Literature DB >> 2078516

Use of fluorescent in situ hybridization to detect chromosomal rearrangements in somatic cell hybrids.

A J Giaccia1, J W Evans, J M Brown.   

Abstract

In situ hybridization of hamster/human hybrids with biotinylated human genomic DNA has revealed that human chromosomal DNA can integrate into the hamster genome and is not always cytologically detectable. This finding helps to explain why discordancy can arise in gene mapping by failing to recognize small pieces of foreign DNA in the rodent genome. Fluorescent in situ hybridization allows one to locate these fragments in rodent chromosomes visually and possibly to identify their chromosome of origin.

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Year:  1990        PMID: 2078516     DOI: 10.1002/gcc.2870020314

Source DB:  PubMed          Journal:  Genes Chromosomes Cancer        ISSN: 1045-2257            Impact factor:   5.006


  3 in total

1.  Chromosome in situ suppression hybridisation in human male meiosis.

Authors:  A S Goldman; M A Hultén
Journal:  J Med Genet       Date:  1992-02       Impact factor: 6.318

2.  The human Ha-ras oncogene induces genomic instability in murine fibroblasts within one cell cycle.

Authors:  N C Denko; A J Giaccia; J R Stringer; P J Stambrook
Journal:  Proc Natl Acad Sci U S A       Date:  1994-05-24       Impact factor: 11.205

3.  Ewing's tumor X mouse hybrids expressing the MIC2 antigen: analyses using fluorescence CDD-banding and non-isotopic ISH.

Authors:  M Dworzak; C Stock; S Strehl; H Gadner; P F Ambros
Journal:  Hum Genet       Date:  1992-01       Impact factor: 4.132

  3 in total

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