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- BAGLIONI C. The fusion of two peptide chains in hemoglobin Lepore and its interpretation as a genetic deletion. Proc Natl Acad Sci U S A. 1962 Nov 15;48:1880–1886. doi: 10.1073/pnas.48.11.1880. [DOI] [PMC free article] [PubMed] [Google Scholar]
- BAILEY I. S., PRANKERD T. A. Studies in thalassaemia. Br J Haematol. 1958 Apr;4(2):150–155. doi: 10.1111/j.1365-2141.1958.tb03845.x. [DOI] [PubMed] [Google Scholar]
- BERLIN N. I., LAWRENCE J. H., LEE H. C. The pathogenesis of the anemia of chronic leukemia; measurement of the life span of the red blood cell with glycine-2-C14. J Lab Clin Med. 1954 Dec;44(6):860–874. [PubMed] [Google Scholar]
- BETKE K., KLEIHAUER E. Fetaler und bleibender Blutfarbstoff in Erythrozyten und Erythroblasten von menschlichen Feten und Neugeborenen. Blut. 1958 Nov;4(5):241–249. doi: 10.1007/BF01630321. [DOI] [PubMed] [Google Scholar]
- BORSOOK H., DEASY C. L., HAAGENSMIT A. J., KEIGHLEY G., LOWY P. H. Incorporation in vitro of labeled amino acids into proteins of rabbit reticulocytes. J Biol Chem. 1952 May;196(2):669–694. [PubMed] [Google Scholar]
- BREATHNACH C. S. Some observations on the erythrocytepigment relationships in neonatal blood and marrow. Q J Exp Physiol Cogn Med Sci. 1962 Apr;47:141–147. doi: 10.1113/expphysiol.1962.sp001585. [DOI] [PubMed] [Google Scholar]
- CHERNOFF A. I. The human hemoglobins in health and disease. N Engl J Med. 1955 Aug 25;253(8):322–contd. doi: 10.1056/NEJM195508252530806. [DOI] [PubMed] [Google Scholar]
- 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]
- FESSAS P. Inclusions of hemoglobin erythroblasts and erythrocytes of thalassemia. Blood. 1963 Jan;21:21–32. [PubMed] [Google Scholar]
- FINCH C. A., STURGEON P. Erythrokinetics in Cooley's anemia. Blood. 1957 Jan;12(1):64–73. [PubMed] [Google Scholar]
- GABUZDA T. G., NATHAN D. G., GARDNER F. H. Comparative metabolism of haemoglobins A and F in thalassaemia. Nature. 1962 Nov 24;196:781–782. doi: 10.1038/196781b0. [DOI] [PubMed] [Google Scholar]
- GIBLETT E. R., COLEMAN D. H., PIRZIOBIROLI G., DONOHUE D. M., MOTULSKY A. G., FINCH C. A. Erythrokinetics: quantitative measurements of red cell production and destruction in normal subjects and patients with anemia. Blood. 1956 Apr;11(4):291–309. [PubMed] [Google Scholar]
- GRINSTEIN M., BANNERMAN R. M., VAVRA J. D., MOORE C. V. Hemoglobin metabolism in thalassemia. In vivo studies. Am J Med. 1960 Jul;29:18–32. doi: 10.1016/0002-9343(60)90004-8. [DOI] [PubMed] [Google Scholar]
- HUISMAN T. H., MARTIS E. A., DOZY A. Chromatography of hemoglobin types on carboxymethylcellulose. J Lab Clin Med. 1958 Aug;52(2):312–327. [PubMed] [Google Scholar]
- INGRAM V. M., STRETTON A. O. Genetic basis of the thalassaemia diseases. Nature. 1959 Dec 19;184:1903–1909. doi: 10.1038/1841903a0. [DOI] [PubMed] [Google Scholar]
- KUNKEL H. G., BEARN A. G. Minor hemoglobin components of normal human blood. Fed Proc. 1957 Sep;16(3):760–762. [PubMed] [Google Scholar]
- MALAMOS B., BELCHER E. H., GYFTAKI E., BINOPOULOS D. Simultaneous radioactive tracer studies of erythropoiesis and red-cell destruction in thalassaemia. Br J Haematol. 1961 Oct;7:411–429. doi: 10.1111/j.1365-2141.1961.tb00352.x. [DOI] [PubMed] [Google Scholar]
- NEUBERGER A., NIVEN J. S. F. Haemoglobin formation in rabbits. J Physiol. 1951 Feb;112(3-4):292–310. doi: 10.1113/jphysiol.1951.sp004530. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 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]
- ROBINSON S., VANIER T., DESFORGES J. F., SCHMID R. Jaundice in thalassemia minor: a consequence of "ineffective erythropoiesis". N Engl J Med. 1962 Sep 13;267:523–529. doi: 10.1056/NEJM196209132671101. [DOI] [PubMed] [Google Scholar]
- SCHROEDER W. A., SHELTON J. R., SHELTON J. B., CORMICK J. Further sequences in the gamma-chain of human fetal hemoglobin. Proc Natl Acad Sci U S A. 1962 Feb;48:284–287. doi: 10.1073/pnas.48.2.284. [DOI] [PMC free article] [PubMed] [Google Scholar]
- SHEPARD M. K., WEATHERALL D. J., CONLEY C. L. Semi-quantitative estimation of the distribution of fetal hemoglobin in red cell populations. Bull Johns Hopkins Hosp. 1962 Jun;110:293–310. [PubMed] [Google Scholar]
- 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]
- THOMAS E. D., LOCHTE H. L., Jr, GREENOUGH W. B., 3rd, WALES M. In vitro synthesis of foetal and adult haemoglobin by foetal haematopoietic tissues. Nature. 1960 Feb 6;185:396–397. doi: 10.1038/185396a0. [DOI] [PubMed] [Google Scholar]
- THOMPSON R. B., MITCHENER J. W., HUISMAN T. H. Studies on the fetal hemoglobin in the persistent high Hb-F anomaly. Blood. 1961 Sep;18:267–284. [PubMed] [Google Scholar]
- 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]