-
2
-
-
0016793039
-
Fetal hemoglobin restriction to a few erythrocytes (F cells) in normal human adults
-
Boyer SH, Belding TK, Margolet L, Noyes AN. Fetal hemoglobin restriction to a few erythrocytes (F cells) in normal human adults. Science 1975;188:361-363.
-
(1975)
Science
, vol.188
, pp. 361-363
-
-
Boyer, S.H.1
Belding, T.K.2
Margolet, L.3
Noyes, A.N.4
-
3
-
-
0016713936
-
F-cells in the adult: Normal values and levels in individuals with hereditary and acquired elevations of Hb F
-
Wood WG, Stamatoyannopoulos G, Lim G, Nute PE. F-cells in the adult: Normal values and levels in individuals with hereditary and acquired elevations of Hb F. Blood 1975;46:671-682.
-
(1975)
Blood
, vol.46
, pp. 671-682
-
-
Wood, W.G.1
Stamatoyannopoulos, G.2
Lim, G.3
Nute, P.E.4
-
4
-
-
0024209310
-
X-linked dominant control of F-cells in normal adult life: Characterization of the Swiss type as hereditary persistence of fetal hemoglobin regulated dominantly by gene(s) on X chromosome
-
Miyoshi K, Kaneto Y, Kawai H, et al. X-linked dominant control of F-cells in normal adult life: Characterization of the Swiss type as hereditary persistence of fetal hemoglobin regulated dominantly by gene(s) on X chromosome. Blood 1988;72:1854-1860.
-
(1988)
Blood
, vol.72
, pp. 1854-1860
-
-
Miyoshi, K.1
Kaneto, Y.2
Kawai, H.3
-
5
-
-
0031871713
-
Molecular basis of hereditary persistence of fetal hemoglobin
-
Forget BG. Molecular basis of hereditary persistence of fetal hemoglobin. Ann NY Acad Sci 1998;850:38-44.
-
(1998)
Ann NY Acad Sci
, vol.850
, pp. 38-44
-
-
Forget, B.G.1
-
6
-
-
0017098798
-
Fetal erythropoiesis following bone marrow transplantation
-
Alter BP, Rappeport JM, Huisman TH, et al. Fetal erythropoiesis following bone marrow transplantation. Blood 1976;48:843-853.
-
(1976)
Blood
, vol.48
, pp. 843-853
-
-
Alter, B.P.1
Rappeport, J.M.2
Huisman, T.H.3
-
7
-
-
0018888401
-
Fetal Hb production during acute erythroid expansion. I. Observations in patients with transient erythroblastopenia and post-phlebotomy
-
Papayannopoulou T, Vichinsky E, Stamatoyannopoulos G. Fetal Hb production during acute erythroid expansion. I. Observations in patients with transient erythroblastopenia and post-phlebotomy. Br J Haematol 1980;44:535-546.
-
(1980)
Br J Haematol
, vol.44
, pp. 535-546
-
-
Papayannopoulou, T.1
Vichinsky, E.2
Stamatoyannopoulos, G.3
-
9
-
-
0027078611
-
A short-term trial of butyrate to stimulate fetal-globin-gene expression in the β-globin disorders
-
Perrine SP, Ginder GD, Faller DV, et al. A short-term trial of butyrate to stimulate fetal-globin-gene expression in the β-globin disorders. N Engl J Med 1993;328:81-86.
-
(1993)
N Engl J Med
, vol.328
, pp. 81-86
-
-
Perrine, S.P.1
Ginder, G.D.2
Faller, D.V.3
-
10
-
-
0030464953
-
Hydroxyurea and sickle cell anemia - Clinical utility of a myelosuppressive "switching" agent
-
Charache S, Barton FB, Moore RD, et al. Hydroxyurea and sickle cell anemia - Clinical utility of a myelosuppressive "switching" agent. Medicine (Baltimore) 1996;75:300-326.
-
(1996)
Medicine (Baltimore)
, vol.75
, pp. 300-326
-
-
Charache, S.1
Barton, F.B.2
Moore, R.D.3
-
11
-
-
35548943647
-
Thalidomide induces γ-globin gene expression through increased reactive oxygen species-mediated p38 MAPK signaling and histone H4 acetylation in adult erythropoiesis
-
Aerbajinai W, Zhu J, Gao Z, et al. Thalidomide induces γ-globin gene expression through increased reactive oxygen species-mediated p38 MAPK signaling and histone H4 acetylation in adult erythropoiesis. Blood 2007;110:2864-2871.
