Penn and CHOP researchers will utilize the new protocol to distribute customizable drugs that target specific genetic disorders.
Scientists at St. Jude Children's Research Hospital and Northwestern University identified a previously unknown treatment ...
Earlier this year, researchers at CHOP and Penn created a first-of-its-kind drug customized to a unique genetic mutation to save an infant named Baby KJ from dying of a rare liver disorder. KJ Muldoon ...
In one of the biggest advances against leukemia and other blood cancers in many years, doctors are reporting unprecedented success by using gene therapy to transform patients' blood cells into ...
The FDA has put a clinical hold on a Tenaya Therapeutics gene therapy study | The FDA has put a clinical hold on a Tenaya ...
Fred Hutch bioengineer Dr. Matthias Stephan is working to develop a special foam that could help make gene therapy for blood ...
The alliance extends a deal streak in genetic medicine for Lilly and hands the company rights to an experimental treatment ...
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Scientists Say They’ve Figured Out a Way to Reprogram the Pancreas to Produce GLP-1s Without Ozempic
Scientists say they've come up with a way for the body to produce its own store of glucagon-like peptide-1 (GLP-1).
Developing new gene therapies for autosomal dominant polycystic kidney disease (ADPKD) is still a challenge to date. A group of researchers from the Johns Hopkins Medicine in Baltimore has presented ...
A rare disease that has cut off children from the outside world now potentially has a cure. A clinical trial to treat severe ...
Earlier this year, researchers at Children's Hospital of Philadelphia and Penn created a first-of-its-kind drug customized to ...
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