First report of polymorphisms in the prion-like protein gene (PRND): implications for human prion diseases (Q28145109)

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J P Brandel

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J M Launay

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J L Laplanche

Demyelinating peripheral neuropathy with Creutzfeldt-Jakob disease and mutation at codon 200 of the prion protein gene

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language of work or name

English

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publication date

2 June 2000

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published in

Neuroscience Letters

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volume

286

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issue

2

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page(s)

144-8

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cites work

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7 January 2021

Normal prion protein has an activity like that of superoxide dismutase.

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Mutation in codon 200 of scrapie amyloid precursor gene linked to Creutzfeldt-Jakob disease in Sephardic Jews of Libyan and non-Libyan origin

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Mutation in codon 200 of scrapie amyloid protein gene in two clusters of Creutzfeldt-Jakob disease in Slovakia

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7 January 2021

Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphism

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7 January 2021

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

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7 January 2021

Ataxia in prion protein (PrP)-deficient mice is associated with upregulation of the novel PrP-like protein doppel

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A knowledge base for predicting protein localization sites in eukaryotic cells

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Identification of prokaryotic and eukaryotic signal peptides and prediction of their cleavage sites

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Prion protein is necessary for latent learning and long-term memory retention

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Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease

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Novel proteinaceous infectious particles cause scrapie

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Loss of cerebellar Purkinje cells in aged mice homozygous for a disrupted PrP gene

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A new method for predicting signal sequence cleavage sites

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