-
(2007)
Blood
, vol.110
, pp. 2864-2871
-
-
Aerbajinai, W.1
Zhu, J.2
Gao, Z.3
-
12
-
-
0027391067
-
c-Kit ligand reactivates fetal hemoglobin synthesis in serum-free culture of stringently purified normal adult burst-forming unit-erythroid
-
Peschle C, Gabbianelli M, Testa U, et al. c-Kit ligand reactivates fetal hemoglobin synthesis in serum-free culture of stringently purified normal adult burst-forming unit-erythroid. Blood 1993;81:328-336.
-
(1993)
Blood
, vol.81
, pp. 328-336
-
-
Peschle, C.1
Gabbianelli, M.2
Testa, U.3
-
13
-
-
29744453274
-
Pharmacological induction of fetal hemoglobin: Why haven't we been more successful in thalassemia?
-
Fathallah H, Sutton M, Atweh GF. Pharmacological induction of fetal hemoglobin: Why haven't we been more successful in thalassemia? Ann NY Acad Sci 2005;1054:228-237.
-
(2005)
Ann NY Acad Sci
, vol.1054
, pp. 228-237
-
-
Fathallah, H.1
Sutton, M.2
Atweh, G.F.3
-
14
-
-
34748864128
-
A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15
-
Menzel S, Garner C, Gut I, et al. A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15. Nat Genet 2007;39:1197-1199.
-
(2007)
Nat Genet
, vol.39
, pp. 1197-1199
-
-
Menzel, S.1
Garner, C.2
Gut, I.3
-
15
-
-
34547450531
-
Intergenic variants of HBS1L-MYB are responsible for a major quantitative trait locus on chromosome 6q23 influencing fetal hemoglobin levels in adults
-
Thein SL, Menzel S, Peng X, et al. Intergenic variants of HBS1L-MYB are responsible for a major quantitative trait locus on chromosome 6q23 influencing fetal hemoglobin levels in adults. Proc Natl Acad Sci USA 2007;104:11346-11351.
-
(2007)
Proc Natl Acad Sci USA
, vol.104
, pp. 11346-11351
-
-
Thein, S.L.1
Menzel, S.2
Peng, X.3
-
16
-
-
27644597215
-
Interaction between two quantitative trait loci affects fetal haemoglobin expression
-
Garner C, Menzel S, Martin C, et al. Interaction between two quantitative trait loci affects fetal haemoglobin expression. Ann Hum Genet 2005;69:707-714.
-
(2005)
Ann Hum Genet
, vol.69
, pp. 707-714
-
-
Garner, C.1
Menzel, S.2
Martin, C.3
-
17
-
-
0026708201
-
Fetal hemoglobin levels in sickle cell disease and normal individuals are partially controlled by an X-linked gene located at Xp22.2
-
Dover GJ, Smith KD, Chang YC, et al. Fetal hemoglobin levels in sickle cell disease and normal individuals are partially controlled by an X-linked gene located at Xp22.2. Blood 1992;80:816-824.
-
(1992)
Blood
, vol.80
, pp. 816-824
-
-
Dover, G.J.1
Smith, K.D.2
Chang, Y.C.3
-
18
-
-
0030905118
-
Prevalence and genotypes of α- and β-thalassemia carriers in Hong Kong - Implications for population screening
-
Lau YL, Chan LC, Chan YYA, et al. Prevalence and genotypes of α- and β-thalassemia carriers in Hong Kong - Implications for population screening. N Engl J Med 1997;336:1298-1301.
-
(1997)
N Engl J Med
, vol.336
, pp. 1298-1301
-
-
Lau, Y.L.1
Chan, L.C.2
Chan, Y.Y.A.3
-
19
-
-
2442556148
-
The prevalence and spectrum of α and β thalassaemia in Guangdong Province: Implications for the future health burden and population screening
-
Xu XM, Zhou YQ, Luo GX, et al. The prevalence and spectrum of α and β thalassaemia in Guangdong Province: Implications for the future health burden and population screening. J Clin Pathol 2004;57:517-522.
