Recent developments in the molecular genetics of human hemoglobin
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[1] J. T. Wilson,et al. Nucleotide sequence of 3' untranslated portion of human alpha globin mRNA. , 1977, Nucleic acids research.
[2] J. B. Clegg,et al. The thalassaemia syndromes , 1965 .
[3] P. Marks,et al. Abnormal or absent β mRNA in β0 Ferrara and gene deletion in δβ thalassaemia , 1976, Nature.
[4] Smith Ew,et al. Study of two abnormal hemoglobins with evidence for a new genetic locus for hemoglobin formation. , 1958 .
[5] D. Charlesworth,et al. A New Hb Variant: Hb F Sardinia γ75 (e 19) Isoieucine→Threonine Found in a Family with Hb G Philadelphia, β-Chain Deficiency and a Lepore-Like Haemoglobin Indistinguishable from Hb A2 , 1975 .
[6] R. Williamson,et al. A direct estimate of the number of human γ-globin genes , 1976, Cell.
[7] J. Clegg,et al. Synthesis in vitro of anti-Lepore haemoglobin. , 1973, Nature: New biology.
[8] H. Varmus,et al. Deletion of α-globin genes in haemoglobin-H disease demonstrates multiple α-globin structural loci , 1975, Nature.
[9] J. Clegg,et al. A Form of Hereditary Persistence of Fetal Haemoglobin Characterized by Uneven Cellular Distribution of Haemoglobin F and the Production of Haemoglobins A and A2 in Homozygotes , 1975, British journal of haematology.
[10] H. Lazarus,et al. Application of endonuclease mapping to the analysis and prenatal diagnosis of thalassemias caused by globin-gene deletion. , 1978, The New England journal of medicine.
[11] J. Lawrence,et al. Chromosomal localization of human β globin gene on human chromosome 11 in somatic cell hybrids , 1978 .
[12] R. Abramson,et al. Homozygous Hb J Tongariki: Evidence for Only One Alpha Chain Structural Locus in Melanesians , 1970, Science.
[13] G. Stamatoyannopoulos,et al. The linkage relationships of the beta and delta hemoglobin genes. , 1977, Hemoglobin.
[14] J. Lawrence,et al. Localization of the human α-globin structural gene to chromosome 16 in somatic cell hybrids by molecular hybridization assay , 1977, Cell.
[15] D. Westaway,et al. Isolation and partial sequence of recombinant plasmids containing human α-, β- and γ-globin cDNA fragments , 1978, Nature.
[16] J. Seidman,et al. Cloning specific segments of the mammalian genome: bacteriophage lambda containing mouse globin and surrounding gene sequences. , 1977, Proceedings of the National Academy of Sciences of the United States of America.
[17] F. Flynn,et al. Two New Hæmoglobin Variants in a Very Young Human Embryo , 1961, Nature.
[18] T. Huisman,et al. Evidence for multiple structural genes for the gamma chain of human fetal hemoglobin. , 1968, Proceedings of the National Academy of Sciences of the United States of America.
[19] P. Rowley,et al. Induction of -globin synthesis in the -thalassaemia of Ferrara. , 1972, Nature: New biology.
[20] A. Bank,et al. Quantitation of human gamma globin genes and gamma globin mRNA with purified gamma globin complementary DNA. , 1976, The Journal of clinical investigation.
[21] G. Stamatoyannopoulos,et al. F-cells in the adult: normal values and levels in individuals with hereditary and acquired elevations of Hb F. , 1975, Blood.
[22] S. Charache,et al. Deletion of the β-globin structure gene in hereditary persistence of foetal haemoglobin , 1975, Nature.
[23] W. Anderson,et al. Isolation and translation of hemoglobin messenger RNA from thalassemia, sickle cell anemia, and normal human reticulocytes. , 1971, The Journal of clinical investigation.
[24] J. Clegg,et al. Characterization of β-globin mRNA in the β0 thalassemias , 1978, Cell.
[25] H. Lazarus,et al. Absence of messenger RNA and gene DNA for β-globin chains in hereditary persistence of fetal hemoglobin , 1976, Cell.
[26] Arthur Bank,et al. Organization of human δ- and β-globin genes in cellular DNA and the presence of intragenic inserts , 1978, Cell.
