Genome editing in stem cells


The development of targeted genome editing technique using custom-engineered sequence-specific nucleases (including CRISPR/Cas9) allowed genetic changes with greater precision. This technique has a widespread application in reprograming of stem cells to study disease outcomes. The rapid evolution of these two techniques over years and their relationship with one another has paved a way for understanding cellular interactions and regulation of transcription at molecular level with appreciable efficiency and flexibility.

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

Quick Links

Are you interested in

Mail us at

Program enquiry
stemcellcongress18@gmail.com
Sponsorship oportunity
stemcellcongress18@gmail.com
General queries
stemcellcongress18@gmail.com
More details about sponsorship:sponsors@alliedacademies.com
Copyright © 2018-2019 Allied Academies, All Rights Reserved.