Chromosomes, Human, Pair 14
"Chromosomes, Human, Pair 14" 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 D CHROMOSOMES of the human chromosome classification.
Descriptor ID |
D002883
|
MeSH Number(s) |
A11.284.187.520.300.370.380 G05.360.162.520.300.370.380
|
Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Chromosomes, Human, Pair 14".
- 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, 13-15 [A11.284.187.520.300.370]
- Chromosomes, Human, Pair 14 [A11.284.187.520.300.370.380]
- 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, 13-15 [G05.360.162.520.300.370]
- Chromosomes, Human, Pair 14 [G05.360.162.520.300.370.380]
Below are MeSH descriptors whose meaning is more specific than "Chromosomes, Human, Pair 14".
This graph shows the total number of publications written about "Chromosomes, Human, Pair 14" by people in this website by year, and whether "Chromosomes, Human, Pair 14" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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1997 | 0 | 1 | 1 |
1998 | 0 | 1 | 1 |
2001 | 0 | 1 | 1 |
2004 | 1 | 1 | 2 |
2006 | 1 | 0 | 1 |
2007 | 1 | 0 | 1 |
2011 | 1 | 0 | 1 |
2012 | 1 | 2 | 3 |
2013 | 2 | 0 | 2 |
2014 | 1 | 0 | 1 |
2016 | 0 | 2 | 2 |
2017 | 1 | 0 | 1 |
2020 | 1 | 0 | 1 |
2021 | 0 | 1 | 1 |
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Below are the most recent publications written about "Chromosomes, Human, Pair 14" 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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Molecular characterization of temple syndrome families with 14q32 epimutations. Eur J Med Genet. 2020 Dec; 63(12):104077.
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New insights into the imprinted MEG8-DMR in 14q32 and clinical and molecular description of novel patients with Temple syndrome. Eur J Hum Genet. 2017 08; 25(8):935-945.
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Novel microdeletions on chromosome 14q32.2 suggest a potential role for non-coding RNAs in Kagami-Ogata syndrome. Eur J Hum Genet. 2016 12; 24(12):1724-1729.
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Examinations of maternal uniparental disomy and epimutations for chromosomes 6, 14, 16 and 20 in Silver-Russell syndrome-like phenotypes. BMC Med Genet. 2016 Mar 11; 17:20.
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Novel deletions affecting the MEG3-DMR provide further evidence for a hierarchical regulation of imprinting in 14q32. Eur J Hum Genet. 2015 Feb; 23(2):180-8.
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Platelet defects in congenital variant of Rett syndrome patients with FOXG1 mutations or reduced expression due to a position effect at 14q12. Eur J Hum Genet. 2013 Dec; 21(12):1349-55.
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The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma. Nat Genet. 2013 May; 45(5):522-525.
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Recurrent mutation of the ID3 gene in Burkitt lymphoma identified by integrated genome, exome and transcriptome sequencing. Nat Genet. 2012 Dec; 44(12):1316-20.
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A phenotype map for 14q32.3 terminal deletions. Am J Med Genet A. 2012 Apr; 158A(4):695-706.