Literature DB >> 8133507

Dynamic mutations on the move.

G R Sutherland1, R I Richards.   

Abstract

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Year:  1993        PMID: 8133507      PMCID: PMC1016627          DOI: 10.1136/jmg.30.12.978

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


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  29 in total

1.  Meiosis-specific RNA splicing in yeast.

Authors:  J A Engebrecht; K Voelkel-Meiman; G S Roeder
Journal:  Cell       Date:  1991-09-20       Impact factor: 41.582

2.  Meiotic stability and genotype-phenotype correlation of the trinucleotide repeat in X-linked spinal and bulbar muscular atrophy.

Authors:  A R La Spada; D B Roling; A E Harding; C L Warner; R Spiegel; I Hausmanowa-Petrusewicz; W C Yee; K H Fischbeck
Journal:  Nat Genet       Date:  1992-12       Impact factor: 38.330

3.  Hereditary unstable DNA: a new explanation for some old genetic questions?

Authors:  G R Sutherland; E A Haan; E Kremer; M Lynch; M Pritchard; S Yu; R I Richards
Journal:  Lancet       Date:  1991-08-03       Impact factor: 79.321

Review 4.  RNA recognition: a family matter?

Authors:  I W Mattaj
Journal:  Cell       Date:  1993-06-04       Impact factor: 41.582

5.  Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome.

Authors:  A J Verkerk; M Pieretti; J S Sutcliffe; Y H Fu; D P Kuhl; A Pizzuti; O Reiner; S Richards; M F Victoria; F P Zhang
Journal:  Cell       Date:  1991-05-31       Impact factor: 41.582

6.  Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy.

Authors:  H G Harley; J D Brook; S A Rundle; S Crow; W Reardon; A J Buckler; P S Harper; D E Housman; D J Shaw
Journal:  Nature       Date:  1992-02-06       Impact factor: 49.962

Review 7.  Systemic treatment of early breast cancer by hormonal, cytotoxic, or immune therapy. 133 randomised trials involving 31,000 recurrences and 24,000 deaths among 75,000 women. Early Breast Cancer Trialists' Collaborative Group.

Authors: 
Journal:  Lancet       Date:  1992-01-04       Impact factor: 79.321

8.  Fragile X syndrome unstable element, p(CCG)n, and other simple tandem repeat sequences are binding sites for specific nuclear proteins.

Authors:  R I Richards; K Holman; S Yu; G R Sutherland
Journal:  Hum Mol Genet       Date:  1993-09       Impact factor: 6.150

9.  Origin of the expansion mutation in myotonic dystrophy.

Authors:  G Imbert; C Kretz; K Johnson; J L Mandel
Journal:  Nat Genet       Date:  1993-05       Impact factor: 38.330

10.  Ubiquitous somatic mutations in simple repeated sequences reveal a new mechanism for colonic carcinogenesis.

Authors:  Y Ionov; M A Peinado; S Malkhosyan; D Shibata; M Perucho
Journal:  Nature       Date:  1993-06-10       Impact factor: 49.962

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  5 in total

Review 1.  Advances in neurology.

Authors:  C R Kennedy
Journal:  Arch Dis Child       Date:  1996-09       Impact factor: 3.791

Review 2.  The genetics of non-insulin-dependent diabetes mellitus: tools and aims.

Authors:  M I McCarthy; P Froguel; G A Hitman
Journal:  Diabetologia       Date:  1994-10       Impact factor: 10.122

3.  Points to consider: ethical, legal, and psychosocial implications of genetic testing in children and adolescents. American Society of Human Genetics Board of Directors, American College of Medical Genetics Board of Directors.

Authors: 
Journal:  Am J Hum Genet       Date:  1995-11       Impact factor: 11.025

4.  Postzygotic instability of the myotonic dystrophy p[AGC] in repeat supported by larger expansions in muscle and reduced amplifications in sperm.

Authors:  A Massari; M Gennarelli; E Menegazzo; A Pizzuti; V Silani; I Mastrogiacomo; E Pagani; C Angelini; G Scarlato; G Novelli
Journal:  J Neurol       Date:  1995-06       Impact factor: 4.849

Review 5.  Genetic mechanisms and mental retardation.

Authors:  R C Trembath
Journal:  J R Coll Physicians Lond       Date:  1994 Mar-Apr
  5 in total

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