BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

166 related articles for article (PubMed ID: 20063986)

  • 1. 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; 21(2):149-56. PubMed ID: 20063986
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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; 1054():103-17. PubMed ID: 16339656
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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; 98(8):1827-1834. PubMed ID: 31190133
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A novel transgenic mouse model produced from lentiviral germline integration for the study of beta-thalassemia gene therapy.
    Li W; Xie S; Guo X; Gong X; Wang S; Lin D; Zhang J; Ren Z; Huang S; Zeng F; Zeng Y
    Haematologica; 2008 Mar; 93(3):356-62. PubMed ID: 18268280
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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; 111(3):352-359. PubMed ID: 31894534
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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; 117(7):1856-65. PubMed ID: 17607360
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Molecular mechanism of AHSP-mediated stabilization of alpha-hemoglobin.
    Feng L; Gell DA; Zhou S; Gu L; Kong Y; Li J; Hu M; Yan N; Lee C; Rich AM; Armstrong RS; Lay PA; Gow AJ; Weiss MJ; Mackay JP; Shi Y
    Cell; 2004 Nov; 119(5):629-40. PubMed ID: 15550245
    [TBL] [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; 55(4):358-62. PubMed ID: 26460260
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Biochemical fates of alpha hemoglobin bound to alpha hemoglobin-stabilizing protein AHSP.
    Zhou S; Olson JS; Fabian M; Weiss MJ; Gow AJ
    J Biol Chem; 2006 Oct; 281(43):32611-8. PubMed ID: 16901899
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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; 45(2):128-32. PubMed ID: 20627634
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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; 85(10):820-2. PubMed ID: 20815047
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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; 50():102239. PubMed ID: 35092867
    [TBL] [Abstract][Full Text] [Related]  

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

  • 19. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 20. AHSP: a novel hemoglobin helper.
    Bank A
    J Clin Invest; 2007 Jul; 117(7):1746-9. PubMed ID: 17607349
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.