Changes in red cell ion transport, reduced intratumoral neovascularization, and some mild motor function abnormalities accompany targeted disruption of the Mouse Kell gene (Kel)
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajh.21453/fullpdf
Reference48 articles.
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2. The value of DNA analysis for antigens of the Kell and Kx blood group systems;Lee;Transfusion,2007
3. Molecular defects underlying the Kell null phenotype;Lee;J Biol Chem,2001
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. Isolation of the gene for McLeod syndrome that encodes a novel membrane transport protein;Ho;Cell,1994
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