-
1
-
-
0002780275
-
Sickle cell anemia - The first molecular disease
-
Wintrobe MM (ed): New York, NY, McGraw-Hill
-
Conley CL: Sickle cell anemia - The first molecular disease, in Wintrobe MM (ed): Blood, Pure and Eloquent: A Story of Discovery, of People, and of Ideas. New York, NY, McGraw-Hill, 1980, p 319
-
(1980)
Blood, Pure and Eloquent: A Story of Discovery, of People, and of Ideas
, pp. 319
-
-
Conley, C.L.1
-
2
-
-
0030853711
-
Pathogenesis and treatment of sickle cell disease
-
Bunn HF: Pathogenesis and treatment of sickle cell disease. N Engl J Med 337:762, 1997
-
(1997)
N Engl J Med
, vol.337
, pp. 762
-
-
Bunn, H.F.1
-
3
-
-
0000420850
-
A specific chemical difference between the globins of normal human and sickle cell anemia haemoglobin
-
Ingram VM: A specific chemical difference between the globins of normal human and sickle cell anemia haemoglobin. Nature 178:792, 1956
-
(1956)
Nature
, vol.178
, pp. 792
-
-
Ingram, V.M.1
-
4
-
-
0021931288
-
Hemoglobin S polymerization. Primary determinant of the hemolytic and clinical severity of the sickling syndromes
-
Brittenham GM, Schechter AN, Noguchi CT: Hemoglobin S polymerization. Primary determinant of the hemolytic and clinical severity of the sickling syndromes. Blood 65:183, 1985
-
(1985)
Blood
, vol.65
, pp. 183
-
-
Brittenham, G.M.1
Schechter, A.N.2
Noguchi, C.T.3
-
5
-
-
0021969576
-
Control of haemoglobin switching by a developmental clock
-
Wood WG, Bunch C, Kelly S, Gunn Y, Breckon G: Control of haemoglobin switching by a developmental clock. Nature 313:320, 1985
-
(1985)
Nature
, vol.313
, pp. 320
-
-
Wood, W.G.1
Bunch, C.2
Kelly, S.3
Gunn, Y.4
Breckon, G.5
-
6
-
-
0026749629
-
Therapeutic approaches to hemoglobin switching in treatment of the hemoglobinopathies
-
Stamatoyannopoulos JA, Nienhuis AW: Therapeutic approaches to hemoglobin switching in treatment of the hemoglobinopathies. Annu Rev Med 43:487, 1992
-
(1992)
Annu Rev Med
, vol.43
, pp. 487
-
-
Stamatoyannopoulos, J.A.1
Nienhuis, A.W.2
-
7
-
-
0006936094
-
Structural bases of the inhibitory effects of Hb F and A2 on the polymerization of Hb S
-
Nagel RL, Bookchin RM: Structural bases of the inhibitory effects of Hb F and A2 on the polymerization of Hb S. Proc Natl Acad Sci USA 76:670, 1979
-
(1979)
Proc Natl Acad Sci USA
, vol.76
, pp. 670
-
-
Nagel, R.L.1
Bookchin, R.M.2
-
8
-
-
0015492354
-
Benign sickle cell anemia
-
Perrine RP: Benign sickle cell anemia. Lancet 2:1163, 1972
-
(1972)
Lancet
, vol.2
, pp. 1163
-
-
Perrine, R.P.1
-
9
-
-
0017365844
-
Sickle cell anemia and trait in a population in southern India
-
Brittenham G, Lozoff B, Harris JW, Sharma VS, Narasimhan S: Sickle cell anemia and trait in a population in southern India. Am J Hematol 2:25, 1977
-
(1977)
Am J Hematol
, vol.2
, pp. 25
-
-
Brittenham, G.1
Lozoff, B.2
Harris, J.W.3
Sharma, V.S.4
Narasimhan, S.5
-
10
-
-
0018969574
-
Hb F synthesis in sickle cell anaemia: A comparison of Saudi Arab cases with those of African origin
-
