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Journal Article
SCIENCE, ISSN 0036-8075, 09/2017, Volume 357, Issue 6357, pp. 1255 - 1255
Mitochondrial and lysosomal dysfunction have been implicated in substantia nigra dopaminergic neurodegeneration in Parkinson's disease (PD), but how these... 
GLUCOCEREBROSIDASE | PACEMAKING | DJ-1 | ALPHA-SYNUCLEIN | SUBSTANTIA-NIGRA | MULTIDISCIPLINARY SCIENCES | Mitochondria - enzymology | Mesencephalon - metabolism | Humans | Protein Deglycase DJ-1 - genetics | Substantia Nigra - metabolism | Melanins - metabolism | Glucosylceramidase - deficiency | Lysosomes - metabolism | Dopaminergic Neurons - metabolism | Tacrolimus - pharmacology | Parkinson Disease - metabolism | Dopamine - metabolism | Disease Models, Animal | Substantia Nigra - enzymology | Cell Line | Calcineurin Inhibitors - pharmacology | Oxidation-Reduction | Mesencephalon - enzymology | Mitochondria - metabolism | Antioxidants - pharmacology | Mitochondria - drug effects | Parkinson Disease - genetics | Mice, Knockout | Animals | Parkinson Disease - enzymology | Mice | Oxidative Stress - drug effects | alpha-Synuclein - metabolism | Oxidation-reduction reaction | Development and progression | Mitochondria | Dopamine | Parkinson's disease | Health aspects | Brain | Energy metabolism | Animal models | Target recognition | Mesencephalon | Pathogenesis | Substantia nigra | Parkinsons disease | Lysosomes | Synuclein | Accumulation | Pathways | Enzymatic activity | Neurodegeneration | Rodents | Oxidation | Degeneration | Species | Movement disorders | Dopamine receptors | Neurodegenerative diseases | Neurons | Medical treatment | Metabolism | Patients | Glucosylceramidase | Index Medicus
Journal Article
PLoS ONE, ISSN 1932-6203, 02/2010, Volume 5, Issue 2, p. e9367
Background: Mitochondrial dysfunction and degradation takes a central role in current paradigms of neurodegeneration in Parkinson's disease (PD). Loss of DJ-1... 
PINK1 | FUSION | GENE | MULTIDISCIPLINARY SCIENCES | ENERGETIC DEPRESSION | CYSTEINE-SULFINIC ACID | MUSCLE | DEGRADATION | MUTATIONS | PATHOLOGY | FISSION | Oncogene Proteins - genetics | Phosphorylation | Reactive Oxygen Species - metabolism | Humans | Intracellular Signaling Peptides and Proteins - metabolism | Autophagy | Fibroblasts - ultrastructure | Lysosomes - metabolism | Intracellular Signaling Peptides and Proteins - genetics | Fibroblasts - metabolism | Parkinson Disease - pathology | Oncogene Proteins - metabolism | Oxidative Phosphorylation | Mitochondria - metabolism | Parkinson Disease - genetics | Microscopy, Electron | Blotting, Western | Mice, Knockout | Peroxiredoxins | Lysosomes - ultrastructure | Protein Deglycase DJ-1 | Animals | Fibroblasts - cytology | Mice | Mutation | Mitogen-Activated Protein Kinase 1 - metabolism | Genes | Genetic aspects | Oxidative stress | Cell culture | Reactive oxygen species | Animal models | Parkinson's disease | Laboratories | Downstream effects | Parkinsons disease | Homeostasis | Lysosomes | Kinases | Accumulation | Degradation | Proteins | Mitochondria | Neurodegeneration | Penicillin | Fibroblasts | Aging | Physiology | Membrane potential | Movement disorders | Neurodegenerative diseases | Extracellular signal-regulated kinase | Organelles | PARK7 protein | Neurology | Brain research | Hypoxia | Electron transport | Respiration | Alzheimers disease | Phagocytosis | Apoptosis | Integrity
Journal Article
Science, ISSN 0036-8075, 09/2017, Volume 357, Issue 6357, pp. 1255 - 1261
Mitochondrial and lysosomal dysfunction have been implicated in substantia nigra dopaminergic neurodegeneration in Parkinson’s disease (PD), but how these... 
Journal Article
Brain, ISSN 0006-8950, 2015, Volume 138, Issue 3, pp. 679 - 693
Journal Article
BMC Medicine, ISSN 1741-7015, 11/2008, Volume 6, Issue 1, pp. 33 - 33
Parkinson's disease is the most common neurodegenerative movement disorder and affects about 2% of the population over the age of 60 years. In 2004, mutations... 
VARIABILITY | PHENOTYPE | MEDICINE, GENERAL & INTERNAL | G2019S | MUTATIONS | GENE | Genetic Predisposition to Disease | Humans | Middle Aged | Protein-Serine-Threonine Kinases - genetics | Heterozygote | Penetrance | Parkinson Disease - genetics | Leucine-Rich Repeat Serine-Threonine Protein Kinase-2 | Genetic aspects | Parkinson's disease | Research | Gene mutations
Journal Article
Annals of Neurology, ISSN 0364-5134, 05/2011, Volume 69, Issue 5, pp. 778 - 792
Journal Article