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L Morlé

Showing results (1-10 of 44) with videos related to

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Pathologie-Biologie|October 1, 1988
[Interaction between various alkylxanthines and the proteins of the erythrocyte skeleton]J Delaunay, B Pothier, F Baklouti, et al.
Human Mutation|January 1, 1996
Spectrin mutations in hereditary elliptocytosis and hereditary spherocytosisP Maillet, N Alloisio, L Morlé, et al.
American Journal of Hematology|April 1, 1984
Thalassemia-like abnormalities of the red cell membrane in hemoglobin E trait and diseaseE Dorléac, L Morlé, O Gentilhomme, et al.
Biochimica Et Biophysica Acta|June 11, 1985
Red cell membrane sialoglycoprotein beta in homozygous and heterozygous 4.1(-) hereditary elliptocytosisN Alloisio, L Morlé, D Bachir, et al.
Blood|May 30, 1998
A large deletion within the protein 4.1 gene associated with a stable truncated mRNA and an unaltered tissue-specific alternative splicingN D Venezia, P Maillet, L Morlé, et al.
Scandinavian Journal of Haematology|September 1, 1984
The Hb F composition in a Moroccan family with beta zero-thalassaemia and Hb O-ArabF Morlé, L Morlé, F Baklouti, et al.
American Journal of Hematology|December 1, 1982
Kinetic alterations of the red cell membrane phosphatase in alpha- and beta-thalassemiaL Morlé, E Dorléac, N Alloisio, et al.
Blood|June 1, 1985
The characterization of protein 4.1 Presles, a shortened variant of RBC membrane protein 4.1L Morlé, M Garbarz, N Alloisio, et al.
Hemoglobin|January 1, 1984
The association of hemoglobin Knossos and hemoglobin Lepore in an Algerian patientL Morlé, F Morlé, E Dorléac, et al.
British Journal of Haematology|January 1, 1989
Reduction of membrane band 7 and activation of volume stimulated (K+, Cl-)-cotransport in a case of congenital stomatocytosisL Morlé, B Pothier, N Alloisio, et al.
Pageof 5

Showing results (1-10 of 44) with videos related to

Sort By:
Pageof 5
Pathologie-Biologie|October 1, 1988
[Interaction between various alkylxanthines and the proteins of the erythrocyte skeleton]J Delaunay, B Pothier, F Baklouti, et al.
Human Mutation|January 1, 1996
Spectrin mutations in hereditary elliptocytosis and hereditary spherocytosisP Maillet, N Alloisio, L Morlé, et al.
American Journal of Hematology|April 1, 1984
Thalassemia-like abnormalities of the red cell membrane in hemoglobin E trait and diseaseE Dorléac, L Morlé, O Gentilhomme, et al.
Biochimica Et Biophysica Acta|June 11, 1985
Red cell membrane sialoglycoprotein beta in homozygous and heterozygous 4.1(-) hereditary elliptocytosisN Alloisio, L Morlé, D Bachir, et al.
Blood|May 30, 1998
A large deletion within the protein 4.1 gene associated with a stable truncated mRNA and an unaltered tissue-specific alternative splicingN D Venezia, P Maillet, L Morlé, et al.
Scandinavian Journal of Haematology|September 1, 1984
The Hb F composition in a Moroccan family with beta zero-thalassaemia and Hb O-ArabF Morlé, L Morlé, F Baklouti, et al.
American Journal of Hematology|December 1, 1982
Kinetic alterations of the red cell membrane phosphatase in alpha- and beta-thalassemiaL Morlé, E Dorléac, N Alloisio, et al.
Blood|June 1, 1985
The characterization of protein 4.1 Presles, a shortened variant of RBC membrane protein 4.1L Morlé, M Garbarz, N Alloisio, et al.
Hemoglobin|January 1, 1984
The association of hemoglobin Knossos and hemoglobin Lepore in an Algerian patientL Morlé, F Morlé, E Dorléac, et al.
British Journal of Haematology|January 1, 1989
Reduction of membrane band 7 and activation of volume stimulated (K+, Cl-)-cotransport in a case of congenital stomatocytosisL Morlé, B Pothier, N Alloisio, et al.
Pageof 5