Wood WG, Pembrey ME, Serjeant GR, Perrine RP, Weatherall DJ: Hb F synthesis in sickle cell anaemia: A comparison of Saudi Arab cases with those of African origin. Br J Haematol 45:431, 1980
-
(1980)
Br J Haematol
, vol.45
, pp. 431
-
-
Wood, W.G.1
Pembrey, M.E.2
Serjeant, G.R.3
Perrine, R.P.4
Weatherall, D.J.5
-
11
-
-
0017880649
-
Natural history of sickle cell anemia in Saudi Arabs
-
Perrine RP: Natural history of sickle cell anemia in Saudi Arabs. Ann Intern Med 88:1, 1978
-
(1978)
Ann Intern Med
, vol.88
, pp. 1
-
-
Perrine, R.P.1
-
12
-
-
0023859033
-
Levels of fetal hemoglobin necessary for treatment of sickle cell disease
-
Noguchi CT, Rodgers GP, Serjeant G, Schechter AN: Levels of fetal hemoglobin necessary for treatment of sickle cell disease. N Engl J Med 318:96, 1988
-
(1988)
N Engl J Med
, vol.318
, pp. 96
-
-
Noguchi, C.T.1
Rodgers, G.P.2
Serjeant, G.3
Schechter, A.N.4
-
13
-
-
0028291736
-
Mortality in sickle cell disease: Life expectancy and risk factors for early death
-
Platt OS, Brambilla DJ, Rosse WF, Milner PF, Castro O, Steinberg MH, Klug PP: Mortality in sickle cell disease: Life expectancy and risk factors for early death. N Engl J Med 330:1639, 1994
-
(1994)
N Engl J Med
, vol.330
, pp. 1639
-
-
Platt, O.S.1
Brambilla, D.J.2
Rosse, W.F.3
Milner, P.F.4
Castro, O.5
Steinberg, M.H.6
Klug, P.P.7
-
14
-
-
0000206049
-
5-Azacytidine stimulates fetal hemoglobin synthesis in anemic baboons
-
DeSimone J, Heller P, Hall L, Zwiers D: 5-Azacytidine stimulates fetal hemoglobin synthesis in anemic baboons. Proc Natl Acad Sci USA 79:4428, 1982
-
(1982)
Proc Natl Acad Sci USA
, vol.79
, pp. 4428
-
-
DeSimone, J.1
Heller, P.2
Hall, L.3
Zwiers, D.4
-
16
-
-
0020563258
-
5-Azacytidine increases γ-globin synthesis and reduces the proportion of dense cells in patients with sickle cell anemia
-
Ley TJ, DeSimone J, Noguchi CT: 5-Azacytidine increases γ-globin synthesis and reduces the proportion of dense cells in patients with sickle cell anemia. Blood 62:370, 1983
-
(1983)
Blood
, vol.62
, pp. 370
-
-
Ley, T.J.1
DeSimone, J.2
Noguchi, C.T.3
-
17
-
-
0026475679
-
Hydroxyurea-induced Hb F production in anemic primates: Augmentation by erythropoietin, growth factors, and sodium butyrate
-
McDonagh KT, Dover GJ, Donahue RE, Nathan DG: Hydroxyurea-induced Hb F production in anemic primates: Augmentation by erythropoietin, growth factors, and sodium butyrate. Exp Hematol 20:1156, 1992
-
(1992)
Exp Hematol
, vol.20
, pp. 1156
-
-
McDonagh, K.T.1
Dover, G.J.2
Donahue, R.E.3
Nathan, D.G.4
-
18
-
-
0022568850
-
Hydroxyurea induction of hemoglobin F production in sickle cell disease: Relationship between cytotoxicity and F-cell production
-
Dover GJ, Humphries RK, Moore JG: Hydroxyurea induction of hemoglobin F production in sickle cell disease: Relationship between cytotoxicity and F-cell production. Blood 67:735, 1986
-
(1986)
Blood
, vol.67
, pp. 735
-
-
Dover, G.J.1
Humphries, R.K.2
Moore, J.G.3
-
19
-
-
0023130331
-
Hydroxyurea-induced augmentation of fetal hemoglobin production in patients with sickle cell anemia
-
Charache S, Dover GJ, Moyer MA, Moore JW: Hydroxyurea-induced augmentation of fetal hemoglobin production in patients with sickle cell anemia. Blood 69:109, 1987
