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The Journal of Biological Chemistry|July 10, 2003
L166P mutant DJ-1, causative for recessive Parkinson's disease, is degraded through the ubiquitin-proteasome systemDavid W Miller, Rili Ahmad, Stephen Hague, et al.The International Journal of Neuropsychopharmacology|December 21, 2012
Age-modulated association between prefrontal NAA and the BDNF geneBasira Salehi, Nora Preuss, Jan Willem van der Veen, et al.Annals of Neurology|August 28, 2018
A comprehensive analysis of SNCA-related genetic risk in sporadic parkinson diseaseLasse Pihlstrøm, Cornelis Blauwendraat, Chiara Cappelletti, et al.Human Molecular Genetics|June 20, 2018
Proteomic analysis reveals co-ordinated alterations in protein synthesis and degradation pathways in LRRK2 knockout miceLaura Pellegrini, David N Hauser, Yan Li, et al.Journal of Neurochemistry|March 19, 2005
Tyrosinase exacerbates dopamine toxicity but is not genetically associated with Parkinson's diseaseElisa Greggio, Elisabetta Bergantino, Donald Carter, et al.Scientific Reports|February 28, 2020
In Vitro CRISPR/Cas9-Directed Gene Editing to Model LRRK2 G2019S Parkinson's Disease in Common MarmosetsScott C Vermilyea, Alexander Babinski, Nina Tran, et al.The Journal of Biological Chemistry|February 24, 2019
Parkinson's disease-associated mutations in the GTPase domain of LRRK2 impair its nucleotide-dependent conformational dynamicsChun-Xiang Wu, Jingling Liao, Yangshin Park, et al.Brain Research|June 16, 2025
Regulation of LRRK2 activity by metabolic stress and heavy metal exposureMichalis Kentros, Jordan Follett, Nitya Subrahmanian, et al.Science Translational Medicine|May 10, 2023
Inhibition of p38α MAPK restores neuronal p38γ MAPK and ameliorates synaptic degeneration in a mouse model of DLB/PDMichiyo Iba, Changyoun Kim, Somin Kwon, et al.Aging Cell|December 23, 2025
Mitochondrial DNA Variation in the Aging Human Cerebral Cortex and CerebellumAudrey A Omidsalar, David R Tyrpak, J Andrew MacKay, et al.Pageof 32