Closing the structure-to-function gap for LRRK2
Author:
Funder
NIH
Michael J Fox Foundation for Parkinson's Research
Publisher
Elsevier BV
Subject
Molecular Biology,Biochemistry
Reference10 articles.
1. Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease;Paisan-Ruiz;Neuron,2004
2. Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology;Zimprich;Neuron,2004
3. Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies;Nalls;Lancet Neurol.,2019
4. LRRK2 Biology from structure to dysfunction: research progresses, but the themes remain the same;Berwick;Mol. Neurogener.,2019
5. Structure of the ROC domain from the Parkinson's disease-associated leucine-rich repeat kinase 2 reveals a dimeric GTPase;Deng;Proc. Natl. Acad. Sci. U. S. A.,2008
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1. Regulation of TIR-1/SARM-1 by miR-71 Protects Dopaminergic Neurons in a C. elegans Model of LRRK2-Induced Parkinson’s Disease;International Journal of Molecular Sciences;2024-08-13
2. R1441C and G2019S LRRK2 knockin mice have distinct striatal molecular, physiological, and behavioral alterations;Communications Biology;2022-11-10
3. The Double-Faceted Role of Leucine-Rich Repeat Kinase 2 in the Immunopathogenesis of Parkinson’s Disease;Frontiers in Aging Neuroscience;2022-05-11
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