[27] R. Dluhy,et al. Hemoglobin Cranston, an unstable variant having an elongated beta chain due to nonhomologous crossover between two normal beta chain genes. , 1975, Proceedings of the National Academy of Sciences of the United States of America.
[28] G. Apell,et al. THE PRESENT STATUS OF THE HETEROGENEITY OF FETAL HEMOGLOBIN IN β‐THALASSEMIA: AN ATTEMPT TO UNIFY SOME OBSERVATIONS IN THALASSEMIA AND RELATED CONDITIONS * , 1974, Annals of the New York Academy of Sciences.
[29] H. Lehmann,et al. Human embryonic haemoglobins including a comparison by homology of the human ζ and α chains , 1975, Nature.
[30] R. Flügel,et al. Malignant transformation of rat embryo fibroblasts by herpes simplex virus types 1 and 2 at suboptimal temperature , 1977, Nature.
[31] R. Williamson,et al. Transcriptional and Post‐transcriptional Defects in β0‐Thalassaemia , 1977 .
[32] Wood Wg,et al. Developmental biology of human hemoglobins. , 1977 .
[33] N. Proudfoot,et al. The 3′ terminal sequences of human α and β globin messenger RNAs: Comparison with rabbit globin messenger RNA , 1976, Cell.
[34] J. Clegg,et al. G gamma beta + type of hereditary persistence of fetal haemoglobin in association with Hb C. , 1979, Journal of medical genetics.
[35] T. Huisman,et al. Hemoglobin Kenya, the product of fusion of amd polypeptide chains. , 1972, Archives of biochemistry and biophysics.
[36] E. Benz,et al. Relative stability of alpha- and beta-globin messenger RNAs in homozygous beta+ thalassemia. , 1977, Proceedings of the National Academy of Sciences of the United States of America.
[37] G. Efremov. Hemoglobins Lepore and anti-Lepore. , 1978, Hemoglobin.
[38] J. Clegg,et al. Linkage relationships between beta- and delta-structural loci and African forms of beta thalassaemia. , 1976, Journal of medical genetics.
[39] E. Huehns,et al. Occurrence of Heterozygotes and Homozygotes for the α-Chain Haemoglobin Variant Hb-J(Tongariki) in New Guinea , 1972, Nature.
[40] R. Williamson,et al. Presence of gene for β globin in homozygous β0 thalassaemia , 1976, Nature.
[41] B. Forget,et al. Defect in messenger RNA for human hemoglobin synthesis in beta thalassemia. , 1971, The Journal of clinical investigation.
[42] J. Clegg,et al. Haemoglobin Constant Spring—A Chain Termination Mutant ? , 1971, Nature.
[43] D. Weatherall,et al. Haemoglobin Synthesis during Human Foetal Development , 1973, Nature.
[44] P. Marks,et al. Decreased globin messenger RNA in thalassemia detected by molecular hybridization. , 1973, Proceedings of the National Academy of Sciences of the United States of America.
[45] P. Leder,et al. An intervening sequence of the mouse β-globin major gene shares extensive homology only with β-globin genes , 1978, Nature.
[46] F. Baralle. Complete nucleotide sequence of the 5′ noncoding region of human α- and β-globin mRNA , 1977, Cell.
[47] J. Clegg,et al. δβ-Thalassemia is due to a gene deletion , 1976, Cell.
[48] A. Jeffreys,et al. The rabbit β-globin gene contains a large insert in the coding sequence , 1977, Cell.
[49] P. Fessas,et al. Hemoglobins of early human embryonic development. , 1966, Science.
[50] Y. Kan,et al. The nucleotide sequence of the 5′ untranslated region of human γ-globin mRNA , 1978 .
[51] R. Williamson,et al. Analysis of the β-δ-globin gene loci in normal and hb lepore DNA: Direct determination of gene linkage and intergene distance , 1978, Cell.
[52] F. Hecht,et al. Predominance of Hemoglobin Gower 1 in Early Human Embryonic Development , 1966, Science.
[53] E. Huehns,et al. Oxygen dissociation properties of human embryonic red cells , 1975, Nature.
[54] H. Varmus,et al. Gene deletion as the cause of α thalassaemia: Genetic lesion in homozygous α thalassaemia (hydrops fetalis) , 1974, Nature.
