Chromosomes, Human, Pair 17
"Chromosomes, Human, Pair 17" 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 E CHROMOSOMES of the human chromosome classification.
Descriptor ID |
D002886
|
MeSH Number(s) |
A11.284.187.520.300.415.425 G05.360.162.520.300.415.425
|
Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Chromosomes, Human, Pair 17".
- 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, 16-18 [A11.284.187.520.300.415]
- Chromosomes, Human, Pair 17 [A11.284.187.520.300.415.425]
- 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, 16-18 [G05.360.162.520.300.415]
- Chromosomes, Human, Pair 17 [G05.360.162.520.300.415.425]
Below are MeSH descriptors whose meaning is more specific than "Chromosomes, Human, Pair 17".
This graph shows the total number of publications written about "Chromosomes, Human, Pair 17" by people in this website by year, and whether "Chromosomes, Human, Pair 17" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2000 | 0 | 1 | 1 |
2001 | 1 | 0 | 1 |
2004 | 0 | 3 | 3 |
2006 | 1 | 0 | 1 |
2009 | 0 | 1 | 1 |
2014 | 1 | 0 | 1 |
2015 | 1 | 2 | 3 |
2017 | 0 | 1 | 1 |
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Below are the most recent publications written about "Chromosomes, Human, Pair 17" by people in Profiles.
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IgM Myeloma with Plasma Cell Leukemia: Case Report and Literature Review. Ann Clin Lab Sci. 2017 Sep; 47(5):611-619.
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Rare copy number variants implicated in posterior urethral valves. Am J Med Genet A. 2016 Mar; 170(3):622-33.
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Externally validated predictive clinical model for untreated del(17p13.1) chronic lymphocytic leukemia patients. Am J Hematol. 2015 Nov; 90(11):967-9.
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A novel Alzheimer disease locus located near the gene encoding tau protein. Mol Psychiatry. 2016 Jan; 21(1):108-17.
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Neurodevelopmental delays and macrocephaly in 17p13.1 microduplication syndrome. Am J Med Genet A. 2014 Nov; 164A(11):2887-91.
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Phase II study of flavopiridol in relapsed chronic lymphocytic leukemia demonstrating high response rates in genetically high-risk disease. J Clin Oncol. 2009 Dec 10; 27(35):6012-8.
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Genomewide linkage scan for opioid dependence and related traits. Am J Hum Genet. 2006 May; 78(5):759-769.
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Feasibility and utility of using chromosomal aneusomy to further define the cytologic categories in nipple aspirate fluid specimens: a preliminary study. Cancer. 2004 Oct 25; 102(5):322-7.
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Systemic lupus erythematosus genome scan: support for linkage at 1q23, 2q33, 16q12-13, and 17q21-23 and novel evidence at 3p24, 10q23-24, 13q32, and 18q22-23. Arthritis Rheum. 2004 Oct; 50(10):3203-10.
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Determination of secondary chromosomal aberrations of chronic myelocytic leukemia. Cancer Genet Cytogenet. 2004 Aug; 153(1):53-6.