Prions in the urine of patients with variant Creutzfeldt-Jakob disease. - Wikidata - awgldk - TriplyDB

Prions in the urine of patients with variant Creutzfeldt-Jakob disease.

Prions in the urine of patients with variant Creutzfeldt-Jakob disease.

http://www.wikidata.org/entity/Q34173236

about

Changes in retinal function and morphology are early clinical signs of disease in cattle with bovine spongiform encephalopathy The Priority position paper: Protecting Europe's food chain from prions Detection of prion seeding activity in the olfactory mucosa of patients with Fatal Familial Insomnia Advanced tests for early and accurate diagnosis of Creutzfeldt-Jakob disease.Distribution and Quantitative Estimates of Variant Creutzfeldt-Jakob Disease Prions in Tissues of Clinical and Asymptomatic Patients Grass plants bind, retain, uptake, and transport infectious prions.Recent US Case of Variant Creutzfeldt-Jakob Disease-Global Implications.2005 Donor Eligibility Requirements: Unintended Consequences for Stem Cell Development.Sialylation of the prion protein glycans controls prion replication rate and glycoform ratio Preclinical detection of infectivity and disease-specific PrP in blood throughout the incubation period of prion disease Role of the biomarkers for the diagnosis of Creutzfeldt-Jakob disease.Guinea Pig Prion Protein Supports Rapid Propagation of Bovine Spongiform Encephalopathy and Variant Creutzfeldt-Jakob Disease Prions.Proteomics applications in prion biology and structure.The transmissible spongiform encephalopathies of livestock.Sporadic and Infectious Human Prion Diseases.Insights from Therapeutic Studies for PrP Prion Disease.Detection of prions in the plasma of presymptomatic and symptomatic patients with variant Creutzfeldt-Jakob disease.Region-specific protein misfolding cyclic amplification reproduces brain tropism of prion strains.Self-propagating, protease-resistant, recombinant prion protein conformers with or without in vivo pathogenicity.CNS infections in 2014: Guns, germs, and will.Detection of prions in blood from patients with variant Creutzfeldt-Jakob disease.Isolation of Exosomes and Microvesicles from Cell Culture Systems to Study Prion Transmission.Diagnosing Sporadic Creutzfeldt-Jakob Disease by the Detection of Abnormal Prion Protein in Patient Urine.Quantitative Real-Time Quaking-Induced Conversion Allows Monitoring of Disease-Modifying Therapy in the Urine of Prion-Infected Mice.Creutzfeldt-Jakob disease: recent developments.Recombinant PrP and Its Contribution to Research on Transmissible Spongiform Encephalopathies.Detection of Prions in Blood of Cervids at the Asymptomatic Stage of Chronic Wasting Disease.Formation and properties of amyloid fibrils of prion protein.Translational Research in Alzheimer's and Prion Diseases.Ante-mortem detection of chronic wasting disease in recto-anal mucosa-associated lymphoid tissues from elk (Cervus elaphus nelsoni) using real-time quaking-induced conversion (RT-QuIC) assay: A blinded collaborative study.Problems with precaution: the transfusion medicine experience.Applications of the real-time quaking-induced conversion assay in diagnosis, prion strain-typing, drug pre-screening and other amyloidopathies.Generation of novel neuroinvasive prions following intravenous challenge.Rapid amplification of prions from variant Creutzfeldt-Jakob disease cerebrospinal fluid.Diagnosis of Methionine/Valine Variant Creutzfeldt-Jakob Disease by Protein Misfolding Cyclic Amplification.Prions activate a p38 MAPK synaptotoxic signaling pathway

P2860

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P2860

Prions in the urine of patients with variant Creutzfeldt-Jakob disease.

http://www.wikidata.org/entity/Q34173236

description

2014 nî lūn-bûn

@nan

2014 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի օգոստոսին հրատարակված գիտական հոդված

@hy

2014年の論文

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2014年論文

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2014年論文

@zh-hant

2014年論文

@zh-hk

2014年論文

@zh-mo

2014年論文

@zh-tw

2014年论文

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name

Prions in the urine of patients with variant Creutzfeldt-Jakob disease.

@ast

Prions in the urine of patients with variant Creutzfeldt-Jakob disease.

@en

Prions in the urine of patients with variant Creutzfeldt-Jakob disease.

@nl

type

label

Prions in the urine of patients with variant Creutzfeldt-Jakob disease.

@ast

Prions in the urine of patients with variant Creutzfeldt-Jakob disease.

@en

Prions in the urine of patients with variant Creutzfeldt-Jakob disease.

@nl

prefLabel

Prions in the urine of patients with variant Creutzfeldt-Jakob disease.

@ast

Prions in the urine of patients with variant Creutzfeldt-Jakob disease.

@en

Prions in the urine of patients with variant Creutzfeldt-Jakob disease.

@nl

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P1433

The New England Journal of Medicine

P1476

Prions in the urine of patients with variant Creutzfeldt-Jakob disease.

@en

P2093

Claudio Soto

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Jean-Philippe Brandel

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Kyung-Won Park

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Pierluigi Gambetti

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Richard Knight

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Silvia Suardi

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Silvio Notari

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Stéphane Haïk

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P2860

Prion hypothesis: the end of the controversy?

Prevalent abnormal prion protein in human appendixes after bovine spongiform encephalopathy epizootic: large scale survey

The physical relationship between infectivity and prion protein aggregates is strain-dependent

Multiorgan detection and characterization of protease-resistant prion protein in a case of variant CJD examined in the United States.

Variant Creutzfeldt-Jakob disease.

Estimating prion concentration in fluids and tissues by quantitative PMCA.

Protein misfolding cyclic amplification of infectious prions.

Iatrogenic Creutzfeldt-Jakob disease at the millennium.

Postmortem findings in a case of variant Creutzfeldt-Jakob disease treated with intraventricular pentosan polysulfate.

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530-539

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scholarly article

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10.1056/NEJMOA1404401

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P433

6

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371

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Luis Concha-Marambio

Emanuela Maderna

Fabrizio Tagliavini

Marcella Catania

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2014-08-01T00:00:00Z

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264644271

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25099577

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Prion protein family

P932

4162740

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