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F Galacteros

Showing results (131-140 of 187) with videos related to

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FEBS Letters|July 9, 1984
Structural study of hemoglobin Hazebrouck, beta 38(C4)Thr----Pro. A new abnormal hemoglobin with instability and low oxygen affinityY Blouquit, J Delanoe-Garin, C Lacombe, et al.
Acta Haematologica|January 1, 1980
Beta O-thalassemia/Hb E association. Hemoglobin synthesis in blood reticulocytes and bone marrow cells fractionated by density gradient and in blood erythroid colonies in cultureU Testa, A Dubart, N Hinard, et al.
Annals of the New York Academy of Sciences|January 1, 1990
Fate of alpha-hemoglobin chains and erythrocyte defects in beta-thalassemiaP Rouyer-Fessard, M D Scott, K Leroy-Viard, et al.
Biomedical & Environmental Mass Spectrometry|October 1, 1988
Identification of some abnormal haemoglobins by fast atom bombardment mass spectrometry and fast atom bombardment tandem mass spectrometryD Prome, J C Prome, F Pratbernou, et al.
Hemoglobin|January 1, 1986
Hemoglobin La Desirade alpha A2 beta 2 129 (H7) Ala----Val: a new unstable hemoglobinG Merault, L Keclard, J Garin, et al.
Hemoglobin|January 1, 1988
Hb Tunis [alpha 2 beta 2 124 (H2)Pro----Ser], a new beta chain variant identified by HPLCA Mrad, Y Blouquit, C Lacombe, et al.
British Journal of Haematology|June 14, 2001
Resveratrol, a natural dietary phytoalexin, possesses similar properties to hydroxyurea towards erythroid differentiationC M Rodrigue, N Arous, D Bachir, et al.
Hemoglobin|October 1, 1993
Identification of Hb Anantharaj [alpha 11(A9)Lys->Glu] as Hb J-Wenchang-Wuming [alpha 11(A9)Lys->Gln]J Svasti, R Surarit, C Srisomsap, et al.
Biochimica Et Biophysica Acta|November 14, 1990
Hemoglobin Calais [beta 76 (E20) Ala----Pro]: a hemoglobin variant with decreased intrinsic oxygen affinityH Wajcman, J Kister, M Marden, et al.
Blood|March 10, 2001
Endothelial dysfunction in patients with sickle cell disease is related to selective impairment of shear stress-mediated vasodilationL Belhassen, G Pelle, S Sediame, et al.
Pageof 19

Showing results (131-140 of 187) with videos related to

Sort By:
Pageof 19
FEBS Letters|July 9, 1984
Structural study of hemoglobin Hazebrouck, beta 38(C4)Thr----Pro. A new abnormal hemoglobin with instability and low oxygen affinityY Blouquit, J Delanoe-Garin, C Lacombe, et al.
Acta Haematologica|January 1, 1980
Beta O-thalassemia/Hb E association. Hemoglobin synthesis in blood reticulocytes and bone marrow cells fractionated by density gradient and in blood erythroid colonies in cultureU Testa, A Dubart, N Hinard, et al.
Annals of the New York Academy of Sciences|January 1, 1990
Fate of alpha-hemoglobin chains and erythrocyte defects in beta-thalassemiaP Rouyer-Fessard, M D Scott, K Leroy-Viard, et al.
Biomedical & Environmental Mass Spectrometry|October 1, 1988
Identification of some abnormal haemoglobins by fast atom bombardment mass spectrometry and fast atom bombardment tandem mass spectrometryD Prome, J C Prome, F Pratbernou, et al.
Hemoglobin|January 1, 1986
Hemoglobin La Desirade alpha A2 beta 2 129 (H7) Ala----Val: a new unstable hemoglobinG Merault, L Keclard, J Garin, et al.
Hemoglobin|January 1, 1988
Hb Tunis [alpha 2 beta 2 124 (H2)Pro----Ser], a new beta chain variant identified by HPLCA Mrad, Y Blouquit, C Lacombe, et al.
British Journal of Haematology|June 14, 2001
Resveratrol, a natural dietary phytoalexin, possesses similar properties to hydroxyurea towards erythroid differentiationC M Rodrigue, N Arous, D Bachir, et al.
Hemoglobin|October 1, 1993
Identification of Hb Anantharaj [alpha 11(A9)Lys->Glu] as Hb J-Wenchang-Wuming [alpha 11(A9)Lys->Gln]J Svasti, R Surarit, C Srisomsap, et al.
Biochimica Et Biophysica Acta|November 14, 1990
Hemoglobin Calais [beta 76 (E20) Ala----Pro]: a hemoglobin variant with decreased intrinsic oxygen affinityH Wajcman, J Kister, M Marden, et al.
Blood|March 10, 2001
Endothelial dysfunction in patients with sickle cell disease is related to selective impairment of shear stress-mediated vasodilationL Belhassen, G Pelle, S Sediame, et al.
Pageof 19