Intracellular assembly of Kell and XK blood group proteins
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Biochemistry,Biophysics
Reference37 articles.
1. Molecular cloning and primary structure of Kell blood group protein;Lee;Proc. Natl. Acad. Sci. USA,1991
2. Isolation of the gene for McLeod syndrome that encodes a novel membrane transport protein;Ho;Cell,1994
3. Purification and partial characterization of the erythrocyte Kx protein deficient in McLeod patients;Khamlichi;Eur. J. Biochem.,1995
4. Immunochemical analysis of the Kx protein from human red cells of different Kell phenotypes using antibodies raised against synthetic peptides;Carbonnet;Br. J. Haematol.,1997
5. The Kell blood group system: a review [Review];Marsh;Transfusion,1990
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1. Case report: Clinical, genetic and immunological characterization of a novel XK variant in a patient with McLeod syndrome;Frontiers in Genetics;2024-08-21
2. Interaction between VPS13A and the XK scramblase is important for VPS13A function in humans;Journal of Cell Science;2022-09-01
3. Interaction between VPS13A and the XK scramblase is required to prevent VPS13A disease in humans;2022-05-10
4. Kell and Kx Blood Group Systems;Human Blood Groups;2013-01-28
5. Neuroacanthocytosis;Handbook of Clinical Neurology;2011
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