Holly Leslie reflects on the origin of this year’s Nobel prize-winning, CRISPR-Cas9 technology, and explores how scientists are beginning to use gene editing approaches on their quest for new medical treatments in hereditary disease.
Sonya explores the field of embryo gene editing which
recently entered unexplored territory with a scientist’s
claim of creating the world’s first genetically edited babies.
Alisha Aman reports on a breakthrough in the cure for Duchenne muscular dystrophy using genome editing.
Pint of Science 2019: The Art of Science
June 21, 2019
Stratonauts Launch theGIST To New Heights… We Went To Space!
March 22, 2019
Press Pause to Begin – TEDx University of Glasgow 2018
April 12, 2018
More
