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ArticlesPeer ReviewedFull Text
Parkinson's disease–associated mutant VPS35 causes mitochondrial dysfunction by recycling DLP1 complexes
Author / Creator:Wang, Wenzhang ; Wang, Xinglong ; Fujioka, Hisashi ; Hoppel, Charles ; Whone, Alan L ; Caldwell, Maeve A ; Cullen, Peter J ; Liu, Jun ; Zhu, Xiongwei
Publisher:New York: Nature Publishing Group US
Journal title:Nature medicine, 2016-01, Vol.22 (1), p.54-63
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Mutation in VPS35 associated with Parkinson’s disease impairs WASH complex association and inhibits autophagy
Author / Creator:Zavodszky, Eszter ; Seaman, Matthew N.J. ; Moreau, Kevin ; Jimenez-Sanchez, Maria ; Breusegem, Sophia Y. ; Harbour, Michael E. ; Rubinsztein, David C.
Publisher:London: Nature Publishing Group UK
Journal title:Nature communications, 2014-05, Vol.5 (1), p.3828-3828, Article 3828
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Parkinson’s disease-linked D620N VPS35 knockin mice manifest tau neuropathology and dopaminergic neurodegeneration
Author / Creator:Chen, Xi ; Kordich, Jennifer K. ; Williams, Erin T. ; Levine, Nathan ; Cole-Strauss, Allyson ; Marshall, Lee ; Labrie, Viviane ; Ma, Jiyan ; Lipton, Jack W. ; Moore, Darren J.
Publisher:United States: National Academy of Sciences
Journal title:Proceedings of the National Academy of Sciences - PNAS, 2019-03, Vol.116 (12), p.5765-5774
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Mitochondrial membrane proteins and VPS35 orchestrate selective removal of mtDNA
Author / Creator:Sen, Ayesha ; Kallabis, Sebastian ; Gaedke, Felix ; Jüngst, Christian ; Boix, Julia ; Nüchel, Julian ; Maliphol, Kanjanamas ; Hofmann, Julia ; Schauss, Astrid C. ; Krüger, Marcus ; Wiesner, Rudolf J. ; Pla-Martín, David
Publisher:London: Nature Publishing Group UK
Journal title:Nature communications, 2022-11, Vol.13 (1), p.6704-6704, Article 6704
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VPS35 D620N knockin mice recapitulate cardinal features of Parkinson’s disease
Author / Creator:Niu, Mengyue ; Zhao, Fanpeng ; Bondelid, Karina ; Siedlak, Sandra L. ; Torres, Sandy ; Fujioka, Hisashi ; Wang, Wenzhang ; Liu, Jun ; Zhu, Xiongwei
Publisher:England: John Wiley & Sons, Inc
Journal title:Aging cell, 2021-05, Vol.20 (5), p.e13347-n/a
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VPS35 regulates tau phosphorylation and neuropathology in tauopathy
Author / Creator:Vagnozzi, Alana N ; Li, Jian-Guo ; Chiu, Jin ; Razmpour, Roshanak ; Warfield, Rebecca ; Ramirez, Servio H ; Praticò, Domenico
Publisher:England: Nature Publishing Group
Journal title:Molecular psychiatry, 2021-11, Vol.26 (11), p.6992-7005
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Microglial VPS35 deficiency impairs Aβ phagocytosis and Aβ-induced disease-associated microglia, and enhances Aβ associated pathology
Author / Creator:Ren, Xiao ; Yao, Lingling ; Wang, YongGang ; Mei, Lin ; Xiong, Wen-Cheng
Publisher:England: BioMed Central
Journal title:Journal of neuroinflammation, 2022-03, Vol.19 (1), p.61-61, Article 61
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Atypical parkinsonism of progressive supranuclear palsy–parkinsonism (PSP-P) phenotype with rare variants in FBXO7 and VPS35 genes associated with Lewy body pathology
Author / Creator:Menšíková, Kateřina ; Tučková, Lucie ; Kolařiková, Kristýna ; Bartoníková, Tereza ; Vodička, Radek ; Ehrmann, Jiri ; Vrtěl, Radek ; Procházka, Martin ; Kaňovský, Petr ; Kovacs, Gabor G.
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Acta neuropathologica, 2019-01, Vol.137 (1), p.171-173
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Vacuolar protein sorting 35 (Vps35) rescues locomotor deficits and shortened lifespan in Drosophila expressing a Parkinson's disease mutant of Leucine-Rich Repeat Kinase 2 (LRRK2)
Author / Creator:Linhart, Radek ; Wong, Sarah Anne ; Cao, Jieyun ; Tran, Melody ; Huynh, Anne ; Ardrey, Casey ; Park, Jong Min ; Hsu, Christine ; Taha, Saher ; Peterson, Rentia ; Shea, Shannon ; Kurian, Jason ; Venderova, Katerina
Publisher:England: BioMed Central
Journal title:Molecular neurodegeneration, 2014-06, Vol.9 (1), p.23-23, Article 23
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KLF7/VPS35 axis contributes to hepatocellular carcinoma progression through CCDC85C-activated β-catenin pathway
Author / Creator:Guo, Yarong ; Chai, Bao ; Jia, Junmei ; Yang, Mudan ; Li, Yanjun ; Zhang, Rui ; Wang, Shunmin ; Xu, Jun
Publisher:England: BioMed Central
Journal title:Cell & bioscience, 2021-04, Vol.11 (1), p.73-73, Article 73
