An Intramolecular Triplex in the Human γ-Globin 5′-Flanking Region Is Altered by Point Mutations Associated with Hereditary Persistence of Fetal Hemoglobin
Open Access
- 1 October 1995
- journal article
- Published by Elsevier
- Vol. 270 (41) , 24556-24563
- https://doi.org/10.1074/jbc.270.41.24556
Abstract
No abstract availableKeywords
This publication has 50 references indexed in Scilit:
- An Intramolecular Triplex Structure From Non-mirror Repeated Sequence Containing BothPy:Pu·Py andPu:Pu·Py TriadsJournal of Molecular Biology, 1995
- Elevated unconstrained supercoiling of plasmid DNA generated by transcription and translation of the tetracycline resistance gene in eubacteriaBiochemistry, 1994
- Physiological Concentration of Magnesium Ions Induces a Strong Macroscopic Curvature in GGGCCC-containing DNAJournal of Molecular Biology, 1994
- The loop sequence plays crucial roles for isomerization of intramolecular DNA triplexes in supercoiled plasmidsJournal of Molecular Biology, 1994
- A single point mutation is the cause of the Greek form of hereditary persistence of fetal haemoglobinNature, 1992
- The β- and δ-Thalassemia RepositoryHemoglobin, 1992
- Solution structure of an oncogenic DNA duplex containing a G.cntdot.A mismatchBiochemistry, 1991
- Nucleosomes are phased along the mouse β-major globin gene in erythroid and nonerythroid cellsCell, 1986
- Folding of the DNA double helix in chromatin-like structures from simian virus 40.Proceedings of the National Academy of Sciences, 1975
- Transitions of DNA homopolymersJournal of Molecular Biology, 1964