129 related articles for article (PubMed ID: 15102476)
1. Expression of alpha-hemoglobin stabilizing protein gene during human erythropoiesis.
dos Santos CO; Duarte AS; Saad ST; Costa FF
Exp Hematol; 2004 Feb; 32(2):157-62. PubMed ID: 15102476
[TBL] [Abstract][Full Text] [Related]
2. 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; 36(3):265-72. PubMed ID: 18179859
[TBL] [Abstract][Full Text] [Related]
3. Expression of alpha-hemoglobin stabilizing protein and cellular prion protein in a subclone of murine erythroleukemia cell line MEL.
Otsuka Y; Ito D; Katsuoka K; Arashiki N; Komatsu T; Inaba M
Jpn J Vet Res; 2008 Aug; 56(2):75-84. PubMed ID: 18828445
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
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. A twins heritability study on alpha hemoglobin stabilizing protein (AHSP) expression variability.
Lai MI; Garner C; Jiang J; Silver N; Best S; Menzel S; Thein SL
Twin Res Hum Genet; 2010 Dec; 13(6):567-72. PubMed ID: 21142933
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. GATA-1 and Oct-1 are required for expression of the human alpha-hemoglobin-stabilizing protein gene.
Gallagher PG; Liem RI; Wong E; Weiss MJ; Bodine DM
J Biol Chem; 2005 Nov; 280(47):39016-23. PubMed ID: 16186125
[TBL] [Abstract][Full Text] [Related]
10. 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; 9(11):e111395. PubMed ID: 25369055
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. 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
[TBL] [Abstract][Full Text] [Related]
14. Hsp90 chaperones hemoglobin maturation in erythroid and nonerythroid cells.
Ghosh A; Garee G; Sweeny EA; Nakamura Y; Stuehr DJ
Proc Natl Acad Sci U S A; 2018 Feb; 115(6):E1117-E1126. PubMed ID: 29358373
[TBL] [Abstract][Full Text] [Related]
15. 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; 417(6890):758-63. PubMed ID: 12066189
[TBL] [Abstract][Full Text] [Related]
16. NF-E2: a novel regulator of alpha-hemoglobin stabilizing protein gene expression.
Guo-wei Z; Rui-feng Y; Xiang L; Mitchell WJ; De-pei L; Chih-chuan L
Chin Med Sci J; 2010 Dec; 25(4):193-8. PubMed ID: 21232177
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. 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]
20. Activation of STAT3 stimulates AHSP expression in K562 cells.
Cao C; Zhao G; Yu W; Xie X; Wang W; Yang R; Lv X; Liu D
Sci China Life Sci; 2014 May; 57(5):488-94. PubMed ID: 24740453
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]