-
1
-
-
0034820416
-
Pharmacologic modulation of fetal hemoglobin
-
Steinberg MH, Rodgers GP. Pharmacologic modulation of fetal hemoglobin. Medicine (Baltimore). 2001;80(5):328-344.
-
(2001)
Medicine (Baltimore)
, vol.80
, Issue.5
, pp. 328-344
-
-
Steinberg, M.H.1
Rodgers, G.P.2
-
2
-
-
20044367676
-
Predicting clinical severity in sickle cell anemia
-
Steinberg MH. Predicting clinical severity in sickle cell anemia. Brit J Haematol. 2005;129(4): 465-481.
-
(2005)
Brit J Haematol
, vol.129
, Issue.4
, pp. 465-481
-
-
Steinberg, M.H.1
-
3
-
-
0015492354
-
Benign sickle anemia
-
Perrine RP, Brown MJ, Clegg JB, Weatherall DJ, May A. Benign sickle anemia. Lancet. 1972;2(7788):1163-1167.
-
(1972)
Lancet
, vol.2
, Issue.7788
, pp. 1163-1167
-
-
Perrine, R.P.1
Brown, M.J.2
Clegg, J.B.3
Weatherall, D.J.4
May, A.5
-
4
-
-
0025770390
-
Pain in sickle cell disease. Rates and risk factors
-
Platt OS, Thorington BD, Brambilla DJ, et al. Pain in sickle cell disease. Rates and risk factors. N Engl J Med. 1991;325(1):11-16.
-
(1991)
N Engl J Med
, vol.325
, Issue.1
, pp. 11-16
-
-
Platt, O.S.1
Thorington, B.D.2
Brambilla, D.J.3
-
5
-
-
0028291736
-
Mortality in sickle cells disease: Life expectancy and risk factors for early death
-
Platt OS, Brambilla DJ, Rosse WF, Milner PF, et al. Mortality in sickle cells disease: Life expectancy and risk factors for early death. N Engl J Med. 1994;330(23):1639-1644.
-
(1994)
N Engl J Med
, vol.330
, Issue.23
, pp. 1639-1644
-
-
Platt, O.S.1
Brambilla, D.J.2
Rosse, W.F.3
Milner, P.F.4
-
6
-
-
0023859033
-
Levels of fetal hemoglobin necessary for treatment of in sickle cell disease
-
Noguchi CT, Rodgers GP, Sergeant G, Schlechter AN. Levels of fetal hemoglobin necessary for treatment of in sickle cell disease. N Engl J Med. 1988;318(2):96-99.
-
(1988)
N Engl J Med
, vol.318
, Issue.2
, pp. 96-99
-
-
Noguchi, C.T.1
Rodgers, G.P.2
Sergeant, G.3
Schlechter, A.N.4
-
7
-
-
33746592856
-
The effect of fetal hemoglobin on the survival characteristics of sickle cells
-
Franco RS, Yasin Z, Palasacak MB, Ciraolo P, Joiner CH, Rucknagel DL. The effect of fetal hemoglobin on the survival characteristics of sickle cells. Blood. 2006;108(3):1073-1076.
-
(2006)
Blood
, vol.108
, Issue.3
, pp. 1073-1076
-
-
Franco, R.S.1
Yasin, Z.2
Palasacak, M.B.3
Ciraolo, P.4
Joiner, C.H.5
Rucknagel, D.L.6
-
8
-
-
33344459039
-
Fetal globin induction - can it cure beta-thalassemia?
-
Perrine SP. Fetal globin induction - can it cure beta-thalassemia? Amer Soc Hematol Education Program. 2005;38-44.
-
(2005)
Amer Soc Hematol Education Program
, pp. 38-44
-
-
Perrine, S.P.1
-
9
-
-
24944465060
-
Beta-thalassemia
-
Rund D, Rachmilewitz E. Beta-thalassemia. N Engl J Med. 2005;353(11):1135-1146.
