Mutations in EKLF/KLF1 form the molecular basis of the rare blood group In(Lu) phenotype
Author:
Affiliation:
1. Bristol Institute for Transfusion Sciences (BITS), National Blood Service, Bristol; and
2. Department of Biochemistry, University of Bristol, Bristol, United Kingdom
Abstract
Publisher
American Society of Hematology
Subject
Cell Biology,Hematology,Immunology,Biochemistry
Link
http://ashpublications.org/blood/article-pdf/112/5/2081/1487511/zh801708002081.pdf
Reference45 articles.
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2. Defective haematopoiesis in fetal liver resulting from inactivation of the EKLF gene.;Nuez;Nature,1995
3. Lethal β-thalassaemia in mice lacking the erythroid CACCC-transcription factor EKLF.;Perkins;Nature,1995
4. Functional synergy and physical interactions of the erythroid transcription factor GATA-1 with the Krüppel family proteins SP1 and EKLF.;Merika;Mol Cell Biol,1995
5. Functional interaction of GATA1 with erythroid Krüppel-like factor and Sp1 at defined erythroid promoters.;Gregory;Blood,1996
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