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 |
|---|
| 1999 | 0 | 1 | 1 |
| 2000 | 1 | 0 | 1 |
| 2003 | 0 | 1 | 1 |
| 2004 | 0 | 1 | 1 |
| 2009 | 1 | 1 | 2 |
| 2010 | 2 | 0 | 2 |
| 2011 | 1 | 0 | 1 |
| 2013 | 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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A mutation in a ganglioside biosynthetic enzyme, ST3GAL5, results in salt & pepper syndrome, a neurocutaneous disorder with altered glycolipid and glycoprotein glycosylation. Hum Mol Genet. 2014 Jan 15; 23(2):418-33.
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The chromosome 2p21 region harbors a complex genetic architecture for association with risk for renal cell carcinoma. Hum Mol Genet. 2012 Mar 01; 21(5):1190-200.
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Genome-wide association study of renal cell carcinoma identifies two susceptibility loci on 2p21 and 11q13.3. Nat Genet. 2011 Jan; 43(1):60-5.
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A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci. Nat Genet. 2010 Nov; 42(11):978-84.
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Pro-opiomelanocortin gene variation related to alcohol or drug dependence: evidence and replications across family- and population-based studies. Biol Psychiatry. 2009 Jul 15; 66(2):128-36.
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Immunoglobulin kappa chain locus on chromosome 2p12 and onchocerciasis. J Infect Dis. 2009 Jan 15; 199(2):286; author reply 286-7.
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Systemic lupus erythematosus genome scan: support for linkage at 1q23, 2q33, 16q12-13, and 17q21-23 and novel evidence at 3p24, 10q23-24, 13q32, and 18q22-23. Arthritis Rheum. 2004 Oct; 50(10):3203-10.
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Evidence for bivariate linkage of obesity and HDL-C levels in the Framingham Heart Study. BMC Genet. 2003 Dec 31; 4 Suppl 1:S52.
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Paternal paracentric inversion of chromosome 2: a possible association with recurrent pregnancy loss and infertility. J Assist Reprod Genet. 2000 May; 17(5):293-6.
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Contribution of interleukin 1beta and KM loci to alopecia areata. Hum Hered. 1999 Mar; 49(2):85-9.