-
(1987)
Blood
, vol.69
, pp. 109
-
-
Charache, S.1
Dover, G.J.2
Moyer, M.A.3
Moore, J.W.4
-
20
-
-
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 328:73, 1993
-
(1993)
N Engl J Med
, vol.328
, pp. 73
-
-
Rodgers, G.P.1
Dover, G.J.2
Uyesaka, N.3
Noguchi, C.T.4
Schechter, A.N.5
Nienhuis, A.W.6
-
21
-
-
0027393050
-
F-reticulocyte response in sickle cell anemia treated with recombinant human erythropoietin: A double blind study
-
Nagel RL, Vichinsky E, Shah M: F-reticulocyte response in sickle cell anemia treated with recombinant human erythropoietin: A double blind study. Blood 81:9, 1993
-
(1993)
Blood
, vol.81
, pp. 9
-
-
Nagel, R.L.1
Vichinsky, E.2
Shah, M.3
-
22
-
-
0029025475
-
Multicenter study of hydroxyurea in sickle cell anemia: Effect of hydroxyurea on the frequency of painful crises in sickle cell anemia
-
Charache S, Terrin ML, Moore RD, Dover GJ, Barton FB, Eckert SV, McMahon RP, Bonds DR: Multicenter study of hydroxyurea in sickle cell anemia: Effect of hydroxyurea on the frequency of painful crises in sickle cell anemia. N Engl J Med 332:1317, 1995
-
(1995)
N Engl J Med
, vol.332
, pp. 1317
-
-
Charache, S.1
Terrin, M.L.2
Moore, R.D.3
Dover, G.J.4
Barton, F.B.5
Eckert, S.V.6
McMahon, R.P.7
Bonds, D.R.8
-
23
-
-
0030893396
-
Fetal hemoglobin in sickle cell anemia: Determinants of response to hydroxyurea
-
Steinberg MH, Lu ZH, Barton FB, Terrin ML, Charache S, Dover GJ, Multicenter Study of Hydroxyurea: Fetal hemoglobin in sickle cell anemia: Determinants of response to hydroxyurea. Blood 89:1078, 1997
-
(1997)
Blood
, vol.89
, pp. 1078
-
-
Steinberg, M.H.1
Lu, Z.H.2
Barton, F.B.3
Terrin, M.L.4
Charache, S.5
Dover, G.J.6
-
24
-
-
0345681889
-
Hydroxyurea increases Hb F production in children with sickle cell disease
-
Ohene-Frempong HK, Bulgarelli W, Schursky HM: Hydroxyurea increases Hb F production in children with sickle cell disease. Blood 82:3258, 1993
-
(1993)
Blood
, vol.82
, pp. 3258
-
-
Ohene-Frempong, H.K.1
Bulgarelli, W.2
Schursky, H.M.3
-
25
-
-
0029845949
-
Hydroxyurea for treatment of severe sickle cell anemia: A pediatric trial
-
Ferster A, Vermylen C, Cornu G: Hydroxyurea for treatment of severe sickle cell anemia: A pediatric trial. Blood 88:1960, 1996
-
(1996)
Blood
, vol.88
, pp. 1960
-
-
Ferster, A.1
Vermylen, C.2
Cornu, G.3
-
26
-
-
0030071882
-
Hydroxyurea in sickle cell disease
-
Schechter AN, Rodgers G: Hydroxyurea in sickle cell disease. N Engl J Med 334:333, 1996
-
(1996)
N Engl J Med
, vol.334
, pp. 333
-
-
Schechter, A.N.1
Rodgers, G.2
-
27
-
-
0031809842
-
Fetal hemoglobin and F-cell responses to long-term hydroxyurea treatment in young sickle cell patients
-
Maier-Redelsperger M, deMontalembert M, Flahault A, Neonato MG, Ducrocq R, Masson M-P, Girot R, Elion J: Fetal hemoglobin and F-cell responses to long-term hydroxyurea treatment in young sickle cell patients. Blood 91:4472, 1998
-
(1998)
Blood
, vol.91
, pp. 4472
-
-
Maier-Redelsperger, M.1
DeMontalembert, M.2
Flahault, A.3
Neonato, M.G.4
Ducrocq, R.5
