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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click here.
Year | Major Topic | Minor Topic | Total |
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1995 | 1 | 1 | 2 |
1997 | 1 | 0 | 1 |
1998 | 0 | 1 | 1 |
2000 | 1 | 0 | 1 |
2003 | 3 | 0 | 3 |
2004 | 1 | 1 | 2 |
2010 | 1 | 2 | 3 |
2011 | 1 | 2 | 3 |
2012 | 3 | 1 | 4 |
2013 | 2 | 0 | 2 |
2014 | 1 | 2 | 3 |
2015 | 1 | 2 | 3 |
2016 | 1 | 1 | 2 |
2018 | 3 | 3 | 6 |
2019 | 1 | 1 | 2 |
2020 | 0 | 2 | 2 |
2021 | 0 | 1 | 1 |
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Below are the most recent publications written about "Chromosomes, Human, Pair 11" by people in Profiles.
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New euchromatic variant dup(11)(p15.3p15.1) transmitted through two generations defined by low coverage whole genome sequencing. Am J Med Genet A. 2021 10; 185(10):3053-3056.
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Heterogeneous phenotypes in families with duplications of the paternal allele within the imprinting center 1 (H19/IGF2:TSS-DMR) in 11p15.5. Clin Genet. 2020 10; 98(4):418-419.
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Paternal 132 bp deletion affecting KCNQ1OT1 in 11p15.5 is associated with growth retardation but does not affect imprinting. J Med Genet. 2021 03; 58(3):173-176.
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Molecular and Clinical Opposite Findings in 11p15.5 Associated Imprinting Disorders: Characterization of Basic Mechanisms to Improve Clinical Management. Int J Mol Sci. 2019 Aug 28; 20(17).
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Novel familial distal imprinting centre 1 (11p15.5) deletion provides further insights in imprinting regulation. Clin Epigenetics. 2019 02 15; 11(1):30.
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The mutational landscape of Burkitt-like lymphoma with 11q aberration is distinct from that of Burkitt lymphoma. Blood. 2019 02 28; 133(9):962-966.
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Genome-wide association analysis identifies a meningioma risk locus at 11p15.5. Neuro Oncol. 2018 10 09; 20(11):1485-1493.
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Search for cis-acting factors and maternal effect variants in Silver-Russell patients with ICR1 hypomethylation and their mothers. Eur J Hum Genet. 2019 01; 27(1):42-48.
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Search for altered imprinting marks in Mayer-Rokitansky-K?ster-Hauser patients. Mol Genet Genomic Med. 2018 11; 6(6):1225-1228.
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Maternal variants in NLRP and other maternal effect proteins are associated with multilocus imprinting disturbance in offspring. J Med Genet. 2018 07; 55(7):497-504.