Instructional Video12:40
SciShow

The First CRISPR Gene Therapy Is Here

12th - Higher Ed
CRISPR is a powerful gene editing tool, but its uses have been purely scientific until now. In 2023, US and UK drug regulators including the FDA approved Casgevy, a CRISPR/Cas9-based therapy for sickle cell disease and beta-thalassemia....
Instructional Video5:35
SciShow

Why Do Some Doctors Still Use Bloodletting?

12th - Higher Ed
Has a doctor ever told you that you just have too much blood? Probably not, but there are a handful of conditions where being a little low might be good for you.
Instructional Video6:04
SciShow

Changing DNA in a Cell With No DNA: Gene Therapy for Blood Disorders

12th - Higher Ed
Lots of genetic diseases come down to a small change in a single gene, but how do you treat those diseases when the cells involved don’t have any DNA?
Instructional Video6:28
Healthcare Triage

Some Unpleasant Facts about Research Priorities

Higher Ed
Sickle Cell Disease affects 100,00 Americans, and has been pretty well understood for a long time. So, why are there only two drugs available for the condition? Why are so few research dollars allocated to the problem? Well, the answers...
Instructional Video3:37
Science360

NSF's 2014 Alan T. Waterman Awardee Feng Zhang discusses his research on the brain

12th - Higher Ed
NSF's 2014 Alan T. Waterman Awardee Feng Zhang discusses the work of his research team on the brain. Zhang is an investigator at the McGovern Institute for Brain Research at MIT and a core member of the Broad Institute of MIT and...
News Clip2:22
Curated Video

FDA Advisers Reviewed a Sickle Cell Treatment

Higher Ed
The Food and Drug Administration says there’s an unmet need for help for patients suffering from severe sickle cell anemia. A new drug that uses gene editing could solve that.
News Clip1:54
Curated Video

Breakthrough Sickle Cell Treatments Come with Health Risks

Higher Ed
The Food and Drug Administration has approved two gene-editing treatments for patients 12 and older suffering from severe sickle cell disease, but they come with health risks doctors want patients to know about.
News Clip4:45
Bloomberg

How Will We Pay For Miracle Cures?

Higher Ed
Gene therapies are considered miracle cures, but their exorbitant costs, which could exceed $12 billion, might hinder access for those in need. Bloomberg Opinion columnist Lisa Jarvis highlights how two gene therapies awaiting FDA...
News Clip6:33
Curated Video

CRISPR Cure For Sickle Cell May Be Slowed By Black Patients' Mistrust

Higher Ed
CRISPR may be a cure, but clinical trials may lack volunteers because of black patients' mistrust of biased and unethical medical practices.
Lesson Plan14:03
Howard Hughes Medical Institute

The Making of the Fittest: Natural Selection in Humans

8th - Higher Ed Standards
Sickle cell disease only occurs when both parents contribute the trait, and mostly in those of African descent. Where did it come from? How did it evolve? Tony Allison, a molecular biologist, noticed a connection between sickle cell and...