From prion diseases to prion-like propagation mechanisms of neurodegenerative diseases. - Wikidata - awgldk - TriplyDB

From prion diseases to prion-like propagation mechanisms of neurodegenerative diseases.

From prion diseases to prion-like propagation mechanisms of neurodegenerative diseases.

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Epigenetics and inheritance of phenotype variation in livestock Human prion diseases: surgical lessons learned from iatrogenic prion transmission Types and Strains: Their Essential Role in Understanding Protein Aggregation in Neurodegenerative Diseases.Proaggregant nuclear factor(s) trigger rapid formation of α-synuclein aggregates in apoptotic neurons.Plasma Exosomes Spread and Cluster Around β-Amyloid Plaques in an Animal Model of Alzheimer's Disease.Impaired endo-lysosomal membrane integrity accelerates the seeding progression of α-synuclein aggregates.Discovery of Therapeutic Approaches for Polyglutamine Diseases: A Summary of Recent Efforts.Potential Pathways of Abnormal Tau and α-Synuclein Dissemination in Sporadic Alzheimer's and Parkinson's Diseases.Low doses of bioherbicide favour prion aggregation and propagation in vivo.Low-volume goat milk transmission of classical scrapie to lambs and goat kids

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From prion diseases to prion-like propagation mechanisms of neurodegenerative diseases.

http://www.wikidata.org/entity/Q38162179

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article científic

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artikel ilmiah

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From prion diseases to prion-like propagation mechanisms of neurodegenerative diseases.

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type

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From prion diseases to prion-like propagation mechanisms of neurodegenerative diseases.

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From prion diseases to prion-like propagation mechanisms of neurodegenerative diseases.

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International Journal of Cell Biology

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From prion diseases to prion-like propagation mechanisms of neurodegenerative diseases

@en

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Isabelle Acquatella-Tran Van Ba

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Conversion of alpha-helices into beta-sheets features in the formation of the scrapie prion proteins

Isolation of phosphatidylethanolamine as a solitary cofactor for prion formation in the absence of nucleic acids

Generating a prion with bacterially expressed recombinant prion protein.

Cofactor molecules maintain infectious conformation and restrict strain properties in purified prions

Spontaneous generation of prion infectivity in fatal familial insomnia knockin mice

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

Transmission and spreading of tauopathy in transgenic mouse brain

Cytoplasmic penetration and persistent infection of mammalian cells by polyglutamine aggregates

Genesis of mammalian prions: from non-infectious amyloid fibrils to a transmissible prion disease

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975832

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scholarly article

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10.1155/2013/975832

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2013

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Thibaut Imberdis

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2013-10-10T00:00:00Z

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258503870

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24222767

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neurodegeneration

Prion protein family

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3810426

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