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124 related items for PubMed ID: 7493679

  • 1. Globin chain turnover in reticulocytes from patients with beta (0) -thalassaemia/Hb E disease.
    Kalpravidh RW, Komolvanich S, Wilairat P, Fucharoen S.
    Eur J Haematol; 1995 Nov; 55(5):322-6. PubMed ID: 7493679
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  • 2. Observations on the relationship between gamma-globin chain content and globin chain precipitation in thalassaemic erythroblasts and on the composition of erythroblastic inclusions in HbE/beta-thalassaemia.
    Wickramasinghe SN, Lee MJ.
    Eur J Haematol; 1997 Nov; 59(5):305-9. PubMed ID: 9414642
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  • 3. Implication of globin gene expression, hemoglobin F and hemoglobin E levels on β-thalassemia/Hb E disease severity.
    Siriworadechkul S, Jindadamrongwech S, Chuncharunee S, Aupparakkitanon S.
    Ann Clin Lab Sci; 2014 Nov; 44(4):437-42. PubMed ID: 25361929
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  • 4. Bone marrow and peripheral blood globin chain synthesis in sickle cell beta zero thalassaemia.
    Costa FF, Zago MA.
    J Med Genet; 1986 Jun; 23(3):252-5. PubMed ID: 3723554
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  • 5. The triplicated alpha-globin gene locus in beta-thalassaemia heterozygotes: clinical, haematological, biosynthetic and molecular studies.
    Traeger-Synodinos J, Kanavakis E, Vrettou C, Maragoudaki E, Michael T, Metaxotou-Mavromati A, Kattamis C.
    Br J Haematol; 1996 Dec; 95(3):467-71. PubMed ID: 8943886
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  • 6. betaS Chain turnover in reticulocytes of sickle trait individuals with high or low concentrations of haemoglobin S.
    Shaeffer JR, Kleve LJ, DeSimone J.
    Br J Haematol; 1976 Mar; 32(3):365-72. PubMed ID: 1252371
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  • 7. Interaction between beta-thalassaemia and Hb G Philadelphia associated with alpha-thalassaemia.
    Stathopoulou R, Sulis E, Lehmann H.
    Acta Haematol; 1979 Mar; 62(2):106-11. PubMed ID: 119398
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  • 8. Unbalanced globin chain synthesis in erythroid precursor cells of heterozygous alpha-thalassaemia.
    Steinberg MH, Coleman M, Dreiling B.
    Br J Haematol; 1976 Sep; 34(1):55-60. PubMed ID: 952769
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  • 9. Globin biosynthesis in erythroid bursts of heterozygous alpha or beta thalassaemia.
    Steinberg MH, Coleman MB, Pressley A, Adams JG.
    Br J Haematol; 1981 Jan; 47(1):57-65. PubMed ID: 7437346
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  • 13. 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; 68(1):118-26. PubMed ID: 6166632
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  • 15. Should we screen for globin gene mutations in blood samples with mean corpuscular volume (MCV) greater than 80 fL in areas with a high prevalence of thalassaemia?
    Chan LC, Ma SK, Chan AY, Ha SY, Waye JS, Lau YL, Chui DH.
    J Clin Pathol; 2001 Apr; 54(4):317-20. PubMed ID: 11304851
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  • 17. Molecular characteristics of a non-deletion alpha-thalassaemia of the Po River Delta.
    del Senno L, Bernardi F, Buzzoni D, Marchetti G, Perrotta C, Conconi F.
    Eur J Biochem; 1981 May; 116(1):127-30. PubMed ID: 7250116
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  • 18. ATP-dependent proteolysis of hemoglobin alpha chains in beta-thalassemic hemolysates is ubiquitin-dependent.
    Shaeffer JR.
    J Biol Chem; 1988 Sep 25; 263(27):13663-9. PubMed ID: 2843527
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  • 19. Mitochondrial Changes in β0-Thalassemia/Hb E Disease.
    Khungwanmaythawee K, Sornjai W, Paemanee A, Jaratsittisin J, Fucharoen S, Svasti S, Lithanatudom P, Roytrakul S, Smith DR.
    PLoS One; 2016 Sep 25; 11(4):e0153831. PubMed ID: 27092778
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