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Best matches for vps35 Parkinson's disease:

VPS35, the Retromer Complex and Parkinson's Disease. Williams ET et al. J Parkinsons Dis. (2017)

Mitochondrial dysfunction in Parkinson's disease. Bose A et al. J Neurochem. (2016)

Genetics of Parkinson's disease. Lill CM et al. Mol Cell Probes. (2016)

Search results

Items: 1 to 20 of 140

1.

Disease model organism for Parkinson Disease: Drosophila melanogaster.

Aryal B, Lee Y.

BMB Rep. 2018 Dec 14. pii: 4331. [Epub ahead of print]

PMID:
30545438
2.

Sphingolipids in the Pathogenesis of Parkinson's Disease and Parkinsonism.

Lin G, Wang L, Marcogliese PC, Bellen HJ.

Trends Endocrinol Metab. 2018 Dec 6. pii: S1043-2760(18)30203-0. doi: 10.1016/j.tem.2018.11.003. [Epub ahead of print] Review.

PMID:
30528460
3.

Synaptic, Mitochondrial, and Lysosomal Dysfunction in Parkinson's Disease.

Nguyen M, Wong YC, Ysselstein D, Severino A, Krainc D.

Trends Neurosci. 2018 Nov 30. pii: S0166-2236(18)30282-0. doi: 10.1016/j.tins.2018.11.001. [Epub ahead of print] Review.

PMID:
30509690
4.

Analysis of RNA Expression Profiles Identifies Dysregulated Vesicle Trafficking Pathways in Creutzfeldt-Jakob Disease.

Bartoletti-Stella A, Corrado P, Mometto N, Baiardi S, Durrenberger PF, Arzberger T, Reynolds R, Kretzschmar H, Capellari S, Parchi P.

Mol Neurobiol. 2018 Nov 16. doi: 10.1007/s12035-018-1421-1. [Epub ahead of print]

PMID:
30446946
5.

Retromer in Synaptic Function and Pathology.

Brodin L, Shupliakov O.

Front Synaptic Neurosci. 2018 Oct 24;10:37. doi: 10.3389/fnsyn.2018.00037. eCollection 2018. Review.

6.

Genotype-phenotype relations for the Parkinson's disease genes SNCA, LRRK2, VPS35: MDSGene systematic review.

Trinh J, Zeldenrust FMJ, Huang J, Kasten M, Schaake S, Petkovic S, Madoev H, Grünewald A, Almuammar S, König IR, Lill CM, Lohmann K, Klein C, Marras C.

Mov Disord. 2018 Oct 24. doi: 10.1002/mds.27527. [Epub ahead of print] Review.

PMID:
30357936
7.

The genetic landscape of Parkinson's disease.

Lunati A, Lesage S, Brice A.

Rev Neurol (Paris). 2018 Nov;174(9):628-643. doi: 10.1016/j.neurol.2018.08.004. Epub 2018 Sep 21. Review.

PMID:
30245141
8.

New endemic familial parkinsonism in south Moravia, Czech Republic and its genetical background.

Bartoníková T, Menšíková K, Kolaříková K, Vodička R, Vrtěl R, Otruba P, Kaiserová M, Vaštík M, Mikulicová L, Ovečka J, Šáchová L, Dvorský F, Krša J, Jugas P, Godava M, Bareš M, Janout V, Hluštík P, Procházka M, Kaňovský P.

Medicine (Baltimore). 2018 Sep;97(38):e12313. doi: 10.1097/MD.0000000000012313.

9.

Sorting Out the Role of α-Synuclein in Retromer-Mediated Endosomal Protein Sorting.

Patel D, Witt SN.

J Exp Neurosci. 2018 Aug 23;12:1179069518796215. doi: 10.1177/1179069518796215. eCollection 2018.

10.

Altered dopamine release and monoamine transporters in Vps35 p.D620N knock-in mice.

Cataldi S, Follett J, Fox JD, Tatarnikov I, Kadgien C, Gustavsson EK, Khinda J, Milnerwood AJ, Farrer MJ.

NPJ Parkinsons Dis. 2018 Aug 21;4:27. doi: 10.1038/s41531-018-0063-3. eCollection 2018.

11.

Phospholipase PLA2G6, a Parkinsonism-Associated Gene, Affects Vps26 and Vps35, Retromer Function, and Ceramide Levels, Similar to α-Synuclein Gain.

Lin G, Lee PT, Chen K, Mao D, Tan KL, Zuo Z, Lin WW, Wang L, Bellen HJ.

Cell Metab. 2018 Oct 2;28(4):605-618.e6. doi: 10.1016/j.cmet.2018.05.019. Epub 2018 Jun 14.

PMID:
29909971
12.

Parkin mediates the ubiquitination of VPS35 and modulates retromer-dependent endosomal sorting.

Williams ET, Glauser L, Tsika E, Jiang H, Islam S, Moore DJ.

Hum Mol Genet. 2018 Sep 15;27(18):3189-3205. doi: 10.1093/hmg/ddy224.

PMID:
29893854
13.

Inhibition of TBC1D5 activates Rab7a and can enhance the function of the retromer cargo-selective complex.

Seaman MNJ, Mukadam AS, Breusegem SY.

J Cell Sci. 2018 Jun 21;131(12). pii: jcs217398. doi: 10.1242/jcs.217398.

14.

Deciphering the role of VPS35 in Parkinson's disease.

Williams ET, Moore DJ.

J Neurosci Res. 2018 Aug;96(8):1339-1340. doi: 10.1002/jnr.24262. Epub 2018 May 18. No abstract available.

PMID:
29775219
15.

Retromer Dysfunction and Neurodegenerative Disease.

Reitz C.

Curr Genomics. 2018 May;19(4):279-288. doi: 10.2174/1389202919666171024122809. Review.

16.

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 6;475(11):1861-1883. doi: 10.1042/BCJ20180248.

17.

Cellular and Molecular Basis of Neurodegeneration in Parkinson Disease.

Zeng XS, Geng WS, Jia JJ, Chen L, Zhang PP.

Front Aging Neurosci. 2018 Apr 17;10:109. doi: 10.3389/fnagi.2018.00109. eCollection 2018. Review.

18.

Pipeline to gene discovery - Analysing familial Parkinsonism in the Queensland Parkinson's Project.

Bentley SR, Bortnick S, Guella I, Fowdar JY, Silburn PA, Wood SA, Farrer MJ, Mellick GD.

Parkinsonism Relat Disord. 2018 Apr;49:34-41. doi: 10.1016/j.parkreldis.2017.12.033. Epub 2018 Jan 3.

PMID:
29329938
19.

Genetics of Parkinson disease.

Domingo A, Klein C.

Handb Clin Neurol. 2018;147:211-227. doi: 10.1016/B978-0-444-63233-3.00014-2.

PMID:
29325612
20.

The emerging role of Rab GTPases in the pathogenesis of Parkinson's disease.

Gao Y, Wilson GR, Stephenson SEM, Bozaoglu K, Farrer MJ, Lockhart PJ.

Mov Disord. 2018 Feb;33(2):196-207. doi: 10.1002/mds.27270. Epub 2018 Jan 9. Review.

PMID:
29315801

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