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Journal Abstract Search

222 related items for PubMed ID: 975241

  • 1. Delta-beta-thalassemia is due to a gene deletion.
    Ottolenghi S, Comi P, Giglioni B, Tolstoshev P, Lanyon WG, Mitchell GJ, Williamson R, Russo G, Musumeci S, Schillro G, Tsistrakis GA, Charache S, Wood WG, Clegg JB, Weatherall DJ.
    Cell; 1976 Sep; 9(1):71-80. PubMed ID: 975241
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  • 2. Molecular comparison of delta beta-thalassemia and hereditary persistence of fetal hemoglobin DNAs: evidence of a regulatory area?
    Ottolenghi S, Giglioni B, Taramelli R, Comi P, Mazza U, Saglio G, Camaschella C, Izzo P, Cao A, Galanello R, Gimferrer E, Baiget M, Gianni AM.
    Proc Natl Acad Sci U S A; 1982 Apr; 79(7):2347-51. PubMed ID: 6179097
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  • 4. Featured Article: Modulation of fetal hemoglobin in hereditary persistence of fetal hemoglobin deletion type-2, compared to Sicilian δβ-thalassemia, by BCL11A and SOX6-targeting microRNAs.
    Fornari TA, Lanaro C, Albuquerque DM, Ferreira R, Costa FF.
    Exp Biol Med (Maywood); 2017 Feb; 242(3):267-274. PubMed ID: 27591578
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  • 7. Globin chain synthesis in the greek type (A gamma) of hereditary persisitence of fetal haemoglobin.
    Sofroniadou K, Wood WG, Nute PE, Stamatoyannopoulos G.
    Br J Haematol; 1975 Jan; 29(1):137-48. PubMed ID: 1201197
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  • 8. Characterisation of deletions which affect the expression of fetal globin genes in man.
    Fritsch EF, Lawn RM, Maniatis T.
    Nature; 1979 Jun 14; 279(5714):598-603. PubMed ID: 450109
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  • 11. Deletion of the A gamma-globin gene in G gamma-delta beta-thalassemia.
    Orkin SH, Alter BP, Altay C.
    J Clin Invest; 1979 Sep 14; 64(3):866-9. PubMed ID: 468997
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  • 12. Molecular basis and hematologic characterization of deltabeta-thalassemia and hereditary persistence of fetal hemoglobin in Thailand.
    Panyasai S, Fucharoen S, Surapot S, Fucharoen G, Sanchaisuriya K.
    Haematologica; 2004 Jul 14; 89(7):777-81. PubMed ID: 15257928
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  • 13. Heterocellular hereditary persistence of fetal hemoglobin (HPFH). Molecular mechanisms of abnormal gamma-gene expression in association with beta thalassemia and linkage relationship with the beta-globin gene cluster.
    Giampaolo A, Mavilio F, Sposi NM, Carè A, Massa A, Cianetti L, Petrini M, Russo R, Cappellini MD, Marinucci M.
    Hum Genet; 1984 Jul 14; 66(2-3):151-6. PubMed ID: 6201431
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  • 15. Occurrence of G gamma Hb F in Greek HPFH: analysis of heterozygotes and compound heterozygotes with beta thalassaemia.
    Clegg JB, Metaxatou-Mavromati A, Kattamis C, Sofroniadou K, Wood WG, Weatherall DJ.
    Br J Haematol; 1979 Dec 14; 43(4):521-36. PubMed ID: 93488
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  • 16. Alpha zero- and beta zero-thalassemia in a Thai family: unusually mild homozygous beta zero-thalassemia without alpha-globin gene deletion.
    Yenchitsomanus P, Summers KM.
    Hum Genet; 1985 Dec 14; 69(4):375-7. PubMed ID: 2580774
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  • 17. A Chinese G gamma + (A gamma delta beta)zero thalassemia deletion: comparison to other deletions in the human beta-globin gene cluster and sequence analysis of the breakpoints.
    Mager DL, Henthorn PS, Smithies O.
    Nucleic Acids Res; 1985 Sep 25; 13(18):6559-75. PubMed ID: 2997715
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