Chromosomes, Human, Pair 6
"Chromosomes, Human, Pair 6" 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 GROUP C CHROMSOMES of the human chromosome classification.
Descriptor ID |
D002896
|
MeSH Number(s) |
A11.284.187.520.300.325.330 G05.360.162.520.300.325.330
|
Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Chromosomes, Human, Pair 6".
- 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 6 [A11.284.187.520.300.325.330]
- 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 6 [G05.360.162.520.300.325.330]
Below are MeSH descriptors whose meaning is more specific than "Chromosomes, Human, Pair 6".
This graph shows the total number of publications written about "Chromosomes, Human, Pair 6" by people in this website by year, and whether "Chromosomes, Human, Pair 6" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2008 | 0 | 1 | 1 |
2018 | 0 | 1 | 1 |
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Below are the most recent publications written about "Chromosomes, Human, Pair 6" by people in Profiles.
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Genetic variation in the SIM1 locus is associated with erectile dysfunction. Proc Natl Acad Sci U S A. 2018 10 23; 115(43):11018-11023.
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GWAS of cerebrospinal fluid tau levels identifies risk variants for Alzheimer's disease. Neuron. 2013 Apr 24; 78(2):256-68.
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SNP combinations in chromosome-wide genes are associated with bone mineral density in Taiwanese women. Chin J Physiol. 2008 Feb 29; 51(1):32-41.
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A complete genomic screen for multiple sclerosis underscores a role for the major histocompatability complex. The Multiple Sclerosis Genetics Group. Nat Genet. 1996 Aug; 13(4):469-71.