Parkinson's disease-linked mutations in VPS35 induce dopaminergic neurodegeneration (Q33991769)

24740878

30 July 2017

title

Parkinson's disease-linked mutations in VPS35 induce dopaminergic neurodegeneration (English)

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30 July 2017

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Rina Bandopadhyay

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Liliane Glauser

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Andrew Lees

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Roger Moser

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31 May 2020

Guillaume Daniel

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Una-Marie Sheerin

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Juan C Troncoso

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publication date

15 April 2014

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24740878

30 July 2017

published in

Human Molecular Genetics

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volume

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issue

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page(s)

4621-4638

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describes a project that uses

31 May 2020

ImageJ

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11 June 2022

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based on heuristic

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cites work

The Vps35 D620N mutation linked to Parkinson's disease disrupts the cargo sorting function of retromer

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The VPS35 gene and Parkinson's disease

5 July 2018

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Pathogenic mutation in VPS35 impairs its protection against MPP(+) cytotoxicity

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RAB7L1 interacts with LRRK2 to modify intraneuronal protein sorting and Parkinson's disease risk

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A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants

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A mutation in VPS35, encoding a subunit of the retromer complex, causes late-onset Parkinson disease

5 July 2018

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VPS35 mutations in Parkinson disease

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Dopaminergic neuronal loss, reduced neurite complexity and autophagic abnormalities in transgenic mice expressing G2019S mutant LRRK2.

5 July 2018

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Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease

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5 July 2018

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Crossref

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21 January 2018

Identifiers

DOI

10.1093/HMG/DDU178

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31 May 2020

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31 May 2020

24740878

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