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Retraction Note: VPS35 regulates tau phosphorylation and neuropathology in tauopathy
Author / Creator:Vagnozzi, Alana N. ; Li, Jian-Guo ; Chiu, Jin ; Razmpour, Roshanak ; Warfield, Rebecca ; Ramirez, Servio H. ; Praticò, Domenico
Publisher:London: Nature Publishing Group UK
Journal title:Molecular psychiatry, 2023-04, Vol.28 (4), p.1828-1828
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(D620N) VPS35 causes the impairment of Wnt/β-catenin signaling cascade and mitochondrial dysfunction in a PARK17 knockin mouse model
Author / Creator:Chiu, Ching-Chi ; Weng, Yi-Hsin ; Huang, Ying-Zu ; Chen, Rou-Shayn ; Liu, Yu-Chuan ; Yeh, Tu-Hsueh ; Lu, Chin-Song ; Lin, Yan-Wei ; Chen, Yu-Jie ; Hsu, Chia-Chen ; Chiu, Chi-Han ; Wang, Yu-Ting ; Chen, Wan-Shia ; Liu, Shu-Yu ; Wang, Hung-Li
Publisher:London: Nature Publishing Group UK
Journal title:Cell death & disease, 2020-11, Vol.11 (11), p.1018-1018, Article 1018
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VPS35 and α-Synuclein fail to interact to modulate neurodegeneration in rodent models of Parkinson's disease
Author / Creator:Chen, Xi ; Tsika, Elpida ; Levine, Nathan ; Moore, Darren J
Publisher:England: BioMed Central
Journal title:Molecular neurodegeneration, 2023-08, Vol.18 (1), p.51-51, Article 51
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DNA and RNA sequencing identified a novel oncogene VPS35 in liver hepatocellular carcinoma
Author / Creator:Zhang, Guiji ; Tang, Xia ; Liang, Li ; Zhang, Wanfeng ; Li, Dewei ; Li, Xiaoyuan ; Zhao, Dachun ; Zheng, Yaqiu ; Chen, Yanhong ; Hao, Bingtao ; Wang, Kai ; Tang, Ni ; Ding, Keyue
Publisher:London: Nature Publishing Group UK
Journal title:Oncogene, 2020-04, Vol.39 (16), p.3229-3244
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Mutant mice with rod-specific VPS35 deletion exhibit retinal α-synuclein pathology-associated degeneration
Author / Creator:Fu, Cheng ; Yang, Nan ; Chuang, Jen-Zen ; Nakajima, Nobuyuki ; Iraha, Satoshi ; Roy, Neeta ; Wu, Zhenquan ; Jiang, Zhichun ; Otsu, Wataru ; Radu, Roxana A. ; Yang, Howard Hua ; Lee, Maxwell Ping ; Worgall, Tilla S. ; Xiong, Wen-Cheng ; Sung, Ching-Hwa
Publisher:London: Nature Publishing Group UK
Journal title:Nature communications, 2024-07, Vol.15 (1), p.5970-19, Article 5970
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Endosomal dysfunction in iPSC-derived neural cells from Parkinson’s disease patients with VPS35 D620N
Author / Creator:Bono, Keiko ; Hara-Miyauchi, Chikako ; Sumi, Shunsuke ; Oka, Hisayoshi ; Iguchi, Yasuyuki ; Okano, Hirotaka James
Publisher:London: BioMed Central Ltd
Journal title:Molecular brain, 2020-10, Vol.13 (1), p.1-137, Article 137
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Parkinson's disease-associated VPS35 mutant reduces mitochondrial membrane potential and impairs PINK1/Parkin-mediated mitophagy
Author / Creator:Ma, Kai Yu ; Fokkens, Michiel R ; Reggiori, Fulvio ; Mari, Muriel ; Verbeek, Dineke S
Publisher:England: BioMed Central
Journal title:Translational neurodegeneration, 2021-06, Vol.10 (1), p.19-19, Article 19
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RETRACTED ARTICLE: VPS35 regulates tau phosphorylation and neuropathology in tauopathy
Author / Creator:Vagnozzi, Alana N. ; Li, Jian-Guo ; Chiu, Jin ; Razmpour, Roshanak ; Warfield, Rebecca ; Ramirez, Servio H. ; Praticò, Domenico
Publisher:London: Nature Publishing Group UK
Journal title:Molecular psychiatry, 2021-11, Vol.26 (11), p.6992-7005
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Altered striatal dopamine levels in Parkinson’s disease VPS35 D620N mutant transgenic aged mice
Author / Creator:Vanan, Sarivin ; Zeng, Xiaoxia ; Chia, Sook Yoong ; Varnäs, Katarina ; Jiang, Mei ; Zhang, Ke ; Saw, Wuan Ting ; Padmanabhan, Parasuraman ; Yu, Wei-Ping ; Zhou, Zhi-Dong ; Halldin, Christer ; Gulyás, Balázs ; Tan, Eng-King ; Zeng, Li
Publisher:London: BioMed Central Ltd
Journal title:Molecular brain, 2020-12, Vol.13 (1), p.1-164, Article 164
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Identification of VPS35 p.D620N mutation-related Parkinson's disease in a Taiwanese family with successful bilateral subthalamic nucleus deep brain stimulation: a case report and literature review
Author / Creator:Chen, Ying-Fa ; Chang, Yung-Yee ; Lan, Min-Yu ; Chen, Pei-Lung ; Lin, Chin-Hsien
Publisher:England: BioMed Central Ltd
Journal title:BMC neurology, 2017-10, Vol.17 (1), p.191-191, Article 191
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Parkinson's disease–associated mutant VPS35 causes mitochondrial dysfunction by recycling DLP1 complexes

