Purification and Partial Characterization of the Erythrocyte Kx Protein Deficient in McLeod Patients
- 1 March 1995
- journal article
- Published by Wiley in European Journal of Biochemistry
- Vol. 228 (3) , 931-934
- https://doi.org/10.1111/j.1432-1033.1995.0931m.x
Abstract
No abstract availableThis publication has 18 references indexed in Scilit:
- Isolation of the gene for McLeod syndrome that encodes a novel membrane transport proteinCell, 1994
- Glycosidase digestion, electrophoresis and chromatographic analysis of recombinant human granulocyte colony-stimulating factor glycoforms produced in Chinese hamster ovary cellsJournal of Chromatography A, 1993
- A low-cost automated device incorporating a hollow fiber filtration cartridge for large-scale production of ghosts from human erythrocytesJournal of Biochemical and Biophysical Methods, 1990
- Molecular cloning and protein structure of a human blood group Rh polypeptide.Proceedings of the National Academy of Sciences, 1990
- Human monoclonal antibodies against blood group antigensJournal of Immunological Methods, 1987
- Recent Developments in the Kell Blood Group SystemTransfusion Medicine Reviews, 1987
- Unmasking of Kx antigen by reduction of disulphide bonds on normal and McLeod red cellsBritish Journal of Haematology, 1985
- Disulfide bonds are a requirement for Kell and Cartwright (Yta) blood group antigen integrityBritish Journal of Haematology, 1983
- Inactivation of Kell blood group antigens by 2‐aminoethylisothiouronium bromideBritish Journal of Haematology, 1982
- A New Phenotype (McLeod) in the Kell Blood‐group System*Vox Sanguinis, 1961