NeuralCipher Open access
Activation Mechanism of LRRK2 and Its Cellular Functions in Parkinson's Disease.
DOI: 10.1155/2016/7351985PMID: 27293958
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15.814 articles found
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LRRK2 phosphorylation level correlates with abnormal motor behaviour in an experimental model of levodopa-induced dyskinesias.
DOI: 10.1186/s13041-016-0234-2PMID: 27169991
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Clinical findings and genetic screening for copy number variation mutations in a cohort of South African patients with Parkinson's disease.
DOI: 10.7196/samj.2016.v106i6.10340PMID: 27245731
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Mitochondrial DNA variants as genetic risk factors for Parkinson disease.
DOI: 10.1111/ene.13020PMID: 27160373
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Alpha-synuclein and familial variants affect the chain order and the thermotropic phase behavior of anionic lipid vesicles.
DOI: 10.1016/j.bbapap.2016.05.003PMID: 27177693
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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Alpha-synuclein structure, functions, and interactions.
DOI: 10.4103/1735-1995.181989PMID: 27904575
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Toxic Dopamine Metabolite DOPAL Forms an Unexpected Dicatechol Pyrrole Adduct with Lysines of α-Synuclein.
DOI: 10.1002/anie.201600277PMID: 27158766
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The contribution of mutant GBA to the development of Parkinson disease in Drosophila.
DOI: 10.1093/hmg/ddw129PMID: 27162249
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Exogenous α-Synuclein Monomers Alter Dopamine Metabolism in Murine Brain.
DOI: 10.1007/s11064-016-1923-zPMID: 27161373
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Geniposide reduces α-synuclein by blocking microRNA-21/lysosome-associated membrane protein 2A interaction in Parkinson disease models.
DOI: 10.1016/j.brainres.2016.05.011PMID: 27173998
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Hereditary chorea - what else to consider when the Huntington's disease genetics test is negative?
DOI: 10.1111/ane.12609PMID: 27150574
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An Expert Diagnosis System for Parkinson Disease Based on Genetic Algorithm-Wavelet Kernel-Extreme Learning Machine.
DOI: 10.1155/2016/5264743PMID: 27274882
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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