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Journal Abstract Search

257 related items for PubMed ID: 21264907

  • 1. 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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  • 4. 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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  • 9. 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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  • 11. Relationship between AHSP gene expression, β/α globin mRNA ratio, and clinical severity of the β-thalassemia patients.
    Ranjbaran R, Okhovat MA, Mobarhanfard A, Aboualizadeh F, Abbasi M, Moezzi L, Golafshan HA, Behzad-Behbahani A, Bagheri M, Sharifzadeh S.
    Ann Clin Lab Sci; 2014 Nov; 44(2):189-93. PubMed ID: 24795058
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  • 12. High-yield expression in Escherichia coli of soluble human alpha-hemoglobin complexed with its molecular chaperone.
    Vasseur-Godbillon C, Hamdane D, Marden MC, Baudin-Creuza V.
    Protein Eng Des Sel; 2006 Mar; 19(3):91-7. PubMed ID: 16390839
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  • 14. Red blood cells free α-haemoglobin pool: a biomarker to monitor the β-thalassemia intermedia variability. The ALPHAPOOL study.
    Vasseur C, Domingues-Hamdi E, Ledudal K, Le Corvoisier P, Barau C, Ghaleh B, Rialland A, Pissard S, Galactéros F, Baudin-Creuza V.
    Br J Haematol; 2017 Oct; 179(1):142-153. PubMed ID: 28643346
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  • 15. Role of alpha-hemoglobin-stabilizing protein in normal erythropoiesis and beta-thalassemia.
    Weiss MJ, Zhou S, Feng L, Gell DA, Mackay JP, Shi Y, Gow AJ.
    Ann N Y Acad Sci; 2005 Oct; 1054():103-17. PubMed ID: 16339656
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  • 16. [Use of capillary electrophoresis to determine hemoglobin A2 in healthy adults and alpha- and beta-thalassemia carriers].
    Hua L, Li J, Liu ZY, Zhong HZ, Liao C, Xu XM.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Oct; 20(5):421-4. PubMed ID: 14556197
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  • 19. Coinheritance of the different copy numbers of alpha-globin gene modifies severity of beta-thalassemia/Hb E disease.
    Sripichai O, Munkongdee T, Kumkhaek C, Svasti S, Winichagoon P, Fucharoen S.
    Ann Hematol; 2008 May; 87(5):375-9. PubMed ID: 18026953
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