Associated Papers
An update on the monogenic causes of Parkinson's disease: Impact on patient stratification and personalised medicine.
Asmi S et al.
Ageing Research Reviews, 2026
Exploring the triad: VPS35, neurogenesis, and neurodegenerative diseases.
Qiu Z et al.
Journal of Neurochemistry, 2024
VPS35 and retromer dysfunction in Parkinson's disease.
Rowlands J et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences, 2024
Genetic Evidence for Endolysosomal Dysfunction in Parkinson's Disease: A Critical Overview.
Yahya V et al.
International Journal of Molecular Sciences, 2023
The Role of VPS35 in the Pathobiology of Parkinson's Disease.
Sassone J et al.
Cellular and Molecular Neurobiology, 2021
VPS35, the core component of the retromer complex, and Parkinson's disease.
Luo AD et al.
Ibrain, 2021
Rare VPS35 A320V Variant in Taiwanese Parkinson's Disease Indicates Disrupted CI-MPR Sorting and Impaired Mitochondrial Morphology.
Wu YR et al.
Brain Sciences, 2020
Parkinson's disease-linked D620N VPS35 knockin mice manifest tau neuropathology and dopaminergic neurodegeneration.
Chen X et al.
Proceedings of the National Academy of Sciences of the United States of America, 2019
Contributions of VPS35 Mutations to Parkinson's Disease.
Rahman AA et al.
Neuroscience, 2019
VPS35-Based Approach: A Potential Innovative Treatment in Parkinson's Disease.
Eleuteri S et al.
Frontiers in Neurology, 2019
The functional roles of retromer in Parkinson's disease.
Cui Y et al.
Febs Letters, 2018
Role of the VPS35 D620N mutation in Parkinson's disease.
Mohan M et al.
Parkinsonism & Related Disorders, 2017
VPS35, the Retromer Complex and Parkinson's Disease.
Williams ET et al.
Journal of Parkinson's Disease, 2017
Parkinson's disease-linked mutations in VPS35 induce dopaminergic neurodegeneration.
Tsika E et al.
Human Molecular Genetics, 2014
Update on novel familial forms of Parkinson's disease and multiple system atrophy.
Fujioka S et al.
Parkinsonism & Related Disorders, 2014
The VPS35 gene and Parkinson's disease.
Deng H et al.
Movement Disorders : Official Journal of the Movement Disorder Society, 2013
VPS35 mutation in Chinese Han patients with late-onset Parkinson's disease.
Deng H et al.
European Journal of Neurology, 2012
Contribution of VPS35 genetic variability to LBD in the Flanders-Belgian population.
Verstraeten A et al.
Neurobiology of Aging, 2012