-
1
-
-
0029025475
-
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. Effect of hydroxyurea on the frequency of painful crises in sickle cell anemia. N Engl J Med 1995; 332(20):1317-1322.
-
(1995)
N Engl J Med
, vol.332
, Issue.20
, pp. 1317-1322
-
-
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
-
2
-
-
27144448031
-
Long-term hydroxyurea therapy for infants with sickle cell anemia: The HUSOFT extension study
-
Hankins JS, Ware RE, Rogers ZR, Wynn LW, Lane PA, Scott JP, Wang WC. Long-term hydroxyurea therapy for infants with sickle cell anemia: the HUSOFT extension study. Blood 2005; 106(7):2269-2275.
-
(2005)
Blood
, vol.106
, Issue.7
, pp. 2269-2275
-
-
Hankins, J.S.1
Ware, R.E.2
Rogers, Z.R.3
Wynn, L.W.4
Lane, P.A.5
Scott, J.P.6
Wang, W.C.7
-
3
-
-
0028038985
-
Hydroxyurea affects cell morphology, cation transport, and red blood cell adhesion in cultured vascular endothelial cells
-
Adragna NC, Fonseca P, Lauf PK. Hydroxyurea affects cell morphology, cation transport, and red blood cell adhesion in cultured vascular endothelial cells. Blood 1994; 83(2):553-560.
-
(1994)
Blood
, vol.83
, Issue.2
, pp. 553-560
-
-
Adragna, N.C.1
Fonseca, P.2
Lauf, P.K.3
-
4
-
-
0036091117
-
Chromatin assembly Cooperation between histone chaperones and ATP-dependent nucleosome remodeling machines
-
Tyler JK. Chromatin assembly Cooperation between histone chaperones and ATP-dependent nucleosome remodeling machines. Eur J Biochem 2002; 269(9):2268-2274.
-
(2002)
Eur J Biochem
, vol.269
, Issue.9
, pp. 2268-2274
-
-
Tyler, J.K.1
-
5
-
-
13344259315
-
Hydroxyurea increases Hemoglobin F levels and improves the effectiveness of erythropoiesis in β-thalassemia/Hemoglobin E disease
-
Fucharoen S, Siritanaratkul N, Winichagoon P, Chowthaworn J, Siriboon W, Muangsup W, Chaicharoen S, Poolsup P, Chindavijak B, Pootrakul P, Piankijagum A, Rodgers GP. Hydroxyurea increases Hemoglobin F levels and improves the effectiveness of erythropoiesis in β-thalassemia/Hemoglobin 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
Chowthaworn, J.4
Siriboon, W.5
Muangsup, W.6
Chaicharoen, S.7
Poolsup, P.8
Chindavijak, B.9
Pootrakul, P.10
Piankijagum, A.11
Rodgers, G.P.12
-
6
-
-
0023663887
-
Position independent, high-level expression of the human β-globin gene in transgenic mice
-
Grosveld F, van Assendelft GB, Greaves DR, Kollias G. Position independent, high-level expression of the human β-globin gene in transgenic mice. Cell 1987; 51(6):975-985.
-
(1987)
Cell
, vol.51
, Issue.6
, pp. 975-985
-
-
Grosveld, F.1
van Assendelft, G.B.2
Greaves, D.R.3
Kollias, G.4
-
7
-
-
2942657608
-
Multiple interactions between regulatory regions are required to stabilize an active chromatin hub
-
Patrinos GP, de Krom M, de Boer E, Langeveld A, Imam AM, Strouboulis J, de Laat W, Grosveld FG. Multiple interactions between regulatory regions are required to stabilize an active chromatin hub. Genes Develop 2004; 18(12):1495-1509.
-
(2004)
Genes Develop
, vol.18
, Issue.12
, pp. 1495-1509
-
-
Patrinos, G.P.1
de Krom, M.2
de Boer, E.3
Langeveld, A.4
Imam, A.M.5
Strouboulis, J.6
de Laat, W.7
Grosveld, F.G.8
-
9
-
-
0003336829
-
The Hemoglobinopathies Techniques of Identification
-
New York: Marcel Dekker, Inc
-
Huisman THJ, Jonxis JHP. The Hemoglobinopathies Techniques of Identification. Clinical and Biochemical Analysis, Vol. 6. New York: Marcel Dekker, Inc., 1977.
-
(1977)
Clinical and Biochemical Analysis
, vol.6
-
-
Huisman, T.H.J.1
Jonxis, J.H.P.2
-
10
-
-
30444432407
-
-
Bank A. Regulation of human fetal hemoglobin: new players, new complexities. 2006; Blood 107(2):435-443.
-
Bank A. Regulation of human fetal hemoglobin: new players, new complexities. 2006; Blood 107(2):435-443.
