Literature DB >> 1671983

Codon 178 mutation in ethnically diverse Creutzfeldt-Jakob disease families.

A Nieto, L G Goldfarb, P Brown, W R McCombie, S Trapp, D M Asher, D C Gajdusek.   

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Year:  1991        PMID： 1671983     DOI： 10.1016/0140-6736(91)91696-r

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


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  17 in total

1.  Research on familial Creutzfeldt-Jakob disease (FCJD) resulting in presymptomatic testing: implications for the Human Genome Project.

Authors:  Janet E Ulm; Cindy L Vnencak-Jones; Patrick Bosque
Journal:  J Genet Couns       Date:  1993-03       Impact factor: 2.537

2.  Presymptomatic detection or exclusion of prion protein gene defects in families with inherited prion diseases.

Authors:  J Collinge; M Poulter; M B Davis; M Baraitser; F Owen; T J Crow; A E Harding
Journal:  Am J Hum Genet       Date:  1991-12       Impact factor: 11.025

3.  Familial Creutzfeldt-Jakob disease in Finland: epidemiological, clinical, pathological and molecular genetic studies.

Authors:  M Haltia; J Kovanen; L G Goldfarb; P Brown; D C Gajdusek
Journal:  Eur J Epidemiol       Date:  1991-09       Impact factor: 8.082

4.  Creutzfeldt-Jacob disease associated with the PRNP codon 200Lys mutation: an analysis of 45 families.

Authors:  L G Goldfarb; P Brown; E Mitrovà; L Cervenáková; L Goldin; A D Korczyn; J Chapman; S Gálvez; L Cartier; R Rubenstein
Journal:  Eur J Epidemiol       Date:  1991-09       Impact factor: 8.082

5.  The phenotypic expression of different mutations in transmissible familial Creutzfeldt-Jakob disease.

Authors:  P Brown; L G Goldfarb; C J Gibbs; D C Gajdusek
Journal:  Eur J Epidemiol       Date:  1991-09       Impact factor: 8.082

Review 6.  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 7.  Prions, beta-sheets and transmissible dementias: is there still something missing?

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

8.  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

Review 9.  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 10.  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
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