Binding of HMG-I(Y) elicits structural changes in a silencer of the human ?-globin gene

This publication has 37 references indexed in Scilit:

• Identification of Upstream Regulatory Elements That Repress Expression of Adult Beta-like Globin Genes in a Primitive Erythroid Environment
  Blood Cells, Molecules, and Diseases, 1998
• Sequence of the —530 region of the β-globin gene of sickle cell anemia patients with the Arabian haplotype
  Human Mutation, 1994
• DNA sequence variation in a negative control region 5' to the beta- globin gene correlates with the phenotypic expression of the beta s mutation
  Blood, 1992
• Increased protein binding to a −530 mutation of the human β‐globin gene associated with decreased β‐globin synthesis
  American Journal of Hematology, 1991
• A common protein binds to two silencers 5′ to the human β-globin gene
  Nucleic Acids Research, 1989
• Structural analysis of the 5' flanking region of the beta-globin gene in African sickle cell anemia patients: further evidence for three origins of the sickle cell mutation in Africa.
  Proceedings of the National Academy of Sciences, 1988
• Evidence for the multicentric origin of the sickle cell hemoglobin gene in Africa.
  Proceedings of the National Academy of Sciences, 1984
• Hemoglobins S and C in Upper Volta
  Human Genetics, 1984
• Natural History of Sickle Cell Anemia in Saudi Arabs
  Annals of Internal Medicine, 1978
• Milder Variant of Sickle‐Cell Disease in Arabs in Kuwait associated with Unusually High Level of Foetal Haemoglobin
  British Journal of Haematology, 1970