-
(2005)
N Engl J Med
, vol.353
, Issue.11
, pp. 1135-1146
-
-
Rund, D.1
Rachmilewitz, E.2
-
10
-
-
0018381031
-
The importance of the genetic picture and globin synthesis in determining the clinical and hematological features of thalassemia intermedia
-
Gallo E, Massero P, Miniero R, David D, Tarella C. The importance of the genetic picture and globin synthesis in determining the clinical and hematological features of thalassemia intermedia. Br J Haematol. 1979;41(2):211-221.
-
(1979)
Br J Haematol
, vol.41
, Issue.2
, pp. 211-221
-
-
Gallo, E.1
Massero, P.2
Miniero, R.3
David, D.4
Tarella, C.5
-
11
-
-
0030908559
-
Pathobiology of thalassemic erythrocytes
-
Schrier SL. Pathobiology of thalassemic erythrocytes. Curr Opin Hematol. 1997;4(2):75-78.
-
(1997)
Curr Opin Hematol
, vol.4
, Issue.2
, pp. 75-78
-
-
Schrier, S.L.1
-
12
-
-
0034538786
-
Ineffective erythropoiesis in beta-thalassemia major is due to apoptosis at the polychromatophilic nomoblast stage
-
Mathias LA, Fisher TC, Zeng L, et al. Ineffective erythropoiesis in beta-thalassemia major is due to apoptosis at the polychromatophilic nomoblast stage. Exp Hematol. 2000;28(12):1343-1353.
-
(2000)
Exp Hematol
, vol.28
, Issue.12
, pp. 1343-1353
-
-
Mathias, L.A.1
Fisher, T.C.2
Zeng, L.3
-
13
-
-
0027181636
-
Accelerated programmed cell death (apoptosis) in erythroid precursors of patients with severe beta-thalassemia
-
Yuan J, Angelucci E, Lucarelli G, et al. Accelerated programmed cell death (apoptosis) in erythroid precursors of patients with severe beta-thalassemia. Blood. 1993;82(7):374-377.
-
(1993)
Blood
, vol.82
, Issue.7
, pp. 374-377
-
-
Yuan, J.1
Angelucci, E.2
Lucarelli, G.3
-
14
-
-
0028006103
-
Serum erythropoietin levels and erythropoiesis in high and low-fetal hemoglobin beta-thalassemia intermedia patients
-
Galanello R, Barella S, Turco MP, et al. Serum erythropoietin levels and erythropoiesis in high and low-fetal hemoglobin beta-thalassemia intermedia patients. Blood. 1994;83(2):561-565.
-
(1994)
Blood
, vol.83
, Issue.2
, pp. 561-565
-
-
Galanello, R.1
Barella, S.2
Turco, M.P.3
-
16
-
-
0034307683
-
A correlation of erythrokinetics, ineffective erythropoiesis, erythroid precursor apoptosis in Thai patients with thalassemia
-
Pootrakul P, Sirankapracha P, Hemsorach S, et al. A correlation of erythrokinetics, ineffective erythropoiesis, erythroid precursor apoptosis in Thai patients with thalassemia. Blood. 2000;96(7):2606-2612.
-
(2000)
Blood
, vol.96
, Issue.7
, pp. 2606-2612
-
-
Pootrakul, P.1
Sirankapracha, P.2
Hemsorach, S.3
-
17
-
-
49549085453
-
-
American Society of Hematology Education program
-
Vichinsky E. Hemoglobin E syndromes. American Society of Hematology Education program, 2007:79-83.
-
(2007)
Hemoglobin E syndromes
, pp. 79-83
-
-
Vichinsky, E.1
-
18
-
-
0028120456
-
Pharmacologic treatment of thalassemia intermedia with hydroxyurea
-
Hajjar FM, Pearson HA. Pharmacologic treatment of thalassemia intermedia with hydroxyurea. J Pediatr. 1994;125(3):490-492.
-
(1994)
J Pediatr
, vol.125
, Issue.3
, pp. 490-492
-
-
Hajjar, F.M.1
Pearson, H.A.2
-
19
-
-
13344259315
-
Hydroxyurea increases Hb F levels and improves the effectiveness of erythropoiesis in beta-thalassemia/Hb E disease
-
Fucharoen S, Siritanaratkul N, Winichagoon P, et al. Hydroxyurea increases Hb F levels and improves the effectiveness of erythropoiesis in beta-thalassemia/Hb E disease. Blood. 1996;87(3):887-892.
