Genomic Editing in Stem Cells

The development of targeted genome editing technique using custom-engineered sequence-specific nucleases(including CRISPR/Cas9) allowed genetic changes with larger exactness. this method contains a widespread application within the reprogramming of stem cells to review disease outcomes. The fast evolution of these two techniques over years and their relationship with each other has made-up the way for understanding cellular interactions and regulation of transcription at a molecular level with considerable potency and flexibility.


  • DNA repair in stem cells
  • Targeting genetic diseases by genome editing in stem cells
  • CRISPR/Cas9 in genome editing
  • Genome editing for designer babies

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