[55] K. Imai,et al. Haemoglobin Tak: a β‐Chain Elongation , 1975 .
[56] G. Stamatoyannopoulos,et al. Hemoglobin F synthesis in vitro: evidence for control at the level of primitive erythroid stem cells. , 1977, Proceedings of the National Academy of Sciences of the United States of America.
[57] D. Housman,et al. Variability in the amount of β-globin mRNA in β 0 thalassemia , 1978, Cell.
[58] F. Baralle,et al. AUG is the only recognisable signal sequence in the 5′ non-coding regions of eukaryotic mRNA , 1978, Nature.
[59] J. Clegg,et al. The alpha-chain-termination mutants and their relation to the alpha-thalassaemias. , 1975, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.
[60] J. Clegg,et al. A Genetically Determined Disorder with Features both of Thalassaemia and Congenital Dyserythropoietic Anaemia , 1973, British journal of haematology.
[61] R. Abramson,et al. Hemoglobin Wayne: a frameshift mutation detected in human hemoglobin alpha chains. , 1976, Proceedings of the National Academy of Sciences of the United States of America.
[62] Y. Kan,et al. Identification of a nondeletion defect in α-thalassemia. , 1977 .
[63] E. Huehns,et al. The Abnormal Haemoglobins in Homozygous α‐Thalassaemia , 1970 .
[64] S. Boyer,et al. Fetal hemoglobin restriction to a few erythrocytes (F cells) in normal human adults. , 1975, Science.
[65] Richard T. Jones,et al. Hemoglobin Portland 1: A New Human Hemoglobin Unique in Structure , 1967, Science.
[66] R. Williamson,et al. Structure of the human fetal globin gene locus , 1979, Nature.
[67] D. Rucknagel,et al. Trimodality in the proportion of hemoglobin G Philadelphia in heterozygotes: evidence for heterogeneity in the number of human alpha chain loci. , 1976, Proceedings of the National Academy of Sciences of the United States of America.
[68] J. Clegg,et al. Haemoglobin J Tongariki is associated with α thalassaemia , 1978, Nature.
[69] J. Clegg,et al. The Haemoglobin Constitution of Infants with the Haemoglobin Bart's Hydrops Foetalis Syndrome , 1970, British journal of haematology.
[70] P. Leder,et al. The intervening sequence of a mouse beta-globin gene is transcribed within the 15S beta-globin mRNA precursor. , 1978, Proceedings of the National Academy of Sciences of the United States of America.
[71] R. Williamson,et al. The severe form of alpha thalassaemia is caused by a haemoglobin gene deletion. , 1974, Nature.
[72] P. Leder,et al. The sequence of the chromosomal mouse β-globin major gene: Homologies in capping, splicing and poly(A) sites , 1978, Cell.
[73] S. Weissman,et al. Human beta-globin messenger RNA. III. Nucleotide sequences derived from complementary DNA. , 1977, The Journal of biological chemistry.
[74] F. Hecht,et al. HUMAN EMBRYONIC HEMOGLOBINS. , 1964, Cold Spring Harbor symposia on quantitative biology.
[75] J. Clegg,et al. Human globin gene expression: Control of β, δ and δβ chain production , 1978, Cell.
[76] Richard T. Jones. Evidence for a New Haemoglobin Chain (ζ-Chain) , 1970, Nature.
[77] C. Baglioni. The fusion of two peptide chains in hemoglobin Lepore and its interpretation as a genetic deletion. , 1962, Proceedings of the National Academy of Sciences of the United States of America.
[78] N. Proudfoot,et al. Nucleotide sequences of globin messenger RNA. , 1976, British medical bulletin.
[79] J. T. Wilson,et al. Insertion of synthetic copies of human globin genes into bacterial plasmids. , 1978, Nucleic acids research.
[80] J. Clegg,et al. Molecular genetics of human hemoglobin. , 1976, Annual review of genetics.
[81] J. Clegg,et al. Hereditary Persistence of Foetal Haemoglobin associated with a γβ Fusion Variant, Haemoglobin Kenya , 1973 .
[82] S. Orkin. The duplicated human alpha globin genes lie close together in cellular DNA. , 1978, Proceedings of the National Academy of Sciences of the United States of America.