Review: Creutzfeldt-Jakob disease: prion protein type, disease phenotype and agent strain.
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The Unfolded Protein Response and the Role of Protein Disulfide Isomerase in NeurodegenerationSelf-propagation of pathogenic protein aggregates in neurodegenerative diseasesRapidly progressive dementia with thalamic degeneration and peculiar cortical prion protein immunoreactivity, but absence of proteinase K resistant PrP: a new disease entity?Targeted discovery and validation of plasma biomarkers of Parkinson's disease.Prion Protein-Hemin Interaction Upregulates Hemoglobin Synthesis: Implications for Cerebral Hemorrhage and Sporadic Creutzfeldt-Jakob DiseaseTypes and Strains: Their Essential Role in Understanding Protein Aggregation in Neurodegenerative Diseases.The Features of Genetic Prion Diseases Based on Chinese Surveillance Program.The Distribution of Prion Protein Allotypes Differs Between Sporadic and Iatrogenic Creutzfeldt-Jakob Disease PatientsCorruption and spread of pathogenic proteins in neurodegenerative diseases.Amyloidosis in Alzheimer's Disease: The Toxicity of Amyloid Beta (A β ), Mechanisms of Its Accumulation and Implications of Medicinal Plants for TherapyAtypical and classical forms of the disease-associated state of the prion protein exhibit distinct neuronal tropism, deposition patterns, and lesion profiles.Laboratory activities involving transmissible spongiform encephalopathy causing agents: risk assessment and biosafety recommendations in Belgium.Management of notifications of donors with Creutzfeldt-Jakob disease (post-donation information).Role of water in protein folding, oligomerization, amyloidosis and miniprotein.Proteomics applications in prion biology and structure.The prion-ZIP connection: From cousins to partners in iron uptake.Sporadic and Infectious Human Prion Diseases.Special needs populations: perioperative care of the patient with creutzfeldt-jakob disease.PrP mRNA and protein expression in brain and PrP(c) in CSF in Creutzfeldt-Jakob disease MM1 and VV2.Epidemiological genetics and meta-analysis of a polymorphism at codon 129 of the PRNP gene in Alzheimer's disease in Brazil.Rapid amplification of prions from variant Creutzfeldt-Jakob disease cerebrospinal fluid.Two-photon absorption of polyfluorene aggregates stabilized by insulin amyloid fibrils
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Review: Creutzfeldt-Jakob disease: prion protein type, disease phenotype and agent strain.
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article científic
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article scientifique
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articol științific
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articolo scientifico
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artigo científico
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artigo científico
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artigo científico
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artículo científico
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Review: Creutzfeldt-Jakob dise ...... se phenotype and agent strain.
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Review: Creutzfeldt-Jakob dise ...... se phenotype and agent strain.
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type
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Review: Creutzfeldt-Jakob dise ...... se phenotype and agent strain.
@en
Review: Creutzfeldt-Jakob dise ...... se phenotype and agent strain.
@nl
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Review: Creutzfeldt-Jakob dise ...... se phenotype and agent strain.
@en
Review: Creutzfeldt-Jakob dise ...... se phenotype and agent strain.
@nl
P2860
P1476
Review: Creutzfeldt-Jakob disease: prion protein type, disease phenotype and agent strain
@en
P2093
J W Ironside
P2860
P304
P356
10.1111/J.1365-2990.2012.01265.X
P577
2012-06-01T00:00:00Z