Lack of prion infectivity in fixed heart tissue from patients with Creutzfeldt-Jakob disease or amyloid heart disease. - Wikidata - wikimedia - TriplyDB

Lack of prion infectivity in fixed heart tissue from patients with Creutzfeldt-Jakob disease or amyloid heart disease.

Lack of prion infectivity in fixed heart tissue from patients with Creutzfeldt-Jakob disease or amyloid heart disease.

http://www.wikidata.org/entity/Q37123552

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Detection and Quantification of CWD Prions in Fixed Paraffin Embedded Tissues by Real-Time Quaking-Induced Conversion.Familial human prion diseases associated with prion protein mutations Y226X and G131V are transmissible to transgenic mice expressing human prion protein.

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P2860

Lack of prion infectivity in fixed heart tissue from patients with Creutzfeldt-Jakob disease or amyloid heart disease.

http://www.wikidata.org/entity/Q37123552

description

article científic

@ca

article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 19 June 2013

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Lack of prion infectivity in f ...... ease or amyloid heart disease.

@en

Lack of prion infectivity in f ...... ease or amyloid heart disease.

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type

label

Lack of prion infectivity in f ...... ease or amyloid heart disease.

@en

Lack of prion infectivity in f ...... ease or amyloid heart disease.

@nl

prefLabel

Lack of prion infectivity in f ...... ease or amyloid heart disease.

@en

Lack of prion infectivity in f ...... ease or amyloid heart disease.

@nl

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Journal of Virology

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Lack of prion infectivity in f ...... ease or amyloid heart disease.

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Anne E Ward

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

Justin T Cruite

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Laura Solforosi

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Matthew Trifilo

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Michael B A Oldstone

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R Anthony Williamson

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Sherman A McCall

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Suzette A Priola

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Young Pyo Choi

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P2860

Transmission of chronic wasting disease identifies a prion strain causing cachexia and heart infection in hamsters

Anchorless prion protein results in infectious amyloid disease without clinical scrapie

Changing a single amino acid in the N-terminus of murine PrP alters TSE incubation time across three species barriers.

Prion protein amyloidosis with divergent phenotype associated with two novel nonsense mutations in PRNP.

Susceptibilities of nonhuman primates to chronic wasting disease.

Entry versus blockade of brain infection following oral or intraperitoneal scrapie administration: role of prion protein expression in peripheral nerves and spleen.

Measuring prions causing bovine spongiform encephalopathy or chronic wasting disease by immunoassays and transgenic mice.

Defining sporadic Creutzfeldt-Jakob disease strains and their transmission properties.

CDR walking mutagenesis for the affinity maturation of a potent human anti-HIV-1 antibody into the picomolar range.

PrPTSE distribution in a primate model of variant, sporadic, and iatrogenic Creutzfeldt-Jakob disease.

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9501-9510

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scholarly article

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10.1128/JVI.00692-13

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17

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2013-06-19T00:00:00Z

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23785217

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Prion protein family

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3754135

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