-
1
-
-
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 188:361-363, 1975.
-
(1975)
Science
, vol.188
, pp. 361-363
-
-
Boyer, S.H.1
Belding, T.K.2
Margolet, L.3
Noyes, A.N.4
-
2
-
-
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 46:671-682, 1975.
-
(1975)
Blood
, vol.46
, pp. 671-682
-
-
Wood, W.G.1
Stamatoyannopoulos, G.2
Lim, G.3
Nute, P.E.4
-
3
-
-
0002398438
-
Hemoglobin switching
-
Stamatoyannopoulos G, Nienhuis AW, Majerus PW, Varmus H (eds): Philadelphia: W.B. Saunders Company
-
Stamatoyannopoulos G, Nienhuis AW: Hemoglobin switching. In Stamatoyannopoulos G, Nienhuis AW, Majerus PW, Varmus H (eds): "The Molecular Basis of Blood Diseases." Philadelphia: W.B. Saunders Company, 1994, pp 107-136.
-
(1994)
The Molecular Basis of Blood Diseases
, pp. 107-136
-
-
Stamatoyannopoulos, G.1
Nienhuis, A.W.2
-
4
-
-
0027204744
-
Increased Hb F in adult life
-
Higgs DR, Weatherall DJ (eds): London: Baillière Tindall
-
Wood WG: Increased Hb F in adult life. In Higgs DR, Weatherall DJ (eds): "The Hemoglobinopathies." London: Baillière Tindall, 1993, pp 177-213.
-
(1993)
The Hemoglobinopathies
, pp. 177-213
-
-
Wood, W.G.1
-
5
-
-
67749125406
-
2-Vermehrung bei der Schweizer Bevölkerung
-
2-Vermehrung bei der Schweizer Bevölkerung. Acta Haematol 26:65-74, 1961.
-
(1961)
Acta Haematol
, vol.26
, pp. 65-74
-
-
Marti, H.R.1
Butler, R.2
-
6
-
-
0017132176
-
Interaction of heterocellular hereditary persistence of fœtal hemoglobin with β-thalassaemia and sickle cell anaemia
-
Wood WG, Weathearall DJ, Clegg JB: Interaction of heterocellular hereditary persistence of fœtal hemoglobin with β-thalassaemia and sickle cell anaemia. Nature 264:247-249, 1976.
-
(1976)
Nature
, vol.264
, pp. 247-249
-
-
Wood, W.G.1
Weathearall, D.J.2
Clegg, J.B.3
-
7
-
-
0018764371
-
Genetic control of F-cells in human adults
-
Zago MA, Wood WG, Clegg JB, Weatherall DJ, O'Sullivan M, Gunson H: Genetic control of F-cells in human adults. Blood 53:977-986, 1979.
-
(1979)
Blood
, vol.53
, pp. 977-986
-
-
Zago, M.A.1
Wood, W.G.2
Clegg, J.B.3
Weatherall, D.J.4
O'Sullivan, M.5
Gunson, H.6
-
8
-
-
0020064422
-
Linkage analysis of nondeletion hereditary persistence of fetal hemoglobin
-
Old JM, Ayyub H, Wood WG: Linkage analysis of nondeletion hereditary persistence of fetal hemoglobin. Science 215:981-982, 1982.
-
(1982)
Science
, vol.215
, pp. 981-982
-
-
Old, J.M.1
Ayyub, H.2
Wood, W.G.3
-
9
-
-
0020985678
-
A gene controlling fetal hemoglobin expression in adults is not linked to the non-α globin cluster
-
Gianni AM, Bregni M, Cappellini MD, Fiorelli G, Taramelli R, Giglioni B, Comi P, Ottolenghi S: A gene controlling fetal hemoglobin expression in adults is not linked to the non-α globin cluster. EMBO J 2:921-925, 1983.
-
(1983)
EMBO J
, vol.2
, pp. 921-925
-
-
Gianni, A.M.1
Bregni, M.2
Cappellini, M.D.3
Fiorelli, G.4
Taramelli, R.5
Giglioni, B.6
Comi, P.7
Ottolenghi, S.8
-
10
-
-
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 M, Kaneto Y, Kawai H, Ohchi H, Niki S, Hasegawa K, Shirakami A, Yamano T: 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 72:1854-1860, 1988.
-
(1988)
Blood
, vol.72
, pp. 1854-1860
-
-
Miyoshi, M.1
Kaneto, Y.2
Kawai, H.3
Ohchi, H.4
Niki, S.5
Hasegawa, K.6
Shirakami, A.7
Yamano, T.8
-
11
-
-
0024385307
-
A case of hereditary persistence of fetal hemoglobin caused by a gene not linked to the β-globin cluster
-
Martinez G, Novelletto A, Di Rienzo A, Felicetti L, Colombo B: A case of hereditary persistence of fetal hemoglobin caused by a gene not linked to the β-globin cluster. Hum Genet 82:335-337, 1989.
-
(1989)
Hum Genet
, vol.82
, pp. 335-337
-
-
Martinez, G.1
Novelletto, A.2
Di Rienzo, A.3
Felicetti, L.4
Colombo, B.5
-
12
-
-
0028897283
-
An analysis of fetal hemoglobin variation in sickle cell disease: The relative contributions of X-linked factor, β-globin haplotypes, α-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 X-linked factor, β-globin haplotypes, α-globin gene number, gender and age. Blood 85:1111-1117, 1994.
