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Results: 1 to 20 of 92

1.

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. doi: 10.1111/tra.12136. Epub 2013 Nov 14.

PMID:
24152121
[PubMed - indexed for MEDLINE]
2.

The VPS35 gene and Parkinson's disease.

Deng H, Gao K, Jankovic J.

Mov Disord. 2013 May;28(5):569-75. doi: 10.1002/mds.25430. Epub 2013 Mar 27. Review.

PMID:
23536430
[PubMed - indexed for MEDLINE]
3.

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

Bi F, Li F, Huang C, Zhou H.

Int J Biol Sci. 2013;9(2):149-55. doi: 10.7150/ijbs.5617. Epub 2013 Jan 26.

PMID:
23411763
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

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

Sharma M, Ioannidis JP, Aasly JO, Annesi G, Brice A, Bertram L, Bozi M, Barcikowska M, Crosiers D, Clarke CE, Facheris MF, Farrer M, Garraux G, Gispert S, Auburger G, Vilariño-Güell C, Hadjigeorgiou GM, Hicks AA, Hattori N, Jeon BS, Jamrozik Z, Krygowska-Wajs A, Lesage S, Lill CM, Lin JJ, Lynch T, Lichtner P, Lang AE, Libioulle C, Murata M, Mok V, Jasinska-Myga B, Mellick GD, Morrison KE, Meitnger T, Zimprich A, Opala G, Pramstaller PP, Pichler I, Park SS, Quattrone A, Rogaeva E, Ross OA, Stefanis L, Stockton JD, Satake W, Silburn PA, Strom TM, Theuns J, Tan EK, Toda T, Tomiyama H, Uitti RJ, Van Broeckhoven C, Wirdefeldt K, Wszolek Z, Xiromerisiou G, Yomono HS, Yueh KC, Zhao Y, Gasser T, Maraganore D, Krüger R; GEOPD consortium.

J Med Genet. 2012 Nov;49(11):721-6. doi: 10.1136/jmedgenet-2012-101155. Erratum in: J Med Genet. 2013 Mar;50(3):202.

PMID:
23125461
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

VPS35 mutation in Japanese patients with typical Parkinson's disease.

Ando M, Funayama M, Li Y, Kashihara K, Murakami Y, Ishizu N, Toyoda C, Noguchi K, Hashimoto T, Nakano N, Sasaki R, Kokubo Y, Kuzuhara S, Ogaki K, Yamashita C, Yoshino H, Hatano T, Tomiyama H, Hattori N.

Mov Disord. 2012 Sep 15;27(11):1413-7. doi: 10.1002/mds.25145. Epub 2012 Sep 18.

PMID:
22991136
[PubMed - indexed for MEDLINE]
6.

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

Deng H, Xu H, Deng X, Song Z, Zheng W, Gao K, Fan X, Tang J.

Eur J Neurol. 2012 Sep;19(9):e96-7. doi: 10.1111/j.1468-1331.2012.03800.x. No abstract available.

PMID:
22891780
[PubMed - indexed for MEDLINE]
7.

Frequency of the D620N mutation in VPS35 in Parkinson disease.

Kumar KR, Weissbach A, Heldmann M, Kasten M, Tunc S, Sue CM, Svetel M, Kostić VS, Segura-Aguilar J, Ramirez A, Simon DK, Vieregge P, Münte TF, Hagenah J, Klein C, Lohmann K.

Arch Neurol. 2012 Oct;69(10):1360-4.

PMID:
22801713
[PubMed - indexed for MEDLINE]
8.

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

Guo JF, Sun QY, Lv ZY, Yu RL, Li K, Zhang YH, Tian JY, Xia K, Yan XX, Tang BS.

Parkinsonism Relat Disord. 2012 Sep;18(8):983-5. doi: 10.1016/j.parkreldis.2012.05.002. Epub 2012 Jun 4.

PMID:
22673036
[PubMed - indexed for MEDLINE]
9.

Identification of VPS35 mutations replicated in French families with Parkinson disease.

Lesage S, Condroyer C, Klebe S, Honoré A, Tison F, Brefel-Courbon C, Dürr A, Brice A; French Parkinson's Disease Genetics Study Group.

Neurology. 2012 May 1;78(18):1449-50. doi: 10.1212/WNL.0b013e318253d5f2. Epub 2012 Apr 18. No abstract available.

PMID:
22517097
[PubMed - indexed for MEDLINE]
10.

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

Zhang Y, Chen S, Xiao Q, Cao L, Liu J, Rong TY, Ma JF, Wang G, Wang Y, Chen SD.

Parkinsonism Relat Disord. 2012 Jun;18(5):638-40. doi: 10.1016/j.parkreldis.2012.02.011. Epub 2012 Mar 10.

PMID:
22410496
[PubMed - indexed for MEDLINE]
11.

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

Verstraeten A, Wauters E, Crosiers D, Meeus B, Corsmit E, Elinck E, Mattheijssens M, Peeters K, Cras P, Pickut B, Vandenberghe R, Engelborghs S, De Deyn PP, Van Broeckhoven C, Theuns J.

