Timmerman Report
Creating lower cost accessible cell & gene therapies
TVC News Nigeria
Managing Sickle Cell Disease: Science Offers New Hope Through Gene Therapy – Experts
The Guardian Nigeria
Experts advocate adoption of gene therapy to treat sickle cell in Nigeria
With an estimated four million Nigerians living with sickle cell disease (SCD) health experts are advocating the adoption of gene therapy as a curative treatment option for patients in the country.
NBC News
The best and brightest young scientists are looking beyond the U.S. as cuts hit home
Top scientists are cutting staff at their labs. Postdocs are leaving the country. Here's how the Trump cuts are playing out at the University of Washington.
Stat
Q&A with Jennifer Adair researcher on a mission to increase global access to gene therapies
Gene and cell therapies have transformed a handful of devastating disorders in the U.S. and Europe with more treatments on the way. But those technologies have largely failed to reach most of the world.
Hutch News
If you want to go far go together
Fred Hutch scientist Dr. Jennifer Adair partners with colleagues around the globe to make gene therapies more effective and more widely available.
ASGCT
Global Gene Therapy Initiative Aims to Bring Gene Therapy Trials to India and Uganda
The Global Gene Therapy Initiative (GGTI) recently published its first report in Gene Therapy which highlights the need for cost-effective gene therapy development strategies in low-and-middle-income countries.
UW Medicine
Dr. Jennifer Adair inaugural recipient of the Fleischauer Family Endowed Chair in Gene Therapy Translation
The new endowed chair will help advance Dr. Adair’s research which focuses on developing safe cost-effective gene therapies that can be delivered worldwide.
Washington State University
5 Questions with School of Molecular Biosciences alumna Jennifer Adair
GeekWire
Fred Hutch scientist on how gold nanoparticles could bring CRISPR to the developing world
Healthcare in Europe
Could gold be the key to making gene therapy for HIV?
A proof-of-principle study shows that gold nanoparticles loaded with CRISPR and other gene-editing tools safely and effectively edited blood stem cells.
Eureka Alert!
Could gold be the key to making gene therapy for HIV blood disorders more accessible?
A proof-of-principle study published in Nature Materials shows that gold nanoparticles loaded with CRISPR and other gene-editing tools safely and effectively edited blood stem cells
MIT Technology review
This Lab-in-a-Box Could Make Gene Therapy Less Elitist
Genetic repairs are curing patients—but only at a few elite centers.
The ASCO Post
Jennifer Adair PhD Recognized as ‘Outstanding New Investigator’
Jennifer Adair PhD of the Fred Hutchinson Cancer Research Center has been named a 2015 Outstanding New Investigator by the American Society of Gene & Cell Therapy (ASGCT). The award recognizes Dr. Adair’s independent research efforts to understand and improve blood stem cell–based gene therapies.