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M J Tanner

Showing results (121-130 of 150) with videos related to

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Cytogenetics and Cell Genetics|January 1, 1992
Assignment of the chromosomal locus of the human 30-kDal Rh (rhesus) blood group-antigen-related protein (Rh30A) to chromosome region 1p36.13----p34C MacGeoch, C J Mitchell, B Carritt, et al.
The Biochemical Journal|March 15, 1986
Identification and partial characterization of the human erythrocyte membrane component(s) that express the antigens of the LW blood-group systemG Mallinson, P G Martin, D J Anstee, et al.
Carbohydrate Research|July 15, 1988
Effect of endoglycosidase F-peptidyl N-glycosidase F preparations on the surface components of the human erythrocyteM J Tanner, D J Anstee, G Mallinson, et al.
The Journal of Biological Chemistry|June 14, 1996
Immunochemical analysis of the human erythrocyte Rh polypeptidesN D Avent, W Liu, K M Warner, et al.
The Biochemical Journal|July 15, 1989
Studies on the defect which causes absence of decay accelerating factor (DAF) from the peripheral blood cells of an individual with the Inab phenotypeC G Tate, M Uchikawa, M J Tanner, et al.
The Biochemical Journal|August 1, 1984
Rhnull human erythrocytes have an abnormal membrane phospholipid organizationF Kuypers, M van Linde-Sibenius-Trip, B Roelofsen, et al.
Transfusion Medicine (Oxford, England)|June 3, 1999
Glycophorin A mutation Ala65 --> Pro gives rise to a novel pair of MNS alleles ENEP (MNS39) and HAG (MNS41) and altered Wrb expression: direct evidence for GPA/band 3 interaction necessary for normal Wrb expressionJ Poole, J Banks, L J Bruce, et al.
Blood|December 15, 1991
Biochemical studies on red blood cells from a patient with the Inab phenotype (decay-accelerating factor deficiency)M E Reid, G Mallinson, R B Sim, et al.
Transfusion|May 29, 2000
The low-frequency MNS blood group antigens Ny(a) (MNS18) and Os(a) (MNS38) are associated with GPA amino acid substitutionsG L Daniels, L J Bruce, W J Mawby, et al.
Vox Sanguinis|February 1, 1980
The rare phenotype En(a-) in a French-Canadian familyV Taliano, R M Guévin, D Hébert, et al.
Pageof 15

Showing results (121-130 of 150) with videos related to

Sort By:
Pageof 15
Cytogenetics and Cell Genetics|January 1, 1992
Assignment of the chromosomal locus of the human 30-kDal Rh (rhesus) blood group-antigen-related protein (Rh30A) to chromosome region 1p36.13----p34C MacGeoch, C J Mitchell, B Carritt, et al.
The Biochemical Journal|March 15, 1986
Identification and partial characterization of the human erythrocyte membrane component(s) that express the antigens of the LW blood-group systemG Mallinson, P G Martin, D J Anstee, et al.
Carbohydrate Research|July 15, 1988
Effect of endoglycosidase F-peptidyl N-glycosidase F preparations on the surface components of the human erythrocyteM J Tanner, D J Anstee, G Mallinson, et al.
The Journal of Biological Chemistry|June 14, 1996
Immunochemical analysis of the human erythrocyte Rh polypeptidesN D Avent, W Liu, K M Warner, et al.
The Biochemical Journal|July 15, 1989
Studies on the defect which causes absence of decay accelerating factor (DAF) from the peripheral blood cells of an individual with the Inab phenotypeC G Tate, M Uchikawa, M J Tanner, et al.
The Biochemical Journal|August 1, 1984
Rhnull human erythrocytes have an abnormal membrane phospholipid organizationF Kuypers, M van Linde-Sibenius-Trip, B Roelofsen, et al.
Transfusion Medicine (Oxford, England)|June 3, 1999
Glycophorin A mutation Ala65 --> Pro gives rise to a novel pair of MNS alleles ENEP (MNS39) and HAG (MNS41) and altered Wrb expression: direct evidence for GPA/band 3 interaction necessary for normal Wrb expressionJ Poole, J Banks, L J Bruce, et al.
Blood|December 15, 1991
Biochemical studies on red blood cells from a patient with the Inab phenotype (decay-accelerating factor deficiency)M E Reid, G Mallinson, R B Sim, et al.
Transfusion|May 29, 2000
The low-frequency MNS blood group antigens Ny(a) (MNS18) and Os(a) (MNS38) are associated with GPA amino acid substitutionsG L Daniels, L J Bruce, W J Mawby, et al.
Vox Sanguinis|February 1, 1980
The rare phenotype En(a-) in a French-Canadian familyV Taliano, R M Guévin, D Hébert, et al.
Pageof 15