Literature DB >> 7460386

Family analysis of Werner's syndrome: a survey of 42 Japanese families with a review of the literature.

M Goto, K Tanimoto, Y Horiuchi, T Sasazuki.   

Abstract

Forty-two Japanese families, including 80 individuals with Werner's syndrome were studied, confirming that this syndrome is inherited as an autosomal recessive trait. The incidence of malignancy was relatively high in these families and individuals with Werner's syndrome, although the incidence was not so high as was reported previously. HLA typing revealed no significant linkage with Werner's syndrome. The frequency of Werner's syndrome in Japan was estimated using two methods which indicated approximately 300 cases among 100 million people.

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Year:  1981        PMID: 7460386     DOI: 10.1111/j.1399-0004.1981.tb00660.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  24 in total

1.  Werner's syndrome protein is required for correct recovery after replication arrest and DNA damage induced in S-phase of cell cycle.

Authors:  P Pichierri; A Franchitto; P Mosesso; F Palitti
Journal:  Mol Biol Cell       Date:  2001-08       Impact factor: 4.138

2.  Sp1-mediated transcription of the Werner helicase gene is modulated by Rb and p53.

Authors:  Y Yamabe; A Shimamoto; M Goto; J Yokota; M Sugawara; Y Furuichi
Journal:  Mol Cell Biol       Date:  1998-11       Impact factor: 4.272

3.  A unique human gene that spans over 230 kb in the human chromosome 8p11-12 and codes multiple family proteins sharing RNA-binding motifs.

Authors:  A Shimamoto; S Kitao; K Ichikawa; N Suzuki; Y Yamabe; O Imamura; Y Tokutake; M Satoh; T Matsumoto; J Kuromitsu; H Kataoka; K Sugawara; M Sugawara; M Sugimoto; M Goto; Y Furuichi
Journal:  Proc Natl Acad Sci U S A       Date:  1996-10-01       Impact factor: 11.205

4.  DNA helicase activity in Werner's syndrome gene product synthesized in a baculovirus system.

Authors:  N Suzuki; A Shimamoto; O Imamura; J Kuromitsu; S Kitao; M Goto; Y Furuichi
Journal:  Nucleic Acids Res       Date:  1997-08-01       Impact factor: 16.971

5.  Mutations in the consensus helicase domains of the Werner syndrome gene. Werner's Syndrome Collaborative Group.

Authors:  C E Yu; J Oshima; E M Wijsman; J Nakura; T Miki; C Piussan; S Matthews; Y H Fu; J Mulligan; G M Martin; G D Schellenberg
Journal:  Am J Hum Genet       Date:  1997-02       Impact factor: 11.025

Review 6.  Genetics and the pathobiology of ageing.

Authors:  G M Martin
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  1997-12-29       Impact factor: 6.237

7.  Human RECQ Helicase Pathogenic Variants, Population Variation and "Missing" Diseases.

Authors:  Wenqing Fu; Alessio Ligabue; Kai J Rogers; Joshua M Akey; Raymond J Monnat
Journal:  Hum Mutat       Date:  2016-12-09       Impact factor: 4.878

8.  Deletion mapping of chromosome 8p in colorectal carcinoma and dysplasia arising in ulcerative colitis, prostatic carcinoma, and malignant fibrous histiocytomas.

Authors:  M Chang; K Tsuchiya; R H Batchelor; P S Rabinovitch; B G Kulander; R C Haggitt; G C Burmer
Journal:  Am J Pathol       Date:  1994-01       Impact factor: 4.307

9.  Improvement of hyperinsulinemic diabetes following removal of a meningioma in Werner's syndrome. A case report.

Authors:  C Montecucco; G Attardo-Parrinello; G Brambilla; E L Chérié-Lignière; E Ascari
Journal:  Acta Diabetol Lat       Date:  1984 Apr-Jun

Review 10.  Soft-tissue mineralization in Werner syndrome.

Authors:  Antonio Leone; Alessandro Maria Costantini; Raffaela Brigida; Onorina Monica Antoniol; Raffaele Antonelli-Incalzi; Lorenzo Bonomo
Journal:  Skeletal Radiol       Date:  2004-05-11       Impact factor: 2.199

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