Chromosomes, Human, Pair 22
"Chromosomes, Human, Pair 22" 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 |
D002892
|
| MeSH Number(s) |
A11.284.187.520.300.505.515 G05.360.162.520.300.505.515
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Chromosomes, Human, Pair 22".
- 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 22 [A11.284.187.520.300.505.515]
- 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 22 [G05.360.162.520.300.505.515]
Below are MeSH descriptors whose meaning is more specific than "Chromosomes, Human, Pair 22".
This graph shows the total number of publications written about "Chromosomes, Human, Pair 22" by people in this website by year, and whether "Chromosomes, Human, Pair 22" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2010 | 1 | 0 | 1 |
| 2011 | 0 | 1 | 1 |
| 2013 | 1 | 0 | 1 |
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Below are the most recent publications written about "Chromosomes, Human, Pair 22" by people in Profiles.
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Mutations in SCO2 are associated with autosomal-dominant high-grade myopia. Am J Hum Genet. 2013 May 02; 92(5):820-6.
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Extraosseous Ewing's sarcoma of the pancreas. Int J Clin Oncol. 2012 Aug; 17(4):399-406.
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Temporal lobe pleomorphic xanthoastrocytoma and acquired BRAF mutation in an adolescent with the constitutional 22q11.2 deletion syndrome. J Neurooncol. 2011 May; 102(3):509-14.
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Cytogenetic and molecular cytogenetic studies of a variant of t(21;22), ins(22;21)(q12;q21q22), with a deletion of the 3' EWSR1 gene in a patient with Ewing sarcoma. Cancer Genet Cytogenet. 2005 Jun; 159(2):177-80.
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Monosomy 22 as a diagnostic aid in a case of late recurrence of adult granulosa cell tumor of the ovary. Cancer Genet Cytogenet. 2005 Jan 01; 156(1):83-5.
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A new genomic duplication syndrome complementary to the velocardiofacial (22q11 deletion) syndrome. Clin Genet. 2004 May; 65(5):400-4.
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Sequence and analysis of the human ABL gene, the BCR gene, and regions involved in the Philadelphia chromosomal translocation. Genomics. 1995 May 01; 27(1):67-82.