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Mutation in VPS35 associated with Parkinson’s disease impairs WASH complex association and inhibits autophagy

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Parkinson’s disease-linked D620N VPS35 knockin mice manifest tau neuropathology and dopaminergic neurodegeneration

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Mitochondrial membrane proteins and VPS35 orchestrate selective removal of mtDNA

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VPS35 D620N knockin mice recapitulate cardinal features of Parkinson’s disease

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VPS35 regulates tau phosphorylation and neuropathology in tauopathy

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Microglial VPS35 deficiency impairs Aβ phagocytosis and Aβ-induced disease-associated microglia, and enhances Aβ associated pathology

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Atypical parkinsonism of progressive supranuclear palsy–parkinsonism (PSP-P) phenotype with rare variants in FBXO7 and VPS35 genes associated with Lewy body pathology

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Vacuolar protein sorting 35 (Vps35) rescues locomotor deficits and shortened lifespan in Drosophila expressing a Parkinson's disease mutant of Leucine-Rich Repeat Kinase 2 (LRRK2)

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KLF7/VPS35 axis contributes to hepatocellular carcinoma progression through CCDC85C-activated β-catenin pathway

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Retraction Note: VPS35 regulates tau phosphorylation and neuropathology in tauopathy

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(D620N) VPS35 causes the impairment of Wnt/β-catenin signaling cascade and mitochondrial dysfunction in a PARK17 knockin mouse model

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VPS35 and α-Synuclein fail to interact to modulate neurodegeneration in rodent models of Parkinson's disease

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DNA and RNA sequencing identified a novel oncogene VPS35 in liver hepatocellular carcinoma

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Mutant mice with rod-specific VPS35 deletion exhibit retinal α-synuclein pathology-associated degeneration

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Endosomal dysfunction in iPSC-derived neural cells from Parkinson’s disease patients with VPS35 D620N

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Parkinson's disease-associated VPS35 mutant reduces mitochondrial membrane potential and impairs PINK1/Parkin-mediated mitophagy

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RETRACTED ARTICLE: VPS35 regulates tau phosphorylation and neuropathology in tauopathy

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Altered striatal dopamine levels in Parkinson’s disease VPS35 D620N mutant transgenic aged mice

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Identification of VPS35 p.D620N mutation-related Parkinson's disease in a Taiwanese family with successful bilateral subthalamic nucleus deep brain stimulation: a case report and literature review

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