Chromosomes, Human, Pair 12
"Chromosomes, Human, Pair 12" 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 |
D002881
|
MeSH Number(s) |
A11.284.187.520.300.325.360 G05.360.162.520.300.325.360
|
Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Chromosomes, Human, Pair 12".
- 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 12 [A11.284.187.520.300.325.360]
- 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 12 [G05.360.162.520.300.325.360]
Below are MeSH descriptors whose meaning is more specific than "Chromosomes, Human, Pair 12".
This graph shows the total number of publications written about "Chromosomes, Human, Pair 12" by people in this website by year, and whether "Chromosomes, Human, Pair 12" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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1997 | 2 | 0 | 2 |
2006 | 1 | 0 | 1 |
2008 | 0 | 1 | 1 |
2010 | 1 | 0 | 1 |
2012 | 1 | 0 | 1 |
2013 | 0 | 1 | 1 |
2014 | 0 | 1 | 1 |
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Below are the most recent publications written about "Chromosomes, Human, Pair 12" by people in Profiles.
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Genomic inverse PCR for exploration of ligated breakpoints (GIPFEL), a new method to detect translocations in leukemia. PLoS One. 2014; 9(8):e104419.
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Androgenetic alopecia: identification of four genetic risk loci and evidence for the contribution of WNT signaling to its etiology. J Invest Dermatol. 2013 Jun; 133(6):1489-96.
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Genome-wide association analysis reveals 12q13.3-q14.1 as new risk locus for sarcoidosis. Eur Respir J. 2013 Apr; 41(4):888-900.
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A genome-wide linkage analysis in 181 German sarcoidosis families using clustered biallelic markers. Chest. 2010 Jul; 138(1):151-7.
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Graft versus leukemia effect after haploidentical HSCT in a MLL-negative infant AML with HLXB9/ETV6 rearrangement. Pediatr Blood Cancer. 2008 Apr; 50(4):921-3.
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Loss-of-function mutations in the keratin 5 gene lead to Dowling-Degos disease. Am J Hum Genet. 2006 Mar; 78(3):510-9.
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Incidence of TEL/AML1 fusion gene analyzed consecutively in children with acute lymphoblastic leukemia in relapse. Blood. 1997 Dec 15; 90(12):4933-7.
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Incidence and clinical relevance of TEL/AML1 fusion genes in children with acute lymphoblastic leukemia enrolled in the German and Italian multicenter therapy trials. Associazione Italiana Ematologia Oncologia Pediatrica and the Berlin-Frankfurt-M?nster Study Group. Blood. 1997 Jul 15; 90(2):571-7.