-
(1996)
Blood
, vol.87
, Issue.3
, pp. 887-892
-
-
Fucharoen, S.1
Siritanaratkul, N.2
Winichagoon, P.3
-
20
-
-
0037414164
-
Effect of hydroxyurea on mortality and morbidity in adult sickle cell anemia: Risks and benefits up to 9 years of treatment
-
Steinberg MH, Barton F, Castro O, et al. Effect of hydroxyurea on mortality and morbidity in adult sickle cell anemia: risks and benefits up to 9 years of treatment. JAMA. 2003;289(13):1645-1651.
-
(2003)
JAMA
, vol.289
, Issue.13
, pp. 1645-1651
-
-
Steinberg, M.H.1
Barton, F.2
Castro, O.3
-
22
-
-
0036096085
-
Predictors of fetal hemoglobin response in children with sickle cell anemia receiving hydroxyurea therapy
-
Ware RE, Eggleston B, Redding-Lallinger R, et al. Predictors of fetal hemoglobin response in children with sickle cell anemia receiving hydroxyurea therapy. Blood. 2002;99(1):10-14.
-
(2002)
Blood
, vol.99
, Issue.1
, pp. 10-14
-
-
Ware, R.E.1
Eggleston, B.2
Redding-Lallinger, R.3
-
23
-
-
1542373662
-
Sustained long-term hematologic efficacy of hydroxyurea at maximum tolerated dose in children with sickle cell disease
-
Zimmerman SA, Schultz WH, Davis JS, et al. Sustained long-term hematologic efficacy of hydroxyurea at maximum tolerated dose in children with sickle cell disease. Blood. 2004;103(6):2039-2045.
-
(2004)
Blood
, vol.103
, Issue.6
, pp. 2039-2045
-
-
Zimmerman, S.A.1
Schultz, W.H.2
Davis, J.S.3
-
24
-
-
0030893396
-
Fetal hemoglobin in sickle cell anemia: Determinants of response to hydroxyurea
-
Steinberg MH, Lu ZH, Barton FB, Terrin ML, Charache S, Dover GJ. Fetal hemoglobin in sickle cell anemia: determinants of response to hydroxyurea. Blood. 1997;89(3):1078-1088.
-
(1997)
Blood
, vol.89
, Issue.3
, pp. 1078-1088
-
-
Steinberg, M.H.1
Lu, Z.H.2
Barton, F.B.3
Terrin, M.L.4
Charache, S.5
Dover, G.J.6
-
25
-
-
0037414164
-
Effects of hydroxyurea on mortality and morbidity in adult sickle cell anemia: Risks and benefits up to 9 years of treatment
-
Steinberg MH, Barton F, Castro O, et al. Effects of hydroxyurea on mortality and morbidity in adult sickle cell anemia: risks and benefits up to 9 years of treatment. JAMA. 2003;289(13):1645-1651.
-
(2003)
JAMA
, vol.289
, Issue.13
, pp. 1645-1651
-
-
Steinberg, M.H.1
Barton, F.2
Castro, O.3
-
26
-
-
0035666461
-
A two year pilot trial of hydroxyurea in very young children with sickle cell anemia
-
Wang WC, et al. A two year pilot trial of hydroxyurea in very young children with sickle cell anemia. J Pediatr. 2001;139:790-796.
-
(2001)
J Pediatr
, vol.139
, pp. 790-796
-
-
Wang, W.C.1
-
27
-
-
0035383785
-
Five years of experience with hydroxyurea in children and young adults with sickle cell disease
-
Ferster C, Tahrir P, Vermylen C, et al. Five years of experience with hydroxyurea in children and young adults with sickle cell disease. Blood. 2001;97(11):3628-3632.
