Propagation of prions causing synucleinopathies in cultured cells - Test2 - elhamkhani - TriplyDB

Propagation of prions causing synucleinopathies in cultured cells

Propagation of prions causing synucleinopathies in cultured cells

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Neuroinflammation in Multiple System Atrophy: Response to and Cause of α-Synuclein Aggregation Evidence for α-synuclein prions causing multiple system atrophy in humans with parkinsonism Genomic Characteristics of Genetic Creutzfeldt-Jakob Disease Patients with V180I Mutation and Associations with Other Neurodegenerative Disorders.Phosphorylation induces distinct alpha-synuclein strain formation.Analysis of the prion protein gene in multiple system atrophy Tau prions from Alzheimer's disease and chronic traumatic encephalopathy patients propagate in cultured cells.Robust Central Nervous System Pathology in Transgenic Mice following Peripheral Injection of α-Synuclein Fibrils.Neuropathological Staging of Brain Pathology in Sporadic Parkinson's disease: Separating the Wheat from the Chaff.The Synucleinopathies: Twenty Years On.Prions and Protein Assemblies that Convey Biological Information in Health and Disease.The Concept of Prodromal Parkinson's Disease.Impaired endo-lysosomal membrane integrity accelerates the seeding progression of α-synuclein aggregates.ɑ-Synuclein strains and the variable pathologies of synucleinopathies.Anle138b Partly Ameliorates Motor Deficits Despite Failure of Neuroprotection in a Model of Advanced Multiple System Atrophy.Pathogenic mechanisms of prion protein, amyloid-β and α-synuclein misfolding: the prion concept and neurotoxicity of protein oligomers.Bioassays and Inactivation of Prions.Potential Pathways of Abnormal Tau and α-Synuclein Dissemination in Sporadic Alzheimer's and Parkinson's Diseases.Potential mechanisms and implications for the formation of tau oligomeric strains.Genetic prion disease: Experience of a rapidly progressive dementia center in the United States and a review of the literature.Prelysosomal Compartments in the Unconventional Secretion of Amyloidogenic Seeds.The Contribution of α-Synuclein Spreading to Parkinson's Disease Synaptopathy.Designer protein disaggregases to counter neurodegenerative disease.Nanomolar oligomerization and selective co-aggregation of α-synuclein pathogenic mutants revealed by single-molecule fluorescence.Molecular and Biological Compatibility with Host Alpha-Synuclein Influences Fibril Pathogenicity.Internalized Tau sensitizes cells to stress by promoting formation and stability of stress granules C-Terminal Truncated α-Synuclein Fibrils Contain Strongly Twisted β-Sheets.The importance of developing strain-specific models of neurodegenerative disease.In vivo models of alpha-synuclein transmission and propagation.Vertebrate food products as a potential source of prion-like α-synuclein.Alpha-synuclein oligomers: a new hope.MSA prions exhibit remarkable stability and resistance to inactivation.A 31-residue peptide induces aggregation of tau's microtubule-binding region in cells.Kinetics of Human Mutant Tau Prion Formation in the Brains of 2 Transgenic Mouse Lines.Alternative Splicing of Alpha- and Beta-Synuclein Genes Plays Differential Roles in Synucleinopathies.Distinct α-Synuclein strains and implications for heterogeneity among α-Synucleinopathies.Is multiple system atrophy an infectious disease?Familial Parkinson's point mutation abolishes multiple system atrophy prion replication.Neurodegeneration and the ordered assembly of α-synuclein.Treatment of autonomic dysfunction in Parkinson disease and other synucleinopathies.Potent prion-like behaviors of pathogenic α-synuclein and evaluation of inactivation methods.

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Propagation of prions causing synucleinopathies in cultured cells

http://www.wikidata.org/entity/Q26269822

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2015 nî lūn-bûn

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2015 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

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2015 թվականի սեպտեմբերին հրատարակված գիտական հոդված

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2015年の論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年论文

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Propagation of prions causing synucleinopathies in cultured cells

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Propagation of prions causing synucleinopathies in cultured cells

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Propagation of prions causing synucleinopathies in cultured cells

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label

Propagation of prions causing synucleinopathies in cultured cells

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Propagation of prions causing synucleinopathies in cultured cells

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Propagation of prions causing synucleinopathies in cultured cells

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prefLabel

Propagation of prions causing synucleinopathies in cultured cells

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Propagation of prions causing synucleinopathies in cultured cells

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Propagation of prions causing synucleinopathies in cultured cells

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Proceedings of the National Academy of Sciences of the United States of America

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Propagation of prions causing synucleinopathies in cultured cells

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Amanda L Woerman

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Atsushi Aoyagi

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Lefkos T Middleton

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Marc I Diamond

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Ryan Rampersaud

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Smita Patel

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P2860

Second consensus statement on the diagnosis of multiple system atrophy

Systematic mutagenesis of α-synuclein reveals distinct sequence requirements for physiological and pathological activities

Evidence for α-synuclein prions causing multiple system atrophy in humans with parkinsonism

Neurodegenerative diseases: expanding the prion concept

Mutation in the alpha-synuclein gene identified in families with Parkinson's disease

alpha-Synuclein locus triplication causes Parkinson's disease

Alpha-synuclein in Lewy bodies

Staging of brain pathology related to sporadic Parkinson's disease

Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease

Lewy body-like pathology in long-term embryonic nigral transplants in Parkinson's disease

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Stanley B. Prusiner

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Prion protein family

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