Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease. - Wikidata - wikimedia - TriplyDB

Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease.

Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease.

http://www.wikidata.org/entity/Q42631333

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Sporadic fatal insomnia in a young woman: a diagnostic challenge: case report Prions A novel human disease with abnormal prion protein sensitive to protease Kuru prions and sporadic Creutzfeldt-Jakob disease prions have equivalent transmission properties in transgenic and wild-type mice The mechanism of prion strain propagation Analysis of prion strains by PrPSc profiling in sporadic Creutzfeldt-Jakob disease.Epidemiological characteristics of human prion diseases Molecular Pathological Classification of Neurodegenerative Diseases: Turning towards Precision Medicine Insoluble cellular prion protein and its association with prion and Alzheimer diseases Distinct α-synuclein strains differentially promote tau inclusions in neurons Strain-specified relative conformational stability of the scrapie prion protein Beyond PrP9res) type 1/type 2 dichotomy in Creutzfeldt-Jakob disease Small ruminant nor98 prions share biochemical features with human gerstmann-sträussler-scheinker disease and variably protease-sensitive prionopathy Racial and ethnic differences in individuals with sporadic Creutzfeldt-jakob disease in the United States of America Charge neutralization of the central lysine cluster in prion protein (PrP) promotes PrP(Sc)-like folding of recombinant PrP amyloids.Rapidly progressive dementia with thalamic degeneration and peculiar cortical prion protein immunoreactivity, but absence of proteinase K resistant PrP: a new disease entity?Getting a grip on prions: oligomers, amyloids, and pathological membrane interactions.Role of magnetic resonance imaging, cerebrospinal fluid, and electroencephalogram in diagnosis of sporadic Creutzfeldt-Jakob disease.Clinical features of variant Creutzfeldt-Jakob disease.Clinical diagnosis and differential diagnosis of CJD and vCJD. With special emphasis on laboratory tests.Rationale for diagnosing human prion disease.Potent inhibition of scrapie prion replication in cultured cells by bis-acridines.Brain-derived proteins in the CSF: do they correlate with brain pathology in CJD?Host PrP glycosylation: a major factor determining the outcome of prion infection.Regulating factors of PrP glycosylation in Creutzfeldt-Jakob disease--implications for the dissemination and the diagnosis of human prion strains.Biochemical characterization of prion strains in bank voles Gerstmann-Sträussler-Scheinker disease subtypes efficiently transmit in bank voles as genuine prion diseases.Cellular biology of prion diseases.Clinical features of genetic Creutzfeldt-Jakob disease with V180I mutation in the prion protein gene.A new method for the characterization of strain-specific conformational stability of protease-sensitive and protease-resistant PrPSc.Filamentous white matter prion protein deposition is a distinctive feature of multiple inherited prion diseases Familial Creutzfeldt-Jakob disease with a V180I mutation: comparative analysis with pathological findings and diffusion-weighted images High-resolution structure of infectious prion protein: the final frontier Experimental verification of a traceback phenomenon in prion infection.A novel form of human disease with a protease-sensitive prion protein and heterozygosity methionine/valine at codon 129: Case report.Novel antibody-lectin enzyme-linked immunosorbent assay that distinguishes prion proteins in sporadic and variant cases of Creutzfeldt-Jakob disease.Gene expression profiling of brains from bovine spongiform encephalopathy (BSE)-infected cynomolgus macaques.Types and Strains: Their Essential Role in Understanding Protein Aggregation in Neurodegenerative Diseases.Variant Creutzfeldt-Jakob disease: immunocytochemical studies and image analysis.Intracerebral distribution of the abnormal isoform of the prion protein in sporadic Creutzfeldt-Jakob disease and fatal insomnia.

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P2860

Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease.

http://www.wikidata.org/entity/Q42631333

description

1996 nî lūn-bûn

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1996年論文

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1996年論文

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1996年论文

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1996年论文

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1996年论文

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name

Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease.

@en

Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease.

@nl

type

label

Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease.

@en

Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease.

@nl

prefLabel

Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease.

@en

Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease.

@nl

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Annals of Neurology

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Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease.

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Capellari S

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Castellani R

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Chen SG

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Farlow M

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Gambetti P

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Young K

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P2860

Proteinase-resistant prion protein accumulation in Syrian hamster brain correlates with regional pathology and scrapie infectivity.

Clinical significance of types of cerebellar amyloid plaques in human spongiform encephalopathies.

Iatrogenic Creutzfeldt-Jakob disease: an example of the interplay between ancient genes and modern medicine.

Ataxic Creutzfeldt-Jakob disease: diagnostic techniques and neuropathologic observations in early disease.

The ataxic form of Creutzfeldt-Jakob disease.

Transmissible spongiform encephalopathy (Creutzfeldt-Jakob disease). Atypical clinical and pathological findings.

Molecular genetics of prion diseases in France. French Research Group on Epidemiology of Human Spongiform Encephalopathies.

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6

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39

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