Molecular biology and pathology of prion strains in sporadic human prion diseases. - Wikidata - wikimedia - TriplyDB

Molecular biology and pathology of prion strains in sporadic human prion diseases.

Molecular biology and pathology of prion strains in sporadic human prion diseases.

http://www.wikidata.org/entity/Q34802620

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Is tau ready for admission to the prion club?An overview of human prion diseases Neurodegenerative diseases: expanding the prion concept Biological and biochemical characterization of mice expressing prion protein devoid of the octapeptide repeat region after infection with prions Critical significance of the region between Helix 1 and 2 for efficient dominant-negative inhibition by conversion-incompetent prion protein Human prion diseases: surgical lessons learned from iatrogenic prion transmission Transmission characteristics of variably protease-sensitive prionopathy.Mathematical models for the diffusion magnetic resonance signal abnormality in patients with prion diseases.Structural determinants of phenotypic diversity and replication rate of human prions.Recent US Case of Variant Creutzfeldt-Jakob Disease-Global Implications.Biochemical classification of tauopathies by immunoblot, protein sequence and mass spectrometric analyses of sarkosyl-insoluble and trypsin-resistant tau Contributions of the Prion Protein Sequence, Strain, and Environment to the Species Barrier.Creationism and evolutionism in prions Identification of misfolded proteins in body fluids for the diagnosis of prion diseases.Prions: Beyond a Single Protein.Molecular barriers to zoonotic transmission of prions.Novel strain properties distinguishing sporadic prion diseases sharing prion protein genotype and prion type.A platform for discovery: The University of Pennsylvania Integrated Neurodegenerative Disease Biobank.Sequential distribution of pTDP-43 pathology in behavioral variant frontotemporal dementia (bvFTD).Polymorphism at 129 dictates metastable conformations of the human prion protein N-terminal β-sheet.Biochemical and strain properties of CJD prions: complexity versus simplicity.Human prion diseases: molecular, cellular and population biology.Mechanisms of prion-induced neurodegeneration.Influence of the blood-CSF-barrier function on S100B in neurodegenerative diseases.Comparison of nanofiltration efficacy in reducing infectivity of centrifuged versus ultracentrifuged 263K scrapie-infected brain homogenates in "spiked" albumin solutions.MM2-thalamic Creutzfeldt-Jakob disease: neuropathological, biochemical and transmission studies identify a distinctive prion strain.Prion seeding activity and infectivity in skin samples from patients with sporadic Creutzfeldt-Jakob disease.Translational Research in Alzheimer's and Prion Diseases.Fluorodeoxyglucose Positron Emission Tomography (FDG-PET) Correlation of Histopathology and MRI in Prion Disease.Epidemiological genetics and meta-analysis of a polymorphism at codon 129 of the PRNP gene in Alzheimer's disease in Brazil.

P2860

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P2860

Molecular biology and pathology of prion strains in sporadic human prion diseases.

http://www.wikidata.org/entity/Q34802620

description

2010 nî lūn-bûn

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2010 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

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2010 թվականի նոյեմբերին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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name

Molecular biology and pathology of prion strains in sporadic human prion diseases.

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Molecular biology and pathology of prion strains in sporadic human prion diseases.

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Molecular biology and pathology of prion strains in sporadic human prion diseases.

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Molecular biology and pathology of prion strains in sporadic human prion diseases.

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Molecular biology and pathology of prion strains in sporadic human prion diseases.

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Molecular biology and pathology of prion strains in sporadic human prion diseases.

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Molecular biology and pathology of prion strains in sporadic human prion diseases.

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Molecular biology and pathology of prion strains in sporadic human prion diseases.

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Molecular biology and pathology of prion strains in sporadic human prion diseases.

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Acta Neuropathologica

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Molecular biology and pathology of prion strains in sporadic human prion diseases

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P2093

Pierluigi Gambetti

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Qingzhong Kong

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Silvio Notari

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Wen-Quan Zou

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Witold K Surewicz

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P2860

Conformational diversity in prion protein variants influences intermolecular beta-sheet formation

Darwinian evolution of prions in cell culture

Generating a prion with bacterially expressed recombinant prion protein.

Recombinant prion protein induces a new transmissible prion disease in wild-type animals.

A novel human disease with abnormal prion protein sensitive to protease

Formation of native prions from minimal components in vitro

Analysis of prion strains by PrPSc profiling in sporadic Creutzfeldt-Jakob disease.

Efficient transmission and characterization of Creutzfeldt-Jakob disease strains in bank voles.

Crystallographic Studies of Prion Protein (PrP) Segments Suggest How Structural Changes Encoded by Polymorphism at Residue 129 Modulate Susceptibility to Human Prion Disease

Fatal familial insomnia, a prion disease with a mutation at codon 178 of the prion protein gene

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10.1007/S00401-010-0761-3

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1

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121

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Prion protein family

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