Google
Trusted Resources: News & Events
Latest announcements and gatherings
U.S. Government Awards Missouri Researcher $4.3 Million to Study Sickle Cell in Teens, Adults
The National Institutes of Health (NIH) has awarded a $4.3 million research grant to Dr. Allison A. King of the Washington University School of Medicine in St. Louis to support her research on sickle cell disease, with particular focus on teens and adults.
The grant — believed to be the first of its kind from the NIH — will let King continue and expand her study as part of an initiative being coordinated by the agency’s National Heart, Lung, and Blood Institute. The NHLBI has now awarded $36 million in sickle cell research grants to investigators at eight sites.
+myBinderRelated Content
-
Piedmont Health Services and Sickle Cell Agency 11th Annual Sickle Cell Charity RideJoin us for a fun and exciting motorcycl...
-
M. Dawn Nelson, PhDDr. M. Dawn Nelson, PhD is an Associate ...
-
Sickle Cell Foundation NigeriaThe formation of the Sickle Cell Foundat...
-
Simone C. Eastman Uwan, MDDr. Simone Eastman Uwan was born in Guya...
-
Meet the oneSCDvoice Community 2020!https://www.onescdvoice.com/wp-content/u...
-
Dr. Doris Wethers, 91, on Front Lines against Sickle Cell, DiesDr. Doris L. Wethers, who broke racial b...
-
The As One FoundationThe As One Foundation was established in...
To improve your experience on this site, we use cookies. This includes cookies essential for the basic functioning of our website, cookies for analytics purposes, and cookies enabling us to personalize site content. By clicking on 'Accept' or any content on this site, you agree that cookies can be placed. You may adjust your browser's cookie settings to suit your preferences. More Information
The cookie settings on this website are set to "allow cookies" to give you the best browsing experience possible. If you continue to use this website without changing your cookie settings or you click "Accept" below then you are consenting to this.
Powered by
Support for this site is provided by
This platform is made possible through a partnership with the Sickle Cell Disease Association of America, Inc. (SCDAA) and its member organizations. SCDAA's mission is to advocate for people affected by sickle cell conditions and empower community-based organizations to maximize quality of life and raise public consciousness while advancing the search for a universal cure.