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314 related items for PubMed ID: 24795058

  • 1. 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; 44(2):189-93. PubMed ID: 24795058
    [Abstract] [Full Text] [Related]

  • 2. Alpha hemoglobin stabilizing protein: Its causal relationship with the severity of beta thalassemia.
    Sagar CS, Kumar R, Sharma DC, Kishor P.
    Blood Cells Mol Dis; 2015 Aug; 55(2):104-7. PubMed ID: 26142324
    [Abstract] [Full Text] [Related]

  • 3. α-Haemoglobin stabilising protein expression is influenced by mean cell haemoglobin and HbF levels in HbE/β-thalassaemia individuals.
    Lim WF, Muniandi L, George E, Sathar J, Teh LK, Gan GG, Lai MI.
    Blood Cells Mol Dis; 2012 Jan 15; 48(1):17-21. PubMed ID: 22079025
    [Abstract] [Full Text] [Related]

  • 4. AHSP and beta-thalassemia: a possible genetic modifier.
    dos Santos CO, Costa FF.
    Hematology; 2005 Apr 15; 10(2):157-61. PubMed ID: 16019463
    [Abstract] [Full Text] [Related]

  • 5. Association of alpha hemoglobin-stabilizing protein (AHSP) gene mutation and disease severity among HbE-beta thalassemia patients.
    Ray R, Kalantri SA, Bhattacharjee S, Biswas A, Shahab A, Biswas S, Bhattacharyya M.
    Ann Hematol; 2019 Aug 15; 98(8):1827-1834. PubMed ID: 31190133
    [Abstract] [Full Text] [Related]

  • 6. Review: Beta-thalassemia and molecular chaperones.
    Sumera A, Radhakrishnan A, Baba AA, George E.
    Blood Cells Mol Dis; 2015 Apr 15; 54(4):348-52. PubMed ID: 25648458
    [Abstract] [Full Text] [Related]

  • 7. 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
    [Abstract] [Full Text] [Related]

  • 8. 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 01; 9(11):e111395. PubMed ID: 25369055
    [Abstract] [Full Text] [Related]

  • 9. 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 01; 55(4):358-62. PubMed ID: 26460260
    [Abstract] [Full Text] [Related]

  • 10. Analysis of alpha-hemoglobin-stabilizing protein (AHSP) gene as a genetic modifier to the phenotype of beta-thalassemia in Southern China.
    Wang Z, Yu W, Li Y, Shang X, Zhang X, Xiong F, Xu X.
    Blood Cells Mol Dis; 2010 Aug 15; 45(2):128-32. PubMed ID: 20627634
    [Abstract] [Full Text] [Related]

  • 11. 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 15; 21(2):149-56. PubMed ID: 20063986
    [Abstract] [Full Text] [Related]

  • 12. Analysis of β/α globin ratio by using relative qRT-PCR for diagnosis of beta-thalassemia carriers.
    Ranjbaran R, Okhovat MA, Mobarhanfard A, Aboualizadeh F, Abbasi M, Moezzi L, Golafshan HA, Behzad-Behbahani A, Bagheri M, Sharifzadeh S.
    J Clin Lab Anal; 2013 Jul 15; 27(4):267-71. PubMed ID: 23852782
    [Abstract] [Full Text] [Related]

  • 13. Impact of α-Globin Gene Expression and α-Globin Modifiers on the Phenotype of β-Thalassemia and Other Hemoglobinopathies: Implications for Patient Management.
    Traeger-Synodinos J, Vrettou C, Sofocleous C, Zurlo M, Finotti A, Gambari R, International Hemoglobinopathy Research Network (INHERENT).
    Int J Mol Sci; 2024 Mar 17; 25(6):. PubMed ID: 38542374
    [Abstract] [Full Text] [Related]

  • 14. α-Hemoglobin stabilizing protein: a modulating factor in thalassemias?
    Wajcman H, Vasseur C, Pissard S, Baudin-Creuza V.
    Hemoglobin; 2011 Mar 17; 35(5-6):463-8. PubMed ID: 21950764
    [Abstract] [Full Text] [Related]

  • 15. Analysis of alpha hemoglobin stabilizing protein overexpression in murine β-thalassemia.
    Nasimuzzaman M, Khandros E, Wang X, Kong Y, Zhao H, Weiss D, Rivella S, Weiss MJ, Persons DA.
    Am J Hematol; 2010 Oct 17; 85(10):820-2. PubMed ID: 20815047
    [Abstract] [Full Text] [Related]

  • 16. Analysis of human alpha globin gene mutations that impair binding to the alpha hemoglobin stabilizing protein.
    Yu X, Mollan TL, Butler A, Gow AJ, Olson JS, Weiss MJ.
    Blood; 2009 Jun 04; 113(23):5961-9. PubMed ID: 19349619
    [Abstract] [Full Text] [Related]

  • 17. Alpha-hemoglobin-stabilizing protein (AHSP): a modulatory factor in β-thalassemia.
    Che Yaacob NS, Islam MA, Alsaleh H, Ibrahim IK, Hassan R.
    Int J Hematol; 2020 Mar 04; 111(3):352-359. PubMed ID: 31894534
    [Abstract] [Full Text] [Related]

  • 18. Molecular analysis of globin gene expression in different thalassaemia disorders: individual variation of β(E) pre-mRNA splicing determine disease severity.
    Tubsuwan A, Munkongdee T, Jearawiriyapaisarn N, Boonchoy C, Winichagoon P, Fucharoen S, Svasti S.
    Br J Haematol; 2011 Sep 04; 154(5):635-43. PubMed ID: 21732929
    [Abstract] [Full Text] [Related]

  • 19. The Chaperones Involved in Hemoglobin Synthesis Take the Spotlight: Analysis of AHSP in the Argentinean Population and Review of the Literature.
    Scheps KG, Varela V, Targovnik HM.
    Hemoglobin; 2018 Sep 04; 42(5-6):310-314. PubMed ID: 30558442
    [Abstract] [Full Text] [Related]

  • 20. 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 Sep 04; 1054():103-17. PubMed ID: 16339656
    [Abstract] [Full Text] [Related]

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