An intramolecular DNA triplex is disrupted by point mutations associated with hereditary persistence of fetal hemoglobin.
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference90 articles.
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5. Demonstration of an S1-nuclease sensitive site near the human β-globin gene, and its protection by HMG 1 and 2
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2. Transcriptional Repressors of Fetal Globin Genes as Novel Therapeutic Targets in Beta-Thalassemia;Beta Thalassemia;2020-09-23
3. The Hemoglobin Regulatory Regions;Gene Regulatory Sequences and Human Disease;2012
4. research paper: Role of the cold shock domain protein A in the transcriptional regulation of HBG expression;British Journal of Haematology;2010-09
5. RecQ and RecG helicases have distinct roles in maintaining the stability of polypurine·polypyrimidine sequences;Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis;2008-08
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