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Inhibition of mTOR induces autophagy and reduces toxicity of polyglutamine expansions in fly and mouse models of Huntington disease

Nature Genetics · 2004 · Vol. 36(6) · pp. 585–595
Brinda RavikumarCorinne VacherZdenek BergerJ. Eric DaviesShouqing LuoLourdes Garcia OrozFrancesco ScaravilliDouglas F. EastonRainer DudenCahir J. O’KaneDavid C. Rubinsztein
Genetic Neurodegenerative DiseasesMitochondrial Function and PathologyMuscle Physiology and DisordersAutophagyHuntingtinHuntington's diseaseNeurodegenerationPI3K/AKT/mTOR pathwayBiologyHuntingtin ProteinPolyglutamine tractCell biologyMechanistic target of rapamycin

MeSH terms

Huntingtin ProteinAnimalsAutophagyDisease Models, AnimalDrosophila melanogasterFemaleHumansHuntington DiseaseMaleMice, TransgenicMutationNerve Tissue ProteinsNuclear ProteinsPeptidesProtein Kinases

Funding

  • Wellcome Trust
  • Commonwealth Scholarship Commission
  • Cambridge Overseas Trust
  • Directorate for Biological Sciences
  • Medical Research Council
  • Biotechnology and Biological Sciences Research Council
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