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MAPT IVS1+124 C>G modifies risk of LRRK2 G2385R for Parkinson's disease in Chinese individuals.

Dan X, Wang C, Ma J, Feng X, Wang T, Zheng Z, Chan P.

Neurobiol Aging · 2014-01-25

DOI: 10.1016/j.neurobiolaging.2014.01.025PMID: 24559644

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Thiol peroxidases ameliorate LRRK2 mutant-induced mitochondrial and dopaminergic neuronal degeneration in Drosophila.

Angeles DC, Ho P, Chua LL, Wang C, Yap YW, Ng C, Zhou Zd, Lim KL, Wszolek ZK, Wang HY, Tan EK.

Hum Mol Genet · 2014-01-23

DOI: 10.1093/hmg/ddu026PMID: 24459295

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The effects of pdr1, djr1.1 and pink1 loss in manganese-induced toxicity and the role of α-synuclein in C. elegans.

Bornhorst J, Chakraborty S, Meyer S, Lohren H, Brinkhaus SG, Knight AL, Caldwell KA, Caldwell GA, Karst U, Schwerdtle T, Bowman A, Aschner M.

Metallomics · 2014-01-22

DOI: 10.1039/c3mt00325fPMID: 24452053

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CSF α-synuclein and UCH-L1 levels in Parkinson's disease and atypical parkinsonian disorders.

Mondello S, Constantinescu R, Zetterberg H, Andreasson U, Holmberg B, Jeromin A.

Parkinsonism Relat Disord · 2014-01-22

DOI: 10.1016/j.parkreldis.2014.01.011PMID: 24507721

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Targeting alpha-synuclein with a microRNA-embedded silencing vector in the rat substantia nigra: positive and negative effects.

Khodr CE, Becerra A, Han Y, Bohn MC.

Brain Res · 2014-01-21

DOI: 10.1016/j.brainres.2014.01.010PMID: 24463035

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Cerebrospinal fluid lysosomal enzymes and alpha-synuclein in Parkinson's disease.

Parnetti L, Chiasserini D, Persichetti E, Eusebi P, Varghese S, Qureshi MM, Dardis A, Deganuto M, De Carlo C, Castrioto A, Balducci C, Paciotti S, Tambasco N, Bembi B, Bonanni L, Onofrj M, Rossi A, Beccari T, El-Agnaf O, Calabresi P.

Mov Disord · 2014-01-16

DOI: 10.1002/mds.25772PMID: 24436092

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Interactions between Tau and α-synuclein augment neurotoxicity in a Drosophila model of Parkinson's disease.

Roy B, Jackson GR.

Hum Mol Genet · 2014-01-14

DOI: 10.1093/hmg/ddu011PMID: 24430504

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Alpha-synuclein transcript isoforms in three different brain regions from Parkinson's disease and healthy subjects in relation to the SNCA rs356165/rs11931074 polymorphisms.

Cardo LF, Coto E, de Mena L, Ribacoba R, Mata IF, Menéndez M, Moris G, Alvarez V.

Neurosci Lett · 2014-01-10

DOI: 10.1016/j.neulet.2014.01.009PMID: 24418406

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c-Abl phosphorylates α-synuclein and regulates its degradation: implication for α-synuclein clearance and contribution to the pathogenesis of Parkinson's disease.

Mahul-Mellier AL, Fauvet B, Gysbers A, Dikiy I, Oueslati A, Georgeon S, Lamontanara AJ, Bisquertt A, Eliezer D, Masliah E, Halliday G, Hantschel O, Lashuel HA.

Hum Mol Genet · 2014-01-09

DOI: 10.1093/hmg/ddt674PMID: 24412932

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Definite familial multiple system atrophy with unknown genetics.

Itoh K, Kasai T, Tsuji Y, Saito K, Mizuta I, Harada Y, Sudoh S, Mizuno T, Nakagawa M, Fushiki S.

Neuropathology · 2014-01-07

DOI: 10.1111/neup.12092PMID: 24397755

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Sexual dimorphism in xenobiotic genetic variants-mediated risk for Parkinson's disease.

Kumudini N, Uma A, Naushad SM, Mridula R, Borgohain R, Kutala VK.

Neurol Sci · 2014-01-04

DOI: 10.1007/s10072-013-1622-3PMID: 24389856

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Multiple organ involvement by alpha-synuclein pathology in Lewy body disorders.

Gelpi E, Navarro-Otano J, Tolosa E, Gaig C, Compta Y, Rey MJ, Martí MJ, Hernández I, Valldeoriola F, Reñé R, Ribalta T.

Mov Disord · 2014-01-02

DOI: 10.1002/mds.25776PMID: 24395122

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