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Acquisition of chromosome 1q duplication in parental and genome-edited human-induced pluripotent stem cell-derived neural stem cells results in their higher proliferation rate in vitro and in vivo.

Narges Zare MehrjardiMarek MolcanyiFiruze Fulya HatayMarco TimmerEbrahim ShahbaziJustus P AckermannStefan HermsStefanie Heilmann-HeimbachThomas F WunderlichNora ProchnowAiden HaghikiaAngelika LampertJürgen HeschelerEdmund A M NeugebauerHossein BaharvandTomo Šarić
Published in: Cell proliferation (2020)
These results demonstrate that, independently of ZFN-editing, hiPSC-NSCs have a propensity for acquiring dup(1)q and this aberration results in increased proliferation which might compromise downstream hiPSC-NSC applications.
Keyphrases
  • neural stem cells
  • crispr cas
  • endothelial cells
  • signaling pathway
  • high glucose
  • diabetic rats
  • induced pluripotent stem cells
  • genome wide
  • copy number
  • oxidative stress
  • dna methylation