Chromosomes, Human, Pair 5
"Chromosomes, Human, Pair 5" 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.
One of the two pairs of human chromosomes in the group B class (CHROMOSOMES, HUMAN, 4-5).
Descriptor ID |
D002895
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MeSH Number(s) |
A11.284.187.520.300.280.290 G05.360.162.520.300.280.290
|
Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Chromosomes, Human, Pair 5".
- 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, 4-5 [A11.284.187.520.300.280]
- Chromosomes, Human, Pair 5 [A11.284.187.520.300.280.290]
- 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, 4-5 [G05.360.162.520.300.280]
- Chromosomes, Human, Pair 5 [G05.360.162.520.300.280.290]
Below are MeSH descriptors whose meaning is more specific than "Chromosomes, Human, Pair 5".
This graph shows the total number of publications written about "Chromosomes, Human, Pair 5" by people in this website by year, and whether "Chromosomes, Human, Pair 5" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2000 | 1 | 0 | 1 |
2001 | 1 | 0 | 1 |
2009 | 1 | 0 | 1 |
2013 | 0 | 1 | 1 |
2014 | 1 | 0 | 1 |
2016 | 0 | 1 | 1 |
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Below are the most recent publications written about "Chromosomes, Human, Pair 5" by people in Profiles.
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Immunochip analysis identifies association of the RAD50/IL13 region with human longevity. Aging Cell. 2016 06; 15(3):585-8.
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Fine-scale mapping of the 5q11.2 breast cancer locus reveals at least three independent risk variants regulating MAP3K1. Am J Hum Genet. 2015 Jan 08; 96(1):5-20.
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Androgenetic alopecia: identification of four genetic risk loci and evidence for the contribution of WNT signaling to its etiology. J Invest Dermatol. 2013 Jun; 133(6):1489-96.
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A novel microdeletion syndrome involving 5q14.3-q15: clinical and molecular cytogenetic characterization of three patients. Eur J Hum Genet. 2009 Dec; 17(12):1592-9.
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Absence of point mutations within the AML-1 gene in patients with MDS/AML and loss of chromosome 5q or 7. Ann Hematol. 2001 Feb; 80(2):72-3.
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The human GRAF gene is fused to MLL in a unique t(5;11)(q31;q23) and both alleles are disrupted in three cases of myelodysplastic syndrome/acute myeloid leukemia with a deletion 5q. Proc Natl Acad Sci U S A. 2000 Aug 01; 97(16):9168-73.