Codon 129 changes in the prion protein gene in Caucasians.
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Updated projections of future vCJD deaths in the UKvCJD risk in the Republic of IrelandSporadic--but not variant--Creutzfeldt-Jakob disease is associated with polymorphisms upstream of PRNP exon 1.Genomic structure of the human prion protein gene.Neurodegeneration in humans caused by prionsCreutzfeldt-Jakob disease with congophilic kuru plaques: CT and pathological findings of the cerebral white matterLive cell fluorescence resonance energy transfer predicts an altered molecular association of heterologous PrPSc with PrPC.Distinct synthetic Aβ prion strains producing different amyloid deposits in bigenic mice.Bovine spongiform encephalopathy and Creutzfeldt-Jakob disease: implications for physicians.The prion hypothesis: from biological anomaly to basic regulatory mechanism.Analyses of the mitochondrial mutations in the Chinese patients with sporadic Creutzfeldt-Jakob diseaseDissociation of pathological and molecular phenotype of variant Creutzfeldt-Jakob disease in transgenic human prion protein 129 heterozygous mice.Mutation and polymorphism of the prion protein gene in Libyan Jews with Creutzfeldt-Jakob disease (CJD).Prion protein gene analysis in three kindreds with fatal familial insomnia (FFI): codon 178 mutation and codon 129 polymorphismProposed three-dimensional structure for the cellular prion proteinEtiology and pathogenesis of prion diseases.Identification of multiple quantitative trait loci linked to prion disease incubation period in mice.Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association studyPrion diseases: what will be next?Laboratory activities involving transmissible spongiform encephalopathy causing agents: risk assessment and biosafety recommendations in Belgium.Experimental Models of Inherited PrP Prion Diseases.Projections of the future course of the primary vCJD epidemic in the UK: inclusion of subclinical infection and the possibility of wider genetic susceptibility.Codon 219 polymorphism of PRNP in healthy Caucasians and Creutzfeldt-Jakob disease patients.Epidemiological determinants of the pattern and magnitude of the vCJD epidemic in Great Britain.Factors determining the pattern of the variant Creutzfeldt-Jakob disease (vCJD) epidemic in the UKAssessment of the prevalence of vCJD through testing tonsils and appendices for abnormal prion proteinStructural basis for the complete resistance of the human prion protein mutant G127V to prion disease
P2860
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P2860
Codon 129 changes in the prion protein gene in Caucasians.
description
1990 nî lūn-bûn
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name
Codon 129 changes in the prion protein gene in Caucasians.
@en
Codon 129 changes in the prion protein gene in Caucasians.
@nl
type
label
Codon 129 changes in the prion protein gene in Caucasians.
@en
Codon 129 changes in the prion protein gene in Caucasians.
@nl
prefLabel
Codon 129 changes in the prion protein gene in Caucasians.
@en
Codon 129 changes in the prion protein gene in Caucasians.
@nl
P2093
P2860
P1476
Codon 129 changes in the prion protein gene in Caucasians.
@en
P2093
P2860
P304
P407
P577
1990-06-01T00:00:00Z