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Alternative to LRRK2-IN-1 for Pharmacological Studies of Parkinson's Disease.

Koshibu K, van Asperen J, Gerets H, Garcia-Ladona J, Lorthioir O, Courade JP.

Pharmacology · 2015-09-18

DOI: 10.1159/000439136PMID: 26382237

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The Parkinson's Disease-Associated Protein Kinase LRRK2 Modulates Notch Signaling through the Endosomal Pathway.

Imai Y, Kobayashi Y, Inoshita T, Meng H, Arano T, Uemura K, Asano T, Yoshimi K, Zhang CL, Matsumoto G, Ohtsuka T, Kageyama R, Kiyonari H, Shioi G, Nukina N, Hattori N, Takahashi R.

PLoS Genet · 2015-09-10

DOI: 10.1371/journal.pgen.1005503PMID: 26355680

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Conformational heterogeneity of the Roc domains in C. tepidum Roc-COR and implications for human LRRK2 Parkinson mutations.

Rudi K, Ho FY, Gilsbach BK, Pots H, Wittinghofer A, Kortholt A, Klare JP.

Biosci Rep · 2015-08-26

DOI: 10.1042/bsr20150128PMID: 26310572

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Greater motor progression in patients with Parkinson disease who carry LRRK2 risk variants.

Oosterveld LP, Allen JC, Ng EY, Seah SH, Tay KY, Au WL, Tan EK, Tan LC.

Neurology · 2015-08-26

DOI: 10.1212/wnl.0000000000001953PMID: 26311745

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Open access

Changes to Intermediary Metabolites in Sporadic and LRRK2 Parkinson's Disease Demonstrated by Proton Magnetic Resonance Spectroscopy.

Aasly JO, Sæther O, Johansen KK, Bathen TF, Giskeødegård GF, White LR.

Parkinsons Dis · 2015-08-18

DOI: 10.1155/2015/264896PMID: 26357583

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Clinical and imaging markers in premotor LRRK2 G2019S mutation carriers.

Vilas D, Ispierto L, Álvarez R, Pont-Sunyer C, Martí MJ, Valldeoriola F, Compta Y, de Fabregues O, Hernández-Vara J, Puente V, Calopa M, Jaumà S, Campdelacreu J, Aguilar M, Quílez P, Casquero P, Lomeña F, Ríos J, Tolosa E.

Parkinsonism Relat Disord · 2015-08-12

DOI: 10.1016/j.parkreldis.2015.08.007PMID: 26306001

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Open access

Cognitive Impairments in LRRK2-Related Parkinson's Disease: A Study in Chinese Individuals.

Zheng Y, Pei Z, Liu Y, Zhou H, Xian W, Fang Y, Chen L, Wu Q.

Behav Neurol · 2015-08-06

DOI: 10.1155/2015/621873PMID: 26346174

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The Parkinson's Disease-Associated Mutation LRRK2-G2019S Impairs Synaptic Plasticity in Mouse Hippocampus.

Sweet ES, Saunier-Rebori B, Yue Z, Blitzer RD.

J Neurosci · 2015-08-01

DOI: 10.1523/jneurosci.0040-15.2015PMID: 26269629

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Association between Parkinson's disease and G2019S and R1441C mutations of the LRRK2 gene.

Li XX, Liao Q, Xia H, Yang XL.

Exp Ther Med · 2015-07-27

DOI: 10.3892/etm.2015.2659PMID: 26622505

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Novel LRRK2 mutations in Parkinsonism.

Trinh J, Guella I, McKenzie M, Gustavsson EK, Szu-Tu C, Petersen MS, Rajput A, Rajput AH, McKeown M, Jeon BS, Aasly JO, Bardien S, Farrer MJ.

Parkinsonism Relat Disord · 2015-07-18

DOI: 10.1016/j.parkreldis.2015.07.011PMID: 26213354

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Open access

Sleep Disorders in Parkinsonian and Nonparkinsonian LRRK2 Mutation Carriers.

Pont-Sunyer C, Iranzo A, Gaig C, Fernández-Arcos A, Vilas D, Valldeoriola F, Compta Y, Fernández-Santiago R, Fernández M, Bayés A, Calopa M, Casquero P, de Fàbregues O, Jaumà S, Puente V, Salamero M, José Martí M, Santamaría J, Tolosa E.

PLoS One · 2015-07-15

DOI: 10.1371/journal.pone.0132368PMID: 26177462

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LRRK2 A419V variant is a risk factor for Parkinson's disease in Asian population.

Li K, Tang BS, Liu ZH, Kang JF, Zhang Y, Shen L, Li N, Yan XX, Xia K, Guo JF.

Neurobiol Aging · 2015-07-11

DOI: 10.1016/j.neurobiolaging.2015.07.012PMID: 26234753

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

1.220 articles found

Alternative to LRRK2-IN-1 for Pharmacological Studies of Parkinson's Disease.

The Parkinson's Disease-Associated Protein Kinase LRRK2 Modulates Notch Signaling through the Endosomal Pathway.

Conformational heterogeneity of the Roc domains in C. tepidum Roc-COR and implications for human LRRK2 Parkinson mutations.

Greater motor progression in patients with Parkinson disease who carry LRRK2 risk variants.

Changes to Intermediary Metabolites in Sporadic and LRRK2 Parkinson's Disease Demonstrated by Proton Magnetic Resonance Spectroscopy.

Clinical and imaging markers in premotor LRRK2 G2019S mutation carriers.

Cognitive Impairments in LRRK2-Related Parkinson's Disease: A Study in Chinese Individuals.

The Parkinson's Disease-Associated Mutation LRRK2-G2019S Impairs Synaptic Plasticity in Mouse Hippocampus.

Association between Parkinson's disease and G2019S and R1441C mutations of the LRRK2 gene.

Novel LRRK2 mutations in Parkinsonism.

Sleep Disorders in Parkinsonian and Nonparkinsonian LRRK2 Mutation Carriers.

LRRK2 A419V variant is a risk factor for Parkinson's disease in Asian population.

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