Targeting of XJB-5-131 to mitochondria suppresses oxidative DNA damage and motor decline in a mouse model of Huntington’s disease

Lignende værker

• Mitochondrial targeting of XJB-5-131 attenuates or improves pathophysiology in HdhQ150 animals with well-developed disease phenotypes
  af: Polyzos, Aris, et al.
  Udgivet: (2016)
• XJB-5-131-mediated improvement in physiology and behaviour of the R6/2 mouse model of Huntington's disease is age- and sex- dependent
  af: Polyzos, Aris A., et al.
  Udgivet: (2018)
• Problems and solutions for the analysis of somatic CAG repeat expansion and their relationship to Huntington's disease toxicity
  af: Budworth, Helen, et al.
  Udgivet: (2016)
• Distinct Pools of Non-Glycolytic Substrates Differentiate Brain Regions and Prime Region-Specific Responses of Mitochondria
  af: Lee, Do Yup, et al.
  Udgivet: (2013)
• Suppression of Somatic Expansion Delays the Onset of Pathophysiology in a Mouse Model of Huntington’s Disease
  af: Budworth, Helen, et al.
  Udgivet: (2015)