Chromosomes, Human, Pair 21
"Chromosomes, Human, Pair 21" 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 GROUP G CHROMOSOMES of the human chromosome classification.
Descriptor ID |
D002891
|
MeSH Number(s) |
A11.284.187.520.300.505.510 G05.360.162.520.300.505.510
|
Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Chromosomes, Human, Pair 21".
- 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, 21-22 and Y [A11.284.187.520.300.505]
- Chromosomes, Human, Pair 21 [A11.284.187.520.300.505.510]
- 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, 21-22 and Y [G05.360.162.520.300.505]
- Chromosomes, Human, Pair 21 [G05.360.162.520.300.505.510]
Below are MeSH descriptors whose meaning is more specific than "Chromosomes, Human, Pair 21".
This graph shows the total number of publications written about "Chromosomes, Human, Pair 21" by people in this website by year, and whether "Chromosomes, Human, Pair 21" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2004 | 0 | 2 | 2 |
2007 | 1 | 0 | 1 |
2010 | 1 | 0 | 1 |
2012 | 1 | 1 | 2 |
2013 | 0 | 1 | 1 |
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Below are the most recent publications written about "Chromosomes, Human, Pair 21" by people in Profiles.
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Down syndrome: genes, model systems, and progress towards pharmacotherapies and clinical trials for cognitive deficits. Cytogenet Genome Res. 2013; 141(4):260-71.
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Immunoglobulin genes and immunity to herpes simplex virus type 1. J Infect Dis. 2012 Jul 01; 206(1):143-4.
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Anthropometric charts for infants with trisomies 21, 18, or 13 born between 22 weeks gestation and term: the VON charts. Am J Med Genet A. 2012 Feb; 158A(2):322-32.
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Identification of candidate loci at 6p21 and 21q22 in a genome-wide association study of cardiac manifestations of neonatal lupus. Arthritis Rheum. 2010 Nov; 62(11):3415-24.
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Autism spectrum disorder, Klinefelter syndrome, and chromosome 3p21.31 duplication: a case report. MedGenMed. 2007 Dec 18; 9(4):60.
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Krtap16, characterization of a new hair keratin-associated protein (KAP) gene complex on mouse chromosome 16 and evidence for regulation by Hoxc13. J Biol Chem. 2004 Dec 03; 279(49):51524-33.
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t(8;21)(q22;q22) in blast phase of chronic myelogenous leukemia. Am J Clin Pathol. 2004 Jun; 121(6):836-42.
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Isolation, characterization, and regional mapping of microclones from a human chromosome 21 microdissection library. Am J Hum Genet. 1992 Aug; 51(2):263-72.
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ETS family of genes in leukemia and Down syndrome. Am J Med Genet Suppl. 1990; 7:251-61.