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See Latest ArticlesMutations in the LRRK2 Roc-COR tandem domain link Parkinson's disease to Wnt signalling pathways
Human Molecular Genetics, 09/24/09
Sancho RM et al. – The findings also link LRRK2 to Wnt signalling pathways, suggesting novel pathogenic mechanisms and new targets for genetic analysis in Parkinson's disease.
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Today in Basic Science/Genetics...keeping you current
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Effect of IFN-beta therapy on the frequency and function of CD4+CD25+ regulatory T cells and Foxp3 gene expression in relapsing–remitting multiple sclerosis (RRMS): A preliminary study
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Skeletal dysplasias due to filamin A mutations result from a gain-of-function mechanism distinct from allelic neurological disorders
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Today in Movement Disorders...keeping you current
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Stimulation-Induced Dyskinesia in the Early Stage after Subthalamic Deep Brain Stimulation
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