Literature DB >> 8874483

No detectable mutations at Werner helicase locus in progeria.

J Oshima, W T Brown, G M Martin.   

Abstract

Entities:  

Mesh：

Substances：

Year:  1996        PMID： 8874483     DOI： 10.1016/S0140-6736(05)64456-X

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


× No keyword cloud information.
  4 in total

1.  POLD1 Germline Mutations in Patients Initially Diagnosed with Werner Syndrome.

Authors:  Davor Lessel; Fuki M Hisama; Katalin Szakszon; Bidisha Saha; Alexander Barrios Sanjuanelo; Bonnie A Salbert; Pamela D Steele; Jennifer Baldwin; W Ted Brown; Charles Piussan; Henri Plauchu; Judit Szilvássy; Edit Horkay; Josef Högel; George M Martin; Alan J Herr; Junko Oshima; Christian Kubisch
Journal:  Hum Mutat       Date:  2015-08-06       Impact factor: 4.878

Review 2.  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

Review 3.  Rapid purification of helicase proteins and in vitro analysis of helicase activity.

Authors:  Kambiz Tahmaseb; Steven W Matson
Journal:  Methods       Date:  2010-02-12       Impact factor: 3.608

4.  Nucleolar localization of the Werner syndrome protein in human cells.

Authors:  R A Marciniak; D B Lombard; F B Johnson; L Guarente
Journal:  Proc Natl Acad Sci U S A       Date:  1998-06-09       Impact factor: 11.205
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.