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2. The impact of VPS35 D620N mutation on alternative autophagy and its reversal by estrogen in Parkinson's disease. Shiraishi T; Bono K; Hiraki H; Manome Y; Oka H; Iguchi Y; Okano HJ Cell Mol Life Sci; 2024 Feb; 81(1):103. PubMed ID: 38409392 [TBL] [Abstract][Full Text] [Related]
3. Parkinson's disease-linked Chen X; Kordich JK; Williams ET; Levine N; Cole-Strauss A; Marshall L; Labrie V; Ma J; Lipton JW; Moore DJ Proc Natl Acad Sci U S A; 2019 Mar; 116(12):5765-5774. PubMed ID: 30842285 [TBL] [Abstract][Full Text] [Related]
4. VPS35 in Dopamine Neurons Is Required for Endosome-to-Golgi Retrieval of Lamp2a, a Receptor of Chaperone-Mediated Autophagy That Is Critical for α-Synuclein Degradation and Prevention of Pathogenesis of Parkinson's Disease. Tang FL; Erion JR; Tian Y; Liu W; Yin DM; Ye J; Tang B; Mei L; Xiong WC J Neurosci; 2015 Jul; 35(29):10613-28. PubMed ID: 26203154 [TBL] [Abstract][Full Text] [Related]
5. VPS35 D620N knockin mice recapitulate cardinal features of Parkinson's disease. Niu M; Zhao F; Bondelid K; Siedlak SL; Torres S; Fujioka H; Wang W; Liu J; Zhu X Aging Cell; 2021 May; 20(5):e13347. PubMed ID: 33745227 [TBL] [Abstract][Full Text] [Related]
6. Endosomal dysfunction in iPSC-derived neural cells from Parkinson's disease patients with VPS35 D620N. Bono K; Hara-Miyauchi C; Sumi S; Oka H; Iguchi Y; Okano HJ Mol Brain; 2020 Oct; 13(1):137. PubMed ID: 33032646 [TBL] [Abstract][Full Text] [Related]
7. The Vps35 D620N mutation linked to Parkinson's disease disrupts the cargo sorting function of retromer. Follett J; Norwood SJ; Hamilton NA; Mohan M; Kovtun O; Tay S; Zhe Y; Wood SA; Mellick GD; Silburn PA; Collins BM; Bugarcic A; Teasdale RD Traffic; 2014 Feb; 15(2):230-44. PubMed ID: 24152121 [TBL] [Abstract][Full Text] [Related]
8. VPS35 and α-Synuclein fail to interact to modulate neurodegeneration in rodent models of Parkinson's disease. Chen X; Tsika E; Levine N; Moore DJ Mol Neurodegener; 2023 Aug; 18(1):51. PubMed ID: 37542299 [TBL] [Abstract][Full Text] [Related]
9. (D620N) VPS35 causes the impairment of Wnt/β-catenin signaling cascade and mitochondrial dysfunction in a PARK17 knockin mouse model. Chiu CC; Weng YH; Huang YZ; Chen RS; Liu YC; Yeh TH; Lu CS; Lin YW; Chen YJ; Hsu CC; Chiu CH; Wang YT; Chen WS; Liu SY; Wang HL Cell Death Dis; 2020 Nov; 11(11):1018. PubMed ID: 33257649 [TBL] [Abstract][Full Text] [Related]
10. VPS35 and retromer dysfunction in Parkinson's disease. Rowlands J; Moore DJ Philos Trans R Soc Lond B Biol Sci; 2024 Apr; 379(1899):20220384. PubMed ID: 38368930 [TBL] [Abstract][Full Text] [Related]
11. Mutant VPS35-D620N induces motor dysfunction and impairs DAT-mediated dopamine recycling pathway. Huang Y; Huang H; Zhou L; Li J; Chen X; Thomas J; He X; Guo W; Zeng Y; Low BC; Liang F; Zeng J; Ross CA; Tan EK; Smith W; Pei Z Hum Mol Genet; 2022 Nov; 31(22):3886-3896. PubMed ID: 35766879 [TBL] [Abstract][Full Text] [Related]