-
-
-
-
11
-
-
0016137085
-
The present status of the heterogeneity of fetal hemoglobin in β-thalassemia: An attempt to unify some observations in thalassemia and related conditions
-
Huisman THJ, Schroeder WA, Efremov GD, Duma H, Mladenovski B, Hyman CB, Rachmilewitz EA, Bouver N, Miller A, Brodie A, Shelton JB, Apell G. The present status of the heterogeneity of fetal hemoglobin in β-thalassemia: an attempt to unify some observations in thalassemia and related conditions. Ann NY Acad Sci 1973; 232:107-124.
-
(1973)
Ann NY Acad Sci
, vol.232
, pp. 107-124
-
-
Huisman, T.H.J.1
Schroeder, W.A.2
Efremov, G.D.3
Duma, H.4
Mladenovski, B.5
Hyman, C.B.6
Rachmilewitz, E.A.7
Bouver, N.8
Miller, A.9
Brodie, A.10
Shelton, J.B.11
Apell, G.12
-
12
-
-
0014684181
-
Hemoglobin F(Malta): A new fetal hemoglobin variant with a high incidence in Maltese infants
-
Cauchi MN, Clegg JB, Weatherall DJ. Hemoglobin F(Malta): a new fetal hemoglobin variant with a high incidence in Maltese infants. Nature 1969; 223(203):311-313.
-
(1969)
Nature
, vol.223
, Issue.203
, pp. 311-313
-
-
Cauchi, M.N.1
Clegg, J.B.2
Weatherall, D.J.3
-
13
-
-
0027450887
-
+ IVS, I-NT no. 6 (T→C) thalassaemia in heterozygotes with an associated Hb Valletta or Hb S heterozygosity in homozygotes from Malta
-
+ IVS, I-NT no. 6 (T→C) thalassaemia in heterozygotes with an associated Hb Valletta or Hb S heterozygosity in homozygotes from Malta. Br J Haematol 1993; 83(4):669-671.
-
(1993)
Br J Haematol
, vol.83
, Issue.4
, pp. 669-671
-
-
Scerri, C.A.1
Abela, W.2
Galdies, R.3
Pizzuto, M.L.4
Grech, J.L.5
Felice, A.E.6
-
15
-
-
0024284028
-
A simple salting out procedure for extracting DNA from human nucleated cells
-
Miller SA, Dykes DD, Polesky HF. A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acid Res 1988; 16(3):1215.
-
(1988)
Nucleic Acid Res
, vol.16
, Issue.3
, pp. 1215
-
-
Miller, S.A.1
Dykes, D.D.2
Polesky, H.F.3
-
17
-
-
0025762744
-
-
2117(G19)His→Arg] in the Maltese population. Hum Genet 1991; 86(6):591-594.
-
2117(G19)His→Arg] in the Maltese population. Hum Genet 1991; 86(6):591-594.
-
-
-
-
18
-
-
0026030540
-
Increased protein binding to a -530 mutation of the human β-globin gene associated with decreased β-globin synthesis
-
Berg PE, Mittelman M, Elion J, Labie D, Schechter AN. Increased protein binding to a -530 mutation of the human β-globin gene associated with decreased β-globin synthesis. Am J Hematol 1991; 36(1)42-47.
-
(1991)
Am J Hematol
, vol.36
, Issue.1
, pp. 42-47
-
-
Berg, P.E.1
Mittelman, M.2
Elion, J.3
Labie, D.4
Schechter, A.N.5
-
19
-
-
0034661406
-
The role of trans-acting factors and DNA-bending in the silencing of human β-globin gene expression
-
Drew LR, Tang DC, Berg PE, Rodgers GP. The role of trans-acting factors and DNA-bending in the silencing of human β-globin gene expression. Nucleic Acids Res 2000; 28(14):2823-2830.
-
(2000)
Nucleic Acids Res
, vol.28
, Issue.14
, pp. 2823-2830
-
-
Drew, L.R.1
Tang, D.C.2
Berg, P.E.3
Rodgers, G.P.4
-
20
-
-
0036205323
-
BP1, a homeodomain-containing isoform of DLX4, represses the β-globin gene
-
Chase MB, Fu S, Haga SB, Davenport G, Stevenson H, Do K, Morgan D, Mah AL, Berg PE. BP1, a homeodomain-containing isoform of DLX4, represses the β-globin gene. Mol Cell Biol 2002; 22(8):2505-2514.
-
(2002)
Mol Cell Biol
, vol.22
, Issue.8
, pp. 2505-2514
-
-
Chase, M.B.1
Fu, S.2
Haga, S.B.3
Davenport, G.4
Stevenson, H.5
Do, K.6
Morgan, D.7
Mah, A.L.8
Berg, P.E.9
-
21
-
-
13044289307
-
+-thalassemia alleles
-
+-thalassemia alleles. Hemoglobin 1999; 23(3):221-229.
