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N Alloisio

Showing results (1-10 of 62) with videos related to

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Human Genetics|January 1, 1981
Analysis of the red cell membrane in a family with hereditary elliptocytosis--total or partial of protein 4.1N Alloisio, E Dorléac, R Girot, et al.
Human Mutation|January 1, 1996
Spectrin mutations in hereditary elliptocytosis and hereditary spherocytosisP Maillet, N Alloisio, L Morlé, et al.
Nouvelle Revue Francaise D'Hematologie|January 1, 1991
The genetic disorders of the red cell skeletonJ Delaunay, N Alloisio, L Morle, et al.
Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|January 1, 1980
[A molecular abnormality of the erythrocyte membrane in beta-thalassemia]F Morle, L Morle, M Aguercif, et al.
Blood|July 1, 1982
A shortened variant of red cell membrane protein 4.1N Alloisio, E Dorléac, J Delaunay, 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.
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.
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.
Biomedica Biochimica Acta|January 1, 1983
The genetic abnormalities involving red cell membrane protein 4.1 with or without elliptocytosisN Alloisio, E Dorleac, L Morle, et al.
Pageof 7

Showing results (1-10 of 62) with videos related to

Sort By:
Pageof 7
Human Genetics|January 1, 1981
Analysis of the red cell membrane in a family with hereditary elliptocytosis--total or partial of protein 4.1N Alloisio, E Dorléac, R Girot, et al.
Human Mutation|January 1, 1996
Spectrin mutations in hereditary elliptocytosis and hereditary spherocytosisP Maillet, N Alloisio, L Morlé, et al.
Nouvelle Revue Francaise D'Hematologie|January 1, 1991
The genetic disorders of the red cell skeletonJ Delaunay, N Alloisio, L Morle, et al.
Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|January 1, 1980
[A molecular abnormality of the erythrocyte membrane in beta-thalassemia]F Morle, L Morle, M Aguercif, et al.
Blood|July 1, 1982
A shortened variant of red cell membrane protein 4.1N Alloisio, E Dorléac, J Delaunay, 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.
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.
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.
Biomedica Biochimica Acta|January 1, 1983
The genetic abnormalities involving red cell membrane protein 4.1 with or without elliptocytosisN Alloisio, E Dorleac, L Morle, et al.
Pageof 7