"Chromosome Banding" 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.
Staining of bands, or chromosome segments, allowing the precise identification of individual chromosomes or parts of chromosomes. Applications include the determination of chromosome rearrangements in malformation syndromes and cancer, the chemistry of chromosome segments, chromosome changes during evolution, and, in conjunction with cell hybridization studies, chromosome mapping.
Descriptor ID |
D002871
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MeSH Number(s) |
E01.370.225.500.385.130 E01.370.225.500.620.670.130 E01.370.225.750.600.670.130 E05.200.500.385.130 E05.200.500.620.670.130 E05.200.750.600.670.130 E05.242.385.130 E05.393.285.130
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Concept/Terms |
Chromosome Banding- Chromosome Banding
- Banding, Chromosome
- Bandings, Chromosome
- Chromosome Bandings
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Below are MeSH descriptors whose meaning is more general than "Chromosome Banding".
Below are MeSH descriptors whose meaning is more specific than "Chromosome Banding".
This graph shows the total number of publications written about "Chromosome Banding" by people in this website by year, and whether "Chromosome Banding" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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1996 | 1 | 0 | 1 |
2000 | 0 | 1 | 1 |
2001 | 1 | 2 | 3 |
2003 | 0 | 1 | 1 |
2008 | 0 | 1 | 1 |
2017 | 0 | 1 | 1 |
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click here.
Below are the most recent publications written about "Chromosome Banding" by people in Profiles.
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Hurd LM, Thacker MM, Okenfuss E, Duker AL, Lou Y, Harty MP, Conard K, Lian JB, Bober MB. Aneurysmal bone cysts and pathologic fracture associated with supernumerary ring chromosome 6 in two unrelated patients. Am J Med Genet A. 2017 Dec; 173(12):3205-3210.
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Sessions SK, St?ck M, Vieites DR, Quarles R, Min MS, Wake DB. Cytogenetic analysis of the Asian plethodontid salamander, Karsenia koreana: evidence for karyotypic conservation, chromosome repatterning, and genome size evolution. Chromosome Res. 2008; 16(4):563-74.
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Shopland LS, Johnson CV, Byron M, McNeil J, Lawrence JB. Clustering of multiple specific genes and gene-rich R-bands around SC-35 domains: evidence for local euchromatic neighborhoods. J Cell Biol. 2003 Sep 15; 162(6):981-90.
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Lee C, Lemyre E, Miron PM, Morton CC. Multicolor fluorescence in situ hybridization in clinical cytogenetic diagnostics. Curr Opin Pediatr. 2001 Dec; 13(6):550-5.
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Chen YZ, Soeda E, Yang HW, Takita J, Chai L, Horii A, Inazawa J, Ohki M, Hayashi Y. Homozygous deletion in a neuroblastoma cell line defined by a high-density STS map spanning human chromosome band 1p36. Genes Chromosomes Cancer. 2001 Aug; 31(4):326-32.
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Lee C, Murray MF, Miron PM, Marsden D, Irons M, Wilkins-Haug LE, Morton CC. Clinical picture: Multicolour karyotyping. Lancet. 2001 Apr 21; 357(9264):1240.
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Bhat M, Morrison PJ, Getty A, McManus D, Tubman R, Nevin NC. First clinical case of small de novo duplication of 19q (13.3-13.4) confirmed by FISH. Am J Med Genet. 2000 Mar 20; 91(3):201-3.
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Braaten D, Wellington S, Warburton D, Luban J. Assignment of cyclophilin A (PPIA) to human chromosome band 7p13by in situ hybridization. Cytogenet Cell Genet. 1996; 74(4):262.
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Ionasescu V, Burns T, Ionasescu R, Searby C, Ginns E. Linkage between the loci for autosomal dominant Charcot-Marie-Tooth neuropathy type 1 and human glucocerebrosidase. Cytogenet Cell Genet. 1988; 47(3):173-4.
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Suomalainen HA, Goldsby RA, Osborne BA, Schr?der J. Mouse/human T-cell hybrids rosetting with sheep erythrocytes. Scand J Immunol. 1980; 11(2):163-8.