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Journal Abstract Search

314 related items for PubMed ID: 24795058

  • 21.
    ; . PubMed ID:
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  • 22. The correlation of α-globin gene mutations and the XmnI polymorphism with clinical severity of Hb E/β-thalassemia.
    Charoenkwan P, Teerachaimahit P, Sanguansermsri T.
    Hemoglobin; 2014; 38(5):335-8. PubMed ID: 25238043
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  • 23.
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  • 24. Evaluation of the free α-hemoglobin pool in red blood cells: a new test providing a scale of β-thalassemia severity.
    Vasseur C, Pissard S, Domingues-Hamdi E, Marden MC, Galactéros F, Baudin-Creuza V.
    Am J Hematol; 2011 Feb; 86(2):199-202. PubMed ID: 21264907
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  • 25. Evaluation of alpha hemoglobin stabilizing protein (AHSP) as a genetic modifier in patients with beta thalassemia.
    Viprakasit V, Tanphaichitr VS, Chinchang W, Sangkla P, Weiss MJ, Higgs DR.
    Blood; 2004 May 01; 103(9):3296-9. PubMed ID: 14715623
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  • 26.
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  • 27. Reduction of AHSP synthesis in hemin-induced K562 cells and EPO-induced CD34(+) cells leads to alpha-globin precipitation, impairment of normal hemoglobin production, and increased cell death.
    Pinho FO, de Albuquerque DM, Olalla Saad ST, Costa FF.
    Exp Hematol; 2008 Mar 01; 36(3):265-72. PubMed ID: 18179859
    [Abstract] [Full Text] [Related]

  • 28. Compensated variability in the expression of globin-related genes in erythroblasts generated ex vivo from different donors.
    Varricchio L, Fabucci ME, Alfani E, Godbold J, Migliaccio AR.
    Transfusion; 2010 Mar 01; 50(3):672-84. PubMed ID: 19891622
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  • 29.
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  • 30. Association of an α-globin gene cluster duplication and heterozygous β-thalassemia in a patient with a severe thalassemia syndrome.
    Jiang H, Liu S, Zhang YL, Wan JH, Li R, Li DZ.
    Hemoglobin; 2015 Mar 01; 39(2):102-6. PubMed ID: 25690803
    [Abstract] [Full Text] [Related]

  • 31.
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  • 32. Biophysical characterization of the alpha-globin binding protein alpha-hemoglobin stabilizing protein.
    Gell D, Kong Y, Eaton SA, Weiss MJ, Mackay JP.
    J Biol Chem; 2002 Oct 25; 277(43):40602-9. PubMed ID: 12192002
    [Abstract] [Full Text] [Related]

  • 33.
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  • 34. Alpha-haemoglobin stabilising protein is a quantitative trait gene that modifies the phenotype of beta-thalassaemia.
    Lai MI, Jiang J, Silver N, Best S, Menzel S, Mijovic A, Colella S, Ragoussis J, Garner C, Weiss MJ, Thein SL.
    Br J Haematol; 2006 Jun 25; 133(6):675-82. PubMed ID: 16704446
    [Abstract] [Full Text] [Related]

  • 35. Nrf2 expands the intracellular pool of the chaperone AHSP in a cellular model of β-thalassemia.
    Han G, Cao C, Yang X, Zhao GW, Hu XJ, Yu DL, Yang RF, Yang K, Zhang YY, Wang WT, Liu XZ, Xu P, Liu XH, Chen P, Xue Z, Liu DP, Lv X.
    Redox Biol; 2022 Apr 25; 50():102239. PubMed ID: 35092867
    [Abstract] [Full Text] [Related]

  • 36. Detection of germline rearrangements in patients with α- and β-thalassemia using high resolution array CGH.
    Blattner A, Brunner-Agten S, Ludin K, Hergersberg M, Herklotz R, Huber AR, Röthlisberger B.
    Blood Cells Mol Dis; 2013 Jun 25; 51(1):39-47. PubMed ID: 23491071
    [Abstract] [Full Text] [Related]

  • 37. [Quantitative analysis of human globin gene expression in beta-thalassemia using real-time RT-PCR].
    Han JY, Zeng RP, Cheng G, Hu B, Li H, Lai YR.
    Yi Chuan; 2005 Jan 25; 27(1):57-64. PubMed ID: 15730961
    [Abstract] [Full Text] [Related]

  • 38. The associations of SEA-alpha thalassemia 1, XmnI-Ggamma polymorphism and beta-globin gene mutations with the clinical severity of beta-thalassemia syndrome in northern Thailand.
    Tatu T, Sritong W, Sa-Nguansermsri T.
    J Med Assoc Thai; 2014 Mar 25; 97(3):300-7. PubMed ID: 25123009
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  • 39.
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  • 40.
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