The VPS35 gene and Parkinson's disease (Q38093808)

28 August 2017

title

The VPS35 gene and Parkinson's disease (English)

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28 August 2017

Joseph Jankovic

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28 August 2017

Hao Deng

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28 August 2017

Kai Gao

series ordinal

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28 August 2017

language of work or name

English

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publication date

27 March 2013

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28 August 2017

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28 August 2017

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28 August 2017

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28 August 2017

page(s)

569-575

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Epidemiology of Parkinson's disease

28 August 2017

cites work

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Parkinson's disease: clinical features and diagnosis

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Initial clinical manifestations of Parkinson's disease: features and pathophysiological mechanisms.

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Therapies in Parkinson's disease

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Role of mendelian genes in "sporadic" Parkinson's disease

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VPS35 mutations in Parkinson disease

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

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Contribution of VPS35 genetic variability to LBD in the Flanders-Belgian population

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Screening for VPS35 mutations in Parkinson's disease

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Vacuolar protein sorting 35 Asp620Asn mutation is rare in the ethnic Chinese population with Parkinson's disease

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VPS35 gene variants are not associated with Parkinson's disease in the mainland Chinese population

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Frequency of the D620N mutation in VPS35 in Parkinson disease

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VPS35 mutation in Chinese Han patients with late-onset Parkinson's disease.

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VPS35 mutation in Japanese patients with typical Parkinson's disease

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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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VPS35 Asp620Asn and EIF4G1 Arg1205His mutations are rare in Parkinson disease from southwest China

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Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic data

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Parkinson's disease in Arabs: a systematic review

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Human homologues of yeast vacuolar protein sorting 29 and 35

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Cloning and characterization of human VPS35 and mouse Vps35 and mapping of VPS35 to human chromosome 16q13-q21

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Recent advances in retromer biology

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Interchangeable but essential functions of SNX1 and SNX2 in the association of retromer with endosomes and the trafficking of mannose 6-phosphate receptors

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Exit from the trans-Golgi network: from molecules to mechanisms

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Role of the mammalian retromer in sorting of the cation-independent mannose 6-phosphate receptor

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Genetic evidence for a mammalian retromer complex containing sorting nexins 1 and 2.

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Retromer is required for apoptotic cell clearance by phagocytic receptor recycling

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A SNX3-dependent retromer pathway mediates retrograde transport of the Wnt sorting receptor Wntless and is required for Wnt secretion

21 January 2018

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Functional architecture of the retromer cargo-recognition complex

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Structural features of vps35p involved in interaction with other subunits of the retromer complex

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Dominant-negative behavior of mammalian Vps35 in yeast requires a conserved PRLYL motif involved in retromer assembly

21 January 2018

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Human orthologs of yeast vacuolar protein sorting proteins Vps26, 29, and 35: assembly into multimeric complexes

21 January 2018

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Vps29 has a phosphoesterase fold that acts as a protein interaction scaffold for retromer assembly

21 January 2018

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Model-guided microarray implicates the retromer complex in Alzheimer's disease

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The location and trafficking routes of the neuronal retromer and its role in amyloid precursor protein transport

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Retromer deficiency observed in Alzheimer's disease causes hippocampal dysfunction, neurodegeneration, and Abeta accumulation

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VPS35 haploinsufficiency increases Alzheimer's disease neuropathology.

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VPS35 regulates developing mouse hippocampal neuronal morphogenesis by promoting retrograde trafficking of BACE1

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Differential regulation of midbrain dopaminergic neuron development by Wnt-1, Wnt-3a, and Wnt-5a

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Emerging roles of Wnts in the adult nervous system

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Inhibition of the canonical Wnt pathway by Dickkopf-1 contributes to the neurodegeneration in 6-OHDA-lesioned rats

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Reactive astrocytes and Wnt/β-catenin signaling link nigrostriatal injury to repair in 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine model of Parkinson's disease

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Gene expression profiling in progressively MPTP-lesioned macaques reveals molecular pathways associated with sporadic Parkinson's disease

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Effects of gender on nigral gene expression and parkinson disease

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Activation of Wnt signaling rescues neurodegeneration and behavioral impairments induced by beta-amyloid fibrils

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Parkin protects dopaminergic neurons from excessive Wnt/beta-catenin signaling

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Mutations in the LRRK2 Roc-COR tandem domain link Parkinson's disease to Wnt signalling pathways

21 January 2018

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What genetics tells us about the causes and mechanisms of Parkinson's disease

21 January 2018

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Wntless, a conserved membrane protein dedicated to the secretion of Wnt proteins from signaling cells

21 January 2018

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Secretion of Wnt ligands requires Evi, a conserved transmembrane protein

21 January 2018

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The retromer complex influences Wnt secretion by recycling wntless from endosomes to the trans-Golgi network

21 January 2018

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Wingless secretion requires endosome-to-Golgi retrieval of Wntless/Evi/Sprinter by the retromer complex

21 January 2018

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Wingless secretion promotes and requires retromer-dependent cycling of Wntless

21 January 2018

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The ins and outs of iron homeostasis

21 January 2018

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Brain iron homeostasis and neurodegenerative disease

21 January 2018

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Iron dysregulation in movement disorders

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Up-regulation of divalent metal transporter 1 in 6-hydroxydopamine intoxication is IRE/IRP dependent

21 January 2018

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Divalent metal transporter 1 (DMT1) contributes to neurodegeneration in animal models of Parkinson's disease

21 January 2018

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Up-regulation of divalent metal transporter 1 is involved in 1-methyl-4-phenylpyridinium (MPP(+))-induced apoptosis in MES23.5 cells

21 January 2018

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DMT1 polymorphism and risk of Parkinson's disease

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Enhanced autophagy from chronic toxicity of iron and mutant A53T α-synuclein: implications for neuronal cell death in Parkinson disease

21 January 2018

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α-Synuclein: membrane interactions and toxicity in Parkinson's disease

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Parkin regulates metal transport via proteasomal degradation of the 1B isoforms of divalent metal transporter 1.

21 January 2018

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Retromer-mediated direct sorting is required for proper endosomal recycling of the mammalian iron transporter DMT1

21 January 2018

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Parkinson's disease: from monogenic forms to genetic susceptibility factors

21 January 2018

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Synaptic vesicle trafficking and Parkinson's disease

21 January 2018

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Lysosome-dependent pathways as a unifying theme in Parkinson's disease.

21 January 2018

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Helping Wingless take flight: how WNT proteins are secreted

21 January 2018

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Wnt signaling requires retromer-dependent recycling of MIG-14/Wntless in Wnt-producing cells

21 January 2018

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LRRK2 mutations and Parkinsonism

21 January 2018

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21 January 2018

Identifiers

DOI

10.1002/MDS.25430

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28 August 2017

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