A Recombinant Human Hemoglobin with Anti-sickling Properties Greater than Fetal Hemoglobin
Open Access
- 1 June 2004
- journal article
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 279 (26) , 27518-27524
- https://doi.org/10.1074/jbc.m402578200
Abstract
No abstract availableKeywords
This publication has 31 references indexed in Scilit:
- Mortality In Sickle Cell Disease -- Life Expectancy and Risk Factors for Early DeathNew England Journal of Medicine, 1994
- Human gamma- to beta-globin gene switching in transgenic mice.Genes & Development, 1990
- Developmental regulation of human fetal-to-adult globin gene switching in transgenic miceNature, 1990
- Levels of Fetal Hemoglobin Necessary for Treatment of Sickle Cell DiseaseNew England Journal of Medicine, 1988
- Hb F Synthesis in Sickle Cell Anaemia: a Comparison of Saudi Arab Cases with those of African OriginBritish Journal of Haematology, 1980
- Three-dimensional reconstruction of the 14-filament fibers of hemoglobin SJournal of Molecular Biology, 1979
- Sickle cell anemia and trait in Southern India: Further studiesAmerican Journal of Hematology, 1979
- Crystal structure of sickle-cell deoxyhemoglobin at 5 Å resolutionJournal of Molecular Biology, 1975
- Gene Mutations in Human Hæmoglobin: the Chemical Difference Between Normal and Sickle Cell HæmoglobinNature, 1957
- A Specific Chemical Difference Between the Globins of Normal Human and Sickle-Cell Anæmia HæmoglobinNature, 1956