Literature DB >> 2068787

Fluorescence in situ hybridization: applications in cytogenetics and gene mapping.

B J Trask1.   

Abstract

Unique sequences, chromosomal subregions, or entire genomes can be specifically highlighted in metaphase or interphase cells by fluorescence in situ hybridization (FISH). This technique can be used to identify chromosomes, detect chromosomal abnormalities or determine the chromosomal location of specific sequences. FISH plays an increasingly important role in a variety of research areas, including cytogenetics, prenatal diagnosis, tumor biology, gene amplification and gene mapping.

Entities:  

Mesh：

Year:  1991        PMID： 2068787     DOI： 10.1016/0168-9525(91)90378-4

Source DB:  PubMed          Journal:  Trends Genet        ISSN： 0168-9525            Impact factor:   11.639


  68 in total

1.  Correlated positioning of homologous chromosomes in daughter fibroblast cells.

Authors:  H B Sun; H Yokota
Journal:  Chromosome Res       Date:  1999       Impact factor: 5.239

2.  Localization of single- and low-copy sequences on tomato synaptonemal complex spreads using fluorescence in situ hybridization (FISH).

Authors:  D G Peterson; N L Lapitan; S M Stack
Journal:  Genetics       Date:  1999-05       Impact factor: 4.562

3.  Primer-mediated in situ detection of the B-hordein gene cluster on barley chromosome 1H.

Authors:  S Abbo; R P Dunford; T E Miller; S M Reader; I P King
Journal:  Proc Natl Acad Sci U S A       Date:  1993-12-15       Impact factor: 11.205

4.  A new structure for the murine Xist gene and its relationship to chromosome choice/counting during X-chromosome inactivation.

Authors:  Y K Hong; S D Ontiveros; C Chen; W M Strauss
Journal:  Proc Natl Acad Sci U S A       Date:  1999-06-08       Impact factor: 11.205

5.  High-resolution mapping of mammalian genes by in situ hybridization to free chromatin.

Authors:  H H Heng; J Squire; L C Tsui
Journal:  Proc Natl Acad Sci U S A       Date:  1992-10-15       Impact factor: 11.205

6.  Quantitative fluorescence in situ hybridization of Aureobasidium pullulans on microscope slides and leaf surfaces.

Authors:  S Li; R N Spear; J H Andrews
Journal:  Appl Environ Microbiol       Date:  1997-08       Impact factor: 4.792

7.  High-resolution genomic profiling of chromosomal aberrations using Infinium whole-genome genotyping.

Authors:  Daniel A Peiffer; Jennie M Le; Frank J Steemers; Weihua Chang; Tony Jenniges; Francisco Garcia; Kirt Haden; Jiangzhen Li; Chad A Shaw; John Belmont; Sau Wai Cheung; Richard M Shen; David L Barker; Kevin L Gunderson
Journal:  Genome Res       Date:  2006-08-09       Impact factor: 9.043

8.  20p12.3 microdeletion predisposes to Wolff-Parkinson-White syndrome with variable neurocognitive deficits.

Authors:  S R Lalani; J V Thakuria; G F Cox; X Wang; W Bi; M S Bray; C Shaw; S W Cheung; A C Chinault; B A Boggs; Z Ou; E K Brundage; J R Lupski; J Gentile; S Waisbren; A Pursley; L Ma; M Khajavi; G Zapata; R Friedman; J J Kim; J A Towbin; P Stankiewicz; S Schnittger; I Hansmann; T Ai; S Sood; X H Wehrens; J F Martin; J W Belmont; L Potocki
Journal:  J Med Genet       Date:  2008-09-23       Impact factor: 6.318

9.  Identification of chromosome abnormalities in subtelomeric regions by microarray analysis: a study of 5,380 cases.

Authors:  Lina Shao; Chad A Shaw; Xin-Yan Lu; Trilochan Sahoo; Carlos A Bacino; Seema R Lalani; Pawel Stankiewicz; Svetlana A Yatsenko; Yinfeng Li; Sarah Neill; Amber N Pursley; A Craig Chinault; Ankita Patel; Arthur L Beaudet; James R Lupski; Sau W Cheung
Journal:  Am J Med Genet A       Date:  2008-09-01       Impact factor: 2.802

10.  Comparison of high resolution cytogenetics, fluorescence in situ hybridisation, and DNA studies to validate the diagnosis of Prader-Willi and Angelman's syndromes.

Authors:  A Smith; M Prasad; Z M Deng; L Robson; T Woodage; R J Trent
Journal:  Arch Dis Child       Date:  1995-05       Impact factor: 3.791
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.