-
(2001)
Blood
, vol.97
, Issue.11
, pp. 3628-3632
-
-
Ferster, C.1
Tahrir, P.2
Vermylen, C.3
-
28
-
-
1542373662
-
Sustained long-term hematologic efficacy of hydroxyurea at maximum tolerated dose in children with sickle cell disease
-
Zimmerman SA, Schultz WH, Davis JS, et al. Sustained long-term hematologic efficacy of hydroxyurea at maximum tolerated dose in children with sickle cell disease. Blood. 2004;103(6):2039-2045.
-
(2004)
Blood
, vol.103
, Issue.6
, pp. 2039-2045
-
-
Zimmerman, S.A.1
Schultz, W.H.2
Davis, J.S.3
-
29
-
-
0027051389
-
Augmentation by erythropoietin of the fetal hemoglobin response to hydroxyurea in sickle cell disease
-
Rodgers GP, Dover GJ, Uyesaka N, Noguchi CT, Schechter AN, Nienhuis AW. Augmentation by erythropoietin of the fetal hemoglobin response to hydroxyurea in sickle cell disease. N Engl J Med. 1993;328(2):73-80.
-
(1993)
N Engl J Med
, vol.328
, Issue.2
, pp. 73-80
-
-
Rodgers, G.P.1
Dover, G.J.2
Uyesaka, N.3
Noguchi, C.T.4
Schechter, A.N.5
Nienhuis, A.W.6
-
30
-
-
0036625004
-
Maintenance of elevated fetal hemoglobin levels by decitabine during dose interval treatment of sickle cell anemia
-
DeSimone J, Koshy M, Dorn L, et al. Maintenance of elevated fetal hemoglobin levels by decitabine during dose interval treatment of sickle cell anemia. Blood. 2002:99(11):3905-3908.
-
(2002)
Blood
, vol.99
, Issue.11
, pp. 3905-3908
-
-
DeSimone, J.1
Koshy, M.2
Dorn, L.3
-
31
-
-
0020466344
-
5-Azacytidine selectively increases gamma-globin synthesis in a patient with beta-thalassemia
-
Ley TJ, DeSimone J, Anagou NP, et al. 5-Azacytidine selectively increases gamma-globin synthesis in a patient with beta-thalassemia. N Eng J Med. 1982;307(24):1469-1475
-
(1982)
N Eng J Med
, vol.307
, Issue.24
, pp. 1469-1475
-
-
Ley, T.J.1
DeSimone, J.2
Anagou, N.P.3
-
32
-
-
0024338898
-
5-Azacytidine treatment in a beta (0)-thalassemic patient unable to be transfused due to multiple allo-antibodies
-
Dunbar C, Travis W, Kan YW, Nienhuis AW. 5-Azacytidine treatment in a beta (0)-thalassemic patient unable to be transfused due to multiple allo-antibodies. Br J Haematol. 1989;72:467-468
-
(1989)
Br J Haematol
, vol.72
, pp. 467-468
-
-
Dunbar, C.1
Travis, W.2
Kan, Y.W.3
Nienhuis, A.W.4
-
33
-
-
0027274649
-
Brief report: Treatment with azacitidine of patients with end-stage beta-thalassemia
-
Lowrey CH, Nienhuis AW. Brief report: treatment with azacitidine of patients with end-stage beta-thalassemia. N Eng J Med. 1993;329(12):845-848.
-
(1993)
N Eng J Med
, vol.329
, Issue.12
, pp. 845-848
-
-
Lowrey, C.H.1
Nienhuis, A.W.2
-
34
-
-
0020563258
-
5-azacytidine increases gamma globin synthesis and reduces the proportion of dense cells in patients with sickle cell anemia
-
Ley TJ, DeSimone J, Noguchi CT. 5-azacytidine increases gamma globin synthesis and reduces the proportion of dense cells in patients with sickle cell anemia. Blood. 1983;62(2):370-380.
-
(1983)
Blood
, vol.62
, Issue.2
, pp. 370-380
-
-
Ley, T.J.1
DeSimone, J.2
Noguchi, C.T.3
-
35
-
-
0034307656
-
2-deoxy 5-azacytidine and fetal hemoglobin induction in sickle cell anemia
-
Koshy M, Dorn L, Bressler L, et al. 2-deoxy 5-azacytidine and fetal hemoglobin induction in sickle cell anemia. Blood. 2000;96(7):2379-2384.
