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.
To see the data from this visualization as text,
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1996 | 0 | 2 | 2 |
| 2001 | 0 | 1 | 1 |
| 2002 | 1 | 0 | 1 |
| 2003 | 1 | 0 | 1 |
| 2004 | 2 | 0 | 2 |
| 2005 | 0 | 1 | 1 |
| 2007 | 1 | 1 | 2 |
| 2008 | 2 | 2 | 4 |
| 2009 | 2 | 0 | 2 |
| 2010 | 1 | 0 | 1 |
| 2011 | 2 | 0 | 2 |
| 2012 | 0 | 1 | 1 |
| 2013 | 2 | 0 | 2 |
| 2015 | 0 | 1 | 1 |
| 2016 | 0 | 1 | 1 |
| 2018 | 1 | 0 | 1 |
| 2019 | 0 | 1 | 1 |
| 2023 | 1 | 0 | 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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Insights into the genomics of iAMP21-ALL. Blood. 2023 08 24; 142(8):682-684.
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The association between maternal occupation and down syndrome: A report from the national Down syndrome project. Int J Hyg Environ Health. 2020 01; 223(1):207-213.
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Analysis of Copy Number Variants on Chromosome 21 in Down Syndrome-Associated Congenital Heart Defects. G3 (Bethesda). 2018 01 04; 8(1):105-111.
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[Superior sagittal sinus thrombosis after intrathecal chemotherapy and intravenous high-dose cytarabine in an acute myeloid leukemia case with t(8;21)(q22;q22)]. Rinsho Ketsueki. 2016 Apr; 57(4):477-82.
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Genome-Wide Association Study of Down Syndrome-Associated Atrioventricular Septal Defects. G3 (Bethesda). 2015 Jul 20; 5(10):1961-71.
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Evidence for dysregulation of genome-wide recombination in oocytes with nondisjoined chromosomes 21. Hum Mol Genet. 2014 Jan 15; 23(2):408-17.
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Intrachromosomal amplification of chromosome 21 is associated with inferior outcomes in children with acute lymphoblastic leukemia treated in contemporary standard-risk children's oncology group studies: a report from the children's oncology group. J Clin Oncol. 2013 Sep 20; 31(27):3397-402.
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Variants in CXADR and F2RL1 are associated with blood pressure and obesity in African-Americans in regions identified through admixture mapping. J Hypertens. 2012 Oct; 30(10):1970-6.
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Myelodysplastic syndrome/acute myeloid leukemia with t(3;21)(q26.2;q22) is commonly a therapy-related disease associated with poor outcome. Am J Clin Pathol. 2012 Jul; 138(1):146-52.
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Altered patterns of multiple recombinant events are associated with nondisjunction of chromosome 21. Hum Genet. 2012 Jul; 131(7):1039-46.