"Chromosome Painting" 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 technique for visualizing CHROMOSOME ABERRATIONS using fluorescently labeled DNA probes which are hybridized to chromosomal DNA. Multiple fluorochromes may be attached to the probes. Upon hybridization, this produces a multicolored, or painted, effect with a unique color at each site of hybridization. This technique may also be used to identify cross-species homology by labeling probes from one species for hybridization with chromosomes from another species.
Descriptor ID |
D020223
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MeSH Number(s) |
E01.370.225.500.620.670.325.350.125 E01.370.225.750.600.670.325.350.125 E05.200.500.620.670.325.350.125 E05.200.750.600.670.325.350.125 E05.393.285.350.125 E05.393.661.475.350.125
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Concept/Terms |
Chromosome Painting- Chromosome Painting
- Chromosome Paintings
- Painting, Chromosome
- Paintings, Chromosome
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Below are MeSH descriptors whose meaning is more general than "Chromosome Painting".
Below are MeSH descriptors whose meaning is more specific than "Chromosome Painting".
This graph shows the total number of publications written about "Chromosome Painting" by people in this website by year, and whether "Chromosome Painting" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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1999 | 0 | 1 | 1 |
2000 | 0 | 1 | 1 |
2002 | 0 | 3 | 3 |
2003 | 0 | 2 | 2 |
2004 | 0 | 3 | 3 |
2007 | 0 | 1 | 1 |
2008 | 0 | 2 | 2 |
2011 | 0 | 1 | 1 |
2012 | 0 | 1 | 1 |
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Below are the most recent publications written about "Chromosome Painting" by people in Profiles.
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Walking along chromosomes with super-resolution imaging, contact maps, and integrative modeling. PLoS Genet. 2018 12; 14(12):e1007872.
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Centromere remodeling in Hoolock leuconedys (Hylobatidae) by a new transposable element unique to the gibbons. Genome Biol Evol. 2012; 4(7):648-58.
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Massive genomic rearrangement acquired in a single catastrophic event during cancer development. Cell. 2011 Jan 07; 144(1):27-40.
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Dynamic changes of territories 17 and 18 during EBV-infection of human lymphocytes. Mol Biol Rep. 2010 Jun; 37(5):2347-54.
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A chromatin-wide transition to H4K20 monomethylation impairs genome integrity and programmed DNA rearrangements in the mouse. Genes Dev. 2008 Aug 01; 22(15):2048-61.
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Genotype, phenotype, and karyotype correlation in the XO mouse model of Turner Syndrome. J Hered. 2008 Sep-Oct; 99(5):512-7.
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Molecular cytogenetic characterization of eight small supernumerary marker chromosomes originating from chromosomes 2, 4, 8, 18, and 21 in three patients. J Appl Genet. 2007; 48(2):167-75.
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Specific chromosome aberrations in peripheral blood lymphocytes are associated with risk of bladder cancer. Genes Chromosomes Cancer. 2004 Dec; 41(4):379-89.
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Major chromatin remodeling in the germinal vesicle (GV) of mammalian oocytes is dispensable for global transcriptional silencing but required for centromeric heterochromatin function. Dev Biol. 2004 Nov 15; 275(2):447-58.
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Frequent amplification and rearrangement of chromosomal bands 6p12-p21 and 17p11.2 in osteosarcoma. Genes Chromosomes Cancer. 2004 Jan; 39(1):11-21.