Masson, M.-P.6
Girot, R.7
Elion, J.8
-
28
-
-
0021694055
-
Human globin gene transcription in injected Xenopus oocytes: Enhancement by sodium butyrate
-
Partington GA, Yarwood NJ, Rutherford TR: Human globin gene transcription in injected Xenopus oocytes: Enhancement by sodium butyrate. EMBO J 3:2787, 1984
-
(1984)
EMBO J
, vol.3
, pp. 2787
-
-
Partington, G.A.1
Yarwood, N.J.2
Rutherford, T.R.3
-
29
-
-
0010308916
-
Butyrate infusions in the ovine fetus delay the biologic clock for globin gene switching
-
Perrine SP, Rudolph A, Faller DV: Butyrate infusions in the ovine fetus delay the biologic clock for globin gene switching. Proc Natl Acad Sci USA 85:8540, 1988
-
(1988)
Proc Natl Acad Sci USA
, vol.85
, pp. 8540
-
-
Perrine, S.P.1
Rudolph, A.2
Faller, D.V.3
-
30
-
-
0024334257
-
Sodium butyrate enhances fetal globin gene expression in erythroid progenitors of patients with Hb SS and β thalassemia
-
Perrine SP, Miller BA, Faller DV, Cohen RA, Vichinsky EP, Hurst D, Lubin BH, Papayannopoulou T: Sodium butyrate enhances fetal globin gene expression in erythroid progenitors of patients with Hb SS and β thalassemia. Blood 74:454, 1989
-
(1989)
Blood
, vol.74
, pp. 454
-
-
Perrine, S.P.1
Miller, B.A.2
Faller, D.V.3
Cohen, R.A.4
Vichinsky, E.P.5
Hurst, D.6
Lubin, B.H.7
Papayannopoulou, T.8
-
31
-
-
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, Stamatoyannopoulous 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 74:1963, 1989
-
(1989)
Blood
, vol.74
, pp. 1963
-
-
Constantoulakis, P.1
Knitter, G.2
Stamatoyannopoulous, G.3
-
32
-
-
0027507268
-
Fetal hemoglobin induction with butyric acid: Efficacy and toxicity
-
Blau A, Constantoulakis P, Shaw CM, Stamatoyannopoulos G: Fetal hemoglobin induction with butyric acid: Efficacy and toxicity. Blood 81:529, 1993
-
(1993)
Blood
, vol.81
, pp. 529
-
-
Blau, A.1
Constantoulakis, P.2
Shaw, C.M.3
Stamatoyannopoulos, G.4
-
33
-
-
0028170946
-
Augmentation of γ globin gene promoter activity by carboxylic acids and components of the human β-globin locus control region
-
Safaya S, Ibrahim A, Reider RF: Augmentation of γ globin gene promoter activity by carboxylic acids and components of the human β-globin locus control region. Blood 84:3929, 1994
-
(1994)
Blood
, vol.84
, pp. 3929
-
-
Safaya, S.1
Ibrahim, A.2
Reider, R.F.3
-
34
-
-
0028845153
-
Stimulation of fetal hemoglobin production by short chain fatty acids
-
Liakopoulou E, Blau C, Li Q: Stimulation of fetal hemoglobin production by short chain fatty acids. Blood 86:3227, 1995
-
(1995)
Blood
, vol.86
, pp. 3227
-
-
Liakopoulou, E.1
Blau, C.2
Li, Q.3
-
35
-
-
0028139130
-
Isobutyramide, an orally bioavailable butyrate analogue, stimulates fetal globin gene expression in vitro and in vivo
-
Perrine SP, Dover GH, Daftari P, Walsh CT, Jin YX, Mays A, Faller DV: Isobutyramide, an orally bioavailable butyrate analogue, stimulates fetal globin gene expression in vitro and in vivo. Br J Haematol 88:555, 1994
-
(1994)
Br J Haematol
, vol.88
, pp. 555
-
-
Perrine, S.P.1
Dover, G.H.2
Daftari, P.3
Walsh, C.T.4
Jin, Y.X.5