12. Parkinson's disease-associated mutant VPS35 causes mitochondrial dysfunction by recycling DLP1 complexes. Wang W; Wang X; Fujioka H; Hoppel C; Whone AL; Caldwell MA; Cullen PJ; Liu J; Zhu X Nat Med; 2016 Jan; 22(1):54-63. PubMed ID: 26618722 [TBL] [Abstract][Full Text] [Related]
13. Parkinson's disease-linked mutations in VPS35 induce dopaminergic neurodegeneration. Tsika E; Glauser L; Moser R; Fiser A; Daniel G; Sheerin UM; Lees A; Troncoso JC; Lewis PA; Bandopadhyay R; Schneider BL; Moore DJ Hum Mol Genet; 2014 Sep; 23(17):4621-38. PubMed ID: 24740878 [TBL] [Abstract][Full Text] [Related]
14. The Parkinson's disease VPS35[D620N] mutation enhances LRRK2-mediated Rab protein phosphorylation in mouse and human. Mir R; Tonelli F; Lis P; Macartney T; Polinski NK; Martinez TN; Chou MY; Howden AJM; König T; Hotzy C; Milenkovic I; Brücke T; Zimprich A; Sammler E; Alessi DR Biochem J; 2018 Jun; 475(11):1861-1883. PubMed ID: 29743203 [TBL] [Abstract][Full Text] [Related]
15. Retromer binding to FAM21 and the WASH complex is perturbed by the Parkinson disease-linked VPS35(D620N) mutation. McGough IJ; Steinberg F; Jia D; Barbuti PA; McMillan KJ; Heesom KJ; Whone AL; Caldwell MA; Billadeau DD; Rosen MK; Cullen PJ Curr Biol; 2014 Jul; 24(14):1670-1676. PubMed ID: 24980502 [TBL] [Abstract][Full Text] [Related]
16. Impaired neurogenesis in the hippocampus of an adult VPS35 mutant mouse model of Parkinson's disease through interaction with APP. Jiang M; Tu HT; Zhang K; Zhang W; Yu WP; Xu J; Tan EK; Guo KH; Zeng L Neurobiol Dis; 2021 Jun; 153():105313. PubMed ID: 33636388 [TBL] [Abstract][Full Text] [Related]
17. VPS35 Deficiency or Mutation Causes Dopaminergic Neuronal Loss by Impairing Mitochondrial Fusion and Function. Tang FL; Liu W; Hu JX; Erion JR; Ye J; Mei L; Xiong WC Cell Rep; 2015 Sep; 12(10):1631-43. PubMed ID: 26321632 [TBL] [Abstract][Full Text] [Related]
18. Formation of retromer transport carriers is disrupted by the Parkinson disease-linked Vps35 D620N variant. Cui Y; Yang Z; Flores-Rodriguez N; Follett J; Ariotti N; Wall AA; Parton RG; Teasdale RD Traffic; 2021 Apr; 22(4):123-136. PubMed ID: 33347683 [TBL] [Abstract][Full Text] [Related]
19. Parkinson's disease-associated VPS35 mutant reduces mitochondrial membrane potential and impairs PINK1/Parkin-mediated mitophagy. Ma KY; Fokkens MR; Reggiori F; Mari M; Verbeek DS Transl Neurodegener; 2021 Jun; 10(1):19. PubMed ID: 34127073 [TBL] [Abstract][Full Text] [Related]
20. Retromer-dependent neurotransmitter receptor trafficking to synapses is altered by the Parkinson's disease VPS35 mutation p.D620N. Munsie LN; Milnerwood AJ; Seibler P; Beccano-Kelly DA; Tatarnikov I; Khinda J; Volta M; Kadgien C; Cao LP; Tapia L; Klein C; Farrer MJ Hum Mol Genet; 2015 Mar; 24(6):1691-703. PubMed ID: 25416282 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]