Neuron dysfunction is induced by prion protein with an insertional mutation via a Fyn kinase and reversed by sirtuin activation in Caenorhabditis elegans

Although prion propagation is well understood, the signaling pathways activated by neurotoxic forms of prion protein (PrP) and those able to mitigate pathological phenotypes remain largely unknown. Here, we identify src-2, a Fyn-related kinase, as a gene required for human PrP with an insertional mu...

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Veröffentlicht in:The Journal of neuroscience 2010-04, Vol.30 (15), p.5394-5403
Hauptverfasser: Bizat, Nicolas, Peyrin, Jean-Michel, Haïk, Stephane, Cochois, Véronique, Beaudry, Patrick, Laplanche, Jean-Louis, Néri, Christian
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Sprache:eng
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