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Parkinson's disease-associated mutations in LRRK2 link enhanced GTP-binding and kinase activities to neuronal toxicity
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Kinase activity is required for the toxic effects of mutant LRRK2/dardarin
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LRRK2 G2019S as a cause of Parkinson's disease in North African Arabs
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LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews
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G2019S dardarin substitution is a common cause of Parkinson's disease in a Portuguese cohort
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Parkinson's disease-associated mutations in leucine-rich repeat kinase 2 augment kinase activity
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Dimerization through the catalytic domain is essential for MEKK2 activation
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Structures of human MAP kinase kinase 1 (MEK1) and MEK2 describe novel noncompetitive kinase inhibition
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Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease
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Mutations in LRRK2 cause autosomal-dominant Parkinsonism with pleomorphic pathology
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