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Journal Abstract Search

300 related items for PubMed ID: 15545996

  • 1. Loss of alpha-hemoglobin-stabilizing protein impairs erythropoiesis and exacerbates beta-thalassemia.
    Kong Y, Zhou S, Kihm AJ, Katein AM, Yu X, Gell DA, Mackay JP, Adachi K, Foster-Brown L, Louden CS, Gow AJ, Weiss MJ.
    J Clin Invest; 2004 Nov; 114(10):1457-66. PubMed ID: 15545996
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  • 3. An abundant erythroid protein that stabilizes free alpha-haemoglobin.
    Kihm AJ, Kong Y, Hong W, Russell JE, Rouda S, Adachi K, Simon MC, Blobel GA, Weiss MJ.
    Nature; 2002 Jun 13; 417(6890):758-63. PubMed ID: 12066189
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  • 5. Impaired binding of AHSP to alpha chain variants: Hb Groene Hart illustrates a mechanism leading to unstable hemoglobins with alpha thalassemic like syndrome.
    Vasseur-Godbillon C, Marden MC, Giordano P, Wajcman H, Baudin-Creuza V.
    Blood Cells Mol Dis; 2006 Jun 13; 37(3):173-9. PubMed ID: 17052927
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  • 6. Transgenic human alpha-hemoglobin stabilizing protein could partially relieve betaIVS-2-654-thalassemia syndrome in model mice.
    Wang B, Fang Y, Guo X, Ren Z, Zhang J.
    Hum Gene Ther; 2010 Feb 13; 21(2):149-56. PubMed ID: 20063986
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  • 7. α-Hemoglobin stabilizing protein: a modulating factor in thalassemias?
    Wajcman H, Vasseur C, Pissard S, Baudin-Creuza V.
    Hemoglobin; 2011 Feb 13; 35(5-6):463-8. PubMed ID: 21950764
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  • 8. [Role of alpha-hemoglobin molecular chaperone in the hemoglobin formation and clinical expression of some hemoglobinopathies].
    Vasseur C, Baudin-Creuza V.
    Transfus Clin Biol; 2015 Mar 13; 22(1):49-57. PubMed ID: 25724329
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  • 9. Dynamics of α-Hb chain binding to its chaperone AHSP depends on heme coordination and redox state.
    Kiger L, Vasseur C, Domingues-Hamdi E, Truan G, Marden MC, Baudin-Creuza V.
    Biochim Biophys Acta; 2014 Jan 13; 1840(1):277-87. PubMed ID: 24060751
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  • 10. 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 13; 36(3):265-72. PubMed ID: 18179859
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  • 11. An erythroid chaperone that facilitates folding of alpha-globin subunits for hemoglobin synthesis.
    Yu X, Kong Y, Dore LC, Abdulmalik O, Katein AM, Zhou S, Choi JK, Gell D, Mackay JP, Gow AJ, Weiss MJ.
    J Clin Invest; 2007 Jul 13; 117(7):1856-65. PubMed ID: 17607360
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  • 12. Oxidative instability of hemoglobin E (β26 Glu→Lys) is increased in the presence of free α subunits and reversed by α-hemoglobin stabilizing protein (AHSP): Relevance to HbE/β-thalassemia.
    Strader MB, Kassa T, Meng F, Wood FB, Hirsch RE, Friedman JM, Alayash AI.
    Redox Biol; 2016 Aug 13; 8():363-74. PubMed ID: 26995402
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  • 14. Study of alpha hemoglobin stabilizing protein expression in patients with β thalassemia and sickle cell anemia and its impact on clinical severity.
    Mahmoud HM, Shoeib AA, Abd El Ghany SM, Reda MM, Ragab IA.
    Blood Cells Mol Dis; 2015 Dec 13; 55(4):358-62. PubMed ID: 26460260
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  • 20. Role of α-globin H helix in the building of tetrameric human hemoglobin: interaction with α-hemoglobin stabilizing protein (AHSP) and heme molecule.
    Domingues-Hamdi E, Vasseur C, Fournier JB, Marden MC, Wajcman H, Baudin-Creuza V.
    PLoS One; 2014 Dec 13; 9(11):e111395. PubMed ID: 25369055
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