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 |
|---|
| 2009 | 1 | 0 | 1 |
| 2011 | 1 | 1 | 2 |
| 2017 | 0 | 4 | 4 |
| 2018 | 3 | 0 | 3 |
| 2019 | 0 | 1 | 1 |
To return to the timeline, click here.
Below are the most recent publications written about "Chromosomes, Human, Pair 6" by people in Profiles.
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Identity-by-Descent Analysis Reveals Susceptibility Loci for Severe Acne in Chinese Han Cohort. J Invest Dermatol. 2019 09; 139(9):2049-2051.e20.
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Genome-wide burden and association analyses implicate copy number variations in asthma risk among children and young adults from Latin America. Sci Rep. 2018 09 27; 8(1):14475.
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Large deletion in 6q associated to A20 haploinsufficiency and thoracoabdominal heterotaxy. Ann Rheum Dis. 2018 11; 77(11):1697-1698.
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TNFAIP3 haploinsufficiency is the cause of autoinflammatory manifestations in a patient with a deletion of 13Mb on chromosome 6. Clin Immunol. 2018 06; 191:44-51.
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Vascular endothelial growth factor A amplification in colorectal cancer is associated with reduced M1 and M2 macrophages and diminished PD-1-expressing lymphocytes. PLoS One. 2017; 12(4):e0175563.
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Activating Killer Immunoglobulin Receptors and HLA-C: a successful combination providing HIV-1 control. Sci Rep. 2017 02 13; 7:42470.
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6q12 and 11p14 variants are associated with postnatal exhaled nitric oxide levels and respiratory symptoms. J Allergy Clin Immunol. 2017 Oct; 140(4):1015-1023.
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Clinicopathological study of 5 cases of renal cell carcinoma with t(6;11)(p21;q12). Pol J Pathol. 2017; 68(1):66-72.
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Array-CGH and clinical characterization in a patient with subtelomeric 6p deletion without ocular dysgenesis. Am J Med Genet A. 2012 Jan; 158A(1):150-4.
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Psoriasis regression analysis of MHC loci identifies shared genetic variants with vitiligo. PLoS One. 2011; 6(11):e23089.