Literature DB >> 8755939

The molecular basis of fragile sites.

C Dobkin, N Zhong, W T Brown.   

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Year:  1996        PMID： 8755939      PMCID： PMC1914742     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN： 0002-9297            Impact factor:   11.025


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  10 in total

1.  FRA3B extends over a broad region and contains a spontaneous HPV16 integration site: direct evidence for the coincidence of viral integration sites and fragile sites.

Authors:  C M Wilke; B K Hall; A Hoge; W Paradee; D I Smith; T W Glover
Journal:  Hum Mol Genet       Date:  1996-02       Impact factor: 6.150

2.  On the formation of nucleosomes within the FMR1 trinucleotide repeat.

Authors:  S Metzenberg
Journal:  Am J Hum Genet       Date:  1996-07       Impact factor: 11.025

3.  Trinucleotide repeats that expand in human disease form hairpin structures in vitro.

Authors:  A M Gacy; G Goellner; N Juranić; S Macura; C T McMurray
Journal:  Cell       Date:  1995-05-19       Impact factor: 41.582

4.  Hairpins are formed by the single DNA strands of the fragile X triplet repeats: structure and biological implications.

Authors:  X Chen; S V Mariappan; P Catasti; R Ratliff; R K Moyzis; A Laayoun; S S Smith; E M Bradbury; G Gupta
Journal:  Proc Natl Acad Sci U S A       Date:  1995-05-23       Impact factor: 11.205

5.  Isolation of a GCC repeat showing expansion in FRAXF, a fragile site distal to FRAXA and FRAXE.

Authors:  J E Parrish; B A Oostra; A J Verkerk; C S Richards; J Reynolds; A S Spikes; L G Shaffer; D L Nelson
Journal:  Nat Genet       Date:  1994-11       Impact factor: 38.330

6.  Implications of FRA16A structure for the mechanism of chromosomal fragile site genesis.

Authors:  J K Nancarrow; E Kremer; K Holman; H Eyre; N A Doggett; D Le Paslier; D F Callen; G R Sutherland; R I Richards
Journal:  Science       Date:  1994-06-24       Impact factor: 47.728

7.  Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation.

Authors:  S J Knight; A V Flannery; M C Hirst; L Campbell; Z Christodoulou; S R Phelps; J Pointon; H R Middleton-Price; A Barnicoat; M E Pembrey
Journal:  Cell       Date:  1993-07-16       Impact factor: 41.582

8.  Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox.

Authors:  Y H Fu; D P Kuhl; A Pizzuti; M Pieretti; J S Sutcliffe; S Richards; A J Verkerk; J J Holden; R G Fenwick; S T Warren
Journal:  Cell       Date:  1991-12-20       Impact factor: 41.582

9.  High functioning fragile X males: demonstration of an unmethylated fully expanded FMR-1 mutation associated with protein expression.

Authors:  R J Hagerman; C E Hull; J F Safanda; I Carpenter; L W Staley; R A O'Connor; C Seydel; M M Mazzocco; K Snow; S N Thibodeau
Journal:  Am J Med Genet       Date:  1994-07-15

10.  Physical linkage of the fragile site FRA11B and a Jacobsen syndrome chromosome deletion breakpoint in 11q23.3.

Authors:  C Jones; P Slijepcevic; S Marsh; E Baker; W Y Langdon; R I Richards; A Tunnacliffe
Journal:  Hum Mol Genet       Date:  1994-12       Impact factor: 6.150
  10 in total

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