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Showing results (131-140 of 150) with videos related to

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FEBS Letters|May 6, 1985
The phospholipid organisation in the membranes of McLeod and Leach phenotype erythrocytesF A Kuypers, M van Linde-Sibenius Trip, B Roelofsen, et al.
British Journal of Haematology|January 1, 1997
Novel band 3 variants (bands 3 Foggia, Napoli I and Napoli II) associated with hereditary spherocytosis and band 3 deficiency: status of the D38A polymorphism within the EPB3 locusE Miraglia del Giudice, A Vallier, P Maillet, et al.
Blood|April 21, 2001
Glycophorin A dimerization and band 3 interaction during erythroid membrane biogenesis: in vivo studies in human glycophorin A transgenic miceI Auffray, S Marfatia, K de Jong, et al.
British Journal of Haematology|April 1, 1995
A point mutation in the protein 4.2 gene (allele 4.2 Tozeur) associated with hereditary haemolytic anaemiaS Hayette, L Morle, M Bozon, et al.
The Journal of Biological Chemistry|July 25, 1992
Localization of the C termini of the Rh (rhesus) polypeptides to the cytoplasmic face of the human erythrocyte membraneN D Avent, S K Butcher, W Liu, et al.
British Journal of Haematology|December 1, 1995
Band 3 Chur: a variant associated with band 3-deficient hereditary spherocytosis and substitution in a highly conserved position of transmembrane segment 11P Maillet, A Vallier, W H Reinhart, et al.
Transfusion|March 1, 1990
Murine monoclonal antibody MB-2D10 recognizes Rh-related glycoproteins in the human red cell membraneG Mallinson, D J Anstee, N D Avent, et al.
The Journal of Clinical Investigation|October 6, 1997
Familial distal renal tubular acidosis is associated with mutations in the red cell anion exchanger (Band 3, AE1) geneL J Bruce, D L Cope, G K Jones, et al.
Biochimica Et Biophysica Acta|January 16, 1999
South-east asian ovalocytic (SAO) erythrocytes have a cold sensitive cation leak: implications for in vitro studies on stored SAO red cellsL J Bruce, S M Ring, K Ridgwell, et al.
Journal of Immunogenetics|December 1, 1979
Two apparently healthy Japanese individuals of type MkMk have erythrocytes which lack both the blood group MN and Ss-active sialoglycoproteinsE Tokunaga, S Sasakawa, K Tamaka, et al.
Pageof 15

Showing results (131-140 of 150) with videos related to

Sort By:
Pageof 15
FEBS Letters|May 6, 1985
The phospholipid organisation in the membranes of McLeod and Leach phenotype erythrocytesF A Kuypers, M van Linde-Sibenius Trip, B Roelofsen, et al.
British Journal of Haematology|January 1, 1997
Novel band 3 variants (bands 3 Foggia, Napoli I and Napoli II) associated with hereditary spherocytosis and band 3 deficiency: status of the D38A polymorphism within the EPB3 locusE Miraglia del Giudice, A Vallier, P Maillet, et al.
Blood|April 21, 2001
Glycophorin A dimerization and band 3 interaction during erythroid membrane biogenesis: in vivo studies in human glycophorin A transgenic miceI Auffray, S Marfatia, K de Jong, et al.
British Journal of Haematology|April 1, 1995
A point mutation in the protein 4.2 gene (allele 4.2 Tozeur) associated with hereditary haemolytic anaemiaS Hayette, L Morle, M Bozon, et al.
The Journal of Biological Chemistry|July 25, 1992
Localization of the C termini of the Rh (rhesus) polypeptides to the cytoplasmic face of the human erythrocyte membraneN D Avent, S K Butcher, W Liu, et al.
British Journal of Haematology|December 1, 1995
Band 3 Chur: a variant associated with band 3-deficient hereditary spherocytosis and substitution in a highly conserved position of transmembrane segment 11P Maillet, A Vallier, W H Reinhart, et al.
Transfusion|March 1, 1990
Murine monoclonal antibody MB-2D10 recognizes Rh-related glycoproteins in the human red cell membraneG Mallinson, D J Anstee, N D Avent, et al.
The Journal of Clinical Investigation|October 6, 1997
Familial distal renal tubular acidosis is associated with mutations in the red cell anion exchanger (Band 3, AE1) geneL J Bruce, D L Cope, G K Jones, et al.
Biochimica Et Biophysica Acta|January 16, 1999
South-east asian ovalocytic (SAO) erythrocytes have a cold sensitive cation leak: implications for in vitro studies on stored SAO red cellsL J Bruce, S M Ring, K Ridgwell, et al.
Journal of Immunogenetics|December 1, 1979
Two apparently healthy Japanese individuals of type MkMk have erythrocytes which lack both the blood group MN and Ss-active sialoglycoproteinsE Tokunaga, S Sasakawa, K Tamaka, et al.
Pageof 15