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Annual Review of Genetics, ISSN 0066-4197, 11/2013, Volume 47, Issue 1, pp. 601 - 623
Prions are proteins that acquire alternative conformations that become self-propagating. Transformation of proteins into prions is generally accompanied by an... 
neurodegeneration | prion | Neurodegeneration | Prion | PROTEIN-TAU TAU | AMYOTROPHIC-LATERAL-SCLEROSIS | CHRONIC TRAUMATIC ENCEPHALOPATHY | CEREBRAL BETA-AMYLOIDOSIS | PATHOLOGICAL ALPHA-SYNUCLEIN | GENETICS & HEREDITY | FAMILIAL ALZHEIMERS-DISEASE | CREUTZFELDT-JAKOB-DISEASE | STRAUSSLER-SCHEINKER DISEASE | PARKINSONS-DISEASE | TRANSGENIC MICE | Fungal Proteins - chemistry | Synucleins - physiology | Amyloidogenic Proteins - classification | Prion Diseases - genetics | Prions - genetics | Transcription Factors - chemistry | Tauopathies - genetics | Neurodegenerative Diseases - etiology | Humans | Virulence | mRNA Cleavage and Polyadenylation Factors - chemistry | Amyloidogenic Proteins - physiology | Amyloidogenic Proteins - chemistry | Neurofibrillary Tangles | mRNA Cleavage and Polyadenylation Factors - classification | Tauopathies - etiology | Plaque, Amyloid | Inclusion Bodies | tau Proteins - genetics | tau Proteins - physiology | Saccharomyces cerevisiae Proteins - classification | Peptide Termination Factors - physiology | Models, Molecular | Neurodegenerative Diseases - genetics | Fungal Proteins - classification | Mammals | Transcription Factors - classification | Peptide Termination Factors - classification | Fungal Proteins - physiology | Animals | Prions - physiology | Prion Diseases - etiology | Age of Onset | Protein Conformation | Peptide Termination Factors - chemistry | Saccharomyces cerevisiae Proteins - physiology | Neurodegenerative Diseases - epidemiology | Saccharomyces cerevisiae Proteins - chemistry | Prions | Physiological aspects | Causes of | Nervous system | Degeneration | Genetic aspects | Health aspects
Journal Article
Trends in Neurosciences, ISSN 0166-2236, 2013, Volume 36, Issue 6, pp. 325 - 335
Highlights • Mitochondria provide energy, buffer calcium ions, and regulate apoptosis. • Mitochondrial dynamics is the term describing their regulated fusion... 
Neurology | dementia | frontotemporal dementia | TAU | actin | synapse | amyloid-β (Aβ) | Synapse | Amyloid-β (Aβ) | Frontotemporal dementia | Actin | Dementia | MITOFUSIN 2 | MICE IMPLICATIONS | IMPAIRED AXONAL-TRANSPORT | SYNAPTIC MITOCHONDRIA | NEUROSCIENCES | S-NITROSYLATION | amyloid-beta (A beta) | AMYLOID-BETA | MOUSE MODEL | A-BETA | FISSION | Axonal Transport | Humans | Receptors, Metabotropic Glutamate - physiology | Mitochondrial Proteins - genetics | Adenosine Triphosphate - biosynthesis | Mitochondria - ultrastructure | Charcot-Marie-Tooth Disease - genetics | Mitochondrial Membrane Transport Proteins - physiology | Neurons - ultrastructure | Membrane Proteins - physiology | tau Proteins - physiology | Neurons - physiology | Mitochondrial Proteins - deficiency | Amyloid beta-Peptides - physiology | Nerve Tissue Proteins - physiology | Membrane Fusion | GTP Phosphohydrolases - physiology | Synapses - physiology | Mitochondrial Proteins - physiology | Neurodegenerative Diseases - metabolism | Microtubule-Associated Proteins - physiology | Animals | Energy Metabolism | GTP Phosphohydrolases - genetics | Alzheimer Disease - metabolism | GTP Phosphohydrolases - deficiency | Mice | Models, Neurological | Mitochondria - physiology | Mitochondrial DNA | Alzheimer's disease | Analysis | Amyloid beta-protein
Journal Article