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Journal Abstract Search

134 related items for PubMed ID: 874650

  • 21. Common haplotype dependency of high G gamma-globin gene expression and high Hb F levels in beta-thalassemia and sickle cell anemia patients.
    Labie D, Pagnier J, Lapoumeroulie C, Rouabhi F, Dunda-Belkhodja O, Chardin P, Beldjord C, Wajcman H, Fabry ME, Nagel RL.
    Proc Natl Acad Sci U S A; 1985 Apr; 82(7):2111-4. PubMed ID: 2580306
    [Abstract] [Full Text] [Related]

  • 22. Variation in beta-alpha synthesis ratios in thalassemia and hemoglobinopathies.
    Rieder RF.
    Ann N Y Acad Sci; 1974 Apr; 232(0):44-53. PubMed ID: 4607338
    [No Abstract] [Full Text] [Related]

  • 23. Variations in globin synthesis in delta-beta-thalassaemia.
    Kinney TR, Friedman S, Cifuentes E, Kim HC, Schwartz E.
    Br J Haematol; 1978 Jan; 38(1):15-22. PubMed ID: 638060
    [Abstract] [Full Text] [Related]

  • 24. Balanced bone marrow globin synthesis in mideastern alpha-thalassemia.
    Zaizov R, Steinherz M, Wollach B, Kirschmann C.
    Acta Haematol; 1980 Jan; 64(3):136-40. PubMed ID: 6778046
    [Abstract] [Full Text] [Related]

  • 25. Chromatographic measurements of hemoglobin A2 in blood samples that contain sickle hemoglobin.
    Shokrani M, Terrell F, Turner EA, Aguinaga MD.
    Ann Clin Lab Sci; 2000 Apr; 30(2):191-4. PubMed ID: 10807164
    [Abstract] [Full Text] [Related]

  • 26. Globin synthesis studies in a person heterozygous for alpha-thalassemia-2, Hb S and Hb G Philadelphia.
    Ballas SK, Walker BK, Atwater J.
    Clin Chim Acta; 1980 Jan 01; 100(1):1-6. PubMed ID: 7351073
    [Abstract] [Full Text] [Related]

  • 27. Variations in globin chain synthesis in hereditary persistence of fetal haemoglobin.
    Friedman S, Schwartz E, Ahern E, Ahern V.
    Br J Haematol; 1976 Mar 01; 32(3):357-64. PubMed ID: 1252370
    [Abstract] [Full Text] [Related]

  • 28. Molecular analysis of the beta-thalassemia phenotype associated with inheritance of hemoglobin E (alpha 2 beta2(26)Glu leads to Lys).
    Benz EJ, Berman BW, Tonkonow BL, Coupal E, Coates T, Boxer LA, Altman A, Adams JG.
    J Clin Invest; 1981 Jul 01; 68(1):118-26. PubMed ID: 6166632
    [Abstract] [Full Text] [Related]

  • 29. Hemoglobin S-O Arab-alpha-thalassemia: globin biosynthesis and clinical picture.
    Ballas SK, Atwater J, Burka ER.
    Hemoglobin; 1977 Jul 01; 1(7):651-62. PubMed ID: 914640
    [Abstract] [Full Text] [Related]

  • 30. Globin synthesis in fractionated Normoblasts of beta-thalassemia heterozygotes.
    Wood WG, Stamatoyannopoulos G.
    J Clin Invest; 1975 Mar 01; 55(3):567-78. PubMed ID: 1167870
    [Abstract] [Full Text] [Related]

  • 31. Preferential binding of beta C relative to beta S globin to stroma in hemoglobin SC disease.
    Natta C, Muir M.
    Hemoglobin; 1980 Mar 01; 4(2):157-63. PubMed ID: 7390861
    [Abstract] [Full Text] [Related]

  • 32. Sickle cell anemia and trait in southern India: further studies.
    Brittenham G, Lozoff B, Harris JW, Mayson SM, Miller A, Huisman TH.
    Am J Hematol; 1979 Mar 01; 6(2):107-23. PubMed ID: 474571
    [Abstract] [Full Text] [Related]

  • 33. Two new sickle cell syndromes: HbS, Hb Camden, and alpha-thalassemia; and HbS in combination with Hb Tacoma.
    Honig GR, Mason RG, Shamsuddin M, Vida LN, Rao KR, Patel AR.
    Blood; 1980 Apr 01; 55(4):655-60. PubMed ID: 7357091
    [Abstract] [Full Text] [Related]

  • 34. Further evidence of a quantitative deficiency of chain-specific globin mRNA in the thalassemia syndromes.
    Kazazian HH, Ginder GD, Snyder PG, Van Beneden RJ, Woodhead AP.
    Proc Natl Acad Sci U S A; 1975 Feb 01; 72(2):567-71. PubMed ID: 1054838
    [Abstract] [Full Text] [Related]

  • 35. Haemoglobin C/alpha thalassaemia: haematological and biosynthetic studies.
    Steinberg MH.
    Br J Haematol; 1975 Jul 01; 30(3):337-42. PubMed ID: 1201216
    [Abstract] [Full Text] [Related]

  • 36. Hereditary Persistence of Fetal Hemoglobin Caused by Single Nucleotide Promoter Mutations in Sickle Cell Trait and Hb SC Disease.
    Akinbami AO, Campbell AD, Han ZJ, Luo HY, Chui DH, Steinberg MH.
    Hemoglobin; 2016 Jul 01; 40(1):64-5. PubMed ID: 26372199
    [Abstract] [Full Text] [Related]

  • 37. Sickle cell disease due to compound heterozygosity for Hb S and a novel 7.7-kb beta-globin gene deletion.
    Andersson BA, Wering ME, Luo HY, Basran RK, Steinberg MH, Smith HP, Chui DH.
    Eur J Haematol; 2007 Jan 01; 78(1):82-5. PubMed ID: 17038017
    [Abstract] [Full Text] [Related]

  • 38. Hb F in sickle cell anemia.
    Adekile AD, Huisman TH.
    Experientia; 1993 Jan 15; 49(1):16-27. PubMed ID: 7679078
    [Abstract] [Full Text] [Related]

  • 39. Prenatal diagnosis of hemoglobinopathies: comparison of the results obtained by isoelectric focusing of hemoglobins and by chromatography of radioactive globin chains.
    Dubart A, Goossens M, Beuzard Y, Monplaisir N, Testa U, Basset P, Rosa J.
    Blood; 1980 Dec 15; 56(6):1092-9. PubMed ID: 6159934
    [Abstract] [Full Text] [Related]

  • 40. Adult hemoglobin levels in newborn babies from different countries and in babies with some significant hemoglobinopathies.
    Kutlar F, Kutlar A, Gu YC, Huisman TH.
    Acta Haematol; 1987 Dec 15; 78(1):28-32. PubMed ID: 3116804
    [Abstract] [Full Text] [Related]

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