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F Galacteros

Showing results (81-90 of 187) with videos related to

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Hemoglobin|January 1, 1994
Hb Poitiers [alpha 45(CE3)His-->Asp]: a new hemoglobin variant with a two-fold increase in oxygen affinityJ Bardakdjian, J Kister, H Wajcman, et al.
Hemoglobin|January 1, 1981
Hemoglobin Hotel-Dieu beta 99 Asp replaced by Gly (g1). A new abnormal hemoglobin with high oxygen affinityY Blouquit, F Braconnier, F Galacteros, et al.
Vox Sanguinis|January 1, 1993
Frozen blood and transfusion-transmitted hepatitis C virusF Norol, D Bachir, F Bernaudin, et al.
The Journal of Laboratory and Clinical Medicine|September 1, 1981
Excess alpha chains are lost from beta-thalassemic reticulocytes by proteolysisU Testa, N Hinard, Y Beuzard, et al.
Blood|February 1, 1992
Hemoglobin variants and activity of the (K+Cl-) cotransport system in human erythrocytesO Olivieri, D Vitoux, F Galacteros, et al.
Presse Medicale (Paris, France : 1983)|June 12, 1993
[Acute aseptic arthritis in major sickle cell syndromes]B Godeau, D Bachir, F Galacteros, et al.
Analytical Biochemistry|May 15, 1996
Perfusion chromatography on reversed-phase column allows fast analysis of human globin chainsH Wajcman, R Ducrocq, J Riou, et al.
The Journal of Biological Chemistry|November 5, 1986
Covalent binding of glutathione to hemoglobin. I. Inhibition of hemoglobin S polymerizationM C Garel, C Domenget, J Caburi-Martin, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 1, 1989
Inhibition of K+ efflux and dehydration of sickle cells by [(dihydroindenyl)oxy]alkanoic acid: an inhibitor of the K+ Cl- cotransport systemD Vitoux, O Olivieri, R P Garay, et al.
Journal Francais D'Ophtalmologie|April 5, 2012
[Sickle-cell retinopathy: Retrospective study of 730 patients followed in a referral center]N Leveziel, F Lalloum, S Bastuji-Garin, et al.
Pageof 19

Showing results (81-90 of 187) with videos related to

Sort By:
Pageof 19
Hemoglobin|January 1, 1994
Hb Poitiers [alpha 45(CE3)His-->Asp]: a new hemoglobin variant with a two-fold increase in oxygen affinityJ Bardakdjian, J Kister, H Wajcman, et al.
Hemoglobin|January 1, 1981
Hemoglobin Hotel-Dieu beta 99 Asp replaced by Gly (g1). A new abnormal hemoglobin with high oxygen affinityY Blouquit, F Braconnier, F Galacteros, et al.
Vox Sanguinis|January 1, 1993
Frozen blood and transfusion-transmitted hepatitis C virusF Norol, D Bachir, F Bernaudin, et al.
The Journal of Laboratory and Clinical Medicine|September 1, 1981
Excess alpha chains are lost from beta-thalassemic reticulocytes by proteolysisU Testa, N Hinard, Y Beuzard, et al.
Blood|February 1, 1992
Hemoglobin variants and activity of the (K+Cl-) cotransport system in human erythrocytesO Olivieri, D Vitoux, F Galacteros, et al.
Presse Medicale (Paris, France : 1983)|June 12, 1993
[Acute aseptic arthritis in major sickle cell syndromes]B Godeau, D Bachir, F Galacteros, et al.
Analytical Biochemistry|May 15, 1996
Perfusion chromatography on reversed-phase column allows fast analysis of human globin chainsH Wajcman, R Ducrocq, J Riou, et al.
The Journal of Biological Chemistry|November 5, 1986
Covalent binding of glutathione to hemoglobin. I. Inhibition of hemoglobin S polymerizationM C Garel, C Domenget, J Caburi-Martin, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 1, 1989
Inhibition of K+ efflux and dehydration of sickle cells by [(dihydroindenyl)oxy]alkanoic acid: an inhibitor of the K+ Cl- cotransport systemD Vitoux, O Olivieri, R P Garay, et al.
Journal Francais D'Ophtalmologie|April 5, 2012
[Sickle-cell retinopathy: Retrospective study of 730 patients followed in a referral center]N Leveziel, F Lalloum, S Bastuji-Garin, et al.
Pageof 19