NeuralCipher Source record
Correlation between LRRK2 gene G2385R polymorphisms and Parkinson's disease.
DOI: 10.3892/mmr.2012.1008PMID: 22842796
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
1.220 articles found
“Parkinson LRRK2” Clear search
Open access
LRRK2 A419V is not associated with Parkinson's disease in different Chinese populations.
DOI: 10.1371/journal.pone.0036123PMID: 22807999
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
Open access
The IkappaB kinase family phosphorylates the Parkinson's disease kinase LRRK2 at Ser935 and Ser910 during Toll-like receptor signaling.
DOI: 10.1371/journal.pone.0039132PMID: 22723946
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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Dyskinesias in patients with Parkinson's disease: effect of the leucine-rich repeat kinase 2 (LRRK2) G2019S mutation.
DOI: 10.1016/j.parkreldis.2012.05.014PMID: 22703868
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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Penetrance of LRRK2 G2385R and R1628P is modified by common PD-associated genetic variants.
DOI: 10.1016/j.parkreldis.2012.05.003PMID: 22658533
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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Atypical tauopathy in a patient with LRRK2-G2019S mutation and tremor-dominant Parkinsonism.
DOI: 10.1111/j.1365-2990.2011.01216.xPMID: 21883375
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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Brain transcriptomic profiling in idiopathic and LRRK2-associated Parkinson's disease.
DOI: 10.1016/j.brainres.2012.05.036PMID: 22634372
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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Leucine-rich repeat kinase 2 (LRRK2) as a potential therapeutic target in Parkinson's disease.
DOI: 10.1016/j.tips.2012.04.001PMID: 22578536
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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Quantitative assessment of the effect of LRRK2 exonic variants on the risk of Parkinson's disease: a meta-analysis.
DOI: 10.1016/j.parkreldis.2012.04.013PMID: 22575234
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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LRRK2 I2020T mutation is associated with tau pathology.
DOI: 10.1016/j.parkreldis.2012.03.024PMID: 22525366
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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Mutation analysis of LRRK2, SCNA, UCHL1, HtrA2 and GIGYF2 genes in Chinese patients with autosomal dorminant Parkinson's disease.
DOI: 10.1016/j.neulet.2012.03.086PMID: 22503729
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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LRRK2: Understanding the role of common and rare variants in Parkinson's disease.
DOI: 10.1002/mds.24937PMID: 22590717
A bibliographic record traceable to Europe PMC.
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