Literature DB >> 8558550

FMR1 triplet arrays: paying the price for perfection.

M C Hirst1.   

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Year:  1995        PMID： 8558550      PMCID： PMC1051695          DOI： 10.1136/jmg.32.10.761

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  16 in total

1.  Unusual (CGG)n expansion and recombination in a family with fragile X and DiGeorge syndrome.

Authors:  J N Macpherson; G Curtis; J A Crolla; N Dennis; B Migeon; P K Grewal; M C Hirst; K E Davies; P A Jacobs
Journal:  J Med Genet       Date:  1995-03       Impact factor: 6.318

2.  Data on the CGG repeat at the fragile X site in the non-retarded Japanese population and family suggest the presence of a subgroup of normal alleles predisposing to mutate.

Authors:  T Arinami; M Asano; K Kobayashi; H Yanagi; H Hamaguchi
Journal:  Hum Genet       Date:  1993-11       Impact factor: 4.132

3.  Frequency and stability of the fragile X premutation.

Authors:  A L Reiss; H H Kazazian; C M Krebs; A McAughan; C D Boehm; M T Abrams; D L Nelson
Journal:  Hum Mol Genet       Date:  1994-03       Impact factor: 6.150

4.  Distribution of FMR-1 and associated microsatellite alleles in a normal Chinese population.

Authors:  N Zhong; X Liu; S Gou; G E Houck; S Li; C Dobkin; W T Brown
Journal:  Am J Med Genet       Date:  1994-07-15

5.  Length of uninterrupted CGG repeats determines instability in the FMR1 gene.

Authors:  E E Eichler; J J Holden; B W Popovich; A L Reiss; K Snow; S N Thibodeau; C S Richards; P A Ward; D L Nelson
Journal:  Nat Genet       Date:  1994-09       Impact factor: 38.330

6.  Evidence for a mechanism predisposing to intergenerational CAG repeat instability in spinocerebellar ataxia type I.

Authors:  M Y Chung; L P Ranum; L A Duvick; A Servadio; H Y Zoghbi; H T Orr
Journal:  Nat Genet       Date:  1993-11       Impact factor: 38.330

7.  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

8.  Haplotype analysis at the FRAXA locus in the Japanese population.

Authors:  R I Richards; I Kondo; K Holman; M Yamauchi; N Seki; K Kishi; A Staples; G R Sutherland; T Hori
Journal:  Am J Med Genet       Date:  1994-07-15

9.  Cryptic and polar variation of the fragile X repeat could result in predisposing normal alleles.

Authors:  C B Kunst; S T Warren
Journal:  Cell       Date:  1994-06-17       Impact factor: 41.582

10.  Apparent regression of the CGG repeat in FMR1 to an allele of normal size.

Authors:  L Vits; K De Boulle; E Reyniers; I Handig; J K Darby; B Oostra; P J Willems
Journal:  Hum Genet       Date:  1994-11       Impact factor: 4.132
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  3 in total

1.  Cloned human FMR1 trinucleotide repeats exhibit a length- and orientation-dependent instability suggestive of in vivo lagging strand secondary structure.

Authors:  M C Hirst; P J White
Journal:  Nucleic Acids Res       Date:  1998-05-15       Impact factor: 16.971

Review 2.  The fragile X syndrome.

Authors:  B B de Vries; D J Halley; B A Oostra; M F Niermeijer
Journal:  J Med Genet       Date:  1998-07       Impact factor: 6.318

3.  Fragile X (CGG)n repeats induce a transcriptional repression in cis upon a linked promoter: evidence for a chromatin mediated effect.

Authors:  Simon P Chandler; Pushpa Kansagra; Mark C Hirst
Journal:  BMC Mol Biol       Date:  2003-03-21       Impact factor: 2.946
  3 in total

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