Generalization of the prion hypothesis to other neurodegenerative diseases: an imperfect fit.
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Role of exosomes/microvesicles in the nervous system and use in emerging therapiesThe prion hypothesis in Parkinson's disease: Braak to the futureExosomes: mediators of neurodegeneration, neuroprotection and therapeuticsProteotoxicity: an underappreciated pathology in cardiac diseaseSystematic review of potential health risks posed by pharmaceutical, occupational and consumer exposures to metallic and nanoscale aluminum, aluminum oxides, aluminum hydroxide and its soluble saltsAberrant localization of FUS and TDP43 is associated with misfolding of SOD1 in amyotrophic lateral sclerosisProtease-resistant SOD1 aggregates in amyotrophic lateral sclerosis demonstrated by paraffin-embedded tissue (PET) blot.Is there a risk of prion-like disease transmission by Alzheimer- or Parkinson-associated protein particles?Fibril-forming motifs are essential and sufficient for the fibrillization of human Tau.TDP-43 or FUS-induced misfolded human wild-type SOD1 can propagate intercellularly in a prion-like fashionMolecular nexopathies: a new paradigm of neurodegenerative disease.Identification of a novel mechanism of blood-brain communication during peripheral inflammation via choroid plexus-derived extracellular vesicles.Selective vulnerability to neurodegenerative disease: the curious case of Prion Protein.Intercellular propagated misfolding of wild-type Cu/Zn superoxide dismutase occurs via exosome-dependent and -independent mechanismsTotal allowable concentrations of monomeric inorganic aluminum and hydrated aluminum silicates in drinking water.Evaluation of the Braak hypothesis: how far can it explain the pathogenesis of Parkinson's disease?Bioinformatics aggregation predictors in the study of protein conformational diseases of the human nervous system.Protein misfolding in the late-onset neurodegenerative diseases: common themes and the unique case of amyotrophic lateral sclerosis.Structural disorder and the loss of RNA homeostasis in aging and neurodegenerative disease.An emerging role for misfolded wild-type SOD1 in sporadic ALS pathogenesis.Is Parkinson's disease truly a prion-like disorder? An appraisal of current evidence.Walking the tightrope: proteostasis and neurodegenerative disease.Potential Pathways of Abnormal Tau and α-Synuclein Dissemination in Sporadic Alzheimer's and Parkinson's Diseases.Functional genomics approach for identification of molecular processes underlying neurodegenerative disorders in prion diseases.p53 Aggregates penetrate cells and induce the co-aggregation of intracellular p53.Exosome-dependent and independent mechanisms are involved in prion-like transmission of propagated Cu/Zn superoxide dismutase misfolding.Military- and sports-related mild traumatic brain injury: clinical presentation, management, and long-term consequences.Reduced Abundance and Subverted Functions of Proteins in Prion-Like Diseases: Gained Functions Fascinate but Lost Functions Affect Aetiology.Clinical Spectrum of Amyotrophic Lateral Sclerosis (ALS).The morphometric co-atrophy networking of schizophrenia, autistic and obsessive spectrum disorders.Induction of IAPP amyloid deposition and associated diabetic abnormalities by a prion-like mechanism.The Pathoconnectivity Profile of Alzheimer's Disease: A Morphometric Coalteration Network Analysis.Propagated protein misfolding: New opportunities for therapeutics, new public health risk.Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
P2860
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P2860
Generalization of the prion hypothesis to other neurodegenerative diseases: an imperfect fit.
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article científic
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article scientifique
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articol științific
@ro
articolo scientifico
@it
artigo científico
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artigo científico
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artigo científico
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artikel ilmiah
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artikull shkencor
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artículo científico
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name
Generalization of the prion hy ...... ve diseases: an imperfect fit.
@en
Generalization of the prion hy ...... ve diseases: an imperfect fit.
@nl
type
label
Generalization of the prion hy ...... ve diseases: an imperfect fit.
@en
Generalization of the prion hy ...... ve diseases: an imperfect fit.
@nl
prefLabel
Generalization of the prion hy ...... ve diseases: an imperfect fit.
@en
Generalization of the prion hy ...... ve diseases: an imperfect fit.
@nl
P2093
P2860
P1476
Generalization of the prion hy ...... ve diseases: an imperfect fit.
@en
P2093
Edward Pokrishevsky
J Maxwell Silverman
Leslie I Grad
Megan A O'Neill
Neil R Cashman
Will C Guest
P2860
P304
P356
10.1080/15287394.2011.618967
P577
2011-01-01T00:00:00Z