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Molecular Pathological Classification of Neurodegenerative Diseases: Turning towards Precision MedicineHuman prion diseases in the Netherlands (1998-2009): clinical, genetic and molecular aspects.Prion protein amyloidosis with divergent phenotype associated with two novel nonsense mutations in PRNP.A Drosophila model of GSS syndrome suggests defects in active zones are responsible for pathogenesis of GSS syndrome.Gerstmann-Sträussler-Scheinker disease subtypes efficiently transmit in bank voles as genuine prion diseases.Agent strain variation in human prion disease: insights from a molecular and pathological review of the National Institutes of Health series of experimentally transmitted disease.A novel seven-octapeptide repeat insertion in the prion protein gene (PRNP) in a Dutch pedigree with Gerstmann-Sträussler-Scheinker disease phenotype: comparison with similar cases from the literature.Intermolecular alignment in Y145Stop human prion protein amyloid fibrils probed by solid-state NMR spectroscopyMicro-imaging of amyloid in mice.Current perspectives on cardiac amyloidosis.Phenotypic variability in human prion diseases.[(11)C]PiB PET in Gerstmann-Sträussler-Scheinker disease.Prions and the potential transmissibility of protein misfolding diseasesConsensus classification of human prion disease histotypes allows reliable identification of molecular subtypes: an inter-rater study among surveillance centres in Europe and USADrosophila melanogaster as a model organism of brain diseasesA novel PRNP-P105S mutation associated with atypical prion disease and a rare PrPSc conformationAnalyses of protease resistance and aggregation state of abnormal prion protein across the spectrum of human prionsClinicopathological Correlates in a PRNP P102L Mutation Carrier with Rapidly Progressing Parkinsonism-dystoniaProteolytic processing of the prion protein in health and disease.Invited review: Neuropathology of tauopathies: principles and practice.Resistance of cell lines to prion toxicity aided by phospho-ERK expression.Transmissibility of Gerstmann-Sträussler-Scheinker syndrome in rodent models: New insights into the molecular underpinnings of prion infectivity.Recombinant PrP and Its Contribution to Research on Transmissible Spongiform Encephalopathies.Tau pathology in Creutzfeldt-Jakob disease revisited.Two novel PRNP truncating mutations broaden the spectrum of prion amyloidosis.
P2860
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P2860
description
2003 nî lūn-bûn
@nan
2003 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի մարտին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
Hereditary prion protein amyloidoses.
@ast
Hereditary prion protein amyloidoses.
@en
type
label
Hereditary prion protein amyloidoses.
@ast
Hereditary prion protein amyloidoses.
@en
prefLabel
Hereditary prion protein amyloidoses.
@ast
Hereditary prion protein amyloidoses.
@en
P2093
P1476
Hereditary prion protein amyloidoses.
@en
P2093
Bernardino Ghetti
Fabrizio Tagliavini
Orso Bugiani
Pedro Piccardo
P304
65-85, viii
P356
10.1016/S0272-2712(02)00064-1
P577
2003-03-01T00:00:00Z