From The Cover: Parkinson's disease-associated mutations in leucine-rich repeat kinase 2 augment kinase activity
Author:
Publisher
Proceedings of the National Academy of Sciences
Subject
Multidisciplinary
Reference20 articles.
1. A new locus for Parkinson's disease (PARK8) maps to chromosome 12p11.2-q13.1
2. Mutations in LRRK2 Cause Autosomal-Dominant Parkinsonism with Pleomorphic Pathology
3. Cloning of the Gene Containing Mutations that Cause PARK8-Linked Parkinson's Disease
4. A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease
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1. Cell biology of Parkinson's disease: Mechanisms of synaptic, lysosomal, and mitochondrial dysfunction;Current Opinion in Neurobiology;2024-04
2. Preclinical Evaluation of Novel Positron Emission Tomography (PET) Probes for Imaging Leucine-Rich Repeat Kinase 2 (LRRK2);Journal of Medicinal Chemistry;2024-02-02
3. Axonal Lysosomal Assays for Characterizing the Effects of LRRK2 G2019S;Biology;2024-01-20
4. Post-translational modification and mitochondrial function in Parkinson’s disease;Frontiers in Molecular Neuroscience;2024-01-11
5. Cellular and subcellular localization of Rab10 and phospho-T73 Rab10 in the mouse and human brain;Acta Neuropathologica Communications;2023-12-18
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