-
(2004)
J Clin Pathol
, vol.57
, pp. 517-522
-
-
Xu, X.M.1
Zhou, Y.Q.2
Luo, G.X.3
-
20
-
-
0033782529
-
_ _SEA) α-globin gene deletion in β-thalassemia carriers and prevention of hydrops fetalis
-
_ _SEA) α-globin gene deletion in β-thalassemia carriers and prevention of hydrops fetalis. Haematologica 2000;85:991-993.
-
(2000)
Haematologica
, vol.85
, pp. 991-993
-
-
Ma, E.S.K.1
Chan, A.Y.Y.2
Ha, S.Y.3
-
22
-
-
37549029778
-
β-Thalassemia intermedia due to compound heterozygosity for two β-globin gene promoter mutations, including a novel TATA box deletion
-
Basran RK, Reiss UM, Luo HY, et al. β-Thalassemia intermedia due to compound heterozygosity for two β-globin gene promoter mutations, including a novel TATA box deletion. Pediatr Blood Cancer 2008;50:363-366.
-
(2008)
Pediatr Blood Cancer
, vol.50
, pp. 363-366
-
-
Basran, R.K.1
Reiss, U.M.2
Luo, H.Y.3
-
23
-
-
0347547003
-
The Molecular Pathology of the Thalassaemias
-
4th ed. Oxford, UK: Blackwell Science;
-
Weatherall DJ, Clegg JB. The Molecular Pathology of the Thalassaemias. The Thalassaemia Syndromes,4th ed. Oxford, UK: Blackwell Science; 2001. p 151.
-
(2001)
The Thalassaemia Syndromes
, pp. 151
-
-
Weatherall, D.J.1
Clegg, J.B.2
-
25
-
-
0033847329
-
Molecular studies of β-thalassemia heterozygotes with raised Hb F levels
-
Vrettou C, Kanavakis E, Traeger-Synodinos J, et al. Molecular studies of β-thalassemia heterozygotes with raised Hb F levels. Hemoglobin 2000;24: 203-220.
-
(2000)
Hemoglobin
, vol.24
, pp. 203-220
-
-
Vrettou, C.1
Kanavakis, E.2
Traeger-Synodinos, J.3
-
26
-
-
0033230344
-
Why are hemoglobin F levels increased in HbE/β thalassemia?
-
Rees DC, Porter JB, Clegg JB, Weatherall DJ. Why are hemoglobin F levels increased in HbE/β thalassemia? Blood 1999;94:3199-3204.
-
(1999)
Blood
, vol.94
, pp. 3199-3204
-
-
Rees, D.C.1
Porter, J.B.2
Clegg, J.B.3
Weatherall, D.J.4
-
27
-
-
0038045578
-
In vitro induction of fetal hemoglobin in human erythroid progenitor cells
-
Ho JA, Pickens CV, Gamcsik MP, et al. In vitro induction of fetal hemoglobin in human erythroid progenitor cells. Exp Hematol 2003;31:586-591.
-
(2003)
Exp Hematol
, vol.31
, pp. 586-591
-
-
Ho, J.A.1
Pickens, C.V.2
Gamcsik, M.P.3
-
28
-
-
33646571213
-
DNA hypomethylation therapy for hemoglobin disorders: Molecular mechanisms and clinical applications
-
Fathallah H, Atweh GF. DNA hypomethylation therapy for hemoglobin disorders: Molecular mechanisms and clinical applications. Blood Rev 2006; 20:227-234.
-
(2006)
Blood Rev
, vol.20
, pp. 227-234
-
-
Fathallah, H.1
Atweh, G.F.2
-
30
-
-
0033966370
-
Genetic influences on F cells and other hematologic variables: A twin heritability study
-
Garner C, Tatu T, Reittie JE, et al. Genetic influences on F cells and other hematologic variables: A twin heritability study. Blood 2000;95:342-346.
-
(2000)
Blood
, vol.95
, pp. 342-346
-
-
Garner, C.1
Tatu, T.2
Reittie, J.E.3
-
31
-
-
0032406849
-
Genetics of Hb F/F cell variance in adults and heterocellular hereditary persistence of fetal hemoglobin
-
Thein SL, Craig JE. Genetics of Hb F/F cell variance in adults and heterocellular hereditary persistence of fetal hemoglobin. Hemoglobin 1998;22:401-414.
