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Molecular Pathological Classification of Neurodegenerative Diseases: Turning towards Precision MedicineFatal prion disease in a mouse model of genetic E200K Creutzfeldt-Jakob diseaseLoss of Octarepeats in two processed prion pseudogenes in the red squirrel, Sciurus vulgarisRapidly progressive dementia with thalamic degeneration and peculiar cortical prion protein immunoreactivity, but absence of proteinase K resistant PrP: a new disease entity?Brain transcriptional stability upon prion protein-encoding gene invalidation in zygotic or adult mouseTranscriptomic analysis brings new insight into the biological role of the prion protein during mouse embryogenesisPathogenic mutations in the hydrophobic core of the human prion protein can promote structural instability and misfolding.Prion protein and Shadoo are involved in overlapping embryonic pathways and trophoblastic developmentTargeting of prion-infected lymphoid cells to the central nervous system accelerates prion infection.A Fluorescent Oligothiophene-Bis-Triazine ligand interacts with PrP fibrils and detects SDS-resistant oligomers in human prion diseases.A specific role for PRND in goat foetal Leydig cells is suggested by prion family gene expression during gonad development in goats and micePrion diseases as transmissible zoonotic diseases.Cerebral amyloid angiopathy in the aetiology and immunotherapy of Alzheimer disease.Molecular diagnosis of human prion disease.Gene expression resulting from PrPC ablation and PrPC overexpression in murine and cellular models.Mechanisms of prion-induced neurodegeneration.Plasma cholesterol level determines in vivo prion propagationThe diversities of PrP(Sc) distributions and pathologic changes in various brain regions from a Chinese patient with G114V genetic CJD.Urodynamic findings in patients with Creutzfeldt-Jakob disease: a case report.Regional and subtype-dependent miRNA signatures in sporadic Creutzfeldt-Jakob disease are accompanied by alterations in miRNA silencing machinery and biogenesis.Protein astrogliopathies in human neurodegenerative diseases and aging.Pellagra encephalopathy as a differential diagnosis for Creutzfeldt-Jakob disease.Tau pathology in Creutzfeldt-Jakob disease revisited.Neurotoxicity of the Cyanotoxin BMAA Through Axonal Degeneration and Intercellular Spreading.
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P2860
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 09 March 2009
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Molecular pathology of human prion diseases.
@en
Molecular pathology of human prion diseases.
@nl
type
label
Molecular pathology of human prion diseases.
@en
Molecular pathology of human prion diseases.
@nl
prefLabel
Molecular pathology of human prion diseases.
@en
Molecular pathology of human prion diseases.
@nl
P2860
P921
P356
P1476
Molecular pathology of human prion diseases.
@en
P2860
P304
P356
10.3390/IJMS10030976
P407
P5008
P577
2009-03-01T00:00:00Z
2009-03-09T00:00:00Z