Search Results - "prion"
Suggested Topics within your search.
Suggested Topics within your search.
- genetics
- Degeneration 2
- Genetic aspects 2
- Nervous system 2
- Neurodegenerative Diseases 2
- Parkinson Disease 2
- Parkinson's disease 2
- Prions 2
- pathology 2
- Alzheimer Disease 1
- Alzheimer's disease 1
- Amyloid 1
- Amyotrophic Lateral Sclerosis 1
- Amyotrophic lateral sclerosis 1
- Ataxins 1
- Diseases 1
- Genetic Predisposition to Disease 1
- Lewy Bodies 1
- Lewy body dementia 1
- Nerve Tissue Proteins 1
- Neuroprotective Agents 1
- Pathology 1
- Pathophysiology 1
- Prion Diseases 1
- Prion diseases 1
- RNA-Binding Proteins 1
- RNA-protein interactions 1
- Risk Factors 1
- Tauopathies 1
- Treatment 1
-
1
Prion-like propagation of Parkinson's disease
Published 2014Table of Contents: “…Contents: Parkinson's disease : symptoms and pathology (PD mutations and risk factors) -- Braak staging of Lewy body-related pathology in PD -- The prion-like hypothesis -- Key steps of alpha-synuclein pathology propagation (Release, Uptake, Seeding, Transport) -- In vivo and cell models from different species -- Therapeutic targets: promoting degradation, antibody aided clearance, and preventing seeding of alpha-synuclein -- Parkinson's disease vaccine: first clinical studies.…”
Get full text
Series
Electronic Video -
2
Expanding roles of RNA-binding proteins in neurodegenerative diseases
Published 2017Table of Contents: “…Contents: Amyotrophic lateral sclerosis (ALS) -- Genetic causes of ALS -- Role of RNA-binding proteins and stress granules in ALS pathogenesis -- Emerging class of RNA-binding proteins with prion-like domains in neurodegenerative disease -- Mechanisms by which C9ORF72 mutations cause ALS.…”
Get full text
Series
Series
Electronic Video -
3
Neurodegenerative disease expression levels of normal sequence pathogenic proteins contribute to risk of disease /
Published 2021Table of Contents: “…Contents: Protein pathology of disease -- Loci underlying autosomal dominant neurodegenerative disease -- Prion mutations causing Gerstmann Straussler syndrome and hereditary Creuzfeldt-Jakob disease -- Tau mutations cause autosomal dominant frontal temporal dementia -- Alpha-synuclein mutations cause autosomal dominant Parkinson's disease -- How genetic variability of these genes contributes to the risk of sporadic disease.…”
Get full text
Series
Electronic Video