Chromosomes, Human, Pair 11
"Chromosomes, Human, Pair 11" 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 C CHROMOSOMES of the human chromosome classification.
| Descriptor ID |
D002880
|
| MeSH Number(s) |
A11.284.187.520.300.325.355 G05.360.162.520.300.325.355
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Chromosomes, Human, Pair 11".
- 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, 6-12 and X [A11.284.187.520.300.325]
- Chromosomes, Human, Pair 11 [A11.284.187.520.300.325.355]
- 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, 6-12 and X [G05.360.162.520.300.325]
- Chromosomes, Human, Pair 11 [G05.360.162.520.300.325.355]
Below are MeSH descriptors whose meaning is more specific than "Chromosomes, Human, Pair 11".
This graph shows the total number of publications written about "Chromosomes, Human, Pair 11" by people in this website by year, and whether "Chromosomes, Human, Pair 11" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1997 | 1 | 0 | 1 |
| 1998 | 1 | 0 | 1 |
| 2002 | 5 | 2 | 7 |
| 2004 | 1 | 0 | 1 |
| 2006 | 1 | 1 | 2 |
| 2008 | 0 | 1 | 1 |
| 2009 | 1 | 0 | 1 |
| 2010 | 1 | 1 | 2 |
| 2011 | 1 | 0 | 1 |
| 2012 | 2 | 0 | 2 |
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Below are the most recent publications written about "Chromosomes, Human, Pair 11" by people in Profiles.
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Deep penetrating nevus-like borderline tumors: A unique subset of ambiguous melanocytic tumors with malignant potential and normal cytogenetics. Eur J Dermatol. 2014 Sep-Oct; 24(5):594-602.
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A novel translocation t(11;13) (q21;q14.2) in a child with suprasellar primitive neuroectodermal tumor and retinoblastoma. Ophthalmic Genet. 2013 Mar-Jun; 34(1-2):97-100.
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A replication study of GWAS-derived lipid genes in Asian Indians: the chromosomal region 11q23.3 harbors loci contributing to triglycerides. PLoS One. 2012; 7(5):e37056.
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Characterization of a novel t(2;5;11) in a patient with concurrent AML and CLL: a case report and literature review. Cancer Genet. 2011 Jun; 204(6):328-33.
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Identification of a systemic lupus erythematosus susceptibility locus at 11p13 between PDHX and CD44 in a multiethnic study. Am J Hum Genet. 2011 Jan 07; 88(1):83-91.
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Genome-wide association scan of Dupuytren's disease. J Hand Surg Am. 2010 Dec; 35(12):2039-45.
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Genetic influence on variation in serum uric acid in American Indians: the strong heart family study. Hum Genet. 2009 Nov; 126(5):667-76.
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Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci. Nat Genet. 2008 Feb; 40(2):204-10.
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Extracellular superoxide production by Enterococcus faecalis promotes chromosomal instability in mammalian cells. Gastroenterology. 2007 Feb; 132(2):551-61.
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A (9;11)(q34;q13) translocation in a hibernoma. Cancer Genet Cytogenet. 2006 Oct 15; 170(2):163-6.