Fatal familial insomnia and familial Creutzfeldt-Jakob disease: different prion proteins determined by a DNA polymorphism.
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Transmissible Spongiform Encephalopathies Affecting HumansPrionsStrain-specified relative conformational stability of the scrapie prion proteinHuman prion diseases: surgical lessons learned from iatrogenic prion transmissionNanopore analysis of wild-type and mutant prion protein (PrP(C)): single molecule discrimination and PrP(C) kinetics.Prionic diseases.Regulating factors of PrP glycosylation in Creutzfeldt-Jakob disease--implications for the dissemination and the diagnosis of human prion strains.Cellular biology of prion diseases.A novel form of human disease with a protease-sensitive prion protein and heterozygosity methionine/valine at codon 129: Case report.Types and Strains: Their Essential Role in Understanding Protein Aggregation in Neurodegenerative Diseases.A comparison of tau and 14-3-3 protein in the diagnosis of Creutzfeldt-Jakob diseaseIntracerebral distribution of the abnormal isoform of the prion protein in sporadic Creutzfeldt-Jakob disease and fatal insomnia.Prion protein genes and prion diseases: studies in transgenic mice.Protease-sensitive conformers in broad spectrum of distinct PrPSc structures in sporadic Creutzfeldt-Jakob disease are indicator of progression rate.Human 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.Prion diseases: epidemiology in man.Molecular biology and pathology of prion strains in sporadic human prion diseases.Peripheral tissue involvement in sporadic, iatrogenic, and variant Creutzfeldt-Jakob disease: an immunohistochemical, quantitative, and biochemical study.Creutzfeldt-Jakob disease (CJD) with a mutation at codon 148 of prion protein gene: relationship with sporadic CJD.Evidence that the penetrance of mutations at the RP11 locus causing dominant retinitis pigmentosa is influenced by a gene linked to the homologous RP11 allele.Inherited prion diseases.Transgenic fatal familial insomnia mice indicate prion infectivity-independent mechanisms of pathogenesis and phenotypic expression of disease.Penetrance and expressivity in the molecular age.Proposed three-dimensional structure for the cellular prion proteinEffect of the E200K mutation on prion protein metabolism. Comparative study of a cell model and human brain.Distinct pathological phenotypes of Creutzfeldt-Jakob disease in recipients of prion-contaminated growth hormone.Requirements for mutant and wild-type prion protein misfolding in vitro.Molecular pathogenesis of sporadic prion diseases in man.Contributions of neuronal prion protein on sleep recovery and stress response following sleep deprivation.Different patterns of truncated prion protein fragments correlate with distinct phenotypes in P102L Gerstmann-Sträussler-Scheinker disease.Mouse-adapted ovine scrapie prion strains are characterized by different conformers of PrPSc.Propagation of prion strains through specific conformers of the prion proteinProtease-sensitive prions with 144-bp insertion mutationsPrion proteins: a biological role beyond prion diseases.Consensus classification of human prion disease histotypes allows reliable identification of molecular subtypes: an inter-rater study among surveillance centres in Europe and USAPrions: Beyond a Single Protein.Failure to detect the presence of prions in the uterine and gestational tissues from a Gravida with Creutzfeldt-Jakob disease.Phosphorylation of prion protein at serine 43 induces prion protein conformational changePolyvariant mutant cystic fibrosis transmembrane conductance regulator genes. The polymorphic (Tg)m locus explains the partial penetrance of the T5 polymorphism as a disease mutation.
P2860
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P2860
Fatal familial insomnia and familial Creutzfeldt-Jakob disease: different prion proteins determined by a DNA polymorphism.
description
1994 nî lūn-bûn
@nan
1994 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
1994 թվականի մարտին հրատարակված գիտական հոդված
@hy
1994年の論文
@ja
1994年論文
@yue
1994年論文
@zh-hant
1994年論文
@zh-hk
1994年論文
@zh-mo
1994年論文
@zh-tw
1994年论文
@wuu
name
Fatal familial insomnia and fa ...... ermined by a DNA polymorphism.
@ast
Fatal familial insomnia and fa ...... ermined by a DNA polymorphism.
@en
type
label
Fatal familial insomnia and fa ...... ermined by a DNA polymorphism.
@ast
Fatal familial insomnia and fa ...... ermined by a DNA polymorphism.
@en
prefLabel
Fatal familial insomnia and fa ...... ermined by a DNA polymorphism.
@ast
Fatal familial insomnia and fa ...... ermined by a DNA polymorphism.
@en
P2093
P2860
P356
P1476
Fatal familial insomnia and fa ...... ermined by a DNA polymorphism.
@en
P2093
P Cortelli
P Montagna
R B Petersen
P2860
P304
P356
10.1073/PNAS.91.7.2839
P407
P577
1994-03-01T00:00:00Z