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Prolyl oligopeptidase inhibition reduces PolyQ aggregation and improves cell viability in cellular model of Huntington’s disease

  • Susanna Norrbacka
  • , Dan Lindholm
  • , Timo T. Myöhänen*
  • *Corresponding author for this work
  • University of Helsinki

Research output: Contribution to journalArticleScientificpeer-review

Original languageEnglish
Pages (from-to)8511-8515
Number of pages5
JournalJournal of Cellular and Molecular Medicine
Volume23
Issue number12
DOIs
Publication statusPublished - 1 Dec 2019
MoE publication typeA1 Journal article-refereed

Funding

This study was supported by Academy of Finland (grants 303833, 267788, and 273799), University of Helsinki 3-year grant, Jane and Aatos Erkko Foundation and Sigrid Juselius Foundation grants for TTM. This study was supported by Academy of Finland (grants 303833, 267788, and 273799), University of Helsinki 3‐year grant, Jane and Aatos Erkko Foundation and Sigrid Juselius Foundation grants for TTM.

Keywords

  • autophagy
  • huntingtin
  • neurodegeneration
  • protein aggregation
  • protein processing

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