Title : Rab11 rescues synaptic dysfunction and behavioural deficits in a Drosophila model of Huntington's disease.

Pub. Date : 2012 Jul 1

PMID : 22466800






1 Functional Relationships(s)
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1 The polyglutamine expansion in the huntingtin (htt) protein that underlies this disorder leads to perturbations in many cellular pathways, including the disruption of Rab11-dependent endosomal recycling. polyglutamine RAB11A, member RAS oncogene family Homo sapiens