Chromosomes, Human, 16-18
"Chromosomes, Human, 16-18" 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.
The short, submetacentric human chromosomes, called group E in the human chromosome classification. This group consists of chromosome pairs 16, 17, and 18.
Descriptor ID |
D002902
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MeSH Number(s) |
A11.284.187.520.300.415 G05.360.162.520.300.415
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Concept/Terms |
Chromosomes, Human, 16-18- Chromosomes, Human, 16-18
- Group E Chromosomes
- Chromosome, Group E
- Chromosomes, Group E
- E Chromosomes, Group
- Group E Chromosome
- Chromosomes E
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Below are MeSH descriptors whose meaning is more general than "Chromosomes, Human, 16-18".
Below are MeSH descriptors whose meaning is more specific than "Chromosomes, Human, 16-18".
This graph shows the total number of publications written about "Chromosomes, Human, 16-18" by people in this website by year, and whether "Chromosomes, Human, 16-18" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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1994 | 0 | 1 | 1 | 2007 | 0 | 1 | 1 |
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Below are the most recent publications written about "Chromosomes, Human, 16-18" by people in Profiles.
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Kim JH, Dhanasekaran SM, Mehra R, Tomlins SA, Gu W, Yu J, Kumar-Sinha C, Cao X, Dash A, Wang L, Ghosh D, Shedden K, Montie JE, Rubin MA, Pienta KJ, Shah RB, Chinnaiyan AM. Integrative analysis of genomic aberrations associated with prostate cancer progression. Cancer Res. 2007 Sep 01; 67(17):8229-39.
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Chiu BC, Dave BJ, Blair A, Gapstur SM, Chmiel JS, Fought AJ, Zahm SH, Weisenburger DD. Cigarette smoking, familial hematopoietic cancer, hair dye use, and risk of t(14;18)-defined subtypes of non-Hodgkin's lymphoma. Am J Epidemiol. 2007 Mar 15; 165(6):652-9.
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Morse HG, Moore GE, Ortiz LM, Gonzalez R, Robinson WA. Malignant melanoma: from subcutaneous nodule to brain metastasis. Cancer Genet Cytogenet. 1994 Jan; 72(1):16-23.
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Smith AC, McGavran L, Robinson J, Waldstein G, Macfarlane J, Zonona J, Reiss J, Lahr M, Allen L, Magenis E. Interstitial deletion of (17)(p11.2p11.2) in nine patients. Am J Med Genet. 1986 Jul; 24(3):393-414.
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Disteche CM, Swisshelm K, Forbes S, Pagon RA. X-inactivation patterns in lymphocytes and skin fibroblasts of three cases of X-autosome translocations with abnormal phenotypes. Hum Genet. 1984; 66(1):71-6.
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Leinwand LA, Fournier RE, Nadal-Ginard B, Shows TB. Multigene family for sarcomeric myosin heavy chain in mouse and human DNA: localization on a single chromosome. Science. 1983 Aug 19; 221(4612):766-9.
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