Article
Combined kinase inhibition modulates parkin inactivation.
Human molecular genetics - 1 Mar 2009
Rubio de la Torre Elena, Luzón-Toro Berta, Forte-Lago Irene, Minguez-Castellanos Adolfo, Ferrer Isidro, Hilfiker Sabine
Abstract excerpt
Mutations in the parkin gene cause autosomal-recessive, juvenile-onset parkinsonism, and parkin dysfunction may also play a role in the pathogenesis of sporadic Parkinson disease (PD). Although its precise function remains largely unknown, parkin seems to play a neuroprotective role. Several studies indicate that changes in parkin solubility induced by post-translational modifications, such as S-nitrosylation or...
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