 Chromosome Banding
"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 UAMS Profiles by year, and whether "Chromosome Banding" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2024 | 1 | 1 | 2 | | 2019 | 0 | 1 | 1 | | 2017 | 0 | 1 | 1 | | 2016 | 0 | 1 | 1 | | 2015 | 0 | 1 | 1 | | 2007 | 0 | 1 | 1 | | 2006 | 1 | 2 | 3 | | 2005 | 0 | 3 | 3 | | 2004 | 0 | 1 | 1 | | 2002 | 0 | 1 | 1 | | 1996 | 0 | 2 | 2 | | 1992 | 0 | 1 | 1 |
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Below are the most recent publications written about "Chromosome Banding" by people in Profiles over the past ten years.
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Binz RL, Pathak R. G-Banding and Molecular Cytogenetics Detect Novel Translocations and Cryptic Aberrations in Human Immortal Endothelial Cells. Int J Mol Sci. 2024 Jul 20; 25(14).
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Binz RL, Burns K, Pathak R. Protocol for preparation and staining of chromosomes isolated from mouse and human tissues for conventional and molecular cytogenetic analysis. STAR Protoc. 2024 Mar 15; 5(1):102897.
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Binz RL, Tian E, Sadhukhan R, Zhou D, Hauer-Jensen M, Pathak R. Identification of novel breakpoints for locus- and region-specific translocations in 293 cells by molecular cytogenetics before and after irradiation. Sci Rep. 2019 07 22; 9(1):10554.
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Sun M, Zhang H, Li G, Guy CJ, Wang X, Lu X, Gong F, Lee J, Hassed S, Li S. Molecular characterization of 20 small supernumerary marker chromosome cases using array comparative genomic hybridization and fluorescence in situ hybridization. Sci Rep. 2017 09 04; 7(1):10395.
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Sawyer JR, Tian E, Shaughnessy JD, Epstein J, Swanson CM, Stangeby C, Hale CL, Parr L, Lynn M, Sammartino G, Lukacs JL, Stein C, Bailey C, Zangari M, Davies FE, Van Rhee F, Barlogie B, Morgan GJ. Hyperhaploidy is a novel high-risk cytogenetic subgroup in multiple myeloma. Leukemia. 2017 03; 31(3):637-644.
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Caponetti GC, Dave BJ, Perry AM, Smith LM, Jain S, Meyer PN, Bast M, Bierman PJ, Bociek RG, Vose JM, Armitage JO, Aoun P, Fu K, Greiner TC, Chan WC, Sanger WG, Weisenburger DD. Isolated MYC cytogenetic abnormalities in diffuse large B-cell lymphoma do not predict an adverse clinical outcome. Leuk Lymphoma. 2015; 56(11):3082-9.
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