-
(2000)
Blood
, vol.96
, Issue.7
, pp. 2379-2384
-
-
Koshy, M.1
Dorn, L.2
Bressler, L.3
-
36
-
-
10744231450
-
Effects of 5-aza-2-deoxycytidine on fetal hemoglobin levels, red cell adhesion, and hematopoietic differentiation in sickle cell disease
-
Sauntharararajah Y, Hillery CA, Lavelle D, et al. Effects of 5-aza-2-deoxycytidine on fetal hemoglobin levels, red cell adhesion, and hematopoietic differentiation in sickle cell disease. Blood. 2003;102(12):3865-3870.
-
(2003)
Blood
, vol.102
, Issue.12
, pp. 3865-3870
-
-
Sauntharararajah, Y.1
Hillery, C.A.2
Lavelle, D.3
-
37
-
-
0027078611
-
A short-term trial of butyrate to stimulate fetal-globin-gene expression in the beta-globin disorders
-
Perrine SP, Ginder G, Faller DV, et al. A short-term trial of butyrate to stimulate fetal-globin-gene expression in the beta-globin disorders. N Eng J Med. 1993;328(2):129-131.
-
(1993)
N Eng J Med
, vol.328
, Issue.2
, pp. 129-131
-
-
Perrine, S.P.1
Ginder, G.2
Faller, D.V.3
-
38
-
-
0033559320
-
Sustained induction of fetal hemoglobin by pulse butyrate therapy in sickle cell disease
-
Atweh GF, Sutton M, Nassif I, et al. Sustained induction of fetal hemoglobin by pulse butyrate therapy in sickle cell disease. Blood. 1999;93(6):1790-1797.
-
(1999)
Blood
, vol.93
, Issue.6
, pp. 1790-1797
-
-
Atweh, G.F.1
Sutton, M.2
Nassif, I.3
-
39
-
-
0028303870
-
Induction of fetal hemoglobin production in subjects with sickle cell anemia by oral sodium phenylbutyrate
-
Dover GJ, Brusilow S, Charache S. Induction of fetal hemoglobin production in subjects with sickle cell anemia by oral sodium phenylbutyrate. Blood. 1994;84(1):339-343.
-
(1994)
Blood
, vol.84
, Issue.1
, pp. 339-343
-
-
Dover, G.J.1
Brusilow, S.2
Charache, S.3
-
40
-
-
0028870221
-
Oral sodium phenylbutyrate therapy in homozygous beta-thalassemia:a clinical trial
-
Collins AF, Pearson HA, Giardina P, McDonagh KT, Brusilow SW, Dover GJ. Oral sodium phenylbutyrate therapy in homozygous beta-thalassemia:a clinical trial. Blood. 1995; 85(1):39-34.
-
(1995)
Blood
, vol.85
, Issue.1
, pp. 39-34
-
-
Collins, A.F.1
Pearson, H.A.2
Giardina, P.3
McDonagh, K.T.4
Brusilow, S.W.5
Dover, G.J.6
-
41
-
-
3543107193
-
Alterations in protein-DNA interactions in the gamma-globin gene promoter in response to butyrate therapy
-
Ikuta T, Kan YW, Swerdlow PS, Faller DV, Perrine SP. Alterations in protein-DNA interactions in the gamma-globin gene promoter in response to butyrate therapy. Blood. 1998;92(8):2924-2933.
-
(1998)
Blood
, vol.92
, Issue.8
, pp. 2924-2933
-
-
Ikuta, T.1
Kan, Y.W.2
Swerdlow, P.S.3
Faller, D.V.4
Perrine, S.P.5
-
42
-
-
0034143867
-
Oral isobutyramide therapy in patients with thalassemia intermedia: Results of a phase II open study
-
Cappellini MD, Graziadei G, Ciceri L, et al. Oral isobutyramide therapy in patients with thalassemia intermedia: Results of a phase II open study. Blood Cells Mol Dis. 2000;26:105-111.
