| scholarly article | Q13442814 |
| P356 | DOI | 10.1007/BF00334457 |
| P698 | PubMed publication ID | 8480516 |
| P2093 | author name string | Y Mizutani | |
| M Yokochi | |||
| K Hayashida | |||
| S Oyanagi | |||
| P2860 | cites work | Idiopathic Parkinson's disease and the Lewy body disorders | Q39503766 |
| Ultrastructure of Lewy bodies in the stellate ganglion | Q39987734 | ||
| Dense core vesicles around the Lewy body in incidental Parkinson's disease: an electron microscopic study | Q40095790 | ||
| Colloid (hyaline) inclusion bodies in the central nervous system: their presence in the substantia nigra is diagnostic of Parkinson's disease | Q48169432 | ||
| The Lewy body in Parkinson's disease. | Q48254020 | ||
| Relationships between Lewy bodies and pale bodies in Parkinson's disease | Q48600286 | ||
| Depigmentation in the nerve cells of the substantia nigra and locus ceruleus in Parkinsonism | Q48603493 | ||
| Juvenile parkinsonism--some clinical, pharmacological, and neuropathological aspects | Q48697227 | ||
| New pathologic observations in juvenile onset parkinsonism with dystonia | Q48710035 | ||
| Juvenile parkinsonism: a case with first clinical manifestation at the age of six years and with neuropathological findings suggesting a new pathogenesis. | Q48772736 | ||
| Ultrastructural observations in Parkinsonism | Q51160729 | ||
| Neuronal inclusions of Parkinson's disease | Q67914362 | ||
| Atypical senile dementia with widespread Lewy type inclusion in the cerebral cortex | Q72848189 | ||
| P433 | issue | 4 | |
| P921 | main subject | substantia nigra | Q753278 |
| Parkinson's disease | Q11085 | ||
| autopsy | Q41482 | ||
| P304 | page(s) | 445-448 | |
| P577 | publication date | 1993-01-01 | |
| P1433 | published in | Acta Neuropathologica | Q343168 |
| P1476 | title | An early cytoplasmic change before Lewy body maturation: an ultrastructural study of the substantia nigra from an autopsy case of juvenile parkinsonism | |
| P478 | volume | 85 |
| Q34989985 | A53T human α-synuclein overexpression in transgenic mice induces pervasive mitochondria macroautophagy defects preceding dopamine neuron degeneration |
| Q35138501 | Aggregation of α-synuclein in S. cerevisiae is associated with defects in endosomal trafficking and phospholipid biosynthesis |
| Q30481396 | Alpha-synuclein-induced aggregation of cytoplasmic vesicles in Saccharomyces cerevisiae |
| Q40262236 | Altered cleavage and localization of PINK1 to aggresomes in the presence of proteasomal stress |
| Q36329444 | Autophagy and neuronal cell death in neurological disorders |
| Q90240136 | Cell models of lipid-rich α-synuclein aggregation validate known modifiers of α-synuclein biology and identify stearoyl-CoA desaturase |
| Q64251001 | Dietary Macronutrient Management to Treat Mitochondrial Dysfunction in Parkinson's Disease |
| Q92576096 | Female Sex and Brain-Selective Estrogen Benefit α-Synuclein Tetramerization and the PD-like Motor Syndrome in 3K Transgenic Mice |
| Q30607522 | Formation of α-synuclein Lewy neurite-like aggregates in axons impedes the transport of distinct endosomes |
| Q44195128 | Genetic epidemiology of Parkinson's disease |
| Q28287237 | Immunoelectron-microscopic demonstration of NACP/alpha-synuclein-epitopes on the filamentous component of Lewy bodies in Parkinson's disease and in dementia with Lewy bodies |
| Q22252807 | Intraneuronal dopamine-quinone synthesis: A review |
| Q34478663 | Lewy bodies |
| Q35840040 | Lewy-body formation is an aggresome-related process: a hypothesis |
| Q47801119 | Loss of native α-synuclein multimerization by strategically mutating its amphipathic helix causes abnormal vesicle interactions in neuronal cells |
| Q34073890 | Lys-63-linked ubiquitination by E3 ubiquitin ligase Nedd4-1 facilitates endosomal sequestration of internalized α-synuclein |
| Q35412397 | Mitochondrial Dysfunction and α-Synuclein Synaptic Pathology in Parkinson's Disease: Who's on First? |
| Q64869820 | Orphan neurones and amine excess: the functional neuropathology of Parkinsonism and neuropsychiatric disease |
| Q50532472 | Pale neurites, premature α-synuclein aggregates with centripetal extension from axon collaterals. |
| Q92465171 | Parkinson's disease: proteinopathy or lipidopathy? |
| Q34995015 | Parkinson's genetics: molecular insights for the new millennium. |
| Q43940212 | Parkinson-like neurodegeneration induced by targeted overexpression of alpha-synuclein in the nigrostriatal system. |
| Q30479870 | Proteomic characterization of an isolated fraction of synthetic proteasome inhibitor (PSI)-induced inclusions in PC12 cells might offer clues to aggresomes as a cellular defensive response against proteasome inhibition by PSI. |
| Q34117600 | The AAA-ATPase VPS4 regulates extracellular secretion and lysosomal targeting of α-synuclein. |
| Q37003482 | The Lewy body in Parkinson's disease: molecules implicated in the formation and degradation of alpha-synuclein aggregates |
| Q36423369 | The Parkinson's disease protein alpha-synuclein disrupts cellular Rab homeostasis |
| Q89790112 | The process of Lewy body formation, rather than simply α-synuclein fibrillization, is one of the major drivers of neurodegeneration |
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