Literature DB >> 2378641

Codon 129 changes in the prion protein gene in Caucasians.

F Owen, M Poulter, J Collinge, T J Crow.   

Abstract

Entities:  

Mesh：

Substances：

Year:  1990        PMID： 2378641      PMCID： PMC1683817     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN： 0002-9297            Impact factor:   11.025


× No keyword cloud information.
  7 in total

1.  Mutations in familial Creutzfeldt-Jakob disease and Gerstmann-Sträussler-Scheinker's syndrome.

Authors:  D Goldgaber; L G Goldfarb; P Brown; D M Asher; W T Brown; S Lin; J W Teener; S M Feinstone; R Rubenstein; R J Kascsak
Journal:  Exp Neurol       Date:  1989-11       Impact factor: 5.330

2.  Insertion in prion protein gene in familial Creutzfeldt-Jakob disease.

Authors:  F Owen; M Poulter; R Lofthouse; J Collinge; T J Crow; D Risby; H F Baker; R M Ridley; K Hsiao; S B Prusiner
Journal:  Lancet       Date:  1989-01-07       Impact factor: 79.321

3.  Pro----leu change at position 102 of prion protein is the most common but not the sole mutation related to Gerstmann-Sträussler syndrome.

Authors:  K Doh-ura; J Tateishi; H Sasaki; T Kitamoto; Y Sakaki
Journal:  Biochem Biophys Res Commun       Date:  1989-09-15       Impact factor: 3.575

4.  Analysis of enzymatically amplified beta-globin and HLA-DQ alpha DNA with allele-specific oligonucleotide probes.

Authors:  R K Saiki; T L Bugawan; G T Horn; K B Mullis; H A Erlich
Journal:  Nature       Date:  1986 Nov 13-19       Impact factor: 49.962

5.  Base composition-independent hybridization in tetramethylammonium chloride: a method for oligonucleotide screening of highly complex gene libraries.

Authors:  W I Wood; J Gitschier; L A Lasky; R M Lawn
Journal:  Proc Natl Acad Sci U S A       Date:  1985-03       Impact factor: 11.205

6.  Diagnosis of Gerstmann-Sträussler syndrome in familial dementia with prion protein gene analysis.

Authors:  J Collinge; A E Harding; F Owen; M Poulter; R Lofthouse; A M Boughey; T Shah; T J Crow
Journal:  Lancet       Date:  1989-07-01       Impact factor: 79.321

7.  Linkage of a prion protein missense variant to Gerstmann-Sträussler syndrome.

Authors:  K Hsiao; H F Baker; T J Crow; M Poulter; F Owen; J D Terwilliger; D Westaway; J Ott; S B Prusiner
Journal:  Nature       Date:  1989-03-23       Impact factor: 49.962
  7 in total
  36 in total

1.  Identification of multiple quantitative trait loci linked to prion disease incubation period in mice.

Authors:  S E Lloyd; O N Onwuazor; J A Beck; G Mallinson; M Farrall; P Targonski; J Collinge; E M Fisher
Journal:  Proc Natl Acad Sci U S A       Date:  2001-05-15       Impact factor: 11.205

2.  Projections of the future course of the primary vCJD epidemic in the UK: inclusion of subclinical infection and the possibility of wider genetic susceptibility.

Authors:  Paul Clarke; Azra C Ghani
Journal:  J R Soc Interface       Date:  2005-03-22       Impact factor: 4.118

3.  Codon 219 polymorphism of PRNP in healthy Caucasians and Creutzfeldt-Jakob disease patients.

Authors:  R Petraroli; M Pocchiari
Journal:  Am J Hum Genet       Date:  1996-04       Impact factor: 11.025

Review 4.  Prion diseases: what will be next?

Authors:  P van der Valk
Journal:  J Clin Pathol       Date:  1998-04       Impact factor: 3.411

5.  Distinct synthetic Aβ prion strains producing different amyloid deposits in bigenic mice.

Authors:  Jan Stöhr; Carlo Condello; Joel C Watts; Lillian Bloch; Abby Oehler; Mimi Nick; Stephen J DeArmond; Kurt Giles; William F DeGrado; Stanley B Prusiner
Journal:  Proc Natl Acad Sci U S A       Date:  2014-06-30       Impact factor: 11.205

6.  Live cell fluorescence resonance energy transfer predicts an altered molecular association of heterologous PrPSc with PrPC.

Authors:  Suparna Mallik; Wenbin Yang; Eric M Norstrom; James A Mastrianni
Journal:  J Biol Chem       Date:  2010-01-19       Impact factor: 5.157

7.  Prion protein gene analysis in three kindreds with fatal familial insomnia (FFI): codon 178 mutation and codon 129 polymorphism.

Authors:  R Medori; H J Tritschler
Journal:  Am J Hum Genet       Date:  1993-10       Impact factor: 11.025

8.  Mutation and polymorphism of the prion protein gene in Libyan Jews with Creutzfeldt-Jakob disease (CJD).

Authors:  R Gabizon; H Rosenmann; Z Meiner; I Kahana; E Kahana; Y Shugart; J Ott; S B Prusiner
Journal:  Am J Hum Genet       Date:  1993-10       Impact factor: 11.025

9.  Creutzfeldt-Jakob disease with codon 129 polymorphism (valine): a comparative study of patients with codon 102 point mutation or without mutations.

Authors:  M Miyazono; T Kitamoto; K Doh-ura; T Iwaki; J Tateishi
Journal:  Acta Neuropathol       Date:  1992       Impact factor: 17.088

10.  Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study.

Authors:  Simon Mead; Mark Poulter; James Uphill; John Beck; Jerome Whitfield; Thomas E F Webb; Tracy Campbell; Gary Adamson; Pelagia Deriziotis; Sarah J Tabrizi; Holger Hummerich; Claudio Verzilli; Michael P Alpers; John C Whittaker; John Collinge
Journal:  Lancet Neurol       Date:  2009-01       Impact factor: 44.182
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.