-
(2000)
Blood Cells Mol Dis
, vol.26
, pp. 105-111
-
-
Cappellini, M.D.1
Graziadei, G.2
Ciceri, L.3
-
43
-
-
24644483851
-
Butyrate + EPO in beta-thalassemia intermedia: Interim findings of a phase II trial [abstract]
-
Perrine SP, Yang YM, Piga A, et al. Butyrate + EPO in beta-thalassemia intermedia: interim findings of a phase II trial [abstract]. Blood. 2002;100:47a.
-
(2002)
Blood
, vol.100
-
-
Perrine, S.P.1
Yang, Y.M.2
Piga, A.3
-
44
-
-
29744433240
-
Induction of fetal globin in beta-thalassemia: Cellular obstacles and molecular progress
-
Perrine SP, Casteneda SA, Boosalis MS. White GL, Jones BM, Bohacek R. Induction of fetal globin in beta-thalassemia: cellular obstacles and molecular progress. Ann NY Acad Sci. 2005;1054:257-265.
-
(2005)
Ann NY Acad Sci
, vol.1054
, pp. 257-265
-
-
Perrine, S.P.1
Casteneda, S.A.2
Boosalis, M.S.3
White, G.L.4
Jones, B.M.5
Bohacek, R.6
-
45
-
-
0034670051
-
Oral isobutyramide reduces transfusion requirements in some patients with homozygous beta-thalassemia
-
Reich S, Bührer C, Henze G, et al. Oral isobutyramide reduces transfusion requirements in some patients with homozygous beta-thalassemia. Blood. 2000;96(10):3357-3363.
-
(2000)
Blood
, vol.96
, Issue.10
, pp. 3357-3363
-
-
Reich, S.1
Bührer, C.2
Henze, G.3
-
46
-
-
0036899584
-
Induction of fetal Hemoglobin synthesis in children with sickle cell anemia on low dose oral sodium phenylbutyrate therapy
-
Resar L, Segal J, Fitzpatric LK, Friedmann A, Brusilow S, Dover GJ. Induction of fetal Hemoglobin synthesis in children with sickle cell anemia on low dose oral sodium phenylbutyrate therapy. J Pediatr Hematol Oncol. 2002;24(9):737-741.
-
(2002)
J Pediatr Hematol Oncol
, vol.24
, Issue.9
, pp. 737-741
-
-
Resar, L.1
Segal, J.2
Fitzpatric, L.K.3
Friedmann, A.4
Brusilow, S.5
Dover, G.J.6
-
47
-
-
0030748791
-
Treatment of thalassaemia major with phenylbutyrate and hydroxyurea
-
Olivieri NF, Rees DC, Ginder GD, et al. Treatment of thalassaemia major with phenylbutyrate and hydroxyurea. Lancet. 1997;350(9076):491-492.
-
(1997)
Lancet
, vol.350
, Issue.9076
, pp. 491-492
-
-
Olivieri, N.F.1
Rees, D.C.2
Ginder, G.D.3
-
48
-
-
0031024827
-
Administration of high doses of recombinant human erythropoietin to patients with beta-thalassemia intermedia: A preliminary trial
-
Bourantas K, Economou G, Georgiou J. Administration of high doses of recombinant human erythropoietin to patients with beta-thalassemia intermedia: a preliminary trial. Eur J Haematol. 1997;58(1):22-25.
-
(1997)
Eur J Haematol
, vol.58
, Issue.1
, pp. 22-25
-
-
Bourantas, K.1
Economou, G.2
Georgiou, J.3
-
49
-
-
0030450965
-
Recombinant human erythropoietin trial in thalassemia intermedia
-
Nisli G, Kavakli K, Vergin C, Oztop S, Cetingul N. Recombinant human erythropoietin trial in thalassemia intermedia. J Trop Pediatr. 1996;42:330-334.
