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Results: 1 to 20 of 24

References for PMC Articles for PubMed (Select 21763482)

1.

Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies.

International Parkinson Disease Genomics Consortium, Nalls MA, Plagnol V, Hernandez DG, Sharma M, Sheerin UM, Saad M, Simón-Sánchez J, Schulte C, Lesage S, Sveinbjörnsdóttir S, Stefánsson K, Martinez M, Hardy J, Heutink P, Brice A, Gasser T, Singleton AB, Wood NW.

Lancet. 2011 Feb 19;377(9766):641-9. doi: 10.1016/S0140-6736(10)62345-8. Epub 2011 Feb 1.

2.

A comparative study of Lrrk2 function in primary neuronal cultures.

Dächsel JC, Behrouz B, Yue M, Beevers JE, Melrose HL, Farrer MJ.

Parkinsonism Relat Disord. 2010 Dec;16(10):650-5. doi: 10.1016/j.parkreldis.2010.08.018. Epub 2010 Sep 17.

3.

Alpha-synuclein promotes SNARE-complex assembly in vivo and in vitro.

Burré J, Sharma M, Tsetsenis T, Buchman V, Etherton MR, Südhof TC.

Science. 2010 Sep 24;329(5999):1663-7. doi: 10.1126/science.1195227. Epub 2010 Aug 26.

4.

Vps35 mediates vesicle transport between the mitochondria and peroxisomes.

Braschi E, Goyon V, Zunino R, Mohanty A, Xu L, McBride HM.

Curr Biol. 2010 Jul 27;20(14):1310-5. doi: 10.1016/j.cub.2010.05.066. Epub 2010 Jul 8.

5.

The retromer component SNX6 interacts with dynactin p150(Glued) and mediates endosome-to-TGN transport.

Hong Z, Yang Y, Zhang C, Niu Y, Li K, Zhao X, Liu JJ.

Cell Res. 2009 Dec;19(12):1334-49. doi: 10.1038/cr.2009.130. Epub 2009 Nov 24.

PMID:
19935774
6.

Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease.

Satake W, Nakabayashi Y, Mizuta I, Hirota Y, Ito C, Kubo M, Kawaguchi T, Tsunoda T, Watanabe M, Takeda A, Tomiyama H, Nakashima K, Hasegawa K, Obata F, Yoshikawa T, Kawakami H, Sakoda S, Yamamoto M, Hattori N, Murata M, Nakamura Y, Toda T.

Nat Genet. 2009 Dec;41(12):1303-7. doi: 10.1038/ng.485. Epub 2009 Nov 15.

PMID:
19915576
7.

Targeted capture and massively parallel sequencing of 12 human exomes.

Ng SB, Turner EH, Robertson PD, Flygare SD, Bigham AW, Lee C, Shaffer T, Wong M, Bhattacharjee A, Eichler EE, Bamshad M, Nickerson DA, Shendure J.

Nature. 2009 Sep 10;461(7261):272-6. doi: 10.1038/nature08250. Epub 2009 Aug 16.

8.

Membrane recruitment of the cargo-selective retromer subcomplex is catalysed by the small GTPase Rab7 and inhibited by the Rab-GAP TBC1D5.

Seaman MN, Harbour ME, Tattersall D, Read E, Bright N.

J Cell Sci. 2009 Jul 15;122(Pt 14):2371-82. doi: 10.1242/jcs.048686. Epub 2009 Jun 16.

9.

DCTN1 mutations in Perry syndrome.

Farrer MJ, Hulihan MM, Kachergus JM, Dächsel JC, Stoessl AJ, Grantier LL, Calne S, Calne DB, Lechevalier B, Chapon F, Tsuboi Y, Yamada T, Gutmann L, Elibol B, Bhatia KP, Wider C, Vilariño-Güell C, Ross OA, Brown LA, Castanedes-Casey M, Dickson DW, Wszolek ZK.

Nat Genet. 2009 Feb;41(2):163-5. doi: 10.1038/ng.293. Epub 2009 Jan 11.

10.

