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Silencing polyglutamine degeneration with RNAi

Journal

NEURON
Volume 48, Issue 5, Pages 715-718

Publisher

CELL PRESS
DOI: 10.1016/j.neuron.2005.11.008

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Nine dominantly inherited neurodegenerative diseases are caused by expansion of a CAG repeat encoding glutamine. An important development in the study of such polyglutamine diseases was the realization that merely shutting off expression of a disease-encoding transgene could arrest progression in animal models with significant disease pathology. Such studies opened the door to a powerful new therapeutic approach now being pioneered: silencing of the dominant disease allele by RNA-mediated interference (RNAi), for the arrest-and potential reversal-of the disease process.

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