Literature DB >> 7745561

The genetic background of anticipation.

P Teisberg1.   

Abstract

Mesh：

Year:  1995        PMID： 7745561      PMCID： PMC1295159     

Source DB:  PubMed          Journal:  J R Soc Med        ISSN： 0141-0768            Impact factor:   5.344


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  12 in total

1.  Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n.

Authors:  E J Kremer; M Pritchard; M Lynch; S Yu; K Holman; E Baker; S T Warren; D Schlessinger; G R Sutherland; R I Richards
Journal:  Science       Date:  1991-06-21       Impact factor: 47.728

2.  Hypervariable 'minisatellite' regions in human DNA.

Authors:  A J Jeffreys; V Wilson; S L Thein
Journal:  Nature       Date:  1985 Mar 7-13       Impact factor: 49.962

3.  Early-onset dystrophia myotonica. Evidence supporting a maternal environmental factor.

Authors:  P S Harper; P R Dyken
Journal:  Lancet       Date:  1972-07-08       Impact factor: 79.321

4.  Decreased expression of myotonin-protein kinase messenger RNA and protein in adult form of myotonic dystrophy.

Authors:  Y H Fu; D L Friedman; S Richards; J A Pearlman; R A Gibbs; A Pizzuti; T Ashizawa; M B Perryman; G Scarlato; R G Fenwick
Journal:  Science       Date:  1993-04-09       Impact factor: 47.728

5.  Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene.

Authors:  M Mahadevan; C Tsilfidis; L Sabourin; G Shutler; C Amemiya; G Jansen; C Neville; M Narang; J Barceló; K O'Hoy
Journal:  Science       Date:  1992-03-06       Impact factor: 47.728

6.  An unstable triplet repeat in a gene related to myotonic muscular dystrophy.

Authors:  Y H Fu; A Pizzuti; R G Fenwick; J King; S Rajnarayan; P W Dunne; J Dubel; G A Nasser; T Ashizawa; P de Jong
Journal:  Science       Date:  1992-03-06       Impact factor: 47.728

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.  Absence of myotonic dystrophy protein kinase (DMPK) mRNA as a result of a triplet repeat expansion in myotonic dystrophy.

Authors:  P Carango; J E Noble; H G Marks; V L Funanage
Journal:  Genomics       Date:  1993-11       Impact factor: 5.736

9.  Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member.

Authors:  J D Brook; M E McCurrach; H G Harley; A J Buckler; D Church; H Aburatani; K Hunter; V P Stanton; J P Thirion; T Hudson
Journal:  Cell       Date:  1992-02-21       Impact factor: 41.582

10.  Patterns of inheritance of the symptoms of Huntington's disease suggestive of an effect of genomic imprinting.

Authors:  R M Ridley; C D Frith; L A Farrer; P M Conneally
Journal:  J Med Genet       Date:  1991-04       Impact factor: 6.318
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  2 in total

1.  Anticipation phenomenon in familial adenomatous polyposis:an analysis of its origin.

Authors:  Takeo Iwama; Joji Utsunomiya
Journal:  World J Gastroenterol       Date:  2000-06       Impact factor: 5.742

2.  Anterior segment mesenchymal dysgenesis in a large Australian family is associated with the recurrent 17 bp duplication in PITX3.

Authors:  Kim M Summers; Stephen J Withers; Glen A Gole; Sara Piras; Peter J Taylor
Journal:  Mol Vis       Date:  2008-11-05       Impact factor: 2.367
  2 in total

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