Mays, A.6
Faller, D.V.7
-
36
-
-
0023709306
-
Butyrate induces selective transcriptional activation of a hypomethylated embryonic globin gene in adult erythroid cells
-
Burns LJ, Glauber JG, Ginder GD: Butyrate induces selective transcriptional activation of a hypomethylated embryonic globin gene in adult erythroid cells. Blood 72:1536, 1988
-
(1988)
Blood
, vol.72
, pp. 1536
-
-
Burns, L.J.1
Glauber, J.G.2
Ginder, G.D.3
-
37
-
-
0021203873
-
Activation of a chicken embryonic globin gene in adult erythroid cells by 5-azacytidine and sodium butyrate
-
Ginder GD, Whitters MJ, Pohlman JK: Activation of a chicken embryonic globin gene in adult erythroid cells by 5-azacytidine and sodium butyrate. Proc Natl Acad Sci USA 81:3954, 1984
-
(1984)
Proc Natl Acad Sci USA
, vol.81
, pp. 3954
-
-
Ginder, G.D.1
Whitters, M.J.2
Pohlman, J.K.3
-
38
-
-
0027078611
-
A short-term trial of butyrate to stimulate fetal-globin-gene expression in the β-globin disorders
-
Perrine SP, Ginder GD, Faller DV, Dover GH, Ikuta T, Witkowska HE, Cai SP, Vichinsky EP, Olivieri NF: A short-term trial of butyrate to stimulate fetal-globin-gene expression in the β-globin disorders. N Engl J Med 328:81, 1993
-
(1993)
N Engl J Med
, vol.328
, pp. 81
-
-
Perrine, S.P.1
Ginder, G.D.2
Faller, D.V.3
Dover, G.H.4
Ikuta, T.5
Witkowska, H.E.6
Cai, S.P.7
Vichinsky, E.P.8
Olivieri, N.F.9
-
39
-
-
0345250310
-
Intravenous arginine butyrate increases γ-globin mRNA, F-reticulocytes and hemoglobin F in patients with sickle cell disease
-
Sher GD, Entsuah B, Ginder G, Dover G, Berkovitch M, Lewis N, Perrine S, Olivieri NF: Intravenous arginine butyrate increases γ-globin mRNA, F-reticulocytes and hemoglobin F in patients with sickle cell disease. 19th Annual Meeting of the National Sickle Cell Disease Program. 1994, p 177
-
(1994)
19th Annual Meeting of the National Sickle Cell Disease Program
, pp. 177
-
-
Sher, G.D.1
Entsuah, B.2
Ginder, G.3
Dover, G.4
Berkovitch, M.5
Lewis, N.6
Perrine, S.7
Olivieri, N.F.8
-
40
-
-
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 84:339, 1994
-
(1994)
Blood
, vol.84
, pp. 339
-
-
Dover, G.J.1
Brusilow, S.2
Charache, S.3
-
41
-
-
0028870221
-
Oral sodium phenylbutyrate therapy in homozygous β thalassemia: A clinical trial
-
Collins AF, Pearson HA, Giardina P, McDonagh KT, Brusilow SW, Dover GJ: Oral sodium phenylbutyrate therapy in homozygous β thalassemia: A clinical trial. Blood 85:43, 1995
-
(1995)
Blood
, vol.85
, pp. 43
-
-
Collins, A.F.1
Pearson, H.A.2
Giardina, P.3
McDonagh, K.T.4
Brusilow, S.W.5
Dover, G.J.6
-
42
-
-
0021053871
-
Butyrate inhibits mouse fibroblasts at a control point in the G1 phase
-
Wintersberger E, Mudrak I, Wintersberger U: Butyrate inhibits mouse fibroblasts at a control point in the G1 phase. J Cell Biochem 21:239, 1983
-
(1983)
J Cell Biochem
, vol.21
, pp. 239
-
-
Wintersberger, E.1
Mudrak, I.2
Wintersberger, U.3
-
43
-
-
0024216822
-
Molecular analysis of sodium butyrate induced growth arrest
-
Toscani A, Soprano DR, Soprano KJ: Molecular analysis of sodium butyrate induced growth arrest. Oncogene Res 3:223, 1988
