Heterogeneous Red Blood Cell Adhesion and Deformability in Sickle Cell Disease
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/srep07173.pdf
Reference68 articles.
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2. Alexy, T. et al. Rheologic behavior of sickle and normal red blood cell mixtures in sickle plasma: implications for transfusion therapy. Transfusion 46, 912–918 (2006).
3. Hebbel, R. P. Beyond hemoglobin polymerization: the red blood cell membrane and sickle disease pathophysiology. Blood 77, 214–237 (1991).
4. Ferrone, F. A. Polymerization and sickle cell disease: a molecular view. Microcirculation 11, 115–128 (2004).
5. Noguchi, C. T. & Schechter, A. N. Sickle hemoglobin polymerization in solution and in cells. Annu Rev Biophys Biophys Chem 14, 239–263 (1985).
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