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• W2071777990 startingPage "e20630" @default.
• W2071777990 abstract "Mutations in LRRK2 are genetically linked to Parkinson's disease (PD) but its normal biological function is largely unknown. Sheng et al. recently reported that deletion of the WD40 domain of LRRK2 in zebrafish specifically causes PD-like loss of neurons and behavior defect. However, our similar early study and recent confirming experiments using the same reagents reported by Sheng et al. failed to reproduce the phenotype of the loss of dopaminergic neurons, although the mRNA of LRRK2 was molecularly disrupted. Our study suggests that function of LRRK2 and its usefulness to generate zebrafish PD model needs further evaluation." @default.
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• W2071777990 date "2011-06-16" @default.
• W2071777990 modified "2023-10-06" @default.
• W2071777990 title "Disruption of LRRK2 Does Not Cause Specific Loss of Dopaminergic Neurons in Zebrafish" @default.
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• W2071777990 doi "https://doi.org/10.1371/journal.pone.0020630" @default.
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