Genomewide association study for susceptibility genes contributing to familial Parkinson disease.

Pankratz N, Wilk JB, Latourelle JC, DeStefano AL, Halter C, Pugh EW, Doheny KF, Gusella JF, Nichols WC, Foroud T, Myers RH; PSG-PROGENI and GenePD Investigators, Coordinators and Molecular Genetic Laboratories.

Hum Genet. 2009 Jan;124(6):593-605. doi: 10.1007/s00439-008-0582-9. Epub 2008 Nov 6.

11.

Genetic variation of Omi/HtrA2 and Parkinson's disease.

Ross OA, Soto AI, Vilariño-Güell C, Heckman MG, Diehl NN, Hulihan MM, Aasly JO, Sando S, Gibson JM, Lynch T, Krygowska-Wajs A, Opala G, Barcikowska M, Czyzewski K, Uitti RJ, Wszolek ZK, Farrer MJ.

Parkinsonism Relat Disord. 2008 Nov;14(7):539-43. doi: 10.1016/j.parkreldis.2008.08.003. Epub 2008 Sep 14.

12.

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

Muhammad A, Flores I, Zhang H, Yu R, Staniszewski A, Planel E, Herman M, Ho L, Kreber R, Honig LS, Ganetzky B, Duff K, Arancio O, Small SA.

Proc Natl Acad Sci U S A. 2008 May 20;105(20):7327-32. doi: 10.1073/pnas.0802545105. Epub 2008 May 14.

13.

Retromer.

Bonifacino JS, Hurley JH.

Curr Opin Cell Biol. 2008 Aug;20(4):427-36. doi: 10.1016/j.ceb.2008.03.009. Epub 2008 May 9. Review.

14.

Autosomal dominant dopa-responsive parkinsonism in a multigenerational Swiss family.

Wider C, Skipper L, Solida A, Brown L, Farrer M, Dickson D, Wszolek ZK, Vingerhoets FJ.

Parkinsonism Relat Disord. 2008 Aug;14(6):465-70. doi: 10.1016/j.parkreldis.2007.11.013. Epub 2008 Mar 14.

PMID:
18342564
15.

Functional architecture of the retromer cargo-recognition complex.

Hierro A, Rojas AL, Rojas R, Murthy N, Effantin G, Kajava AV, Steven AC, Bonifacino JS, Hurley JH.

Nature. 2007 Oct 25;449(7165):1063-7. Epub 2007 Sep 23.

16.

Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data.

Fung HC, Scholz S, Matarin M, Simón-Sánchez J, Hernandez D, Britton A, Gibbs JR, Langefeld C, Stiegert ML, Schymick J, Okun MS, Mandel RJ, Fernandez HH, Foote KD, Rodríguez RL, Peckham E, De Vrieze FW, Gwinn-Hardy K, Hardy JA, Singleton A.

Lancet Neurol. 2006 Nov;5(11):911-6.

PMID:
17052657
17.

Complex segregation analysis of Parkinson's disease: The Mayo Clinic Family Study.

McDonnell SK, Schaid DJ, Elbaz A, Strain KJ, Bower JH, Ahlskog JE, Maraganore DM, Rocca WA.

Ann Neurol. 2006 May;59(5):788-95.

PMID:
16634030
18.

Genetics of Parkinson disease: paradigm shifts and future prospects.

Farrer MJ.

Nat Rev Genet. 2006 Apr;7(4):306-18. Review.

PMID:
16543934
19.

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

Small SA, Kent K, Pierce A, Leung C, Kang MS, Okada H, Honig L, Vonsattel JP, Kim TW.

Ann Neurol. 2005 Dec;58(6):909-19.

PMID:
16315276
20.

High-resolution whole-genome association study of Parkinson disease.

Maraganore DM, de Andrade M, Lesnick TG, Strain KJ, Farrer MJ, Rocca WA, Pant PV, Frazer KA, Cox DR, Ballinger DG.

Am J Hum Genet. 2005 Nov;77(5):685-93. Epub 2005 Sep 9.

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