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D Labie

Showing results (61-70 of 212) with videos related to

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European Journal of Biochemistry|April 1, 1986
Differences in DNase I sensitivity and methylation within the human beta-globin gene domain and correlation with expressionC Arapinis, J Elion, D Labie, et al.
Biochemical and Biophysical Research Communications|November 30, 1981
Isolation and characterization of the vitamin K dependent domain of human prothrombinC Dode, A Thiesce, D Labie, et al.
Hemoglobin|January 1, 1978
Association of Hb Hope with beta (0) thalassemiaJ Pagnier, G Gacon, H Wajcman, et al.
Biochimica Et Biophysica Acta|April 27, 1971
Hemoglobin toulouse alpha 2 beta 2 66 (E 10) LysGlu. Structure and consequences in molecular pathologyD Labie, J Rosa, O Belkhodja, et al.
Nouvelle Revue Francaise D'Hematologie|January 1, 1986
Hémoglobinopathies in FranceD Labie, F Galacteros, R Girot, et al.
Nouvelle Revue Francaise D'Hematologie|May 1, 1971
[Hemoglobin Köln: physiopathology of a hemoglobin with spontaneous loss of its heme]H Wajcman, J Pagnier, D Labie, et al.
Biochimica Et Biophysica Acta|June 15, 1973
Two variants of hemoglobin D in the algerian population: hemoglobin D Ouled Rabah 19 (BI) Asn leads to Lys and hemoglobin D Iran 22 (Br) Glu leads to GlnJ Elion, O Belkhodja, H Wajcman, et al.
American Journal of Hematology|February 1, 1985
Membrane expansion as a mechanism explaining the antisickling action of ticlopidine observed in vitroM Sablayrolles, H Wajcman, J P Castaigne, et al.
FEBS Letters|July 15, 1970
Familial diphosphoglyceratemutase deficiency. Influence on the oxygen affinity curves of hemoglobinD Labie, J -P. Leroux, A Najman, et al.
Biochimica Et Biophysica Acta|August 19, 1975
Hemoglobin Cochin-Port-Royal: consequences of the replacement of the beta chain C-terminal by an arginineH Wajcman, J V Kilmartin, A Najman, et al.
Pageof 22

Showing results (61-70 of 212) with videos related to

Sort By:
Pageof 22
European Journal of Biochemistry|April 1, 1986
Differences in DNase I sensitivity and methylation within the human beta-globin gene domain and correlation with expressionC Arapinis, J Elion, D Labie, et al.
Biochemical and Biophysical Research Communications|November 30, 1981
Isolation and characterization of the vitamin K dependent domain of human prothrombinC Dode, A Thiesce, D Labie, et al.
Hemoglobin|January 1, 1978
Association of Hb Hope with beta (0) thalassemiaJ Pagnier, G Gacon, H Wajcman, et al.
Biochimica Et Biophysica Acta|April 27, 1971
Hemoglobin toulouse alpha 2 beta 2 66 (E 10) LysGlu. Structure and consequences in molecular pathologyD Labie, J Rosa, O Belkhodja, et al.
Nouvelle Revue Francaise D'Hematologie|January 1, 1986
Hémoglobinopathies in FranceD Labie, F Galacteros, R Girot, et al.
Nouvelle Revue Francaise D'Hematologie|May 1, 1971
[Hemoglobin Köln: physiopathology of a hemoglobin with spontaneous loss of its heme]H Wajcman, J Pagnier, D Labie, et al.
Biochimica Et Biophysica Acta|June 15, 1973
Two variants of hemoglobin D in the algerian population: hemoglobin D Ouled Rabah 19 (BI) Asn leads to Lys and hemoglobin D Iran 22 (Br) Glu leads to GlnJ Elion, O Belkhodja, H Wajcman, et al.
American Journal of Hematology|February 1, 1985
Membrane expansion as a mechanism explaining the antisickling action of ticlopidine observed in vitroM Sablayrolles, H Wajcman, J P Castaigne, et al.
FEBS Letters|July 15, 1970
Familial diphosphoglyceratemutase deficiency. Influence on the oxygen affinity curves of hemoglobinD Labie, J -P. Leroux, A Najman, et al.
Biochimica Et Biophysica Acta|August 19, 1975
Hemoglobin Cochin-Port-Royal: consequences of the replacement of the beta chain C-terminal by an arginineH Wajcman, J V Kilmartin, A Najman, et al.
Pageof 22