Alteration of the genes for glycophorin A and B in glycophorin-A-deficient individuals
Author:
Publisher
Wiley
Subject
Biochemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1432-1033.1988.tb14413.x/fullpdf
Reference27 articles.
1. 1. W. Dahr, V. Vengelen-Tyler, and W. J. Judd (1986 ) inRecent advances in blood group biochemistry (, eds) pp.23 -65 , American Association of Blood Banks, Arlington, VA.
2. Primary structure of human erythrocyte glycophorin A. Isolation and characterization of peptides and complete amino acid sequence
3. Glycophorins B and C from human erythrocyte membranes. Purification and sequence analysis.
4. Isolation and characterization of human glycophorin A cDNA clones by a synthetic oligonucleotide approach: nucleotide sequence and mRNA structure.
5. Human glycophorin A and B are encoded by separate, single copy genes coordinately regulated by a tumor-promoting phorbol ester.
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