Chromosomes, Human, Pair 19
"Chromosomes, Human, Pair 19" 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 F CHROMOSOMES of the human chromosome classification.
Descriptor ID |
D002888
|
MeSH Number(s) |
A11.284.187.520.300.460.465 G05.360.162.520.300.460.465
|
Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Chromosomes, Human, Pair 19".
- 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, 19-20 [A11.284.187.520.300.460]
- Chromosomes, Human, Pair 19 [A11.284.187.520.300.460.465]
- 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, 19-20 [G05.360.162.520.300.460]
- Chromosomes, Human, Pair 19 [G05.360.162.520.300.460.465]
Below are MeSH descriptors whose meaning is more specific than "Chromosomes, Human, Pair 19".
This graph shows the total number of publications written about "Chromosomes, Human, Pair 19" by people in this website by year, and whether "Chromosomes, Human, Pair 19" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2002 | 1 | 1 | 2 |
2008 | 0 | 1 | 1 |
2012 | 0 | 1 | 1 |
2014 | 1 | 0 | 1 |
2017 | 1 | 0 | 1 |
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Below are the most recent publications written about "Chromosomes, Human, Pair 19" by people in Profiles.
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Comment on Long-term effects of bariatric surgery on patients with obesity and chromosome 19.11-2 microdeletion. Surg Obes Relat Dis. 2017 08; 13(8):1325-1326.
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Smoking dysregulates the human airway basal cell transcriptome at COPD risk locus 19q13.2. PLoS One. 2014; 9(2):e88051.
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Pyrosequencing of IDH1 and IDH2 mutations in brain tumors and non-neoplastic conditions. Diagn Mol Pathol. 2012 Dec; 21(4):214-20.
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Analysis of positional candidate genes in the AAA1 susceptibility locus for abdominal aortic aneurysms on chromosome 19. BMC Med Genet. 2011 Jan 19; 12:14.
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Genome-wide linkage analysis of pulse pressure in American Indians: the Strong Heart Study. Am J Hypertens. 2008 Feb; 21(2):194-9.
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Genome scan stratified by the presence of anti-double-stranded DNA (dsDNA) autoantibody in pedigrees multiplex for systemic lupus erythematosus (SLE) establishes linkages at 19p13.2 (SLED1) and 18q21.1 (SLED2). Genes Immun. 2002 Oct; 3 Suppl 1:S35-41.
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Apolipoprotein E polymorphism and cardiovascular disease: a HuGE review. Am J Epidemiol. 2002 Mar 15; 155(6):487-95.