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Alpha-synuclein misfolding and neurodegenerative diseases.

Uversky VN.

Curr Protein Pept Sci · 2008-10-01

DOI: 10.2174/138920308785915218PMID: 18855701

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Screening of LRRK2 interactants by yeast 2-hybrid analysis.

Zheng XY, Yang M, Tan JQ, Pan Q, Long ZG, Dai HP, Xia K, Xia JH, Zhang ZH.

Zhong Nan Da Xue Xue Bao Yi Xue Ban · 2008-10-01

PMID: 19001729

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Premotor Gray Matter Volume is Associated with Clinical Findings in Idiopathic and Genetically Determined Parkinson's Disease.

Reetz K, Siebner HR, Gaser C, Hagenah J, Buechel C, Kasten M, Petersen D, Pramstaller PP, Klein C, Binkofksi F.

Open Neuroimag J · 2008-09-27

DOI: 10.2174/1874440000802010102PMID: 19526072

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Alpha-synuclein multiplications with parkinsonism, dementia or progressive myoclonus?

Puschmann A, Wszolek ZK, Farrer M, Gustafson L, Widner H, Nilsson C.

Parkinsonism Relat Disord · 2008-09-27

DOI: 10.1016/j.parkreldis.2008.08.002PMID: 18824390

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Mathematical approach to understand the kinetics of alpha-synuclein aggregation: relevance to Parkinson's disease.

Bharathi P, Nagabhushan P, Rao KS.

Comput Biol Med · 2008-09-26

DOI: 10.1016/j.compbiomed.2008.08.008PMID: 18823621

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Genetic polymorphism of Angiotensin-Converting Enzyme is not associated with the development of Parkinson's disease and of L-dopa-induced adverse effects.

Pascale E, Purcaro C, Passarelli E, Guglielmi R, Vestri AR, Passarelli F, Meco G.

J Neurol Sci · 2008-09-20

DOI: 10.1016/j.jns.2008.08.017PMID: 18805557

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Genetic analysis for five LRRK2 mutations in a Sardinian parkinsonian population: importance of G2019S and R1441C mutations in sporadic Parkinson's disease patients.

Floris G, Cannas A, Solla P, Murru MR, Tranquilli S, Corongiu D, Rolesu M, Cuccu S, Sardu C, Marrosu F, Marrosu MG.

Parkinsonism Relat Disord · 2008-09-20

DOI: 10.1016/j.parkreldis.2008.06.009PMID: 18805725

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Neurodegeneration associated with genetic defects in phospholipase A(2).

Gregory A, Westaway SK, Holm IE, Kotzbauer PT, Hogarth P, Sonek S, Coryell JC, Nguyen TM, Nardocci N, Zorzi G, Rodriguez D, Desguerre I, Bertini E, Simonati A, Levinson B, Dias C, Barbot C, Carrilho I, Santos M, Malik I, Gitschier J, Hayflick SJ.

Neurology · 2008-09-17

DOI: 10.1212/01.wnl.0000327094.67726.28PMID: 18799783

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alpha-Synuclein: a therapeutic target for Parkinson's disease?

Maguire-Zeiss KA.

Pharmacol Res · 2008-09-16

DOI: 10.1016/j.phrs.2008.09.006PMID: 18840530

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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 · 2008-09-14

DOI: 10.1016/j.parkreldis.2008.08.003PMID: 18790661

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LRRK2 R1628P increases risk of Parkinson's disease: replication evidence.

Tan EK, Tan LC, Lim HQ, Li R, Tang M, Yih Y, Pavanni R, Prakash KM, Fook-Chong S, Zhao Y.

Hum Genet · 2008-09-10

DOI: 10.1007/s00439-008-0544-2PMID: 18781329

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Striatal 19S Rpt6 deficit is related to alpha-synuclein accumulation in MPTP-treated mice.

Liu B, Shi Q, Ma S, Feng N, Li J, Wang L, Wang X.

Biochem Biophys Res Commun · 2008-09-07

DOI: 10.1016/j.bbrc.2008.08.142PMID: 18782562

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

14.936 articles found

Alpha-synuclein misfolding and neurodegenerative diseases.

Screening of LRRK2 interactants by yeast 2-hybrid analysis.

Premotor Gray Matter Volume is Associated with Clinical Findings in Idiopathic and Genetically Determined Parkinson's Disease.

Alpha-synuclein multiplications with parkinsonism, dementia or progressive myoclonus?

Mathematical approach to understand the kinetics of alpha-synuclein aggregation: relevance to Parkinson's disease.

Genetic polymorphism of Angiotensin-Converting Enzyme is not associated with the development of Parkinson's disease and of L-dopa-induced adverse effects.

Genetic analysis for five LRRK2 mutations in a Sardinian parkinsonian population: importance of G2019S and R1441C mutations in sporadic Parkinson's disease patients.

Neurodegeneration associated with genetic defects in phospholipase A(2).

alpha-Synuclein: a therapeutic target for Parkinson's disease?

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

LRRK2 R1628P increases risk of Parkinson's disease: replication evidence.

Striatal 19S Rpt6 deficit is related to alpha-synuclein accumulation in MPTP-treated mice.

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