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Journal Abstract Search

156 related items for PubMed ID: 17052927

  • 1. 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; 37(3):173-9. PubMed ID: 17052927
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  • 2. α-Hemoglobin stabilizing protein: a modulating factor in thalassemias?
    Wajcman H, Vasseur C, Pissard S, Baudin-Creuza V.
    Hemoglobin; 2011; 35(5-6):463-8. PubMed ID: 21950764
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  • 3. The alpha-hemoglobin stabilizing protein and expression of unstable alpha-Hb variants.
    Vasseur C, Domingues-Hamdi E, Brillet T, Marden MC, Baudin-Creuza V.
    Clin Biochem; 2009 Dec; 42(18):1818-23. PubMed ID: 19482015
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  • 5. 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; 1840(1):277-87. PubMed ID: 24060751
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  • 7. 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 Jan; 9(11):e111395. PubMed ID: 25369055
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  • 14. Distinct phenotypic expression associated with a new hyperunstable alpha globin variant (Hb heraklion, alpha1cd37(C2)Pro>0): comparison to other alpha-thalassemic hemoglobinopathies.
    Traeger-Synodinos J, Papassotiriou I, Metaxotou-Mavrommati A, Vrettou C, Stamoulakatou A, Kanavakis E.
    Blood Cells Mol Dis; 2000 Aug; 26(4):276-84. PubMed ID: 11042028
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  • 15. Transfer of human alpha- to beta-hemoglobin via its chaperone protein: evidence for a new state.
    Baudin-Creuza V, Vasseur-Godbillon C, Pato C, Préhu C, Wajcman H, Marden MC.
    J Biol Chem; 2004 Aug 27; 279(35):36530-3. PubMed ID: 15220346
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  • 16. Alpha-hemoglobin stabilizing protein: molecular function and clinical correlation.
    Turbpaiboon C, Wilairat P.
    Front Biosci (Landmark Ed); 2010 Jan 01; 15(1):1-11. PubMed ID: 20036801
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  • 17. 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 01; 114(10):1457-66. PubMed ID: 15545996
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  • 19. 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 01; 21(2):149-56. PubMed ID: 20063986
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  • 20. Hb Foggia or alpha 117(GH5)Phe -> Ser: a new alpha 2 globin allele affecting the alpha Hb-AHSP interaction.
    Lacerra G, Scarano C, Musollino G, Flagiello A, Pucci P, Carestia C.
    Haematologica; 2008 Jan 01; 93(1):141-2. PubMed ID: 18166800
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