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C A Hillery

Showing results (1-10 of 15) with videos related to

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Current Opinion in Hematology|May 7, 1998
Potential therapeutic approaches for the treatment of vaso-occlusion in sickle cell diseaseC A Hillery
Blood|June 25, 1999
The carboxy-terminal cell-binding domain of thrombospondin is essential for sickle red blood cell adhesionC A Hillery, J P Scott, M C Du
The Journal of Biological Chemistry|August 5, 1992
Fibrinogen binding to purified platelet glycoprotein IIb-IIIa (integrin alpha IIb beta 3) is modulated by lipidsS S Smyth, C A Hillery, L V Parise
The Journal of Biological Chemistry|August 5, 1991
Phosphorylation of human platelet glycoprotein IIIa (GPIIIa). Dissociation from fibrinogen receptor activation and phosphorylation of GPIIIa in vitroC A Hillery, S S Smyth, L V Parise
Transfusion Medicine (Oxford, England)|January 31, 2017
Phosphatidylethanolamine is progressively exposed in RBCs during storageM C Larson, M S Karafin, C A Hillery, et al.
British Journal of Haematology|June 10, 2000
Hydroxyurea therapy decreases the in vitro adhesion of sickle erythrocytes to thrombospondin and lamininC A Hillery, M C Du, W C Wang, et al.
Blood|June 1, 1996
Increased adhesion of erythrocytes to components of the extracellular matrix: isolation and characterization of a red blood cell lipid that binds thrombospondin and lamininC A Hillery, M C Du, R R Montgomery, et al.
The Journal of Pediatrics|June 1, 1996
Hydroxyurea therapy in children severely affected with sickle cell diseaseJ P Scott, C A Hillery, E R Brown, et al.
Journal of Pediatric Hematology/Oncology|April 25, 2000
Low-molecular-weight heparin in thrombotic disease in children and adolescentsR C Punzalan, C A Hillery, R R Montgomery, et al.
The Pediatric Infectious Disease Journal|December 1, 1993
Unsuspected brucellosis diagnosed in a child as a result of an outbreak of laboratory-acquired brucellosisM J Chusid, S K Russler, B A Mohr, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Current Opinion in Hematology|May 7, 1998
Potential therapeutic approaches for the treatment of vaso-occlusion in sickle cell diseaseC A Hillery
Blood|June 25, 1999
The carboxy-terminal cell-binding domain of thrombospondin is essential for sickle red blood cell adhesionC A Hillery, J P Scott, M C Du
The Journal of Biological Chemistry|August 5, 1992
Fibrinogen binding to purified platelet glycoprotein IIb-IIIa (integrin alpha IIb beta 3) is modulated by lipidsS S Smyth, C A Hillery, L V Parise
The Journal of Biological Chemistry|August 5, 1991
Phosphorylation of human platelet glycoprotein IIIa (GPIIIa). Dissociation from fibrinogen receptor activation and phosphorylation of GPIIIa in vitroC A Hillery, S S Smyth, L V Parise
Transfusion Medicine (Oxford, England)|January 31, 2017
Phosphatidylethanolamine is progressively exposed in RBCs during storageM C Larson, M S Karafin, C A Hillery, et al.
British Journal of Haematology|June 10, 2000
Hydroxyurea therapy decreases the in vitro adhesion of sickle erythrocytes to thrombospondin and lamininC A Hillery, M C Du, W C Wang, et al.
Blood|June 1, 1996
Increased adhesion of erythrocytes to components of the extracellular matrix: isolation and characterization of a red blood cell lipid that binds thrombospondin and lamininC A Hillery, M C Du, R R Montgomery, et al.
The Journal of Pediatrics|June 1, 1996
Hydroxyurea therapy in children severely affected with sickle cell diseaseJ P Scott, C A Hillery, E R Brown, et al.
Journal of Pediatric Hematology/Oncology|April 25, 2000
Low-molecular-weight heparin in thrombotic disease in children and adolescentsR C Punzalan, C A Hillery, R R Montgomery, et al.
The Pediatric Infectious Disease Journal|December 1, 1993
Unsuspected brucellosis diagnosed in a child as a result of an outbreak of laboratory-acquired brucellosisM J Chusid, S K Russler, B A Mohr, et al.
Pageof 2