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R P Hebbel

Showing results (101-110 of 116) with videos related to

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British Journal of Anaesthesia|July 4, 2013
Morphine stimulates platelet-derived growth factor receptor-β signalling in mesangial cells in vitro and transgenic sickle mouse kidney in vivoM L Weber, C Chen, Y Li, et al.
Experimental Cell Research|March 6, 1999
VEGF prevents apoptosis of human microvascular endothelial cells via opposing effects on MAPK/ERK and SAPK/JNK signalingK Gupta, S Kshirsagar, W Li, et al.
The Journal of Clinical Investigation|September 18, 1997
Removal of erythrocyte membrane iron in vivo ameliorates the pathobiology of murine thalassemiaP V Browne, O Shalev, F A Kuypers, et al.
Blood|September 1, 1995
Deferiprone (L1) chelates pathologic iron deposits from membranes of intact thalassemic and sickle red blood cells both in vitro and in vivoO Shalev, T Repka, A Goldfarb, et al.
Blood|November 15, 1993
Nonrandom association of free iron with membranes of sickle and beta-thalassemic erythrocytesT Repka, O Shalev, R Reddy, et al.
The Journal of Laboratory and Clinical Medicine|June 9, 1999
Low-density lipoprotein susceptibility to oxidation and cytotoxicity to endothelium in sickle cell anemiaJ D Belcher, P H Marker, P Geiger, et al.
The American Journal of Pathology|March 10, 2001
Oxidative stress and induction of heme oxygenase-1 in the kidney in sickle cell diseaseK A Nath, J P Grande, J J Haggard, et al.
Thrombosis and Haemostasis|March 15, 2001
Whole blood tissue factor procoagulant activity remains detectable during severe aplasia following bone marrow and peripheral blood stem cell transplantationM Ozcan, C T Morton, A Solovey, et al.
American Journal of Physiology. Regulatory, Integrative and Comparative Physiology|November 18, 2000
Mechanisms of vascular instability in a transgenic mouse model of sickle cell diseaseK A Nath, V Shah, J J Haggard, et al.
The Journal of Clinical Investigation|April 1, 1993
Effect of excess alpha-hemoglobin chains on cellular and membrane oxidation in model beta-thalassemic erythrocytesM D Scott, J J van den Berg, T Repka, et al.
Pageof 12

Showing results (101-110 of 116) with videos related to

Sort By:
Pageof 12
British Journal of Anaesthesia|July 4, 2013
Morphine stimulates platelet-derived growth factor receptor-β signalling in mesangial cells in vitro and transgenic sickle mouse kidney in vivoM L Weber, C Chen, Y Li, et al.
Experimental Cell Research|March 6, 1999
VEGF prevents apoptosis of human microvascular endothelial cells via opposing effects on MAPK/ERK and SAPK/JNK signalingK Gupta, S Kshirsagar, W Li, et al.
The Journal of Clinical Investigation|September 18, 1997
Removal of erythrocyte membrane iron in vivo ameliorates the pathobiology of murine thalassemiaP V Browne, O Shalev, F A Kuypers, et al.
Blood|September 1, 1995
Deferiprone (L1) chelates pathologic iron deposits from membranes of intact thalassemic and sickle red blood cells both in vitro and in vivoO Shalev, T Repka, A Goldfarb, et al.
Blood|November 15, 1993
Nonrandom association of free iron with membranes of sickle and beta-thalassemic erythrocytesT Repka, O Shalev, R Reddy, et al.
The Journal of Laboratory and Clinical Medicine|June 9, 1999
Low-density lipoprotein susceptibility to oxidation and cytotoxicity to endothelium in sickle cell anemiaJ D Belcher, P H Marker, P Geiger, et al.
The American Journal of Pathology|March 10, 2001
Oxidative stress and induction of heme oxygenase-1 in the kidney in sickle cell diseaseK A Nath, J P Grande, J J Haggard, et al.
Thrombosis and Haemostasis|March 15, 2001
Whole blood tissue factor procoagulant activity remains detectable during severe aplasia following bone marrow and peripheral blood stem cell transplantationM Ozcan, C T Morton, A Solovey, et al.
American Journal of Physiology. Regulatory, Integrative and Comparative Physiology|November 18, 2000
Mechanisms of vascular instability in a transgenic mouse model of sickle cell diseaseK A Nath, V Shah, J J Haggard, et al.
The Journal of Clinical Investigation|April 1, 1993
Effect of excess alpha-hemoglobin chains on cellular and membrane oxidation in model beta-thalassemic erythrocytesM D Scott, J J van den Berg, T Repka, et al.
Pageof 12