Chromosomes, Human, 6-12 and X
"Chromosomes, Human, 6-12 and X" 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 medium-sized, submetacentric human chromosomes, called group C in the human chromosome classification. This group consists of chromosome pairs 6, 7, 8, 9, 10, 11, and 12 and the X chromosome.
| Descriptor ID |
D002906
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| MeSH Number(s) |
A11.284.187.520.300.325 G05.360.162.520.300.325
|
| Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Chromosomes, Human, 6-12 and X".
Below are MeSH descriptors whose meaning is more specific than "Chromosomes, Human, 6-12 and X".
- Chromosomes, Human, 6-12 and X
- Chromosomes, Human, Pair 10
- Chromosomes, Human, Pair 11
- Chromosomes, Human, Pair 12
- Chromosomes, Human, Pair 6
- Chromosomes, Human, Pair 7
- Chromosomes, Human, Pair 8
- Chromosomes, Human, Pair 9
- Chromosomes, Human, X
This graph shows the total number of publications written about "Chromosomes, Human, 6-12 and X" by people in this website by year, and whether "Chromosomes, Human, 6-12 and X" was a major or minor topic of these publications.
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Below are the most recent publications written about "Chromosomes, Human, 6-12 and X" by people in Profiles.
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Molecular cloning of the breakpoint junction of a human chromosomal 8;14 translocation involving the T-cell receptor alpha-chain gene and sequences on the 3' side of MYC. Proc Natl Acad Sci U S A. 1986 Sep; 83(17):6636-40.
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Interferon-regulated human 2-5A synthetase gene maps to chromosome 12. Somat Cell Mol Genet. 1986 Jul; 12(4):403-8.
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The beta-subunit of follicle-stimulating hormone is deleted in patients with aniridia and Wilms' tumour, allowing a further definition of the WAGR locus. Nature. 1986 Jun 26-Jul 2; 321(6073):882-7.
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Prognostic implications of morphology and karyotype in primary myelodysplastic syndromes. Blood. 1986 Jun; 67(6):1765-72.
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Gene encoding the alpha chain of the T-cell receptor is moved immediately downstream of c-myc in a chromosomal 8;14 translocation in a cell line from a human T-cell leukemia. Proc Natl Acad Sci U S A. 1986 May; 83(10):3439-43.
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Clinical and cytogenetic correlations in 63 patients with therapy-related myelodysplastic syndromes and acute nonlymphocytic leukemia: further evidence for characteristic abnormalities of chromosomes no. 5 and 7. J Clin Oncol. 1986 Mar; 4(3):325-45.
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Interferon and c-ets-1 genes in the translocation (9;11)(p22;q23) in human acute monocytic leukemia. Science. 1986 Jan 17; 231(4735):265-7.
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Linkage of cystic fibrosis to the pro alpha 2(I) collagen gene, COL1A2, on chromosome 7. Cytogenet Cell Genet. 1986; 41(4):234-9.
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Chromosomal localization and characterization of c-abl in the t(6;9) of acute nonlymphocytic leukemia. Proc Natl Acad Sci U S A. 1985 Dec; 82(24):8742-6.
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The human met oncogene is related to the tyrosine kinase oncogenes. Nature. 1985 Nov 28-Dec 4; 318(6044):385-8.