Neurobiol Aging. 2012 Aug;33(8):1844.e11-3. doi: 10.1016/j.neurobiolaging.2012.01.006. Epub 2012 Feb 14.

PMID:
22336192
[PubMed - indexed for MEDLINE]
12.

The Asp620asn mutation in VPS35 is not a common cause of familial Parkinson's disease.

Guella I, Soldà G, Cilia R, Pezzoli G, Asselta R, Duga S, Goldwurm S.

Mov Disord. 2012 May;27(6):800-1. doi: 10.1002/mds.24927. Epub 2012 Jan 25. No abstract available.

PMID:
22278960
[PubMed - indexed for MEDLINE]
13.

Screening for VPS35 mutations in Parkinson's disease.

Sheerin UM, Charlesworth G, Bras J, Guerreiro R, Bhatia K, Foltynie T, Limousin P, Silveira-Moriyama L, Lees A, Wood N.

Neurobiol Aging. 2012 Apr;33(4):838.e1-5. doi: 10.1016/j.neurobiolaging.2011.10.032. Epub 2011 Dec 7.

PMID:
22154191
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Inhibition of retromer activity by herpesvirus saimiri tip leads to CD4 downregulation and efficient T cell transformation.

Kingston D, Chang H, Ensser A, Lee HR, Lee J, Lee SH, Jung JU, Cho NH.

J Virol. 2011 Oct;85(20):10627-38. doi: 10.1128/JVI.00757-11. Epub 2011 Aug 17.

PMID:
21849449
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

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

Zimprich A, Benet-Pagès A, Struhal W, Graf E, Eck SH, Offman MN, Haubenberger D, Spielberger S, Schulte EC, Lichtner P, Rossle SC, Klopp N, Wolf E, Seppi K, Pirker W, Presslauer S, Mollenhauer B, Katzenschlager R, Foki T, Hotzy C, Reinthaler E, Harutyunyan A, Kralovics R, Peters A, Zimprich F, Brücke T, Poewe W, Auff E, Trenkwalder C, Rost B, Ransmayr G, Winkelmann J, Meitinger T, Strom TM.

Am J Hum Genet. 2011 Jul 15;89(1):168-75. doi: 10.1016/j.ajhg.2011.06.008.

PMID:
21763483
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

VPS35 mutations in Parkinson disease.

Vilariño-Güell C, Wider C, Ross OA, Dachsel JC, Kachergus JM, Lincoln SJ, Soto-Ortolaza AI, Cobb SA, Wilhoite GJ, Bacon JA, Behrouz B, Melrose HL, Hentati E, Puschmann A, Evans DM, Conibear E, Wasserman WW, Aasly JO, Burkhard PR, Djaldetti R, Ghika J, Hentati F, Krygowska-Wajs A, Lynch T, Melamed E, Rajput A, Rajput AH, Solida A, Wu RM, Uitti RJ, Wszolek ZK, Vingerhoets F, Farrer MJ.

Am J Hum Genet. 2011 Jul 15;89(1):162-7. doi: 10.1016/j.ajhg.2011.06.001. Erratum in: Am J Hum Genet. 2011 Aug 12;89(2):347.

PMID:
21763482
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

VPS35 and EIF4G1 mutations are rare in Parkinson's disease among Indians.

Sudhaman S, Behari M, Govindappa ST, Muthane UB, Juyal RC, Thelma BK.

Neurobiol Aging. 2013 Oct;34(10):2442.e1-3. doi: 10.1016/j.neurobiolaging.2013.04.025. Epub 2013 May 28.

PMID:
23726718
[PubMed - indexed for MEDLINE]
18.

A global analysis of SNX27-retromer assembly and cargo specificity reveals a function in glucose and metal ion transport.

Steinberg F, Gallon M, Winfield M, Thomas EC, Bell AJ, Heesom KJ, Tavaré JM, Cullen PJ.

Nat Cell Biol. 2013 May;15(5):461-71. doi: 10.1038/ncb2721. Epub 2013 Apr 7.

PMID:
23563491
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

Whole exome sequencing of rare variants in EIF4G1 and VPS35 in Parkinson disease.

Nuytemans K, Bademci G, Inchausti V, Dressen A, Kinnamon DD, Mehta A, Wang L, Züchner S, Beecham GW, Martin ER, Scott WK, Vance JM.

Neurology. 2013 Mar 12;80(11):982-9. doi: 10.1212/WNL.0b013e31828727d4. Epub 2013 Feb 13.

PMID:
23408866
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

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

Chen Y, Chen K, Song W, Chen X, Cao B, Huang R, Zhao B, Guo X, Burgunder J, Li J, Shang HF.

Neurobiol Aging. 2013 Jun;34(6):1709.e7-8. doi: 10.1016/j.neurobiolaging.2012.11.003. Epub 2012 Dec 20.

PMID:
23261770
[PubMed - indexed for MEDLINE]

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