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gene therapy

  • DART VADAR harnesses the force of enzymes for better RNA drugs
    March 23, 2023

    DART VADAR harnesses the force of enzymes for better RNA drugs

    bricemarsters
  • Modified CRISPR-based enzymes improve the prospect of inserting entire genes into the genome to overcome diverse disease-causing mutations
    January 24, 2023

    Modified CRISPR-based enzymes improve the prospect of inserting entire genes into the genome to overcome diverse disease-causing mutations

    bricemarsters
  • Stem cell-gene therapy shows promise in ALS safety trial
    September 7, 2022

    Stem cell-gene therapy shows promise in ALS safety trial

    bricemarsters
  • Industry Matters: Nessan Bermingham on Triplet Therapeutics and the keys to startup success.
    June 15, 2022

    Industry Matters: Nessan Bermingham on Triplet Therapeutics and the keys to startup success.

    scientificinquirer
  • Old skins cells reprogrammed to regain youthful function.
    April 19, 2022

    Old skins cells reprogrammed to regain youthful function.

    bricemarsters
  • WVU research suggests interrupting immune response improves multiple sclerosis outcomes.
    March 29, 2022

    WVU research suggests interrupting immune response improves multiple sclerosis outcomes.

    bricemarsters
  • Cellular therapy improves signs and symptoms of Duchenne muscular dystrophy.
    March 18, 2022

    Cellular therapy improves signs and symptoms of Duchenne muscular dystrophy.

    bricemarsters
  • New study identifies the genes most likely to lead to heart attacks.
    February 22, 2022

    New study identifies the genes most likely to lead to heart attacks.

    bricemarsters
  • DAILY DOSE: Discovery makes natural origin of COVID-19 virus the most likely explanation; Fishing fleet threatens the Galapagos Islands.
    September 24, 2021

    DAILY DOSE: Discovery makes natural origin of COVID-19 virus the most likely explanation; Fishing fleet threatens the Galapagos Islands.

    scientificinquirer
  • CRISPR-Cas9 delivered by adenovirus may revolutionize gene therapy.
    August 6, 2021

    CRISPR-Cas9 delivered by adenovirus may revolutionize gene therapy.

    bricemarsters
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