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21. Full Text Huntington's disease
by Ha, Ainhi D and Fung, Victor S.C
Current opinion in neurology, ISSN 1350-7540, 08/2012, Volume 25, Issue 4, pp. 491 - 498
Biomarker | Premanifest Huntington's disease | Huntington's disease | Neurodegeneration | Prodromal Huntington's disease | Neurosciences | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Humans | Trinucleotide Repeats - genetics | Nerve Tissue Proteins - genetics | Mitochondrial Diseases - etiology | Huntington Disease - complications | Huntington Disease - therapy | Huntingtin Protein | Magnetic Resonance Imaging | Animals | Cognition Disorders - etiology | Brain - pathology | Huntington Disease - genetics | Huntington Disease - diagnosis | Index Medicus | Neuroprotection | Animal models | Reviews | biomarkers
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22. Full Text Oligomeric Aβ-induced synaptic dysfunction in Alzheimer's disease
by Tu, Shichun and Tu, Shichun and Okamoto, Shu-ichi and Okamoto, Shu-Ichi and Lipton, Stuart A and Lipton, Stuart A and Xu, Huaxi and Xu, Huaxi
Molecular neurodegeneration, ISSN 1750-1326, 11/2014, Volume 9, Issue 1, pp. 48 - 48
Cognitive decline | Mitochondrial dysfunction | Tau hyperphosphorylation | Calcium | Aberrant neuronal network activity | Synaptic loss | NMDA receptors | PSD-95 | Alzheimer's disease | Aβ oligomers | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Alzheimer Disease - physiopathology | Animals | Synapses - metabolism | Humans | Alzheimer Disease - metabolism | Amyloid beta-Peptides - metabolism | Synapses - pathology | Alzheimer Disease - pathology | Index Medicus
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23. Full Text Proteinopathy, oxidative stress and mitochondrial dysfunction: Cross talk in alzheimer’s disease and parkinson’s disease
by Ganguly, Gargi and Chakrabarti, Sasanka and Chatterjee, Uttara and Saso, Luciano
Drug design, development and therapy, ISSN 1177-8881, 03/2017, Volume 11, pp. 797 - 810
Oxidative stress | Proteinopathy | Amyloid beta | Mitochondrial dysfunction | α-synuclein | Pharmacology & Pharmacy | Life Sciences & Biomedicine | Chemistry, Medicinal | Science & Technology | Parkinson Disease - pathology | Proteins - metabolism | Oxidative Stress | Humans | Alzheimer Disease - metabolism | Mitochondria - metabolism | Parkinson Disease - metabolism | Mitochondria - pathology | Alzheimer Disease - pathology | Proteins | Mitochondria | Parkinson's disease | Development and progression | Comparative analysis | Alzheimer's disease | Health aspects | Conformation | Brain | Neuroprotection | Reactive oxygen species | Transition metals | Nuclear magnetic resonance--NMR | Peptides | Pathogenesis | Crosstalk | Parkinsons disease | Impairment | Cognitive ability | Kinases | Synuclein | Oligomers | Histopathology | Neurodegeneration | Autopsy | Etiology | Protein folding | Older people | Dementia disorders | Aging | Movement disorders | Metal ions | Dopamine | Neurodegenerative diseases | Morbidity | Diseases | Neurological diseases | Commonality | Brain research | β-Amyloid | Mutation | Alzheimers disease | Geriatrics | Apoptosis | Dementia | Animal cognition | Index Medicus | proteinopathy | α-Synuclein | mitochondrial dysfunction | amyloid beta | oxidative stress
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24. Full Text The roles of PINK1, Parkin, and mitochondrial fidelity in parkinson's disease
by Pickrell, Alicia M and Youle, Richard J
Neuron (Cambridge, Mass.), ISSN 0896-6273, 01/2015, Volume 85, Issue 2, pp. 257 - 273
Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Protein Kinases - metabolism | Protein Kinases - genetics | Proteolysis | Humans | Ubiquitin-Protein Ligases - metabolism | Parkinsonian Disorders - genetics | Mitochondria - metabolism | Parkinson Disease - metabolism | Parkinson Disease - genetics | Ubiquitin-Protein Ligases - genetics | Mitochondrial Degradation - physiology | Ubiquitin | Mitochondrial DNA | Gene mutations | Cells | Membrane proteins | Ligases | Development and progression | Disease susceptibility | Neurons | Genes | Motor ability | Parkinsons disease | Biology | Kinases | Proteins | Mitochondria | Insects | Neurodegeneration | Quality control | Mutation | Alzheimers disease | Index Medicus
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25. Full Text Mitochondrial DNA and disease
by Greaves, Laura C and Reeve, Amy K and Taylor, Robert W and Turnbull, Doug M
The Journal of pathology, ISSN 0022-3417, 01/2012, Volume 226, Issue 2, pp. 274 - 286
mutation | disease | mitochondrial DNA | oxidative phosphorylation | mitochondrion | Pathology | Oncology | Life Sciences & Biomedicine | Science & Technology | Mitochondrial Diseases - genetics | Point Mutation - genetics | Phenotype | DNA, Mitochondrial - genetics | Aging - genetics | Neoplasms - genetics | Gene Deletion | Humans | Oxidative Phosphorylation | Oxidative Stress - genetics | Neurodegenerative Diseases - genetics | Mutation - genetics | Index Medicus
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