Interaction of Hemoglobin Siriraj with Hemoglobin S: A Mild Sickle Cell Syndrome
- 1 January 1986
- journal article
- research article
- Published by Taylor & Francis in Hemoglobin
- Vol. 10 (1) , 21-31
- https://doi.org/10.3109/03630268609072468
Abstract
Hb Siriraj is a .beta. chain variant in which .beta.7 (A4) Glu is replaced by a lysine. It has been encountered in association with Hb S in a black man from Martinique. Some properties of Hb Siriraj are compared, particularly, with Hb C [.alpha.2.beta.26(A3)Glu .fwdarw. Lys], and a study of its in vitro interaction with Hb S is discussed.This publication has 15 references indexed in Scilit:
- The Human Alpha-Globin Gene. The Protein Products of the Duplicated Genes Are IdenticalEuropean Journal of Biochemistry, 1980
- Globin Chain Electrophoresis: a New Approach to the Determination of the Gγ/Aγ Ratio in Fetal Haemoglobin and to Studies of Globin SynthesisBritish Journal of Haematology, 1980
- β-Chain contact sites in the haemoglobin S polymerNature, 1980
- Structural bases of the inhibitory effects of hemoglobin F and hemoglobin A2 on the polymerization of hemoglobin S.Proceedings of the National Academy of Sciences, 1979
- Isoelectric focusing of human hemoglobin: its application to screening, to the characterization of 70 variants, and to the study of modified fractions of normal hemoglobinsBlood, 1978
- Haemoglobin Siriraj, β-7 (βA4) Glu→ Lys, in a Chinese Subject in TaiwanVox Sanguinis, 1972
- A Simple Method for the Detection of Unstable HaemoglobinsBritish Journal of Haematology, 1972
- Studies on the heterogeneity of hemoglobinJournal of Chromatography A, 1968
- A New Haemoglobin in a Thai Family. A Case of Haemoglobin Siriraj- ThalassaemiaBMJ, 1965
- Estimation of Small Percentages of Fœtal HæmoglobinNature, 1959