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Annual review of cell and developmental biology, ISSN 1081-0706, 10/2018, Volume 34, Issue 1, pp. 545 - 568
Journal Article
Science (American Association for the Advancement of Science), ISSN 1095-9203, 2002, Volume 296, Issue 5575, pp. 1991 - 1995
...Neurodegenerative disorders as diverse as Alzheimer's disease, Parkinson's disease, priori diseases, Huntington's disease, frontotemporal dementia, and motor... 
Nervous system diseases | Reviews | Neurodegenerative diseases | Disease models | Huntington disease | Parkinson disease | Prion diseases | Amyotrophic lateral sclerosis | Nervous system heredodegenerative disorders | Alzheimers disease | Genetic mutation | Parkinson Disease - therapy | Neurons - pathology | Prion Diseases - genetics | Humans | Peptides - genetics | Tauopathies - pathology | Alzheimer Disease - pathology | Peptides - metabolism | Tauopathies - therapy | Neurons - metabolism | Parkinson Disease - metabolism | Inclusion Bodies - metabolism | Prion Diseases - therapy | Parkinson Disease - pathology | Neurodegenerative Diseases - pathology | Amyotrophic Lateral Sclerosis - therapy | Amyotrophic Lateral Sclerosis - genetics | Alzheimer Disease - therapy | Neurodegenerative Diseases - genetics | Neurodegenerative Diseases - therapy | Prion Diseases - pathology | Neurodegenerative Diseases - metabolism | Parkinson Disease - genetics | Protein Folding | Trinucleotide Repeat Expansion | Proteins - genetics | Amyotrophic Lateral Sclerosis - pathology | Tauopathies - metabolism | Animals | Proteins - metabolism | Alzheimer Disease - metabolism | Amyotrophic Lateral Sclerosis - metabolism | Mutation | Proteins - chemistry | Alzheimer Disease - genetics | Prion Diseases - metabolism | Parkinson's disease | Nervous system | Degeneration | Research | Alzheimer's disease | Proteins | Neurological disorders
Journal Article
EMBO Molecular Medicine, ISSN 1757-4676, 10/2015, Volume 7, Issue 10, pp. 1307 - 1326
Mitochondrial dysfunction is implicated in multiple neurodegenerative diseases. In order to maintain a healthy population of functional mitochondria in cells... 
glyceraldehyde‐3‐phosphate dehydrogenase | mitophagy | Huntington's disease | polyglutamine repeats | mitochondria | Glyceraldehyde-3-phosphate dehydrogenase | Mitochondria | Mitophagy | Polyglutamine repeats | MEDICINE, RESEARCH & EXPERIMENTAL | ALZHEIMERS-DISEASE | MUTANT HUNTINGTIN | N-ACETYLCYSTEINE | AUTOPHAGY | CELL-DEATH | ABNORMAL MITOCHONDRIAL DYNAMICS | glyceraldehyde-3-phosphate dehydrogenase | GLYCERALDEHYDE-3-PHOSPHATE DEHYDROGENASE GAPDH | RAT-BRAIN | POLYGLUTAMINE EXPANSIONS | MOLECULAR-MECHANISMS | Glyceraldehyde 3-Phosphate Dehydrogenase (NADP+) - genetics | Polyglutamic Acid - metabolism | Cell Survival | Humans | Rats | Mitochondria - metabolism | Nerve Tissue Proteins | Huntington Disease - metabolism | PC12 Cells | Mice, Knockout | Mitochondrial Degradation | Nuclear Proteins | Huntingtin Protein | Animals | Mice | Huntington Disease - physiopathology | Glyceraldehyde 3-Phosphate Dehydrogenase (NADP+) - biosynthesis | Phosphates | Nervous system diseases | Mitochondrial DNA | Analysis | Sugars | Monosaccharides | Huntingtons disease | Cell culture | Oxidative stress | Dehydrogenases | Glyceraldehyde | Lysosomes | Kinases | Autophagy | Experiments | Proteins | Fibroblasts | Physiology | Trinucleotide repeat diseases | Cell survival | Polyglutamine | Neurodegenerative diseases | Metabolism | Pathology | Molecular modelling | Cell death | Mutation | Apoptosis | Huntington’s disease
Journal Article
Journal Article
Journal Article
Journal of Alzheimer's Disease, ISSN 1387-2877, 2008, Volume 15, Issue 3, pp. 473 - 493
Journal Article
Human molecular genetics, ISSN 1460-2083, 2008, Volume 17, Issue 1, pp. 119 - 129
Journal Article