CD55base mutation publications
Search PubMed latest citations for CD55 mutations
2005
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Novel molecular basis of an Inab phenotype.
Hue-Roye K, Powell VI, Patel G, Lane D, Maguire M, Chung A, Reid ME
Immunohematol 2005(2): 53-5
[PubMed abstract].
1998
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Decay-accelerating factor (CD55) deficiency phenotypes in Japanese.
Daniels GL, Green CA, Mallinson G, Okubo Y, Hori Y, Kataoka A, Kaihara M
Transfus Med 1998(2): 141-7
[PubMed abstract].
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Molecular cloning and characterization of decay-accelerating factor deficiency in Cromer blood group Inab phenotype.
Wang L, Uchikawa M, Tsuneyama H, Tokunaga K, Tadokoro K, Juji T
Blood 1998(2): 680-4
[PubMed abstract].
1994
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Molecular basis of reduced or absent expression of decay-accelerating factor in Cromer blood group phenotypes.
Lublin DM, Mallinson G, Poole J, Reid ME, Thompson ES, Ferdman BR, Telen MJ, Anstee DJ, Tanner MJ
Blood 1994(4): 1276-82
[PubMed abstract].
1991
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Biochemical studies on red blood cells from a patient with the Inab phenotype (decay-accelerating factor deficiency).
Reid ME, Mallinson G, Sim RB, Poole J, Pausch V, Merry AH, Liew YW, Tanner MJ
Blood 1991(12): 3291-7
[PubMed abstract].
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Dr(a-) polymorphism of decay accelerating factor. Biochemical, functional, and molecular characterization and production of allele-specific transfectants.
Lublin DM, Thompson ES, Green AM, Levene C, Telen MJ
J Clin Invest 1991(6): 1945-52
[PubMed abstract].
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