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M Sorette

Showing results (1-10 of 7) with videos related to

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American Journal of Clinical Pathology|August 1, 1997
Reticulocyte hemoglobin: an integrated parameter for evaluation of erythropoietic activityC Brugnara, D Zelmanovic, M Sorette, et al.
Blood|July 1, 1995
Generation of normal human red cell volume, hemoglobin content, and membrane area distributions by "birth" or regulation?V L Lew, J E Raftos, M Sorette, et al.
Blood|November 8, 2001
Temporal differences in membrane loss lead to distinct reticulocyte features in hereditary spherocytosis and in immune hemolytic anemiaL Da Costa, N Mohandas, M Sorette, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 22, 2000
Identification and characterization of a newly recognized population of high-Na+, low-K+, low-density sickle and normal red cellsR M Bookchin, Z Etzion, M Sorette, et al.
Blood|November 1, 1994
Sickle cell disease of transgenic SAD miceM Trudel, M E De Paepe, N Chrétien, et al.
Nature Medicine|February 2, 2000
Genetic correction of sickle cell disease: insights using transgenic mouse modelsM J Blouin, H Beauchemin, A Wright, et al.
Proteome Science|December 16, 2004
Development and standardization of multiplexed antibody microarrays for use in quantitative proteomicsL T Perlee, J Christiansen, R Dondero, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
American Journal of Clinical Pathology|August 1, 1997
Reticulocyte hemoglobin: an integrated parameter for evaluation of erythropoietic activityC Brugnara, D Zelmanovic, M Sorette, et al.
Blood|July 1, 1995
Generation of normal human red cell volume, hemoglobin content, and membrane area distributions by "birth" or regulation?V L Lew, J E Raftos, M Sorette, et al.
Blood|November 8, 2001
Temporal differences in membrane loss lead to distinct reticulocyte features in hereditary spherocytosis and in immune hemolytic anemiaL Da Costa, N Mohandas, M Sorette, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 22, 2000
Identification and characterization of a newly recognized population of high-Na+, low-K+, low-density sickle and normal red cellsR M Bookchin, Z Etzion, M Sorette, et al.
Blood|November 1, 1994
Sickle cell disease of transgenic SAD miceM Trudel, M E De Paepe, N Chrétien, et al.
Nature Medicine|February 2, 2000
Genetic correction of sickle cell disease: insights using transgenic mouse modelsM J Blouin, H Beauchemin, A Wright, et al.
Proteome Science|December 16, 2004
Development and standardization of multiplexed antibody microarrays for use in quantitative proteomicsL T Perlee, J Christiansen, R Dondero, et al.
Pageof 1