Corrigendum: The Generation of Mouse and Human Huntington Disease iPS Cells Suitable for In vitro Studies on Huntingtin Function

Samankaltaisia teoksia

• The Generation of Mouse and Human Huntington Disease iPS Cells Suitable for In vitro Studies on Huntingtin Function
  Tekijä: Szlachcic, Wojciech J., et al.
  Julkaistu: (2017)
• Huntington Disease as a Neurodevelopmental Disorder and Early Signs of the Disease in Stem Cells
  Tekijä: Wiatr, Kalina, et al.
  Julkaistu: (2017)
• Huntington disease iPSCs show early molecular changes in intracellular signaling, the expression of oxidative stress proteins and the p53 pathway
  Tekijä: Szlachcic, Wojciech J., et al.
  Julkaistu: (2015)
• Mouse polyQ database: a new online resource for research using mouse models of neurodegenerative diseases
  Tekijä: Szlachcic, Wojciech J., et al.
  Julkaistu: (2015)
• Identification of Altered Developmental Pathways in Human Juvenile HD iPSC With 71Q and 109Q Using Transcriptome Profiling
  Tekijä: Świtońska, Karolina, et al.
  Julkaistu: (2019)