A novel human disease with abnormal prion protein sensitive to protease - Wikidata - wikimedia - TriplyDB

A novel human disease with abnormal prion protein sensitive to protease

A novel human disease with abnormal prion protein sensitive to protease

http://www.wikidata.org/entity/Q24648865

about

Prions, prion-like prionoids, and neurodegenerative disorders Molecular Pathological Classification of Neurodegenerative Diseases: Turning towards Precision Medicine An overview of human prion diseases Insoluble cellular prion protein and its association with prion and Alzheimer diseases Prions in variably protease-sensitive prionopathy: an update De novo generation of prion strains In vivo generation of neurotoxic prion protein: role for hsp70 in accumulation of misfolded isoforms Small ruminant nor98 prions share biochemical features with human gerstmann-sträussler-scheinker disease and variably protease-sensitive prionopathy Styryl-based and tricyclic compounds as potential anti-prion agents Isolation of proteinase K-sensitive prions using pronase E and phosphotungstic acid The Priority position paper: Protecting Europe's food chain from prions Human prion diseases: surgical lessons learned from iatrogenic prion transmission Rapidly progressive dementia with thalamic degeneration and peculiar cortical prion protein immunoreactivity, but absence of proteinase K resistant PrP: a new disease entity?Human prion diseases in the Netherlands (1998-2009): clinical, genetic and molecular aspects.Role of magnetic resonance imaging, cerebrospinal fluid, and electroencephalogram in diagnosis of sporadic Creutzfeldt-Jakob disease.Prionic diseases.Biochemical characterization of prion strains in bank voles Evaluation of the possible transmission of BSE and scrapie to gilthead sea bream (Sparus aurata)Deficient high-affinity binding of Pittsburgh compound B in a case of Alzheimer's disease Immunopurification of pathological prion protein aggregates Human prion diseases in the United States.Multiorgan detection and characterization of protease-resistant prion protein in a case of variant CJD examined in the United States.Protease-sensitive synthetic prions.Altered Ca2+ homeostasis induces Calpain-Cathepsin axis activation in sporadic Creutzfeldt-Jakob disease A new method for the characterization of strain-specific conformational stability of protease-sensitive and protease-resistant PrPSc.Application of "omics" to prion biomarker discovery.A novel form of human disease with a protease-sensitive prion protein and heterozygosity methionine/valine at codon 129: Case report.Chemical induction of misfolded prion protein conformers in cell culture.PrP conformational transitions alter species preference of a PrP-specific antibody.Redox control of prion and disease pathogenesis.Protease-sensitive conformers in broad spectrum of distinct PrPSc structures in sporadic Creutzfeldt-Jakob disease are indicator of progression rate.Creutzfeldt-Jakob disease surveillance in Argentina, 1997-2008.Report of the Working Group 'Overall Blood Supply Strategy with Regard to Variant Creutzfeldt-Jakob Disease (vCJD)': Statement on the Development and Implementation of Test Systems Suitable for the Screening of Blood Donors for vCJD - Dated Septembe Variably protease-sensitive prionopathy: a new sporadic disease of the prion protein.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.Concurrent variably protease-sensitive prionopathy and amyotrophic lateral sclerosis.Allelic origin of protease-sensitive and protease-resistant prion protein isoforms in Gerstmann-Sträussler-Scheinker disease with the P102L mutation.Distinct stability states of disease-associated human prion protein identified by conformation-dependent immunoassay Small protease sensitive oligomers of PrPSc in distinct human prions determine conversion rate of PrP(C).The prion protein protease sensitivity, stability and seeding activity in variably protease sensitive prionopathy brain tissue suggests molecular overlaps with sporadic Creutzfeldt-Jakob disease.

P2860

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P2860

A novel human disease with abnormal prion protein sensitive to protease

http://www.wikidata.org/entity/Q24648865

description

2008 nî lūn-bûn

@nan

2008 թուականի Յունիսին հրատարակուած գիտական յօդուած

@hyw

2008 թվականի հունիսին հրատարակված գիտական հոդված

@hy

2008年の論文

@ja

2008年論文

@yue

2008年論文

@zh-hant

2008年論文

@zh-hk

2008年論文

@zh-mo

2008年論文

@zh-tw

2008年论文

@wuu

name

A novel human disease with abnormal prion protein sensitive to protease

@ast

A novel human disease with abnormal prion protein sensitive to protease

@en

A novel human disease with abnormal prion protein sensitive to protease

@nl

type

label

A novel human disease with abnormal prion protein sensitive to protease

@ast

A novel human disease with abnormal prion protein sensitive to protease

@en

A novel human disease with abnormal prion protein sensitive to protease

@nl

prefLabel

A novel human disease with abnormal prion protein sensitive to protease

@ast

A novel human disease with abnormal prion protein sensitive to protease

@en

A novel human disease with abnormal prion protein sensitive to protease

@nl

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P1433

Annals of Neurology

P1476

A novel human disease with abnormal prion protein sensitive to protease

@en

P2093

Amer Alshekhlee

http://www.w3.org/2001/XMLSchema#string

Carrie Harris

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Christine M Hulette

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Claudio Soto

http://www.w3.org/2001/XMLSchema#string

D Gonzalez-Romero

http://www.w3.org/2001/XMLSchema#string

James A Mastrianni

http://www.w3.org/2001/XMLSchema#string

Jue Yuan

http://www.w3.org/2001/XMLSchema#string

Karen Marder

http://www.w3.org/2001/XMLSchema#string

Lawrence B Schonberger

http://www.w3.org/2001/XMLSchema#string

Mark Cohen

http://www.w3.org/2001/XMLSchema#string

P2860

Deciphering the genetic basis of Alzheimer's disease

Exogenous induction of cerebral beta-amyloidogenesis is governed by agent and host

Eight prion strains have PrP(Sc) molecules with different conformations

Distinct PrP properties suggest the molecular basis of strain variation in transmissible mink encephalopathy.

Transmissible and genetic prion diseases share a common pathway of neurodegeneration.

Diagnosis of human prion disease

Sporadic and familial CJD: classification and characterisation.

A transmembrane form of the prion protein in neurodegenerative disease.

Creutzfeldt-Jakob disease (CJD) with a mutation at codon 148 of prion protein gene: relationship with sporadic CJD.

Comparison of four staining methods on the detection of neuritic plaques.

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697-708

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scholarly article

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2527421

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10.1002/ANA.21420

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P433

6

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63

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Dennis W. Dickson

Thomas Wisniewski

Marcelo A Barria

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2008-06-01T00:00:00Z

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5284262

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18571782

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Prion protein family

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2767200

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