Literature DB >> 14984099

Reverse painting highlights the origin of chromosome aberrations.

Elisabeth Blennow1.   

Abstract

Reverse chromosome painting, as the opposite of forward chromosome painting, means that an abnormal chromosome of interest is recovered by flow sorting or by chromosome microdissection, amplified and labelled by DOP-PCR and hybridized onto normal metaphases of optimal quality. This provides rapid and unequivocal information about the chromosomal origin on the aberrant chromosome in one hybridization. Not only will the specific chromosome(s) involved be identified, but also the subchromosomal origin, including the breakpoints. The method has been used for over 10 years and has proven to be very useful for resolving complex chromosome rearrangements in a variety of different applications, both as a research tool and for clinical purposes in pre- and postnatal diagnosis.

Mesh:

Year:  2004        PMID: 14984099     DOI: 10.1023/b:chro.0000009277.42798.9a

Source DB:  PubMed          Journal:  Chromosome Res        ISSN: 0967-3849            Impact factor:   5.239


  40 in total

1.  Highly comprehensive karyotype analysis by a combination of spectral karyotyping (SKY), microdissection, and reverse painting (SKY-MD).

Authors:  J Weimer; M R Koehler; U Wiedemann; P Attermeyer; A Jacobsen; D Karow; M Kiechl; W Jonat; N Arnold
Journal:  Chromosome Res       Date:  2001       Impact factor: 5.239

2.  Reverse chromosome painting: a method for the rapid analysis of aberrant chromosomes in clinical cytogenetics.

Authors:  N P Carter; M A Ferguson-Smith; M T Perryman; H Telenius; A H Pelmear; M A Leversha; M T Glancy; S L Wood; K Cook; H M Dyson
Journal:  J Med Genet       Date:  1992-05       Impact factor: 6.318

3.  Degenerate oligonucleotide-primed PCR: general amplification of target DNA by a single degenerate primer.

Authors:  H Telenius; N P Carter; C E Bebb; M Nordenskjöld; B A Ponder; A Tunnacliffe
Journal:  Genomics       Date:  1992-07       Impact factor: 5.736

4.  Application of micro-FISH to delineate deletions.

Authors:  J J Engelen; J C Albrechts; W J Loots; B H Hollanders-Crombach; A J Hamers; J P Geraedts
Journal:  Cytogenet Cell Genet       Date:  1996

5.  Microdissection of banded human chromosomes.

Authors:  G Senger; H J Lüdecke; B Horsthemke; U Claussen
Journal:  Hum Genet       Date:  1990-05       Impact factor: 4.132

6.  Trisomy 5q12-->q13.3 in a patient with add(13q): characterization of an interchromosomal insertion by forward and reverse chromosome painting.

Authors:  A Nordgren; S Arver; U Kvist; N Carter; E Blennow
Journal:  Am J Med Genet       Date:  1997-12-19

7.  A mitotically stable marker chromosome negative for whole chromosome libraries, centromere probes and chromosome specific telomere regions: a novel class of supernumerary marker chromosome?

Authors:  C Mackie Ogilvie; R H Harrison; S W Horsley; S V Hodgson; L Kearney
Journal:  Cytogenet Cell Genet       Date:  2001

8.  Rapid detection of human chromosome 21 aberrations by in situ hybridization.

Authors:  P Lichter; T Cremer; C J Tang; P C Watkins; L Manuelidis; D C Ward
Journal:  Proc Natl Acad Sci U S A       Date:  1988-12       Impact factor: 11.205

9.  Swedish survey on extra structurally abnormal chromosomes in 39 105 consecutive prenatal diagnoses: prevalence and characterization by fluorescence in situ hybridization.

Authors:  E Blennow; T H Bui; U Kristoffersson; M Vujic; G Annerén; E Holmberg; M Nordenskjöld
Journal:  Prenat Diagn       Date:  1994-11       Impact factor: 3.050

10.  Detection of amplified DNA sequences by reverse chromosome painting using genomic tumor DNA as probe.

Authors:  S Joos; H Scherthan; M R Speicher; J Schlegel; T Cremer; P Lichter
Journal:  Hum Genet       Date:  1993-02       Impact factor: 4.132

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  2 in total

Review 1.  Canine cytogenetics--from band to basepair.

Authors:  M Breen
Journal:  Cytogenet Genome Res       Date:  2008-04-30       Impact factor: 1.636

Review 2.  Chromosomes in the flow to simplify genome analysis.

Authors:  Jaroslav Doležel; Jan Vrána; Jan Safář; Jan Bartoš; Marie Kubaláková; Hana Simková
Journal:  Funct Integr Genomics       Date:  2012-08-16       Impact factor: 3.410

  2 in total

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