Sorted by: Date | Title

Matthew Heeney, sickle cell program director

Therapy Directed Against Platelets Does Not Significantly Reduce Painful Crises in Sickle Cell Disease

December 08, 2015
Treatment with the antiplatelet agent prasugrel does not significantly reduce the rate of pain crises or severe lung complications in children with sickle cell disease, according to a report published in the New England Journal of Medicine describing one of the largest and most geographically diverse international clinical trials on sickle cell disease to date.
Sickle Cell Photo

Gene Editing Study Reveals Possible "Achilles Heel" of Sickle Cell Disease

September 16, 2015
Researchers from Dana-Farber/Boston Children's, using CRISPR-based gene editing tools, have found that changes to a small stretch of DNA may circumvent the genetic defect behind sickle cell disease (SCD). The discovery, published in the journal Nature, creates a path for developing gene editing approaches for treating SCD and other hemoglobin disorders, such as thalassemia.
Venee Tubman, MD

Liberia’s Response to Ebola

October 14, 2014
New England Cable News interviewed Venee Tubman, MD, about the Ebola outbreak in Liberia, where she has done extensive work on sickle cell disease.
Venee Tubman, MD

Blood Work

August 11, 2014
Harvard Medical School interviewed Venee Tubman, MD, a pediatric hematologist, about her sickle cell work in Liberia.

Hope Grows for Patients with Sickle Cell Disease

March 03, 2014
Advances in research and treatment are changing sickle cell disease from an inherited condition that often condemned children to painful and short lives into a condition that can be managed with less pain and a longer life expectancy, the Washington Post reports.
Sickle Cell Photo

Newly Discovered Gene Regulator Could Precisely Target Sickle Cell Disease

October 10, 2013
(News release) A research team from Dana-Farber/Boston Children's and other institutions has discovered a new genetic target for potential therapy of sickle cell disease. The target, called an enhancer, controls a molecular switch in red blood cells called BCL11A that, in turn, regulates hemoglobin production. The researchers – led by Daniel Bauer, MD, PhD, and Stuart Orkin, MD, of Dana-Farber/Boston Children's – reported their findings in Science.

Potential gene therapy approach to sickle cell disease highlighted at ASH

December 11, 2012
Proof-of-concept animal study selected as one of the best presentations at 54th American Society of Hematology Annual Meeting and Exposition
Showing 11-17 of 17 items