Erythrocytes in sickle cell anemia are heterogeneous in their rheological and hemodynamic characteristics.Dhananjay K. Kaul, R L Nagel, M E Fabry et al.|Journal of Clinical Investigation|1983Cited by 228
Monoclonal antibodies to αVβ3 (7E3 and LM609) inhibit sickle red blood cell–endothelium interactions induced by platelet-activating factorDhananjay K. Kaul, Barry S. Coller, Han‐Mou Tsai et al.|Blood|2000Cited by 183
In vivo demonstration of red cell-endothelial interaction, sickling and altered microvascular response to oxygen in the sickle transgenic mouse.Dhananjay K. Kaul, R L Nagel, M E Fabry et al.|Journal of Clinical Investigation|1995Cited by 132
Heterogeneity of red cells in the sickler: a characteristic with practical clinical and pathophysiological implications.M E Fabry, R L Nagel|PubMed|1982Cited by 111
High expression of human beta S- and alpha-globins in transgenic mice: erythrocyte abnormalities, organ damage, and the effect of hypoxia.M E Fabry, R L Nagel, Frank Costantini et al.|Proceedings of the National Academy of Sciences|1992Cited by 100