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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| Year | Major Topic | Minor Topic | Total |
|---|
| 1997 | 0 | 1 | 1 |
| 2009 | 1 | 1 | 2 |
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Below are the most recent publications written about "Chromosomes, Human, Pair 10" by people in Profiles.
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Fine mapping and functional analysis of a common variant in MSMB on chromosome 10q11.2 associated with prostate cancer susceptibility. Proc Natl Acad Sci U S A. 2009 May 12; 106(19):7933-8.
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Linkage analysis of albuminuria. J Am Soc Nephrol. 2009 Jul; 20(7):1597-606.
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A polymorphism in intron 6 of the CYP17 gene. Clin Genet. 1997 Jul; 52(1):68-9.
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A clinically homogeneous group of families with facioscapulohumeral (Landouzy-Déjérine) muscular dystrophy: linkage analysis of six autosomes. Am J Hum Genet. 1990 Sep; 47(3):376-88.