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Journal Abstract Search

268 related items for PubMed ID: 274714

  • 1.
    ; . PubMed ID:
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  • 2. Organization of human delta--and beta-globin genes in cellular DNA and the presence of intragenic inserts.
    Mears JG, Ramirez F, Leibowitz D, Bank A.
    Cell; 1978 Sep; 15(1):15-23. PubMed ID: 699038
    [Abstract] [Full Text] [Related]

  • 3. Partial deletion of beta-globin gene DNA in certain patients with beta 0-thalassemia.
    Orkin SH, Old JM, Weatherall DJ, Nathan DG.
    Proc Natl Acad Sci U S A; 1979 May; 76(5):2400-4. PubMed ID: 287080
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  • 4. Analysis of globin gene structure in patients with beta thalassemia by restriction endonuclease mapping.
    Tam JW, Kaufman RE, Nienhuis AW.
    Hemoglobin; 1981 May; 5(3):209-15. PubMed ID: 6164667
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  • 5. Application of endonuclease mapping to the analysis and prenatal diagnosis of thalassemias caused by globin-gene deletion.
    Orkin SH, Alter BP, Altay C, Mahoney MJ, Lazarus H, Hobbins JC, Nathan DG.
    N Engl J Med; 1978 Jul 27; 299(4):166-72. PubMed ID: 661890
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  • 6. 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 27; 79(7):2347-51. PubMed ID: 6179097
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  • 7. [Construction of a genome library from a beta-0-thalassemic individual from Ferrara: characterization of clones containing beta globin genes].
    Marchetti G, Evangelisti A, Bernardi F, Perrotta C, Conconi F, Del Senno L.
    Boll Soc Ital Biol Sper; 1983 Jun 30; 59(6):758-64. PubMed ID: 6309196
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  • 8. The organization of the gamma-delta-beta gene complex in normal and thalassemia cells.
    Bank A, Mears JG, Ramirez F, Burns AL, Spence S, Feldenzer J, Baird M.
    Hemoglobin; 1980 Jun 30; 4(3-4):497-507. PubMed ID: 6252123
    [Abstract] [Full Text] [Related]

  • 9. 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
    [Abstract] [Full Text] [Related]

  • 10. gamma-beta-Thalassaemia studies showing that deletion of the gamma- and delta-genes influences beta-globin gene expression in man.
    Van der Ploeg LH, Konings A, Oort M, Roos D, Bernini L, Flavell RA.
    Nature; 1980 Feb 14; 283(5748):637-42. PubMed ID: 6153459
    [Abstract] [Full Text] [Related]

  • 11. Identification of novel candidate genes for globin regulation in erythroid cells containing large deletions of the human beta-globin gene cluster.
    de Andrade TG, Peterson KR, Cunha AF, Moreira LS, Fattori A, Saad ST, Costa FF.
    Blood Cells Mol Dis; 2006 Feb 14; 37(2):82-90. PubMed ID: 16952470
    [Abstract] [Full Text] [Related]

  • 12. Deletion of a region that is a candidate for the difference between the deletion forms of hereditary persistence of fetal hemoglobin and deltabeta-thalassemia affects beta- but not gamma-globin gene expression.
    Calzolari R, McMorrow T, Yannoutsos N, Langeveld A, Grosveld F.
    EMBO J; 1999 Feb 15; 18(4):949-58. PubMed ID: 10022837
    [Abstract] [Full Text] [Related]

  • 13. Cloning and direct examination of a structurally abnormal human beta 0-thalassemia globin gene.
    Orkin SH, Kolodner R, Michelson A, Husson R.
    Proc Natl Acad Sci U S A; 1980 Jun 15; 77(6):3558-62. PubMed ID: 6251466
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  • 14.
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  • 15.
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  • 16. Organization of the alpha-globin genes in the Chinese alpha-thalassemia syndromes.
    Embury SH, Lebo RV, Dozy AM, Kan YW.
    J Clin Invest; 1979 Jun 15; 63(6):1307-10. PubMed ID: 447845
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  • 17. Gene analysis in delta beta and delta (0) thalassemia.
    Baird M, Driscoll MC, Ben-Bassat I, Ohta Y, Nakamura F, Bloom A, Bank A.
    J Biol Chem; 1984 Jan 10; 259(1):512-5. PubMed ID: 6323412
    [Abstract] [Full Text] [Related]

  • 18. 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 10; 242(3):267-274. PubMed ID: 27591578
    [Abstract] [Full Text] [Related]

  • 19. Base substitution in an intervening sequence of a beta+-thalassemic human globin gene.
    Spritz RA, Jagadeeswaran P, Choudary PV, Biro PA, Elder JT, deRiel JK, Manley JL, Gefter ML, Forget BG, Weissman SM.
    Proc Natl Acad Sci U S A; 1981 Apr 10; 78(4):2455-9. PubMed ID: 6264477
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  • 20. Allele-specific transcription of fetal genes in primary erythroid cell cultures from Lepore and deltabeta degrees thalassemia patients.
    Di Marzo R, Acuto S, Calzolari R, Maggio A.
    Exp Hematol; 2005 Nov 10; 33(11):1363-70. PubMed ID: 16263421
    [Abstract] [Full Text] [Related]

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