-
(1988)
Oncogene Res
, vol.3
, pp. 223
-
-
Toscani, A.1
Soprano, D.R.2
Soprano, K.J.3
-
44
-
-
0025130589
-
Butyrate blocks the accumulation of CDC2 mRNA in late G1 phase but inhibits both the early and late G1 progression in chemically transformed mouse fibroblasts BP-A31
-
Charollais RH, Buguet C, Mester J: Butyrate blocks the accumulation of CDC2 mRNA in late G1 phase but inhibits both the early and late G1 progression in chemically transformed mouse fibroblasts BP-A31. J Cell Physiol 145:46, 1990
-
(1990)
J Cell Physiol
, vol.145
, pp. 46
-
-
Charollais, R.H.1
Buguet, C.2
Mester, J.3
-
45
-
-
0027496417
-
Enhanced fetal hemoglobin production by phenylacetate and 4 phenylbutyrate in erythroid precursors derived from normal donors and patients with sickle cell anemia and β-thalassemia
-
Fibach E, Prosmanne J, Rodgers GP, Samid D: Enhanced fetal hemoglobin production by phenylacetate and 4 phenylbutyrate in erythroid precursors derived from normal donors and patients with sickle cell anemia and β-thalassemia. Blood 82:2203, 1993
-
(1993)
Blood
, vol.82
, pp. 2203
-
-
Fibach, E.1
Prosmanne, J.2
Rodgers, G.P.3
Samid, D.4
-
46
-
-
0031596491
-
Butyrate-induced G1 arrest results from p21-independent disruption of retinoblastoma-mediated signals
-
Vaziri C, Stice LL, Faller DV: Butyrate-induced G1 arrest results from p21-independent disruption of retinoblastoma-mediated signals. Cell Growth Differ 9:465, 1998
-
(1998)
Cell Growth Differ
, vol.9
, pp. 465
-
-
Vaziri, C.1
Stice, L.L.2
Faller, D.V.3
-
47
-
-
0029257858
-
Butyrate in the treatment of sickle cell disease and β thalassemia
-
Faller DV, Perrine SP: Butyrate in the treatment of sickle cell disease and β thalassemia. Curr Opin Hematol 2:109, 1995
-
(1995)
Curr Opin Hematol
, vol.2
, pp. 109
-
-
Faller, D.V.1
Perrine, S.P.2
-
48
-
-
0028099605
-
Fetal hemoglobin induction by acetate, a product of butyrate catabolism
-
Stamatoyannopoulos G, Blau CA, Nakamoto B, Josephson B, Li Q, Liakopoulou E, Pace B, Papayannopoulou T, Brusilow SW, Dover G: Fetal hemoglobin induction by acetate, a product of butyrate catabolism. Blood 84:3198, 1994
-
(1994)
Blood
, vol.84
, pp. 3198
-
-
Stamatoyannopoulos, G.1
Blau, C.A.2
Nakamoto, B.3
Josephson, B.4
Li, Q.5
Liakopoulou, E.6
Pace, B.7
Papayannopoulou, T.8
Brusilow, S.W.9
Dover, G.10
-
49
-
-
0030464953
-
Hydroxyurea and sickle cell anemia: Clinical utility of a myelosuppressive "switching" agent: The Multicenter Study of Hydroxyurea in Sickle Cell Anemia
-
Charache S, Barton FB, Moore RD: Hydroxyurea and sickle cell anemia: Clinical utility of a myelosuppressive "switching" agent: The Multicenter Study of Hydroxyurea in Sickle Cell Anemia. Medicine 75:300, 1996
-
(1996)
Medicine
, vol.75
, pp. 300
-
-
Charache, S.1
Barton, F.B.2
Moore, R.D.3
-
50
-
-
0025821277
-
Effects of hydroxyurea on hemoglobin F and water content in the red blood cells of dogs and of patients with sickle cell anemia
-
Orringer EP, Blythe DS, Johnson AE, Phillips GJ, Dover GJ, Parker JC: Effects of hydroxyurea on hemoglobin F and water content in the red blood cells of dogs and of patients with sickle cell anemia. Blood 78:212, 1991
