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J B Porter

Showing results (31-40 of 99) with videos related to

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American Journal of Public Health|December 1, 1986
Drugs and stillbirthJ B Porter, J Hunter-Mitchell, H Jick, et al.
Clinical and Laboratory Haematology|September 13, 2001
Flow cytometric method for simultaneous assay of foetal haemoglobin containing red cells, reticulocytes and foetal haemoglobin containing reticulocytesY Mundee, N C Bigelow, B H Davis, et al.
Cytometry|January 3, 2001
Simplified flow cytometric method for fetal hemoglobin containing red blood cellsY Mundee, N C Bigelow, B H Davis, et al.
British Journal of Haematology|May 1, 1995
Low plasma heparin cofactor II levels in thalassaemia syndromes are corrected by chronic blood transfusionA O'Driscoll, I J Mackie, J B Porter, et al.
British Medical Journal (Clinical Research Ed.)|February 6, 1982
Pruritus after administration of hetastarchN E Parker, J B Porter, H J Williams, et al.
Medicinal Chemistry (Shariqah (United Arab Emirates))|June 19, 2009
Efficacy of curcuminoids in alleviation of iron overload and lipid peroxidation in thalassemic miceC Thephinlap, C Phisalaphong, S Fucharoen, et al.
Hematology (Amsterdam, Netherlands)|July 16, 2016
Technical Report: Triple-Colour Staining Flow Cytometry for Co-Distribution of Thrombospondin Receptor (CD36), Ribonucleic Acid (RNA) and Fetal Haemoglobin (HbF) in Sickle Red Blood CellsY Mundee, N C Bigelow, B H Davis, et al.
Medicinal Chemistry (Shariqah (United Arab Emirates))|September 28, 2007
Curcumin contributes to in vitro removal of non-transferrin bound iron by deferiprone and desferrioxamine in thalassemic plasmaS Srichairatanakool, C Thephinlap, C Phisalaphong, et al.
Annals of the New York Academy of Sciences|January 1, 1990
The development of hydroxypyridin-4-ones as orally active iron chelatorsR C Hider, S Singh, J B Porter, et al.
Blood|November 11, 1999
Why are hemoglobin F levels increased in HbE/beta thalassemia?D C Rees, J B Porter, J B Clegg, et al.
Pageof 10

Showing results (31-40 of 99) with videos related to

Sort By:
Pageof 10
American Journal of Public Health|December 1, 1986
Drugs and stillbirthJ B Porter, J Hunter-Mitchell, H Jick, et al.
Clinical and Laboratory Haematology|September 13, 2001
Flow cytometric method for simultaneous assay of foetal haemoglobin containing red cells, reticulocytes and foetal haemoglobin containing reticulocytesY Mundee, N C Bigelow, B H Davis, et al.
Cytometry|January 3, 2001
Simplified flow cytometric method for fetal hemoglobin containing red blood cellsY Mundee, N C Bigelow, B H Davis, et al.
British Journal of Haematology|May 1, 1995
Low plasma heparin cofactor II levels in thalassaemia syndromes are corrected by chronic blood transfusionA O'Driscoll, I J Mackie, J B Porter, et al.
British Medical Journal (Clinical Research Ed.)|February 6, 1982
Pruritus after administration of hetastarchN E Parker, J B Porter, H J Williams, et al.
Medicinal Chemistry (Shariqah (United Arab Emirates))|June 19, 2009
Efficacy of curcuminoids in alleviation of iron overload and lipid peroxidation in thalassemic miceC Thephinlap, C Phisalaphong, S Fucharoen, et al.
Hematology (Amsterdam, Netherlands)|July 16, 2016
Technical Report: Triple-Colour Staining Flow Cytometry for Co-Distribution of Thrombospondin Receptor (CD36), Ribonucleic Acid (RNA) and Fetal Haemoglobin (HbF) in Sickle Red Blood CellsY Mundee, N C Bigelow, B H Davis, et al.
Medicinal Chemistry (Shariqah (United Arab Emirates))|September 28, 2007
Curcumin contributes to in vitro removal of non-transferrin bound iron by deferiprone and desferrioxamine in thalassemic plasmaS Srichairatanakool, C Thephinlap, C Phisalaphong, et al.
Annals of the New York Academy of Sciences|January 1, 1990
The development of hydroxypyridin-4-ones as orally active iron chelatorsR C Hider, S Singh, J B Porter, et al.
Blood|November 11, 1999
Why are hemoglobin F levels increased in HbE/beta thalassemia?D C Rees, J B Porter, J B Clegg, et al.
Pageof 10