Accumulation and distribution of α-synuclein and ubiquitin in the CNS of Gaucher disease mouse models
Top Cited Papers
- 31 December 2010
- journal article
- Published by Elsevier in Molecular Genetics and Metabolism
- Vol. 102 (4), 436-447
- https://doi.org/10.1016/j.ymgme.2010.12.014
Abstract
No abstract availableKeywords
This publication has 70 references indexed in Scilit:
- Glucocerebrosidase is present in α-synuclein inclusions in Lewy body disordersActa Neuropathologica, 2010
- Specific saposin C deficiency: CNS impairment and acid -glucosidase effects in the mouseHuman Molecular Genetics, 2009
- Multicenter Analysis of Glucocerebrosidase Mutations in Parkinson's DiseaseNew England Journal of Medicine, 2009
- Dependence of reversibility and progression of mouse neuronopathic Gaucher disease on acid β-glucosidase residual activity levelsMolecular Genetics and Metabolism, 2008
- Progression of multiple behavioral deficits with various ages of onset in a murine model of Hurler syndromeBrain Research, 2007
- Glucocerebrosidase mutations in Chinese subjects from Taiwan with sporadic Parkinson diseaseMolecular Genetics and Metabolism, 2007
- Suppression of basal autophagy in neural cells causes neurodegenerative disease in miceNature, 2006
- Loss of autophagy in the central nervous system causes neurodegeneration in miceNature, 2006
- Mice Lacking α-Synuclein Display Functional Deficits in the Nigrostriatal Dopamine SystemNeuron, 2000
- AlaSOPro mutation in the gene encoding α-synuclein in Parkinson's diseaseNature Genetics, 1998