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1. Full Text Prion-like spreading of pathological α-synuclein in brain
by Masuda-Suzukake, Masami and Nonaka, Takashi and Hosokawa, Masato and Oikawa, Takayuki and Arai, Tetsuaki and Akiyama, Haruhiko and Mann, David M. A and Hasegawa, Masato
Brain (London, England : 1878), ISSN 0006-8950, 2013, Volume 136, Issue 4, pp. 1128 - 1138
Parkinson's disease | propagation | α-synuclein | Lewy bodies | Neurosciences | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Neurology | Biological and medical sciences | Medical sciences | Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases | Prions - metabolism | alpha-Synuclein - administration & dosage | alpha-Synuclein - toxicity | Brain - physiopathology | Humans | Mice, Inbred C57BL | Injections, Intraventricular | Lewy Body Disease - pathology | Behavior, Animal - physiology | Administration, Intranasal | Recombinant Proteins - administration & dosage | Brain - metabolism | Lewy Body Disease - metabolism | Animals | Time Factors | Brain - pathology | Recombinant Proteins - toxicity | Female | Mice | alpha-Synuclein - metabolism | Disease Models, Animal | Lewy Body Disease - physiopathology | Index Medicus | Abridged Index Medicus | Original | Parkinson’s disease
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2. Full Text Self-propagation of pathogenic protein aggregates in neurodegenerative diseases
by Jucker, Mathias and Walker, Lary C
Nature (London), ISSN 0028-0836, 2013, Volume 501, Issue 7465, pp. 45 - 51
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Fundamental and applied biological sciences. Psychology | Vertebrates: nervous system and sense organs | Neurology | Biological and medical sciences | Medical sciences | Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases | Prions - metabolism | Neurodegenerative Diseases - pathology | Prion Diseases - drug therapy | Humans | Prions - classification | tau Proteins - metabolism | Prion Diseases - pathology | Amyloid - chemistry | Neurodegenerative Diseases - metabolism | Prions - chemistry | Neurodegenerative Diseases - drug therapy | tau Proteins - chemistry | Alzheimer Disease - pathology | alpha-Synuclein - chemistry | Animals | Amyloid - metabolism | Alzheimer Disease - metabolism | alpha-Synuclein - metabolism | Prion Diseases - metabolism | Evaluation | Prion diseases | Genetic aspects | Properties | Prions | Proteins | Seeds | Aggregates | Propagation | Creutzfeldt-Jakob disease | Spongiform encephalopathies | Index Medicus
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3. Full Text Sustained translational repression by eIF2α-P mediates prion neurodegeneration
by Moreno, Julie A and Radford, Helois and Peretti, Diego and Steinert, Joern R and Verity, Nicholas and Martin, Maria Guerra and Halliday, Mark and Morgan, Jason and Dinsdale, David and Ortori, Catherine A and Barrett, David A and Tsaytler, Pavel and Bertolotti, Anne and Willis, Anne E and Bushell, Martin and Mallucci, Giovanna R
Nature (London), ISSN 0028-0836, 05/2012, Volume 485, Issue 7399, pp. 507 - 511
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Neurology | Organic mental disorders. Neuropsychology | Psychology. Psychoanalysis. Psychiatry | Adult and adolescent clinical studies | Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases | Psychopathology. Psychiatry | Biological and medical sciences | Medical sciences | Neurons - pathology | Neuroprotective Agents | Phosphorylation | Prions - genetics | Eukaryotic Initiation Factor-2 - chemistry | Neurodegenerative Diseases - etiology | PrPSc Proteins - analysis | Synapses - pathology | Thiourea - pharmacology | Phosphoproteins - metabolism | Repressor Proteins - analysis | PrPSc Proteins - metabolism | Synapses - metabolism | Phosphoproteins - analysis | Protein Folding - drug effects | Protein Phosphatase 1 - genetics | Eukaryotic Initiation Factor-2 - metabolism | Synaptic Transmission - drug effects | Cell Death - drug effects | PrPSc Proteins - toxicity | Neurons - drug effects | Repressor Proteins - metabolism | Prions - metabolism | Synapses - drug effects | Repressor Proteins - chemistry | Neurodegenerative Diseases - pathology | Mice, Inbred C57BL | Kaplan-Meier Estimate | Hippocampus - pathology | Prion Diseases - pathology | Neurodegenerative Diseases - metabolism | Hippocampus - cytology | Cinnamates - pharmacology | Eukaryotic Initiation Factor-2 - analysis | Hippocampus - metabolism | Protein Phosphatase 1 - metabolism | Animals | Prions - biosynthesis | Protein Biosynthesis - drug effects | Mice | Unfolded Protein Response - physiology | Thiourea - analogs & derivatives | Index Medicus
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4. Full Text Prion-like mechanisms in neurodegenerative diseases
by Diamond, Marc I and Frost, Bess
Nature reviews. Neuroscience, ISSN 1471-003X, 03/2010, Volume 11, Issue 3, pp. 155 - 159
Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Fundamental and applied biological sciences. Psychology | Neurology | Effects of various physical factors on living matter (vibrations, electric field, ultrasound, sound...) | Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases | Biological and medical sciences | Tissues, organs and organisms biophysics | Medical sciences | Brain - metabolism | Prions - metabolism | Neurodegenerative Diseases - pathology | Humans | Amyloid beta-Peptides - metabolism | Brain - pathology | tau Proteins - metabolism | Protein Conformation | Neurodegenerative Diseases - metabolism | alpha-Synuclein - metabolism | Disease Progression | Protein folding | Physiological aspects | Nervous system | Development and progression | Glycoproteins | Genetic aspects | Degeneration | Research | Risk factors | Index Medicus
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5. Full Text The propagation of prion-like protein inclusions in neurodegenerative diseases
by Goedert, Michel and Clavaguera, Florence and Tolnay, Markus
Trends in neurosciences (Regular ed.), ISSN 0166-2236, 2010, Volume 33, Issue 7, pp. 317 - 325
Neurology | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Fundamental and applied biological sciences. Psychology | Vertebrates: nervous system and sense organs | Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases | Biological and medical sciences | General aspects. Models. Methods | Medical sciences | Prions - metabolism | Prion Diseases - genetics | Neurodegenerative Diseases - pathology | Prions - genetics | Inclusion Bodies - chemistry | Humans | tau Proteins - metabolism | Neurodegenerative Diseases - genetics | Prion Diseases - pathology | Neurodegenerative Diseases - metabolism | Protein Folding | Animals | tau Proteins - genetics | Inclusion Bodies - metabolism | Prion Diseases - metabolism | Brain | Neurodegeneration | Neurons | Protein folding | Prions | Nervous system | Index Medicus | Alzheimer's disease
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6. Full Text Prions in the Urine of Patients with Variant Creutzfeldt–Jakob Disease
by Moda, Fabio and Gambetti, Pierluigi and Notari, Silvio and Concha-Marambio, Luis and Catania, Marcella and Park, Kyung-Won and Maderna, Emanuela and Suardi, Silvia and Haïk, Stéphane and Brandel, Jean-Philippe and Ironside, James and Knight, Richard and Tagliavini, Fabrizio and Soto, Claudio
The New England journal of medicine, ISSN 0028-4793, 08/2014, Volume 371, Issue 6, pp. 530 - 539
Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Neurology | Biological and medical sciences | General aspects | Medical sciences | Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases | Young Adult | Creutzfeldt-Jakob Syndrome - diagnosis | PrPSc Proteins - urine | Protein Engineering - methods | Humans | Sensitivity and Specificity | Adolescent | Creutzfeldt-Jakob Syndrome - urine | Adult | Electrophoresis | Brain Chemistry | Protein Folding | Urine | Analysis | Creutzfeldt-Jakob disease | Research | Diagnosis | Health aspects | Risk factors | Prisoners | Food contamination | Nervous system | Infections | Transmissible spongiform encephalopathy | Meat | Neurological diseases | Proteins | Body fluids | Protein folding | Prions | Prion protein | Public health | Index Medicus | Abridged Index Medicus
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7. Full Text Cellular prion protein mediates impairment of synaptic plasticity by amyloid-Î’ oligomers
by Laurén, Juha and Gimbel, David A and Nygaard, Haakon B and Gilbert, John W and Strittmatter, Stephen M
Nature (London), ISSN 0028-0836, 02/2009, Volume 457, Issue 7233, pp. 1128 - 1132
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Fundamental and applied biological sciences. Psychology | Non conventional transmissible agents | Neurology | Organic mental disorders. Neuropsychology | Psychology. Psychoanalysis. Psychiatry | Microbiology | Adult and adolescent clinical studies | Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases | Psychopathology. Psychiatry | Biological and medical sciences | Medical sciences | Prions - genetics | Humans | Protein Multimerization | Cercopithecus aethiops | Synapses - pathology | Alzheimer Disease - pathology | Synapses - metabolism | Amyloid beta-Peptides - metabolism | Long-Term Potentiation - physiology | Neurons - metabolism | Prions - metabolism | Alzheimer Disease - physiopathology | Peptide Fragments - metabolism | Mice, Inbred C57BL | Receptors, Cell Surface - metabolism | Hippocampus - cytology | Hippocampus - metabolism | Amyloid Precursor Protein Secretases - metabolism | Peptide Fragments - chemistry | Animals | Neuronal Plasticity | Alzheimer Disease - metabolism | Protein Binding | Mice | Amyloid beta-Peptides - chemistry | COS Cells | Amyloidosis - metabolism | Receptors, Cell Surface - genetics | Index Medicus
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