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Journal Article
Molecular neurodegeneration, ISSN 1750-1326, 01/2012, Volume 7, Issue 1, pp. 2 - 2
Journal Article
Nature, ISSN 0028-0836, 09/2018, Volume 561, Issue 7722, pp. 258 - 262
Although serum from patients with Parkinson's disease contains elevated levels of numerous pro-inflammatory cytokines including IL-6, TNF, IL-1 beta, and IFN... 
OXIDATIVE STRESS | ACTIVATION | MUTANTS | MULTIDISCIPLINARY SCIENCES | IN-VIVO MITOPHAGY | DISEASE | NEURONS | DEFICIENT MICE | MUTATIONS | MITOCHONDRIAL-DNA | Protein Kinases - metabolism | Protein Kinases - genetics | Humans | Stress, Physiological | Receptor, Interferon alpha-beta - antagonists & inhibitors | Membrane Proteins - deficiency | Inflammation - metabolism | DNA, Mitochondrial - genetics | Membrane Proteins - metabolism | Parkinson Disease - metabolism | Protein Kinases - deficiency | Physical Conditioning, Animal | Membrane Proteins - genetics | Mice, Inbred C57BL | Alarmins - metabolism | Ubiquitin-Protein Ligases - metabolism | Immunity, Innate | DNA, Mitochondrial - blood | Mitochondrial Degradation | Animals | Receptor, Interferon alpha-beta - immunology | Inflammation - genetics | Ubiquitin-Protein Ligases - deficiency | Inflammation - prevention & control | Mice | Ubiquitin-Protein Ligases - genetics | Inflammation | Genetic aspects | Research | Gene mutations | Risk factors | Ubiquitin | Heart | Cell culture | Oxidative stress | Animal models | Parkinson's disease | Substantia nigra | Parkinsons disease | Innate immunity | Mitochondrial DNA | Kinases | Immunity | Interleukin 6 | Mitochondria | Movement disorders | Ubiquitin-protein ligase | Deoxyribonucleic acid--DNA | Dopamine receptors | Enzymes | Phenotypes | Dopamine | Cytokines | Neurodegenerative diseases | Body temperature | Damage patterns | Insects | Tumor necrosis factor | PTEN-induced putative kinase | Proteomics | Interferon | Parkin protein | Mutation | Methods | Index Medicus
Journal Article
Communicative and Integrative Biology, 09/2010, Volume 3, Issue 5, pp. 396 - 400
The mutations in the LRRK2 gene cause clinically typical, late-onset Parkinson disease, strengthening the idea that the familial forms of the disease represent... 
ERM | Neuronal morphogenesis | Phosphorylation | Tubulin | LRRK2 | Parkinson disease | G2019S | Microtubule | Filamentous actin | Golgi apparatus | microtubule | filamentous actin | tubulin | neuronal morphogenesis | golgi apparatus | Mini-Reviews | phosphorylation
Journal Article
Journal Article
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2018, Volume 8, Issue 1, pp. 1 - 15
Amyotrophic lateral sclerosis (ALS) is a fatal neurological disease characterized by progressive loss of motor neurons. There are no definitive pathogenic... 
Neuroprotection | Motor neurons | Muscles | Traditional Chinese medicine | Amyotrophic lateral sclerosis | Inflammation | High-performance liquid chromatography | Sclerosis | Atrophy | Chinese medicine | Fingerprinting | Life span | Rodents | Apoptosis | Index Medicus
Journal Article
Brain Pathology, ISSN 1015-6305, 01/2018, Volume 28, Issue 1, pp. 3 - 13
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2019, Volume 9, Issue 1, pp. 4857 - 14
Journal Article
Journal of Clinical Investigation, ISSN 0021-9738, 07/2014, Volume 124, Issue 7, pp. 3032 - 3046
Subpopulations of dopaminergic (DA) neurons within the substantia nigra pars compacta (SNpc) display a differential vulnerability to loss in Parkinson's... 
PATHOGENESIS | MEDICINE, RESEARCH & EXPERIMENTAL | 3,4-DIHYDROXYPHENYLACETALDEHYDE | VULNERABILITY | MUTANT ALPHA-SYNUCLEIN | MICE | SUBSTANTIA-NIGRA | METABOLITE | NEUROTOXICITY | BRAIN | PARKINSONS-DISEASE | Substantia Nigra - pathology | Dopaminergic Neurons - pathology | Humans | Protein Multimerization | Nerve Degeneration - genetics | Male | Dopaminergic Neurons - classification | Mutation, Missense | Substantia Nigra - metabolism | Nerve Degeneration - metabolism | Mice, Mutant Strains | Dopaminergic Neurons - metabolism | Aldehyde Dehydrogenase - deficiency | Female | Parkinson Disease - metabolism | alpha-Synuclein - genetics | Aldehyde Dehydrogenase - metabolism | Disease Models, Animal | Recombinant Proteins - metabolism | Parkinson Disease - pathology | Mutant Proteins - genetics | Recombinant Proteins - chemistry | Aldehyde Dehydrogenase - genetics | Mice, Transgenic | Mutant Proteins - metabolism | Recombinant Proteins - genetics | Parkinson Disease - genetics | Nerve Degeneration - pathology | Mice, Knockout | alpha-Synuclein - chemistry | Animals | Mutant Proteins - chemistry | Mice | alpha-Synuclein - metabolism | Brain research | Nervous system | Genetic aspects | Degeneration | Oxidoreductases | Research | Dopaminergic mechanisms | Properties | Dopamine | Dehydrogenases | Neurodegeneration | Neurons | Rodents | Cytotoxicity | Index Medicus | Abridged Index Medicus
Journal Article
The EMBO Journal, ISSN 0261-4189, 10/2014, Volume 33, Issue 20, pp. 2314 - 2331
Journal Article