Spectral Karyotyping

"Spectral Karyotyping" 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.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

The simultaneous identification of all chromosomes from a cell by fluorescence in situ hybridization (IN SITU HYBRIDIZATION, FLUORESCENCE) with chromosome-specific florescent probes that are discerned by their different emission spectra.

Descriptor ID

D032681

MeSH Number(s)

E01.370.225.500.385.315.800

E05.200.500.385.315.800

E05.242.385.315.800

E05.393.285.350.125.800

E05.393.285.475.800

E05.393.661.475.350.125.800

Concept/Terms

Spectral Karyotyping

Below are MeSH descriptors whose meaning is more general than "Spectral Karyotyping".

Analytical, Diagnostic and Therapeutic Techniques and Equipment [E]
Investigative Techniques [E05]
Genetic Techniques [E05.393]
Cytogenetic Analysis [E05.393.285]
In Situ Hybridization, Fluorescence [E05.393.285.350]
Chromosome Painting [E05.393.285.350.125]
Spectral Karyotyping [E05.393.285.350.125.800]
Karyotyping [E05.393.285.475]
Spectral Karyotyping [E05.393.285.475.800]
Nucleic Acid Hybridization [E05.393.661]
In Situ Hybridization [E05.393.661.475]
In Situ Hybridization, Fluorescence [E05.393.661.475.350]
Chromosome Painting [E05.393.661.475.350.125]
Spectral Karyotyping [E05.393.661.475.350.125.800]

Below are MeSH descriptors whose meaning is related to "Spectral Karyotyping".

Below are MeSH descriptors whose meaning is more specific than "Spectral Karyotyping".

publications

Timeline | Most Recent

This graph shows the total number of publications written about "Spectral Karyotyping" by people in Harvard Catalyst Profiles by year, and whether "Spectral Karyotyping" was a major or minor topic of these publication.

Bar chart showing 8 publications over 6 distinct years, with a maximum of 2 publications in 2004 and 2010

To see the data from this visualization as text, click here.

Year	Minor Topic	Total
2003	1	1
2004	2	2
2005	1	1
2006	1	1
2010	2	2
2019	1	1

Below are the most recent publications written about "Spectral Karyotyping" by people in Profiles.

Detection of a novel CBFB-MYH11 fusion transcript in acute myeloid leukemia M1 with inv(16)(p13q22). Cancer Genet. 2020 02; 241:72-76.

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Cytogenetic analysis of a low-grade secondary peripheral chondrosarcoma arising in synovial chondromatosis. In Vivo. 2013 Jan-Feb; 27(1):57-60.

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The TLX1 oncogene drives aneuploidy in T cell transformation. Nat Med. 2010 Nov; 16(11):1321-7.

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PARK2 deletions occur frequently in sporadic colorectal cancer and accelerate adenoma development in Apc mutant mice. Proc Natl Acad Sci U S A. 2010 Aug 24; 107(34):15145-50.

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Genetic instability and mammary tumor formation in mice carrying mammary-specific disruption of Chk1 and p53. Oncogene. 2010 Jul 15; 29(28):4007-17.

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Increased genomic instability and altered chromosomal protein phosphorylation timing in HRAS-transformed mouse fibroblasts. Genes Chromosomes Cancer. 2009 May; 48(5):397-409.

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Architectures of somatic genomic rearrangement in human cancer amplicons at sequence-level resolution. Genome Res. 2007 Sep; 17(9):1296-303.

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Characterization of trisomy 8 in pediatric undifferentiated sarcomas using advanced molecular cytogenetic techniques. Cancer Genet Cytogenet. 2007 Apr 01; 174(1):35-41.

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Overexpression of PRDM16 in the presence and absence of the RUNX1/PRDM16 fusion gene in myeloid leukemias. Genes Chromosomes Cancer. 2006 Nov; 45(11):1072-6.

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A deletion at the mouse Xist gene exposes trans-effects that alter the heterochromatin of the inactive X chromosome and the replication time and DNA stability of both X chromosomes. Genetics. 2006 Nov; 174(3):1115-33.

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