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The search for genetic mouse models of prodromal Parkinson's disease.

Smith GA, Isacson O, Dunnett SB.

Exp Neurol · 2012-07-14

DOI: 10.1016/j.expneurol.2012.06.035PMID: 22819262

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Genetic heterogeneity in Parkinson disease: the meaning of GWAS and replication studies.

Pastor P.

Neurology · 2012-07-11

DOI: 10.1212/wnl.0b013e318264e3d2PMID: 22786592

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Large-scale replication and heterogeneity in Parkinson disease genetic loci.

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

Neurology · 2012-07-11

DOI: 10.1212/wnl.0b013e318264e353PMID: 22786590

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Mice overexpressing wild-type human alpha-synuclein display alterations in colonic myenteric ganglia and defecation.

Wang L, Magen I, Yuan PQ, Subramaniam SR, Richter F, Chesselet MF, Taché Y.

Neurogastroenterol Motil · 2012-07-11

DOI: 10.1111/j.1365-2982.2012.01974.xPMID: 22779732

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Open access

LRRK2 A419V is not associated with Parkinson's disease in different Chinese populations.

Wu YR, Tan LC, Fu X, Chen CM, Au WL, Chen L, Chen YC, Prakash KM, Zheng Y, Lee-Chen GJ, Zhao Y, Zeng JS, Tan EK, Pei Z.

PLoS One · 2012-07-10

DOI: 10.1371/journal.pone.0036123PMID: 22807999

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Open access

Oxidative stress in genetic mouse models of Parkinson's disease.

Varçin M, Bentea E, Michotte Y, Sarre S.

Oxid Med Cell Longev · 2012-07-08

DOI: 10.1155/2012/624925PMID: 22829959

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The LRRK2 G2019S mutant exacerbates basal autophagy through activation of the MEK/ERK pathway.

Bravo-San Pedro JM, Niso-Santano M, Gómez-Sánchez R, Pizarro-Estrella E, Aiastui-Pujana A, Gorostidi A, Climent V, López de Maturana R, Sanchez-Pernaute R, López de Munain A, Fuentes JM, González-Polo RA.

Cell Mol Life Sci · 2012-07-08

DOI: 10.1007/s00018-012-1061-yPMID: 22773119

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Phosphorylation of α-synuclein is crucial in compensating for proteasomal dysfunction.

Choi HS, Liew H, Jang A, Kim YM, Lashuel H, Suh YH.

Biochem Biophys Res Commun · 2012-07-07

DOI: 10.1016/j.bbrc.2012.06.159PMID: 22776201

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A model of nitric oxide induced α-synuclein misfolding in Parkinson's disease.

Stone DK, Kiyota T, Mosley RL, Gendelman HE.

Neurosci Lett · 2012-07-07

DOI: 10.1016/j.neulet.2012.06.070PMID: 22776646

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GSK2578215A; a potent and highly selective 2-arylmethyloxy-5-substitutent-N-arylbenzamide LRRK2 kinase inhibitor.

Reith AD, Bamborough P, Jandu K, Andreotti D, Mensah L, Dossang P, Choi HG, Deng X, Zhang J, Alessi DR, Gray NS.

Bioorg Med Chem Lett · 2012-07-07

DOI: 10.1016/j.bmcl.2012.06.104PMID: 22863203

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Biophysical properties and cellular toxicity of covalent crosslinked oligomers of α-synuclein formed by photoinduced side-chain tyrosyl radicals.

Borsarelli CD, Falomir-Lockhart LJ, Ostatná V, Fauerbach JA, Hsiao HH, Urlaub H, Paleček E, Jares-Erijman EA, Jovin TM.

Free Radic Biol Med · 2012-07-06

DOI: 10.1016/j.freeradbiomed.2012.06.035PMID: 22771470

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Remodeling of lipid vesicles into cylindrical micelles by α-synuclein in an extended α-helical conformation.

Mizuno N, Varkey J, Kegulian NC, Hegde BG, Cheng N, Langen R, Steven AC.

J Biol Chem · 2012-07-05

DOI: 10.1074/jbc.m112.365817PMID: 22767608

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Records come from scientific sources. Bibliographic counts do not represent completed translations or editorial approvals.

15.286 articles found

The search for genetic mouse models of prodromal Parkinson's disease.

Genetic heterogeneity in Parkinson disease: the meaning of GWAS and replication studies.

Large-scale replication and heterogeneity in Parkinson disease genetic loci.

Mice overexpressing wild-type human alpha-synuclein display alterations in colonic myenteric ganglia and defecation.

LRRK2 A419V is not associated with Parkinson's disease in different Chinese populations.

Oxidative stress in genetic mouse models of Parkinson's disease.

The LRRK2 G2019S mutant exacerbates basal autophagy through activation of the MEK/ERK pathway.

Phosphorylation of α-synuclein is crucial in compensating for proteasomal dysfunction.

A model of nitric oxide induced α-synuclein misfolding in Parkinson's disease.

GSK2578215A; a potent and highly selective 2-arylmethyloxy-5-substitutent-N-arylbenzamide LRRK2 kinase inhibitor.

Biophysical properties and cellular toxicity of covalent crosslinked oligomers of α-synuclein formed by photoinduced side-chain tyrosyl radicals.

Remodeling of lipid vesicles into cylindrical micelles by α-synuclein in an extended α-helical conformation.

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