Literature DB >> 7959730

An integrated physical map of 210 markers assigned to the short arm of human chromosome 11.

E Redeker1, J M Hoovers, M Alders, C J van Moorsel, A C Ivens, S Gregory, L Kalikin, J Bliek, L de Galan, R van den Bogaard.   

Abstract

Using a panel of patient cell lines with chromosomal breakpoints, we constructed a physical map for the short arm of human chromosome 11. We focused on 11p15, a chromosome band harboring at least 25 known genes and associated with the Beckwith-Wiedemann syndrome, several childhood tumors, and genomic imprinting. This underlines the need for a physical map for this region. We divided the short arm of chromosome 11 into 18 breakpoint regions, and a large series of new and previously described genes and markers was mapped within these intervals using fluorescence in situ hybridization. Cosmid fingerprint analysis showed that 19 of these markers were included in cosmid contigs. A detailed 10-Mb pulsed-field physical map of the region 11p15.3-pter was constructed. These three different approaches enabled the high-resolution mapping of 210 markers, including 22 known genes.

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Year:  1994        PMID: 7959730     DOI: 10.1006/geno.1994.1312

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  6 in total

1.  Disruption of a novel imprinted zinc-finger gene, ZNF215, in Beckwith-Wiedemann syndrome.

Authors:  M Alders; A Ryan; M Hodges; J Bliek; A P Feinberg; O Privitera; A Westerveld; P F Little; M Mannens
Journal:  Am J Hum Genet       Date:  2000-04-10       Impact factor: 11.025

2.  A common region of loss of heterozygosity in Wilms' tumor and embryonal rhabdomyosarcoma distal to the D11S988 locus on chromosome 11p15.5.

Authors:  C Besnard-Guérin; I Newsham; R Winqvist; W K Cavenee
Journal:  Hum Genet       Date:  1996-02       Impact factor: 4.132

3.  Loss of heterozygosity on chromosome 11p15 during histological progression in microdissected ductal carcinoma of the breast.

Authors:  J H Lichy; M Zavar; M M Tsai; T J O'Leary; J K Taubenberger
Journal:  Am J Pathol       Date:  1998-07       Impact factor: 4.307

4.  Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments.

Authors:  J M Hoovers; L M Kalikin; L A Johnson; M Alders; B Redeker; D J Law; J Bliek; M Steenman; M Benedict; J Wiegant; C Lengauer; P Taillon-Miller; D Schlessinger; M C Edwards; S J Elledge; A Ivens; A Westerveld; P Little; M Mannens; A P Feinberg
Journal:  Proc Natl Acad Sci U S A       Date:  1995-12-19       Impact factor: 11.205

5.  Gene density and transcription influence the localization of chromatin outside of chromosome territories detectable by FISH.

Authors:  Nicola L Mahy; Paul E Perry; Wendy A Bickmore
Journal:  J Cell Biol       Date:  2002-12-09       Impact factor: 10.539

6.  11p15.4 Microdeletion Associates with Hemihypertrophy.

Authors:  Surasak Puvabanditsin; Mehrin Sadiq; Marianne Jacob; Maaz Jalil; Kenya Cabrera; Omer Choudry; Rajeev Mehta
Journal:  Case Rep Genet       Date:  2018-10-30
  6 in total

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