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
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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.
To see the data from this visualization as text,
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Year | Major Topic | Minor Topic | Total |
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1998 | 1 | 0 | 1 |
2000 | 1 | 0 | 1 |
2003 | 1 | 1 | 2 |
2005 | 0 | 1 | 1 |
2007 | 1 | 0 | 1 |
2008 | 0 | 2 | 2 |
2010 | 1 | 1 | 2 |
2011 | 1 | 0 | 1 |
2013 | 2 | 1 | 3 |
2014 | 0 | 1 | 1 |
2015 | 1 | 0 | 1 |
2016 | 1 | 1 | 2 |
2017 | 1 | 0 | 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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Alpha gene upregulates TFEB expression in renal cell carcinoma with t(6;11) translocation, which promotes cell canceration. Int J Oncol. 2018 Mar; 52(3):933-944.
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The maternal uniparental disomy of chromosome 6?(upd(6)mat) "phenotype": result of placental trisomy?6?mosaicism? Mol Genet Genomic Med. 2017 11; 5(6):668-677.
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Examinations of maternal uniparental disomy and epimutations for chromosomes 6, 14, 16 and 20 in Silver-Russell syndrome-like phenotypes. BMC Med Genet. 2016 Mar 11; 17:20.
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Genome-wide association study identifies variation at 6q25.1 associated with survival in multiple myeloma. Nat Commun. 2016 Jan 08; 7:10290.
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Novel evidence of association with nonsyndromic cleft lip with or without cleft palate was shown for single nucleotide polymorphisms in FOXF2 gene in an Asian population. Birth Defects Res A Clin Mol Teratol. 2015 Oct; 103(10):857-62.
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Heritability estimates on Hodgkin's lymphoma: a genomic- versus population-based approach. Eur J Hum Genet. 2015 Jun; 23(6):824-30.
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Sporadic and reversible chromothripsis in chronic lymphocytic leukemia revealed by longitudinal genomic analysis. Leukemia. 2013 Dec; 27(12):2376-9.
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Risk loci for coronary artery calcification replicated at 9p21 and 6q24 in the Heinz Nixdorf Recall Study. BMC Med Genet. 2013 Feb 08; 14:23.
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Variation at 3p24.1 and 6q23.3 influences the risk of Hodgkin's lymphoma. Nat Commun. 2013; 4:2549.
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A genome-wide association study reveals evidence of association with sarcoidosis at 6p12.1. Eur Respir J. 2011 Nov; 38(5):1127-35.