Contributions of VPS35 Mutations to Parkinson’s Disease
Author:
Funder
National Institute of General Medical Sciences
National Institute of Neurological Disorders and Stroke
Publisher
Elsevier BV
Subject
General Neuroscience
Reference119 articles.
1. VPS35 mutation in Japanese patients with typical Parkinson’s disease;Ando;Mov Disord,2012
2. Increased microglial activity, impaired adult hippocampal neurogenesis, and depressive-like behavior in microglial VPS35-depleted mice;Appel;J Neurosci,2018
3. Role of the mammalian retromer in sorting of the cation-independent mannose 6-phosphate receptor;Arighi;J Cell Biol,2004
4. The epidemiology of Parkinson’s disease: risk factors and prevention;Ascherio;Lancet Neurol,2016
5. The pathways of mitophagy for quality control and clearance of mitochondria;Ashrafi;Cell Death Differ,2013
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