Latest hemoglobin Stories
Changing a single letter of the human red blood cell DNA could be the key to curing sickle-cell anemia and other blood disorders.
Development Decision Leverages Recent Data with New ZFN-mediated Genome Editing Approach for Both Sickle Cell Disease and Beta-Thalassemia Programs RICHMOND, Calif., May 13, 2015 /PRNewswire/
RICHMOND, Calif., Feb. 4, 2015 /PRNewswire/ -- Sangamo BioSciences, Inc.
With YrysView you will know the levels of good cholesterol, bad cholesterol, triglycerides, blood pressure, hemoglobin, glucose and protein levels ...
Researchers from the University of Southern Denmark have synthesized crystalline materials that can bind and store oxygen in high concentrations. The stored oxygen can be released again when and where it is needed.
An international team of researchers, led by the University of Leicester, has solved a long-standing mystery in biology, by identifying the molecular structure of a vital biological chemical.
In patients with a traumatic brain injury (TBI), neither the administration of the hormone erythropoietin (EPO) or maintaining a higher hemoglobin concentration through blood transfusion resulted in improved neurological outcome at 6 months.
The presence of sickle cell trait among African Americans may help explain why those on dialysis require higher doses of an anemia medication than patients of other ethnicities.
--Partnership to Focus on Developing Novel Therapies for Sickle Cell Disease and Beta-Thalassemia-- CAMBRIDGE, Mass. and RICHMOND, Calif., Jan.
New research presented today during the 55th American Society of Hematology Annual Meeting and Exposition in New Orleans uncovers several important insights into the pathophysiology of sickle cell disease and thalassemia that may soon translate into the development of better, more targeted treatments for hundreds of thousands of patients worldwide.
- A hairdresser.