CRISPR Genome Editing for Sickle Cell Disease Therapies - Dr. Shengdar Tsai

Поделиться
HTML-код
  • Опубликовано: 5 авг 2024
  • Dr. Shengdar Tsai, Assistant Member, Experimental Hematology, St. Jude Children’s Research Hospital

Комментарии • 5

  • @Rene-uz3eb
    @Rene-uz3eb 6 месяцев назад

    The thing is with any inherited trait you can almost guarantee when it spread there were conditions that made it benign and advantageous, otherwise it wouldn't have spread. So instead of figure out how to undo evolution, maybe find and replicate the conditions, if that's easier.

  • @allknight7905
    @allknight7905 Год назад

    I would love to be in the clinical trials for my thalassemia .. where do I sign up please help !

  • @numeda-ala5203
    @numeda-ala5203 Год назад

    Pls help my 7year old of sickle cell disease.

  • @davidharrison1927
    @davidharrison1927 2 года назад

    God will continue to bless #dridedia for getting rid of my hsv1&2 am so happy right now with my partner.