Gerstmann-Sträussler-Scheinker disease and "anchorless prion protein" mice share prion conformational properties diverging from sporadic Creutzfeldt-Jakob disease. - Wikidata - awgldk - TriplyDB

Gerstmann-Sträussler-Scheinker disease and "anchorless prion protein" mice share prion conformational properties diverging from sporadic Creutzfeldt-Jakob disease.

Gerstmann-Sträussler-Scheinker disease and "anchorless prion protein" mice share prion conformational properties diverging from sporadic Creutzfeldt-Jakob disease.

http://www.wikidata.org/entity/Q37596331

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Prion Strain Characterization of a Novel Subtype of Creutzfeldt-Jakob Disease.C-Terminal-Deleted Prion Protein Fragment Is a Major Accumulated Component of Systemic PrP Deposits in Hereditary Prion Disease With a 2-Bp (CT) Deletion in PRNP Codon 178.

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P2860

Gerstmann-Sträussler-Scheinker disease and "anchorless prion protein" mice share prion conformational properties diverging from sporadic Creutzfeldt-Jakob disease.

http://www.wikidata.org/entity/Q37596331

description

article científic

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article scientifique

@fr

articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 07 January 2014

@en

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

Gerstmann-Sträussler-Scheinker ...... dic Creutzfeldt-Jakob disease.

@en

Gerstmann-Sträussler-Scheinker ...... dic Creutzfeldt-Jakob disease.

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type

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Gerstmann-Sträussler-Scheinker ...... dic Creutzfeldt-Jakob disease.

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Gerstmann-Sträussler-Scheinker ...... dic Creutzfeldt-Jakob disease.

@nl

prefLabel

Gerstmann-Sträussler-Scheinker ...... dic Creutzfeldt-Jakob disease.

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Gerstmann-Sträussler-Scheinker ...... dic Creutzfeldt-Jakob disease.

@nl

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JBC.M113.531335

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Journal of Biological Chemistry

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Gerstmann-Sträussler-Scheinker ...... dic Creutzfeldt-Jakob disease.

@en

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Bernardino Ghetti

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

Emiliana Brocchi

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Ilaria Barbieri

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Kimberly Meade-White

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Sergio Ferrari

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P2860

Anchorless prion protein results in infectious amyloid disease without clinical scrapie

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

Getting a grip on prions: oligomers, amyloids, and pathological membrane interactions.

Mapping the prion protein using recombinant antibodies.

Vascular variant of prion protein cerebral amyloidosis with tau-positive neurofibrillary tangles: the phenotype of the stop codon 145 mutation in PRNP.

Characterization of the prion protein in human urine.

Structural organization of mammalian prions as probed by limited proteolysis.

Familial prion disease with Alzheimer disease-like tau pathology and clinical phenotype.

Spontaneous generation of anchorless prions in transgenic mice.

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4870-4881

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scholarly article

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10.1074/JBC.M113.531335

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8

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289

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Gianluigi Zanusso

Salvatore Monaco

Michele Fiorini

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2014-01-07T00:00:00Z

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24398683

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Prion protein family

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3931049

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