-
(1999)
Hemoglobin
, vol.23
, Issue.3
, pp. 221-229
-
-
Marwan, M.M.1
Scerri, C.A.2
Zarroag, S.O.3
Cao, A.4
Kalogirou, E.5
Kleanthous, M.6
Ioannou, P.7
Angastiniotis, M.8
Felice, A.E.9
-
22
-
-
0000206049
-
5-Azacytidine stimulates fetal hemoglobin synthesis in anemic baboons
-
DeSimone J, Heller P, Hall L, Wiers DZ. 5-Azacytidine stimulates fetal hemoglobin synthesis in anemic baboons. Proc Natl Acad Sci USA 1982; 79(14):4428-4431.
-
(1982)
Proc Natl Acad Sci USA
, vol.79
, Issue.14
, pp. 4428-4431
-
-
DeSimone, J.1
Heller, P.2
Hall, L.3
Wiers, D.Z.4
-
23
-
-
0020466344
-
+-thalassemia
-
+-thalassemia. N Engl J Med 1982; 307(24):1469-1475.
-
(1982)
N Engl J Med
, vol.307
, Issue.24
, pp. 1469-1475
-
-
Ley, T.J.1
DeSimone, J.2
Anagnou, N.P.3
Keller, G.H.4
Humphries, R.K.5
Turner, P.H.6
Young, N.S.7
Heller, P.8
Nienhuis, A.W.9
-
24
-
-
33751166387
-
Short-chain fatty acids induce γ-globin gene expression bydisplacement of a HDAC3-NCoR repressor complex
-
Mankidy R, Faller DV, Malbaaera R, Lowrey CH, Boosalis MS, White GL, Castaneda SA, Perrine SP. Short-chain fatty acids induce γ-globin gene expression bydisplacement of a HDAC3-NCoR repressor complex. Blood 2006; 108(9):3179-3186.
-
(2006)
Blood
, vol.108
, Issue.9
, pp. 3179-3186
-
-
Mankidy, R.1
Faller, D.V.2
Malbaaera, R.3
Lowrey, C.H.4
Boosalis, M.S.5
White, G.L.6
Castaneda, S.A.7
Perrine, S.P.8
-
25
-
-
0021956121
-
-
Perrine SP, Greene MF, Faller DV. Delay in the fetal globin switch in infants of diabetic mothers. N Engl J Med 1985; 312(6):334-338.
-
Perrine SP, Greene MF, Faller DV. Delay in the fetal globin switch in infants of diabetic mothers. N Engl J Med 1985; 312(6):334-338.
-
-
-
-
26
-
-
0021335219
-
Perturbations in the erythroid marrow progenitor cell pools may play a role in the augmentation of HbF by 5-azacytidine
-
Torrealba-de Ron AT, Papayannopoulou Th, Knapp MS, Fu MF, Knitter G, Stamatoyannopoulos G. Perturbations in the erythroid marrow progenitor cell pools may play a role in the augmentation of HbF by 5-azacytidine. Blood 1984; 63(1):201-210.
-
(1984)
Blood
, vol.63
, Issue.1
, pp. 201-210
-
-
Torrealba-de Ron, A.T.1
Papayannopoulou, T.2
Knapp, M.S.3
Fu, M.F.4
Knitter, G.5
Stamatoyannopoulos, G.6
-
27
-
-
0031832011
-
Regression of extramedullary haemopoiesis and augmentation of fetal haemoglobin concentration during hydroxyurea therapy in α thalassaemia
-
Saxon BR, Rees D, Olivieri NF. Regression of extramedullary haemopoiesis and augmentation of fetal haemoglobin concentration during hydroxyurea therapy in α thalassaemia. Br J Haematol 1998; 101(3):416-419.
-
(1998)
Br J Haematol
, vol.101
, Issue.3
, pp. 416-419
-
-
Saxon, B.R.1
Rees, D.2
Olivieri, N.F.3
-
28
-
-
34248149731
-
-
B.Pharm Thesis, Department of Pharmacy, Faculty of Medicine and Surgery, University of Malta, Msida, Malta
-
Galea M. Low dose hydroxyurea therapy in thalassaemia patients for the pharmacological induction of haemoglobin. B.Pharm Thesis, Department of Pharmacy, Faculty of Medicine and Surgery, University of Malta, Msida, Malta, 2005.
-
(2005)
Low dose hydroxyurea therapy in thalassaemia patients for the pharmacological induction of haemoglobin
-
-
Galea, M.1
|