Chromosomes, Human, Pair 2
"Chromosomes, Human, Pair 2" 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 human chromosomes in group A (CHROMOSOMES, HUMAN, 1-3) of the human chromosome classification.
| Descriptor ID |
D002889
|
| MeSH Number(s) |
A11.284.187.520.300.235.245 G05.360.162.520.300.235.245
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Chromosomes, Human, Pair 2".
- 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, 1-3 [A11.284.187.520.300.235]
- Chromosomes, Human, Pair 2 [A11.284.187.520.300.235.245]
- 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, 1-3 [G05.360.162.520.300.235]
- Chromosomes, Human, Pair 2 [G05.360.162.520.300.235.245]
Below are MeSH descriptors whose meaning is more specific than "Chromosomes, Human, Pair 2".
This graph shows the total number of publications written about "Chromosomes, Human, Pair 2" by people in this website by year, and whether "Chromosomes, Human, Pair 2" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2008 | 0 | 1 | 1 |
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Below are the most recent publications written about "Chromosomes, Human, Pair 2" by people in Profiles.
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Linkage analysis of glomerular filtration rate in American Indians. Kidney Int. 2008 Nov; 74(9):1185-91.
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Interaction of gender and body mass index (BMI) reveals evidence of linkage for hypertension in the Framingham Heart Study. BMC Genet. 2003 Dec 31; 4 Suppl 1:S45.
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Genome-wide search for CLN2, the gene causing late-infantile neuronal ceroid-lipofuscinosis (LNCL). Am J Med Genet. 1995 Jun 05; 57(2):344-7.
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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.