Detecting Hemoglobin Variants during Sickle Cell Disease Research
$ 15.99 · 4.6 (587) · In stock
#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. […]
Fixing the sickle cell disease gene National Institutes of Health (NIH)
Micromachines, Free Full-Text
Fifteen years of newborn sickle cell disease screening in Madrid, Spain: an emerging disease in a European country
Identifying genetic variants and pathways associated with extreme levels of fetal hemoglobin in sickle cell disease in Tanzania, BMC Medical Genetics
Clot Club #20 - DiaPharma
Identifying genetic variants and pathways associated with extreme levels of fetal hemoglobin in sickle cell disease in Tanzania, BMC Medical Genetics
Frontiers Gender-Related Differences in Sickle Cell Disease in a Pediatric Cohort: A Single-Center Retrospective Study
Rapid Result Test On Track to Transform Sickle Cell Disease Screening for Millions
New Technology Diagnoses Sickle Cell Disease in Record Time
Frontiers Evaluation of Microchip-Based Point-Of-Care Device “Gazelle” for Diagnosis of Sickle Cell Disease in India
Introductory Chapter: Introduction to the History, Pathology and Clinical Management of Sickle Cell Disease
Sickle Cell Anemia: Genetics and Carrier Information - 23andMe
Automated screening of sickle cells using a smartphone-based microscope and deep learning
Multispectral Imaging for MicroChip Electrophoresis Enables Point-of-Care Newborn Hemoglobin Variant Screening