-
(1998)
Hemoglobin
, vol.22
, pp. 401-414
-
-
Thein, S.L.1
Craig, J.E.2
-
33
-
-
0034671361
-
Simplified flow cytometric method for fetal hemoglobin containing red blood cells
-
Mundee Y, Bigelow NC, Davis BH, Porter JB. Simplified flow cytometric method for fetal hemoglobin containing red blood cells. Cytometry 2000;42: 389-393.
-
(2000)
Cytometry
, vol.42
, pp. 389-393
-
-
Mundee, Y.1
Bigelow, N.C.2
Davis, B.H.3
Porter, J.B.4
-
34
-
-
0035724650
-
Flow cytometric method for simultaneous assay of foetal haemoglobin containing red cells, reticulocytes and foetal haemoglobin containing reticulocytes
-
Mundee Y, Bigelow NC, Davis BH, Porter JB. Flow cytometric method for simultaneous assay of foetal haemoglobin containing red cells, reticulocytes and foetal haemoglobin containing reticulocytes. Clin Lab Haematol 2001;23: 149-154.
-
(2001)
Clin Lab Haematol
, vol.23
, pp. 149-154
-
-
Mundee, Y.1
Bigelow, N.C.2
Davis, B.H.3
Porter, J.B.4
-
35
-
-
0036261355
-
Flow cytometric measurement of hemoglobin F in RBCs: Diagnostic usefulness in the distinction of hereditary persistence of fetal hemoglobin (HPFH) and hemoglobin S-HPFH from other conditions with elevated levels of hemoglobin F
-
Hoyer JD, Penz CS, Fairbanks VF, et al. Flow cytometric measurement of hemoglobin F in RBCs: Diagnostic usefulness in the distinction of hereditary persistence of fetal hemoglobin (HPFH) and hemoglobin S-HPFH from other conditions with elevated levels of hemoglobin F. Am J Clin Pathol 2002;117: 857-863.
-
(2002)
Am J Clin Pathol
, vol.117
, pp. 857-863
-
-
Hoyer, J.D.1
Penz, C.S.2
Fairbanks, V.F.3
-
36
-
-
0031023806
-
Gγ-globin promoter with delayed switchover from fetal to adult hemoglobin synthesis
-
Gγ-globin promoter with delayed switchover from fetal to adult hemoglobin synthesis. Pediatr Res 1997;41:214-217.
-
(1997)
Pediatr Res
, vol.41
, pp. 214-217
-
-
Peri, K.G.1
Gagnon, J.2
Gagnon, C.3
Bard, H.4
-
37
-
-
0035412399
-
A rapid and reliable 7-deletion multiplex polymerase chain reaction assay for α-thalassemia
-
Tan ASC, Quah TC, Low PS, Chong SS. A rapid and reliable 7-deletion multiplex polymerase chain reaction assay for α-thalassemia. Blood 2001;98:250-251.
-
(2001)
Blood
, vol.98
, pp. 250-251
-
-
Tan, A.S.C.1
Quah, T.C.2
Low, P.S.3
Chong, S.S.4
-
38
-
-
0035728091
-
Detection of severe nondeletional α-thalassemia mutations using a single-tube multiplex ARMS assay
-
Eng B, Patterson M, Walker L, et al. Detection of severe nondeletional α-thalassemia mutations using a single-tube multiplex ARMS assay. Genet Test 2001;5:327-329.
-
(2001)
Genet Test
, vol.5
, pp. 327-329
-
-
Eng, B.1
Patterson, M.2
Walker, L.3
-
39
-
-
0141615757
-
Single-tube multiplex-PCR screen for anti-3.7 and anti-4.2 α-globin gene triplications
-
Wang W, Ma ES, Chan AY, et al. Single-tube multiplex-PCR screen for anti-3.7 and anti-4.2 α-globin gene triplications. Clin Chem 2003;49:1679-1682.
-
(2003)
Clin Chem
, vol.49
, pp. 1679-1682
-
-
Wang, W.1
Ma, E.S.2
Chan, A.Y.3
-
40
-
-
44349136613
-
-
Blangero J, Almasey L, Dyer T, et al. Sequential Oligogenic Linkage Analysis Routines, SOLAR version 4.0.7 ed, 2007
-
Blangero J, Almasey L, Dyer T, et al. Sequential Oligogenic Linkage Analysis Routines, SOLAR version 4.0.7 ed., 2007.
-
-
-
|