Detecting Hemoglobin Variants during Sickle Cell Disease Research

#8211; Contributed by Abi Kasberg, PhD   Hemoglobins are protein molecules found in red blood cells (RBCs) that functionally transport oxygen from the lungs to the cells of the body and to shuttle carbon dioxide back to the lungs. Hemoglobins also play important roles in maintaining RBC shape by dynamically changing conformation through binding oxygen. […]

Sickle cell disease - Wikipedia

PDF] Potential Pithfalls in Using HPLC and its Interpretation in Diagnosing HbS

Gene therapy for sickle cell disease: moving from the bench to the bedside - ScienceDirect

News Archives - DiaPharma

Prevalence of hemoglobin variants and hemoglobinopathies using cation-exchange high-performance liquid chromatography in central reference laboratory of India: A report of 65779 cases

Gene-Editing Treatment for Sickle Cell Disease Moves Closer to Approval, Smart News

Micromachines, Free Full-Text

Sickle Cell Anemia, Blood Disorders

Sickle Cell (Hemoglobin SS) Disease: Acute & Chronic Presentation

New Technology Diagnoses Sickle Cell Disease in Record Time

Identifying genetic variants and pathways associated with extreme levels of fetal hemoglobin in sickle cell disease in Tanzania, BMC Medical Genetics