Literature DB >> 1469441

Familial Creutzfeldt-Jakob disease in Chile is associated with the codon 200 mutation of the PRNP amyloid precursor gene on chromosome 20.

P Brown1, S Gálvez, L G Goldfarb, A Nieto, L Cartier, C J Gibbs, D C Gajdusek.   

Abstract

We have found the codon 200Lys mutation in 6 Chilean CJD families, including a family in the rural case cluster in Chillán. Thus, all 3 of the known clusters of CJD, in Slovakia, Libyan-born Israeli Jews, and Chile, are linked to the presence of the same mutation. The phenotypic features of the disease in these families are similar to those reported for other clustered or individual families elsewhere in the world. The heterogeneous genetic composition of the Chilean population interpreted in light of historical migration patterns suggests that the mutation may have entered Chile by Jewish emigration from Spain.

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Year:  1992        PMID: 1469441     DOI: 10.1016/0022-510x(92)90133-6

Source DB:  PubMed          Journal:  J Neurol Sci        ISSN: 0022-510X            Impact factor:   3.181


  10 in total

1.  Ancestral origins and worldwide distribution of the PRNP 200K mutation causing familial Creutzfeldt-Jakob disease.

Authors:  H S Lee; N Sambuughin; L Cervenakova; J Chapman; M Pocchiari; S Litvak; H Y Qi; H Budka; T del Ser; H Furukawa; P Brown; D C Gajdusek; J C Long; A D Korczyn; L G Goldfarb
Journal:  Am J Hum Genet       Date:  1999-04       Impact factor: 11.025

Review 2.  The transmissible amyloidoses: genetical control of spontaneous generation of infectious amyloid proteins by nucleation of configurational change in host precursors: kuru-CJD-GSS-scrapie-BSE.

Authors:  D C Gajdusek
Journal:  Eur J Epidemiol       Date:  1991-09       Impact factor: 8.082

Review 3.  Prions, beta-sheets and transmissible dementias: is there still something missing?

Authors:  P P Liberski
Journal:  Acta Neuropathol       Date:  1995       Impact factor: 17.088

4.  Creutzfeldt-Jakob disease with E200K PRNP mutation: a case report and revision of the literature.

Authors:  Michelangelo Mancuso; Gabriele Siciliano; Sabina Capellari; Daniele Orsucci; Policarpo Moretti; Giuseppe Di Fede; Silvia Suardi; Rosaria Strammiello; Piero Parchi; Fabrizio Tagliavini; Luigi Murri
Journal:  Neurol Sci       Date:  2009-07-14       Impact factor: 3.307

5.  Absence of spontaneous disease and comparative prion susceptibility of transgenic mice expressing mutant human prion proteins.

Authors:  Emmanuel A Asante; Ian Gowland; Andrew Grimshaw; Jacqueline M Linehan; Michelle Smidak; Richard Houghton; Olufunmilayo Osiguwa; Andrew Tomlinson; Susan Joiner; Sebastian Brandner; Jonathan D F Wadsworth; John Collinge
Journal:  J Gen Virol       Date:  2009-03       Impact factor: 3.891

Review 6.  Spontaneous generation of infectious nucleating amyloids in the transmissible and nontransmissible cerebral amyloidoses.

Authors:  D C Gajdusek
Journal:  Mol Neurobiol       Date:  1994-02       Impact factor: 5.590

Review 7.  Molecular genetic studies of Creutzfeldt-Jakob disease.

Authors:  L G Goldfarb; P Brown; L Cervenakova; D C Gajdusek
Journal:  Mol Neurobiol       Date:  1994 Apr-Jun       Impact factor: 5.590

8.  Altered Prion protein expression pattern in CSF as a biomarker for Creutzfeldt-Jakob disease.

Authors:  Mauricio Torres; Luis Cartier; José Manuel Matamala; Nancy Hernández; Ute Woehlbier; Claudio Hetz
Journal:  PLoS One       Date:  2012-04-27       Impact factor: 3.240

9.  Creutzfeldt-Jakob disease associated with a missense mutation at codon 200 of the prion protein gene in Brazil.

Authors:  Jerusa Smid; Vilma Regina Martins; Michele Christine Landemberger; Daniele Riva; Renato Anghinah; Ricardo Nitrini
Journal:  Dement Neuropsychol       Date:  2007 Apr-Jun

Review 10.  Prions and related neurological diseases.

Authors:  M Pocchiari
Journal:  Mol Aspects Med       Date:  1994
  10 in total

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