Sporadic and familial CJD: classification and characterisation.
about
Sporadic fatal insomnia in a young woman: a diagnostic challenge: case reportThe genetic epidemiology of neurodegenerative disease.Insights into the management of emerging infections: regulating variant Creutzfeldt-Jakob disease transfusion risk in the UK and the USA novel human disease with abnormal prion protein sensitive to proteaseEfficient transmission and characterization of Creutzfeldt-Jakob disease strains in bank voles.Prion diseases: immunotargets and therapyEpidemiological characteristics of human prion diseasesGenetics of Prion Disease in CattleAn overview of human prion diseasesPrions in variably protease-sensitive prionopathy: an updatePRNP haplotype associated with classical BSE incidence in European Holstein cattleAtypical BSE (BASE) transmitted from asymptomatic aging cattle to a primateHuman prion diseases: surgical lessons learned from iatrogenic prion transmissionHuman 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.Cytoplasmic prion protein induces forebrain neurotoxicityAssociation of hsp70 polymorphisms with risk of noise-induced hearing loss in Chinese automobile workers.Role of magnetic resonance imaging, cerebrospinal fluid, and electroencephalogram in diagnosis of sporadic Creutzfeldt-Jakob disease.Profoundly different prion diseases in knock-in mice carrying single PrP codon substitutions associated with human diseases.Genetic cross-interaction between APOE and PRNP in sporadic Alzheimer's and Creutzfeldt-Jakob diseases.Advanced tests for early and accurate diagnosis of Creutzfeldt-Jakob disease.Creutzfeldt-Jakob disease.Genomic and post-genomic analyses of human prion diseasesAccelerated high fidelity prion amplification within and across prion species barriers.Surveillance for Creutzfeldt-Jakob disease in China from 2006 to 2007.Loss of anti-Bax function in Gerstmann-Sträussler-Scheinker syndrome-associated prion protein mutantsA 2cM genome-wide scan of European Holstein cattle affected by classical BSE.Transmission and detection of prions in fecesAltered Ca2+ homeostasis induces Calpain-Cathepsin axis activation in sporadic Creutzfeldt-Jakob diseaseGenetic studies in human prion diseases.Clinical features of genetic Creutzfeldt-Jakob disease with V180I mutation in the prion protein gene.Paradoxical role of prion protein aggregates in redox-iron induced toxicity.A novel form of human disease with a protease-sensitive prion protein and heterozygosity methionine/valine at codon 129: Case report.Endogenous proteolytic cleavage of disease-associated prion protein to produce C2 fragments is strongly cell- and tissue-dependent.Chemical induction of misfolded prion protein conformers in cell culture.PrP conformational transitions alter species preference of a PrP-specific antibody.A comparison of tau and 14-3-3 protein in the diagnosis of Creutzfeldt-Jakob diseaseAbsence of spontaneous disease and comparative prion susceptibility of transgenic mice expressing mutant human prion proteinsTreatable neurological disorders misdiagnosed as Creutzfeldt-Jakob diseaseProtease-sensitive conformers in broad spectrum of distinct PrPSc structures in sporadic Creutzfeldt-Jakob disease are indicator of progression rate.
P2860
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P2860
Sporadic and familial CJD: classification and characterisation.
description
2003 nî lūn-bûn
@nan
2003 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի հունվարին 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
Sporadic and familial CJD: classification and characterisation.
@ast
Sporadic and familial CJD: classification and characterisation.
@en
Sporadic and familial CJD: classification and characterisation.
@nl
type
label
Sporadic and familial CJD: classification and characterisation.
@ast
Sporadic and familial CJD: classification and characterisation.
@en
Sporadic and familial CJD: classification and characterisation.
@nl
prefLabel
Sporadic and familial CJD: classification and characterisation.
@ast
Sporadic and familial CJD: classification and characterisation.
@en
Sporadic and familial CJD: classification and characterisation.
@nl
P2093
P356
P1476
Sporadic and familial CJD: classification and characterisation
@en
P2093
Pierluigi Gambetti
Qingzhong Kong
Wenquan Zou
P304
P356
10.1093/BMB/66.1.213
P577
2003-01-01T00:00:00Z