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Journal Article
Journal Article
NEUROCHEMISTRY INTERNATIONAL, ISSN 0197-0186, 02/2016, Volume 93, pp. 6 - 25
Journal Article
Neurobiology of Disease, ISSN 0969-9961, 07/2019, Volume 127, pp. 1 - 12
While the link between and Parkinson's disease (PD) was initially unexpected, it is now well established that mutations are the most frequent genetic risk for... 
Induced pluripotent stem cells | Parkinson's disease | GBA | LYSOSOMAL STORAGE | RISK | ALPHA-SYNUCLEIN | GLUCOCEREBROSIDASE MUTATIONS | NEUROSCIENCES | GAUCHER-DISEASE | GLUCOSYLCERAMIDE LEVELS | MOUSE MODEL | MITOCHONDRIAL DYSFUNCTION | ENDOPLASMIC-RETICULUM | BRAIN | Medical research | Brain research | Analysis | Genomics | Stem cells | Medicine, Experimental | Lipids | Models | Transplantation | Drug discovery | Dementia
Journal Article
Neurochemistry International, ISSN 0197-0186, 02/2016, Volume 93, pp. 6 - 25
mutations are to date the most common genetic risk factor for Parkinson's disease. The gene encodes the lysomal hydrolase glucocerebrosidase. Whilst bi-allelic... 
α-Synuclein | Glucocerebrosidase | Gaucher disease | Parkinson's disease | LIMP-2 | Parkinson Disease - therapy | Glucosylceramidase - genetics | Parkinson Disease - pathology | Humans | Adult | Mutation | Parkinson Disease - genetics | Enzymes | Genetics | Health aspects | Aquaporins
Journal Article
Journal Article
Journal Article
PLoS ONE, ISSN 1932-6203, 02/2010, Volume 5, Issue 2, p. e9313
Background: Lewy body disease is a heterogeneous group of neurodegenerative disorders characterized by alpha-synuclein accumulation that includes dementia with... 
WILD-TYPE | CHAPERONE-MEDIATED AUTOPHAGY | ALZHEIMERS-DISEASE | MOUSE MODEL | FRONTOTEMPORAL DEMENTIA | BIOLOGY | AGGREGATE-PRONE PROTEINS | NEURONAL EXPRESSION | PARKINSONS-DISEASE | TRANSGENIC MICE | GAUCHER-DISEASE | Pyramidal Cells - metabolism | Humans | Nerve Degeneration - genetics | Male | Autophagy | Nerve Degeneration - metabolism | Alzheimer Disease - pathology | Brain - metabolism | Lewy Body Disease - genetics | RNA Interference | Brain - ultrastructure | Aged, 80 and over | Female | alpha-Synuclein - genetics | Pyramidal Cells - ultrastructure | Disease Models, Animal | Cell Line | Ubiquitin-Activating Enzymes - genetics | Signal Transduction | Lewy Body Disease - pathology | Mice, Transgenic | Microscopy, Electron | Ubiquitin-Activating Enzymes - metabolism | Blotting, Western | Nerve Degeneration - pathology | Lewy Body Disease - metabolism | Microscopy, Confocal | Autophagy-Related Protein 7 | Animals | Alzheimer Disease - metabolism | Brain - pathology | Cell Line, Tumor | Pyramidal Cells - pathology | Aged | Mice | Alzheimer Disease - genetics | alpha-Synuclein - metabolism | TOR protein | Neurosciences | Animal models | Parkinson's disease | Pathogenesis | Toxicity | Parkinsons disease | Phagosomes | Nervous system | Synuclein | Neuromodulation | Accumulation | Modulators | Proteins | Infusion | Alterations | Neurodegeneration | Dementia disorders | Alzheimer's disease | Movement disorders | Enzymes | Neurodegenerative diseases | Neurons | Immunomodulation | Lewy body disease | Transgenic mice | Rapamycin | Patients | Lewy bodies | Studies | Pathology | Mutation | Alzheimers disease | Phagocytosis | Apoptosis | Dementia
Journal Article