-
(1991)
Blood
, vol.78
, pp. 212
-
-
Orringer, E.P.1
Blythe, D.S.2
Johnson, A.E.3
Phillips, G.J.4
Dover, G.J.5
Parker, J.C.6
-
51
-
-
0024469605
-
Effect of hydroxyurea on the rheological properties of sickle erythrocytes in vivo
-
Ballas SK, Dover GJ, Charache S: Effect of hydroxyurea on the rheological properties of sickle erythrocytes in vivo. Am J Hematol 32:104, 1989
-
(1989)
Am J Hematol
, vol.32
, pp. 104
-
-
Ballas, S.K.1
Dover, G.J.2
Charache, S.3
-
52
-
-
0021956121
-
Delay in the fetal globin switch in infants of diabetic mothers
-
Perrine SP, Greene MF, Faller DV: Delay in the fetal globin switch in infants of diabetic mothers. N Engl J Med 312:334, 1985
-
(1985)
N Engl J Med
, vol.312
, pp. 334
-
-
Perrine, S.P.1
Greene, M.F.2
Faller, D.V.3
-
53
-
-
0030923438
-
Induction of γ-globin by histone deacetylase inhibitors
-
McCaffrey PG, Newsome DA, Fibach E, Yoshida M, Su MS: Induction of γ-globin by histone deacetylase inhibitors. Blood 90:2075, 1997
-
(1997)
Blood
, vol.90
, pp. 2075
-
-
McCaffrey, P.G.1
Newsome, D.A.2
Fibach, E.3
Yoshida, M.4
Su, M.S.5
-
54
-
-
17744413444
-
A complex containing N-CoR, mSin3 and histone deacetylase mediates transcriptional repression
-
Heinzel T, Lavinsky RM, Mullen TM, Soderstrom M, Laherty CD, Torchia J, Yang WM, Brard G, Ngo SD, Davie JR, Seto E, Eisenman RN, Rose DW, Glass CK, Rosenfeld MG: A complex containing N-CoR, mSin3 and histone deacetylase mediates transcriptional repression. Nature 387:43, 1997
-
(1997)
Nature
, vol.387
, pp. 43
-
-
Heinzel, T.1
Lavinsky, R.M.2
Mullen, T.M.3
Soderstrom, M.4
Laherty, C.D.5
Torchia, J.6
Yang, W.M.7
Brard, G.8
Ngo, S.D.9
Davie, J.R.10
Seto, E.11
Eisenman, R.N.12
Rose, D.W.13
Glass, C.K.14
Rosenfeld, M.G.15
-
55
-
-
0030969516
-
Histone deacetylases associated with the mSin3 corepressor mediate mad transciptional repression
-
Laherty CD, Yang WM, Sun JM, Davie JR, Seto E, Eisenman RN: Histone deacetylases associated with the mSin3 corepressor mediate mad transciptional repression. Cell 89:349, 1997
-
(1997)
Cell
, vol.89
, pp. 349
-
-
Laherty, C.D.1
Yang, W.M.2
Sun, J.M.3
Davie, J.R.4
Seto, E.5
Eisenman, R.N.6
-
56
-
-
0030221901
-
Erythroid progenitor proliferation is stimulated by phenoxyacetic and phenylalkyl acids
-
Torkelson S, White GL, Phipps K: Erythroid progenitor proliferation is stimulated by phenoxyacetic and phenylalkyl acids. Blood Cells Mol Dis 20:150, 1996
-
(1996)
Blood Cells Mol Dis
, vol.20
, pp. 150
-
-
Torkelson, S.1
White, G.L.2
Phipps, K.3
-
57
-
-
0031427861
-
Abrogation of IL-3 requirements and stimulation of hematopoietic cell proliferation in vitro and in vivo by carboxylic acids
-
Boosalis MS, Ikuta T, Pace BS: Abrogation of IL-3 requirements and stimulation of hematopoietic cell proliferation in vitro and in vivo by carboxylic acids. Blood Cells Mol Dis 23:434, 1997
-
(1997)
Blood Cells Mol Dis
, vol.23
, pp. 434
-
-
Boosalis, M.S.1
Ikuta, T.2
Pace, B.S.3
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