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Hemoglobin

Showing results (681-690 of 2,379) with videos related to

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Hemoglobin|January 1, 1982
Functional properties of Hb Pasadena, alpha 2 beta 2 75(E 19) Leu replaced by ArgT B Shih, R T Jones, C S Johnson
Hemoglobin|January 1, 1981
Induction of Heinz body formation by sodium dithioniteH Imanishi, K Hosokawa, H A Itano
Hemoglobin|January 1, 1981
Novel studies on a "silent" high affinity mutant hemoglobin (San Diego, beta 109 Val replaced by Met)D R Harkness, C K Yu, M Goldberg, et al.
Hemoglobin|January 1, 1981
Effect of some physical features and of amino acid substitutions on the mechanical precipitation of hemoglobinM L North, J Thillet, J Rosa
Hemoglobin|January 1, 1989
Hb Evans or alpha 262(E11)Val----Met beta 2; an unstable hemoglobin causing a mild hemolytic anemiaJ B Wilson, B B Webber, A Kutlar, et al.
Hemoglobin|January 1, 1989
Inhibition of oxygen-linked anion binding in Hb Camperdown [alpha 2 beta 2(104)(G6)Arg----Ser]J Kister, J Barbadjian, Y Blouquit, et al.
Hemoglobin|January 1, 1989
Studies of beta-thalassemia mutations in families living in three provinces in southern ChinaJ Z Liu, Q S Gao, Z Jiang, et al.
Hemoglobin|January 1, 1989
Frameshift codon 5 [Fsc-5 (-CT)] thalassemia; a novel mutation detected in a Greek patientP Kollia, J M Gonzalez-Redondo, T A Stoming, et al.
Hemoglobin|June 16, 2015
Clinical to Molecular Screening Paradigm for β-Thalassemia CarriersIbrahim Y Abdel-Messih, Soha R Youssef, Galila M Mokhtar, et al.
Hemoglobin|June 16, 2015
Red Cell Indices and Formulas Used in Differentiation of β-Thalassemia Trait from Iron Deficiency in Thai AdultsSoontharee Plengsuree, Manoo Punyamung, Jintana Yanola, et al.
Pageof 238

Showing results (681-690 of 2,379) with videos related to

Sort By:
Pageof 238
Hemoglobin|January 1, 1982
Functional properties of Hb Pasadena, alpha 2 beta 2 75(E 19) Leu replaced by ArgT B Shih, R T Jones, C S Johnson
Hemoglobin|January 1, 1981
Induction of Heinz body formation by sodium dithioniteH Imanishi, K Hosokawa, H A Itano
Hemoglobin|January 1, 1981
Novel studies on a "silent" high affinity mutant hemoglobin (San Diego, beta 109 Val replaced by Met)D R Harkness, C K Yu, M Goldberg, et al.
Hemoglobin|January 1, 1981
Effect of some physical features and of amino acid substitutions on the mechanical precipitation of hemoglobinM L North, J Thillet, J Rosa
Hemoglobin|January 1, 1989
Hb Evans or alpha 262(E11)Val----Met beta 2; an unstable hemoglobin causing a mild hemolytic anemiaJ B Wilson, B B Webber, A Kutlar, et al.
Hemoglobin|January 1, 1989
Inhibition of oxygen-linked anion binding in Hb Camperdown [alpha 2 beta 2(104)(G6)Arg----Ser]J Kister, J Barbadjian, Y Blouquit, et al.
Hemoglobin|January 1, 1989
Studies of beta-thalassemia mutations in families living in three provinces in southern ChinaJ Z Liu, Q S Gao, Z Jiang, et al.
Hemoglobin|January 1, 1989
Frameshift codon 5 [Fsc-5 (-CT)] thalassemia; a novel mutation detected in a Greek patientP Kollia, J M Gonzalez-Redondo, T A Stoming, et al.
Hemoglobin|June 16, 2015
Clinical to Molecular Screening Paradigm for β-Thalassemia CarriersIbrahim Y Abdel-Messih, Soha R Youssef, Galila M Mokhtar, et al.
Hemoglobin|June 16, 2015
Red Cell Indices and Formulas Used in Differentiation of β-Thalassemia Trait from Iron Deficiency in Thai AdultsSoontharee Plengsuree, Manoo Punyamung, Jintana Yanola, et al.
Pageof 238