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Effects of mutant huntingtin inactivation on Huntington disease-related behaviours in the BACHD mouse model.

Rachel Y CheongBarbara BaldoMuhammad U SajjadDeniz KirikÅsa Petersén
Published in: Neuropathology and applied neurobiology (2021)
Our results indicate that widespread targeting and the timing of interventions aimed at reducing mutant HTT are important factors to consider when developing disease-modifying therapies for HD.
Keyphrases
  • mouse model
  • wild type
  • physical activity
  • cancer therapy
  • drug delivery