Detecting Hemoglobin Variants during Sickle Cell Disease Research: Which  Method is Best? - DiaPharma

Detecting Hemoglobin Variants during Sickle Cell Disease Research: Which Method is Best? - DiaPharma

4.6
(121)
Write Review
More
$ 25.50
Add to Cart
In stock
Description

#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. […]

Applications of genome editing technology in the targeted therapy

A Portable Smartphone-linked Device for Direct, Rapid and Chemical

Frontiers Evaluation of Microchip-Based Point-Of-Care Device

Applications of genome editing technology in the targeted therapy

Frontiers Breaking genetic shackles: The advance of base editing

JCM, Free Full-Text

Micromachines, Free Full-Text

Identifying genetic variants and pathways associated with extreme

Marcus, Author at DiaPharma

Glycosylation in health and disease

TAT is correlated with D-dimer in sickle cell disease. Plasma TAT

The role of MRI-R2* in the detection of subclinical pancreatic