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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.

Blood|August 15, 1994

Molecular basis of reduced or absent expression of decay-accelerating factor in Cromer blood group phenotypesD M Lublin, G Mallinson, J Poole, et al.

Blood|July 1, 1997

Modulation of clinical expression and band 3 deficiency in hereditary spherocytosisN Alloisio, P Texier, A Vallier, et al.

Transfusion|January 1, 1981

Studies on the blood of an MiV homozygoteV Vengelen-Tyler, D J Anstee, P D Issitt, et al.

The Biochemical Journal|April 15, 1988

Monoclonal antibodies that recognize different membrane proteins that are deficient in Rhnull human erythrocytes. One group of antibodies reacts with a variety of cells and tissues whereas the other group is erythroid-specificN Avent, P A Judson, S F Parsons, et al.

The Biochemical Journal|March 1, 1984

Two individuals with elliptocytic red cells apparently lack three minor erythrocyte membrane sialoglycoproteinsD J Anstee, S F Parsons, K Ridgwell, et al.

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Showing results (141-150 of 155) with videos related to

Sort By:

Pageof 16

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.

Blood|August 15, 1994

Molecular basis of reduced or absent expression of decay-accelerating factor in Cromer blood group phenotypesD M Lublin, G Mallinson, J Poole, et al.

Blood|July 1, 1997

Modulation of clinical expression and band 3 deficiency in hereditary spherocytosisN Alloisio, P Texier, A Vallier, et al.

Transfusion|January 1, 1981

Studies on the blood of an MiV homozygoteV Vengelen-Tyler, D J Anstee, P D Issitt, et al.

The Biochemical Journal|April 15, 1988

Monoclonal antibodies that recognize different membrane proteins that are deficient in Rhnull human erythrocytes. One group of antibodies reacts with a variety of cells and tissues whereas the other group is erythroid-specificN Avent, P A Judson, S F Parsons, et al.

The Biochemical Journal|March 1, 1984

Two individuals with elliptocytic red cells apparently lack three minor erythrocyte membrane sialoglycoproteinsD J Anstee, S F Parsons, K Ridgwell, et al.

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