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Items: 1 to 20 of 25

1.

Meta-analysis in genome-wide association datasets: strategies and application in Parkinson disease.

Evangelou E, Maraganore DM, Ioannidis JP.

PLoS One. 2007 Feb 7;2(2):e196.

PMID:
17332845
2.

Parkin mediates nonclassical, proteasomal-independent ubiquitination of synphilin-1: implications for Lewy body formation.

Lim KL, Chew KC, Tan JM, Wang C, Chung KK, Zhang Y, Tanaka Y, Smith W, Engelender S, Ross CA, Dawson VL, Dawson TM.

J Neurosci. 2005 Feb 23;25(8):2002-9.

PMID:
15728840
3.

Haploview: analysis and visualization of LD and haplotype maps.

Barrett JC, Fry B, Maller J, Daly MJ.

Bioinformatics. 2005 Jan 15;21(2):263-5. Epub 2004 Aug 5.

PMID:
15297300
4.

Ubiquitylation of synphilin-1 and alpha-synuclein by SIAH and its presence in cellular inclusions and Lewy bodies imply a role in Parkinson's disease.

Liani E, Eyal A, Avraham E, Shemer R, Szargel R, Berg D, Bornemann A, Riess O, Ross CA, Rott R, Engelender S.

Proc Natl Acad Sci U S A. 2004 Apr 13;101(15):5500-5. Epub 2004 Apr 2.

PMID:
15064394
5.

Case-control study of the alpha-synuclein interacting protein gene and Parkinson's disease.

Maraganore DM, Farrer MJ, Lesnick TG, de Andrade M, Bower JH, Hernandez D, Hardy JA, Rocca WA.

Mov Disord. 2003 Nov;18(11):1233-9.

PMID:
14639662
6.

Identification and functional characterization of a novel R621C mutation in the synphilin-1 gene in Parkinson's disease.

Marx FP, Holzmann C, Strauss KM, Li L, Eberhardt O, Gerhardt E, Cookson MR, Hernandez D, Farrer MJ, Kachergus J, Engelender S, Ross CA, Berger K, Schöls L, Schulz JB, Riess O, Krüger R.

Hum Mol Genet. 2003 Jun 1;12(11):1223-31.

PMID:
12761037
7.

A susceptibility gene for late-onset idiopathic Parkinson's disease.

Hicks AA, Pétursson H, Jónsson T, Stefánsson H, Jóhannsdóttir HS, Sainz J, Frigge ML, Kong A, Gulcher JR, Stefánsson K, Sveinbjörnsdóttir S.

Ann Neurol. 2002 Nov;52(5):549-55.

PMID:
12402251
8.

Genome screen to identify susceptibility genes for Parkinson disease in a sample without parkin mutations.

Pankratz N, Nichols WC, Uniacke SK, Halter C, Rudolph A, Shults C, Conneally PM, Foroud T; Parkinson Study Group.

Am J Hum Genet. 2002 Jul;71(1):124-35. Epub 2002 Jun 7.

PMID:
12058349
9.

The structure of haplotype blocks in the human genome.

Gabriel SB, Schaffner SF, Nguyen H, Moore JM, Roy J, Blumenstiel B, Higgins J, DeFelice M, Lochner A, Faggart M, Liu-Cordero SN, Rotimi C, Adeyemo A, Cooper R, Ward R, Lander ES, Daly MJ, Altshuler D.

Science. 2002 Jun 21;296(5576):2225-9. Epub 2002 May 23.

PMID:
12029063
10.

Sequence conservation between mouse and human synphilin-1.

O'Farrell C, Pickford F, Vink L, McGowan E, Cookson MR.

Neurosci Lett. 2002 Mar 29;322(1):9-12.

PMID:
11958831
11.

Synphilin-1 is developmentally localized to synaptic terminals, and its association with synaptic vesicles is modulated by alpha-synuclein.

Ribeiro CS, Carneiro K, Ross CA, Menezes JR, Engelender S.

J Biol Chem. 2002 Jun 28;277(26):23927-33. Epub 2002 Apr 15. Erratum in: J Biol Chem 2002 Sep 13;277(37):34651-4.

PMID:
11956199
12.

Immunocytochemical localization of synphilin-1, an alpha-synuclein-associated protein, in neurodegenerative disorders.

Wakabayashi K, Engelender S, Tanaka Y, Yoshimoto M, Mori F, Tsuji S, Ross CA, Takahashi H.

Acta Neuropathol. 2002 Mar;103(3):209-14. Epub 2001 Oct 16.

PMID:
11907799
13.

Complete genomic screen in Parkinson disease: evidence for multiple genes.

Scott WK, Nance MA, Watts RL, Hubble JP, Koller WC, Lyons K, Pahwa R, Stern MB, Colcher A, Hiner BC, Jankovic J, Ondo WG, Allen FH Jr, Goetz CG, Small GW, Masterman D, Mastaglia F, Laing NG, Stajich JM, Slotterbeck B, Booze MW, Ribble RC, Rampersaud E, West SG, Gibson RA, Middleton LT, Roses AD, Haines JL, Scott BL, Vance JM, Pericak-Vance MA.

JAMA. 2001 Nov 14;286(18):2239-44.

PMID:
11710888
14.

Parkin ubiquitinates the alpha-synuclein-interacting protein, synphilin-1: implications for Lewy-body formation in Parkinson disease.

Chung KK, Zhang Y, Lim KL, Tanaka Y, Huang H, Gao J, Ross CA, Dawson VL, Dawson TM.

Nat Med. 2001 Oct;7(10):1144-50.

PMID:
11590439
15.

No pathogenic mutations in the synphilin-1 gene in Parkinson's disease.

Bandopadhyay R, de Silva R, Khan N, Graham E, Vaughan J, Engelender S, Ross C, Morris H, Morris C, Wood NW, Daniel S, Lees A.

Neurosci Lett. 2001 Jul 13;307(2):125-7.

PMID:
11427316
16.

Genetic analysis of synphilin-1 in familial Parkinson's disease.

Farrer M, Destée A, Levecque C, Singleton A, Engelender S, Becquet E, Mouroux V, Richard F, Defebvre L, Crook R, Hernandez D, Ross CA, Hardy J, Amouyel P, Chartier-Harlin MC.

Neurobiol Dis. 2001 Apr;8(2):317-23.

PMID:
11300726
17.

Organization of the human synphilin-1 gene, a candidate for Parkinson's disease.

Engelender S, Wanner T, Kleiderlein JJ, Wakabayashi K, Tsuji S, Takahashi H, Ashworth R, Margolis RL, Ross CA.

Mamm Genome. 2000 Sep;11(9):763-6.

PMID:
10967135
18.

Synphilin-1 is present in Lewy bodies in Parkinson's disease.

Wakabayashi K, Engelender S, Yoshimoto M, Tsuji S, Ross CA, Takahashi H.

Ann Neurol. 2000 Apr;47(4):521-3.

PMID:
10762166
19.

Synphilin-1 associates with alpha-synuclein and promotes the formation of cytosolic inclusions.

Engelender S, Kaminsky Z, Guo X, Sharp AH, Amaravi RK, Kleiderlein JJ, Margolis RL, Troncoso JC, Lanahan AA, Worley PF, Dawson VL, Dawson TM, Ross CA.

Nat Genet. 1999 May;22(1):110-4.

PMID:
10319874
20.

Diagnostic criteria for Parkinson disease.

Gelb DJ, Oliver E, Gilman S.

Arch Neurol. 1999 Jan;56(1):33-9. Review.

PMID:
9923759

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