NeuralCipher Open access
G2019S selective LRRK2 kinase inhibitor abrogates mitochondrial DNA damage.
DOI: 10.1038/s41531-024-00660-yPMID: 38429321
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
1.241 articles found
“Parkinson LRRK2” Clear search
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GBA1-and LRRK2-directed Treatments: The Way Forward.
DOI: 10.1016/j.parkreldis.2024.106039PMID: 38438297
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Open access
The Parkinson's disease related mutant VPS35 (D620N) amplifies the LRRK2 response to endolysosomal stress.
DOI: 10.1042/bcj20230492PMID: 38299383
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Phosphorylation of AQP4 by LRRK2 R1441G impairs glymphatic clearance of IFNγ and aggravates dopaminergic neurodegeneration.
DOI: 10.1038/s41531-024-00643-zPMID: 38296953
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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Genetic Modifiers of LRRK2 Parkinson's Disease: A Replication Study in Arab-Berbers.
DOI: 10.1002/mds.29735PMID: 38291980
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Are LRRK2 p.G2019S or GBA1 variants associated with long-term outcomes of deep brain stimulation for Parkinson's disease?
DOI: 10.1016/j.parkreldis.2024.106008PMID: 38242744
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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A potential patient stratification biomarker for Parkinson´s disease based on LRRK2 kinase-mediated centrosomal alterations in peripheral blood-derived cells.
DOI: 10.1038/s41531-023-00624-8PMID: 38191886
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New Pyrrolopyrimidines as LRRK2 Inhibitors for Treating Parkinson's Disease.
DOI: 10.2174/0929867331666230821101247PMID: 37605404
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Comprehensive analysis of clinical and biological features in Parkinson's disease associated with the LRRK2 G2019S mutation: Data from the PPMI study.
DOI: 10.1111/cts.13720PMID: 38266062
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LRRK2; Communicative Role in the Treatment of Parkinson's Disease and Ulcerative Colitis Overlapping.
DOI: 10.2174/0118715273270874231205050727PMID: 38279762
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The Effect of p.G2019S Mutation in the <i>LRRK2</i> Gene on the Activity of Lysosomal Hydrolases and the Clinical Features of Parkinson's Disease Associated with p.N370S Mutation in the <i>GBA1</i> Gene.
DOI: 10.31083/j.jin2301016PMID: 38287861
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Oculomotor Dysfunction in Idiopathic and LRRK2-Parkinson's Disease and At-Risk Individuals.
DOI: 10.3233/jpd-230416PMID: 38701160
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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