipomatous tumor: report of a case providing further evidence for a pathogenetic link. Am J Surg Pathol. 2010 Nov; 34(11):1723-7.
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Hadley D, Orlin A, Brown G, Brucker AJ, Ho AC, Regillo CD, Donoso LA, Tian L, Kaderli B, Stambolian D. Analysis of six genetic risk factors highly associated with AMD in the region surrounding ARMS2 and HTRA1 on chromosome 10, region q26. Invest Ophthalmol Vis Sci. 2010 Apr; 51(4):2191-6.
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Annable K, Donnenfeld AE, Fischer RL, Knops J. Prenatal diagnosis of a jumping translocation. Prenat Diagn. 2008 Aug; 28(8):767-9.
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Fogt F, Selim AM, Xu GX, Prinz MK, Eagle RC, Budimlija ZM. Uveal melanocytomas: genetic comparison with uveal and dermal melanomas. Arch Ophthalmol. 2005 Mar; 123(3):377-80.
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Bullrich F, Fernandes-Alnemri T, Litwack G, Alnemri ES, Croce CM. Chromosomal mapping of cell death proteases CPP32, MCH2, and MCH3. Genomics. 1996 Sep 1; 36(2):362-5.