-
(1996)
J Trop Pediatr
, vol.42
, pp. 330-334
-
-
Nisli, G.1
Kavakli, K.2
Vergin, C.3
Oztop, S.4
Cetingul, N.5
-
50
-
-
0031876330
-
The role of recombinant human erythropoietin in the treatment of thalassemia
-
Rachmilewitz EA, Aker M. The role of recombinant human erythropoietin in the treatment of thalassemia. Ann N Y Acad Sci. 1998;850:129-138.
-
(1998)
Ann N Y Acad Sci
, vol.850
, pp. 129-138
-
-
Rachmilewitz, E.A.1
Aker, M.2
-
51
-
-
45349099429
-
The effect of single and combination drug therapy on previously transfused E/beta-thalassemia patients: Implications on decision-making for therapy
-
Singer ST, Kuypers FA, Coates TD, et al. The effect of single and combination drug therapy on previously transfused E/beta-thalassemia patients: Implications on decision-making for therapy. Blood. 2002;100:119a-120a.
-
(2002)
Blood
, vol.100
-
-
Singer, S.T.1
Kuypers, F.A.2
Coates, T.D.3
-
52
-
-
0029794641
-
Erythropoietin can promote erythroid progenitor survival by repressing apoptosis through Bcl-XL and Bcl-2
-
Silva M, Grillot D, Benito A, Richard C, Nunez G, Fernandez-Luna JL. Erythropoietin can promote erythroid progenitor survival by repressing apoptosis through Bcl-XL and Bcl-2. Blood. 1996;88:1576-1582
-
(1996)
Blood
, vol.88
, pp. 1576-1582
-
-
Silva, M.1
Grillot, D.2
Benito, A.3
Richard, C.4
Nunez, G.5
Fernandez-Luna, J.L.6
-
53
-
-
0024466232
-
On the induction of fetal hemoglobin by butyrates: In vivo and in vitro studies with sodium butyrate and comparison of combination treatments with 5-AzaC and AraC
-
Constantoulakis P, Knitter G, Stamatoyannopoulos G. On the induction of fetal hemoglobin by butyrates: in vivo and in vitro studies with sodium butyrate and comparison of combination treatments with 5-AzaC and AraC. Blood. 1989;74(6):1963-1971.
-
(1989)
Blood
, vol.74
, Issue.6
, pp. 1963-1971
-
-
Constantoulakis, P.1
Knitter, G.2
Stamatoyannopoulos, G.3
-
54
-
-
0035874544
-
Short-chain fatty acid derivatives stimulate cell proliferation and induce STAT-5 activation
-
Boosalis MS, Bandyopadhyay R, Bresnick EH, et al. Short-chain fatty acid derivatives stimulate cell proliferation and induce STAT-5 activation. Blood. 2001;97(10):3259-3267.
-
(2001)
Blood
, vol.97
, Issue.10
, pp. 3259-3267
-
-
Boosalis, M.S.1
Bandyopadhyay, R.2
Bresnick, E.H.3
-
56
-
-
0037114756
-
Short-chain fatty acid derivatives induce fetal globin expression and erythropoiesis in vivo
-
Pace BS, White GL, Dover GJ, Boosalis MS, Faller DV, Perrine SP. Short-chain fatty acid derivatives induce fetal globin expression and erythropoiesis in vivo. Blood. 2002;100(13):4640-4648.
-
(2002)
Blood
, vol.100
, Issue.13
, pp. 4640-4648
-
-
Pace, B.S.1
White, G.L.2
Dover, G.J.3
Boosalis, M.S.4
Faller, D.V.5
Perrine, S.P.6
-
57
-
-
0026708201
-
-
Dover GJ, Smith KD, Chang YC, Purvis S, Mays A, Meyers DA, Sheils C, Serjeant G. Fetal hemoglobin levels in sickle cell disease and normal individuals are partially controlled by an X-linked gene located at Xp22.2 Blood. 1992;80(3):816-824.
-
Dover GJ, Smith KD, Chang YC, Purvis S, Mays A, Meyers DA, Sheils C, Serjeant G. Fetal hemoglobin levels in sickle cell disease and normal individuals are partially controlled by an X-linked gene located at Xp22.2 Blood. 1992;80(3):816-824.
