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. 1965 Jan;44(1):42–50. doi: 10.1172/JCI105125

Studies on Hemoglobin Biosynthesis: Asynchronous Synthesis of Hemoglobin A and Hemoglobin A2 by Erythrocyte Precursors *

Ronald F Rieder 1, David J Weatherall 1
PMCID: PMC442017  PMID: 14254255

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. CONLEY C. L., WEATHERALL D. J., RICHARDSON S. N., SHEPARD M. K., CHARACHE S. Hereditary persistence of fetal hemoglobin: a study of 79 affected persons in 15 Negro families in Baltimore. Blood. 1963 Mar;21:261–281. [PubMed] [Google Scholar]
  2. GERALD P. S., DIAMOND L. K. The diagnosis of thalassemia trait by starch block electrophoresis of the hemoglobin. Blood. 1958 Jan;13(1):61–69. [PubMed] [Google Scholar]
  3. GOLDSTEIN M. A., PATPONGPANIJ N., MINNICH V. THE INCIDENCE OF ELEVATED HEMOGLOBIN A2 LEVELS IN THE AMERICAN NEGRO. Ann Intern Med. 1964 Jan;60:95–99. doi: 10.7326/0003-4819-60-1-95. [DOI] [PubMed] [Google Scholar]
  4. GREENOUGH W. B., 3rd, PETERS T., Jr, THOMAS E. D. An intracellular protein intermediate for hemoglobin formation. J Clin Invest. 1962 May;41:1116–1124. doi: 10.1172/JCI104563. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Gabuzda T. G., Nathan D. G., Gardner F. H. THE TURNOVER OF HEMOGLOBINS A, F, AND A(2) IN THE PERIPHERAL BLOOD OF THREE PATIENTS WITH THALASSEMIA. J Clin Invest. 1963 Nov;42(11):1678–1688. doi: 10.1172/JCI104854. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. JOSEPHSON A. M., MASRI M. S., SINGER L., DWORKIN D., SINGER K. Starch block electrophoretic studies of human hemoglobin solutions. II. Results in cord blood, thalassemia and other hematologic disorders: comparison with Tiselius electrophoresis. Blood. 1958 Jun;13(6):543–551. [PubMed] [Google Scholar]
  7. KUNKEL H. G., BEARN A. G. Minor hemoglobin components of normal human blood. Fed Proc. 1957 Sep;16(3):760–762. [PubMed] [Google Scholar]
  8. KUNKEL H. G., CEPPELLINI R., MULLER-EBERHARD U., WOLF J. Observations on the minor basic hemoglobin component in the blood of normal individuals and patients with thalassemia. J Clin Invest. 1957 Nov;36(11):1615–1625. doi: 10.1172/JCI103561. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. MARKS P. A., BURKA E. R. HEMOGLOBINS A AND F: FORMATION IN THALASSEMIA AND OTHER HEMOLYTIC ANEMIAS. Science. 1964 May 1;144(3618):552–553. doi: 10.1126/science.144.3618.552. [DOI] [PubMed] [Google Scholar]
  10. POULIK M. D. Starch gel electrophoresis in a discontinous system of buffers. Nature. 1957 Dec 28;180(4600):1477–1479. doi: 10.1038/1801477a0. [DOI] [PubMed] [Google Scholar]
  11. RANNEY H. M., KONO P. Studies of the incoporation of Fe59 into normal and abnormal hemoglobins. J Clin Invest. 1959 Mar;38(3):508–515. doi: 10.1172/JCI103828. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. SINGER K., FISHER B. Studies on abnormal hemoglobins. V. The distribution of type S, sickle cell, hemoglobin and type F, alkali resistant, hemoglobin within the red cell population in sickle cell anemia. Blood. 1952 Dec;7(12):1216–1226. [PubMed] [Google Scholar]
  13. SMITHIES O. An improved procedure for starch-gel electrophoresis: further variations in the serum proteins of normal individuals. Biochem J. 1959 Mar;71(3):585–587. doi: 10.1042/bj0710585. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. VINOGRAD J., HUTCHINSON W. D. Carbon-14 labelled hybrids of haemoglobin. Nature. 1960 Jul 16;187:216–218. doi: 10.1038/187216a0. [DOI] [PubMed] [Google Scholar]
  15. WHEELER J. T., KREVANS J. R. The homozygous state of persistent fetal hemoglobin and the interaction of persistent fetal hemoglobin with thalassemia. Bull Johns Hopkins Hosp. 1961 Nov;109:217–233. [PubMed] [Google Scholar]

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