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R P Hebbel

Showing results (51-60 of 116) with videos related to

Pageof 12
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Blood|March 1, 1990
Synergistic effects of oxidation and deformation on erythrocyte monovalent cation leakP A Ney, M M Christopher, R P Hebbel
Blood|November 1, 1981
Modulation of erythrocyte-endothelial interactions and the vasocclusive severity of sickling disordersR P Hebbel, C F Moldow, M H Steinberg
Blood|June 1, 1980
Effect of increased maternal hemoglobin oxygen affinity on fetal growth in the ratR P Hebbel, E M Berger, J W Eaton
Progress in Clinical and Biological Research|January 1, 1981
Erythrocyte calcium abnormalities in sickle cell diseaseR P Hebbel, M H Steinberg, J W Eaton
Blood|November 15, 1992
Thrombospondin mediates adherence of CD36+ sickle reticulocytes to endothelial cellsK Sugihara, T Sugihara, N Mohandas, et al.
Experimental Cell Research|June 24, 2004
The relative magnitudes of endothelial force generation and matrix stiffness modulate capillary morphogenesis in vitroA L Sieminski, R P Hebbel, K J Gooch
Biochimica Et Biophysica Acta|February 16, 1999
Mechanism of interaction of thrombospondin with human endothelium and inhibition of sickle erythrocyte adhesion to human endothelial cells by heparinK Gupta, P Gupta, A Solovey, et al.
Progress in Clinical and Biological Research|January 1, 1989
Iron compartments associated with sickle RBC membranes: a mechanism for the targeting of oxidative damageS A Kuross, B H Rank, R P Hebbel
Experimental Cell Research|March 14, 1998
Thrombin-stimulated calcium mobilization is inhibited by thrombospondin via CD36J Enenstein, K Gupta, G M Vercellotti, et al.
American Journal of Hematology|June 1, 1985
Erythrocyte (Ca+2 + Mg+2)-ATPase activity: increased sensitivity to oxidative stress in glucose-6-phosphate dehydrogenase deficiencyO Shalev, V Lavi, R P Hebbel, et al.
Pageof 12

Showing results (51-60 of 116) with videos related to

Sort By:
Pageof 12
Blood|March 1, 1990
Synergistic effects of oxidation and deformation on erythrocyte monovalent cation leakP A Ney, M M Christopher, R P Hebbel
Blood|November 1, 1981
Modulation of erythrocyte-endothelial interactions and the vasocclusive severity of sickling disordersR P Hebbel, C F Moldow, M H Steinberg
Blood|June 1, 1980
Effect of increased maternal hemoglobin oxygen affinity on fetal growth in the ratR P Hebbel, E M Berger, J W Eaton
Progress in Clinical and Biological Research|January 1, 1981
Erythrocyte calcium abnormalities in sickle cell diseaseR P Hebbel, M H Steinberg, J W Eaton
Blood|November 15, 1992
Thrombospondin mediates adherence of CD36+ sickle reticulocytes to endothelial cellsK Sugihara, T Sugihara, N Mohandas, et al.
Experimental Cell Research|June 24, 2004
The relative magnitudes of endothelial force generation and matrix stiffness modulate capillary morphogenesis in vitroA L Sieminski, R P Hebbel, K J Gooch
Biochimica Et Biophysica Acta|February 16, 1999
Mechanism of interaction of thrombospondin with human endothelium and inhibition of sickle erythrocyte adhesion to human endothelial cells by heparinK Gupta, P Gupta, A Solovey, et al.
Progress in Clinical and Biological Research|January 1, 1989
Iron compartments associated with sickle RBC membranes: a mechanism for the targeting of oxidative damageS A Kuross, B H Rank, R P Hebbel
Experimental Cell Research|March 14, 1998
Thrombin-stimulated calcium mobilization is inhibited by thrombospondin via CD36J Enenstein, K Gupta, G M Vercellotti, et al.
American Journal of Hematology|June 1, 1985
Erythrocyte (Ca+2 + Mg+2)-ATPase activity: increased sensitivity to oxidative stress in glucose-6-phosphate dehydrogenase deficiencyO Shalev, V Lavi, R P Hebbel, et al.
Pageof 12