-
-
-
-
58
-
-
0346497365
-
Common haplotype dependency of Ggamma globin gene expression and high HbF levels in beta-thalassemia and sickle cell anemia patients
-
Labie D, Pagnier J, Lapoumerolie C, et al. Common haplotype dependency of Ggamma globin gene expression and high HbF levels in beta-thalassemia and sickle cell anemia patients. Proc Natl Acad Sci U S A. 1985;82(7):2111-2114.
-
(1985)
Proc Natl Acad Sci U S A
, vol.82
, Issue.7
, pp. 2111-2114
-
-
Labie, D.1
Pagnier, J.2
Lapoumerolie, C.3
-
59
-
-
0028012604
-
Detection of a major gene for heterocellular heriditary persistence of fetal hemoglobin after accounting for genetic modifiers
-
Thein SL, Sampietro M, Rohde K, et al. Detection of a major gene for heterocellular heriditary persistence of fetal hemoglobin after accounting for genetic modifiers. Am J Hum Genet. 1994;54(2):214-228.
-
(1994)
Am J Hum Genet
, vol.54
, Issue.2
, pp. 214-228
-
-
Thein, S.L.1
Sampietro, M.2
Rohde, K.3
-
60
-
-
0028897283
-
An analysis of fetal hemoglobin variation in sickle cell disease: The relative contributions of the x-linked factors, beta globin haplotypes, alpha globin gene number, gender, and age
-
Chang YC, Smith KD, Moore RD, Serjeant GR, Dover GJ. An analysis of fetal hemoglobin variation in sickle cell disease: the relative contributions of the x-linked factors, beta globin haplotypes, alpha globin gene number, gender, and age. Blood. 1995;85(4):111-1117.
-
(1995)
Blood
, vol.85
, Issue.4
, pp. 111-1117
-
-
Chang, Y.C.1
Smith, K.D.2
Moore, R.D.3
Serjeant, G.R.4
Dover, G.J.5
-
61
-
-
0031779292
-
Haplotype mapping of a major quantitative trait locus for fetal hemoglobin production on chromosome 6q23
-
Garner C, Mitchel J, Hatzis T, Reittie J, Farrail M, Thein SL. Haplotype mapping of a major quantitative trait locus for fetal hemoglobin production on chromosome 6q23. Am J Hum Gen. 1998;62(6):1468-1474.
-
(1998)
Am J Hum Gen
, vol.62
, Issue.6
, pp. 1468-1474
-
-
Garner, C.1
Mitchel, J.2
Hatzis, T.3
Reittie, J.4
Farrail, M.5
Thein, S.L.6
-
62
-
-
45349103518
-
Fetal hemoglobin in sickle cell anemia: Associations with single nucleotide polymorphisms in quantitative trait loci on chromosome 8q12 and Xp22
-
Steinberg MH, Kutlar A, Farrer LA, Baldwin CT. Fetal hemoglobin in sickle cell anemia: associations with single nucleotide polymorphisms in quantitative trait loci on chromosome 8q12 and Xp22. Blood. 2006;108:306a.
-
(2006)
Blood
, vol.108
-
-
Steinberg, M.H.1
Kutlar, A.2
Farrer, L.A.3
Baldwin, C.T.4
-
63
-
-
33746632097
-
cMYB is involved in the regulation of fetal hemoglobin production in adults
-
Jiang J, Best S, Menzel S, et al. cMYB is involved in the regulation of fetal hemoglobin production in adults. Blood. 2006;108(3):1077-1083.
-
(2006)
Blood
, vol.108
, Issue.3
, pp. 1077-1083
-
-
Jiang, J.1
Best, S.2
Menzel, S.3
-
64
-
-
19444376971
-
Drug metabolism and variability among patients in drug response
-
Wilkinson GR. Drug metabolism and variability among patients in drug response. N Eng J Med. 2005;352(21):2211-2221.
-
(2005)
N Eng J Med
, vol.352
, Issue.21
, pp. 2211-2221
-
-
Wilkinson, G.R.1
|