-
(1994)
Blood
, vol.85
, pp. 1111-1117
-
-
Chang, Y.C.1
Smith, K.D.2
Moore, R.D.3
Serjeant, G.R.4
Dover, G.J.5
-
13
-
-
0028012604
-
Detection of a major gene for heterocellular hereditary persistence of fetal hemoglobin after accounting for genetic modifiers
-
Thein SL, Sampietro M, Rohde K, Rochette J, Weatherall DJ, Lathrop GM, Demenais F: Detection of a major gene for heterocellular hereditary persistence of fetal hemoglobin after accounting for genetic modifiers. Am J Hum Genet 54:214-228, 1994.
-
(1994)
Am J Hum Genet
, vol.54
, pp. 214-228
-
-
Thein, S.L.1
Sampietro, M.2
Rohde, K.3
Rochette, J.4
Weatherall, D.J.5
Lathrop, G.M.6
Demenais, F.7
-
14
-
-
0030065604
-
Dissecting the loci controlling fetal hemoglobin production on chromosome 11 p and 6 q by the regressive approach
-
Craig JE, Rochette J, Fisher CA, Weatherall DJ, Marc S, Lathrop GM, Demenais F, Thein SL: Dissecting the loci controlling fetal hemoglobin production on chromosome 11 p and 6 q by the regressive approach. Nature Genet 12:58-64, 1996.
-
(1996)
Nature Genet
, vol.12
, pp. 58-64
-
-
Craig, J.E.1
Rochette, J.2
Fisher, C.A.3
Weatherall, D.J.4
Marc, S.5
Lathrop, G.M.6
Demenais, F.7
Thein, S.L.8
-
15
-
-
0022006714
-
DNA sequence variation associated with elevated Gγ-globin production
-
Gilman JG, Huisman THJ: DNA sequence variation associated with elevated Gγ-globin production. Blood 66:783-787, 1985.
-
(1985)
Blood
, vol.66
, pp. 783-787
-
-
Gilman, J.G.1
Huisman, T.H.J.2
-
16
-
-
0022352518
-
The -158 site 5′ to the Gγ-gene and Gγ expression
-
Labie D, Dunda-Belkhodja O, Rouabhi F, Pagnier J, Ragusa A, Nagel RL: The -158 site 5′ to the Gγ-gene and Gγ expression. Blood 66: 1463-1465, 1985.
-
(1985)
Blood
, vol.66
, pp. 1463-1465
-
-
Labie, D.1
Dunda-Belkhodja, O.2
Rouabhi, F.3
Pagnier, J.4
Ragusa, A.5
Nagel, R.L.6
-
17
-
-
0026557081
-
Variation of Hb F and F-cell number with the Gγ XmnI (C → T) polymorphism in normal individuals
-
Sampietro M, Thein SL, Contreras M, Pazmany L: Variation of Hb F and F-cell number with the Gγ XmnI (C → T) polymorphism in normal individuals. Blood 79:832-833, 1992.
-
(1992)
Blood
, vol.79
, pp. 832-833
-
-
Sampietro, M.1
Thein, S.L.2
Contreras, M.3
Pazmany, L.4
-
18
-
-
0026502027
-
s chromosomes are associated with different levels of fetal globin in hemoglobin S homozygotes
-
s chromosomes are associated with different levels of fetal globin in hemoglobin S homozygotes. Blood 79:813-819, 1992.
-
(1992)
Blood
, vol.79
, pp. 813-819
-
-
Öner, C.1
Dimovski, A.J.2
Altay, C.3
Gurgey, A.4
Gu, Y.C.5
Huisman, T.H.J.6
Lanclos, K.D.7
-
19
-
-
0026665430
-
Black β-thalassemia homozygotes with specific sequence variations in the 5′ hypersensitive site-2 of the locus control region have high levels of fetal hemoglobin
-
Beris P, Kitundu MN, Baysal E. Öner C, Lanclos KD, Dimovski AJ, Kutlar F, Huisman THJ: Black β-thalassemia homozygotes with specific sequence variations in the 5′ hypersensitive site-2 of the locus control region have high levels of fetal hemoglobin. Am J Hematol 41:97-101, 1992.
-
(1992)
Am J Hematol
, vol.41
, pp. 97-101
-
-
Beris, P.1
Kitundu, M.N.2
Baysal, E.3
Öner, C.4
Lanclos, K.D.5
Dimovski, A.J.6
Kutlar, F.7
Huisman, T.H.J.8
-
20
-
-
0029979388
-
Variation of fetal hemoglobin and F-cell number with the LCR-HS2 polymorphism in nonanemic individuals
-
Merghoub T, Périchon B, Maier-Redelsperger M, Labie D, Feingold N, Dibenedetto, SP, Samperi P, Schiliro G, Ducrocq R, Elion J, Krishnamoorthy R: Variation of fetal hemoglobin and F-cell number with the LCR-HS2 polymorphism in nonanemic individuals. Blood 87:2607-2609, 1996.
-
(1996)
Blood
, vol.87
, pp. 2607-2609
-
-
Merghoub, T.1
Périchon, B.2
Maier-Redelsperger, M.3
Labie, D.4
Feingold, N.5
Dibenedetto, S.P.6
Samperi, P.7
Schiliro, G.8
Ducrocq, R.9
Elion, J.10
Krishnamoorthy, R.11
-
21
-
-
0346497365
-
Common haplotype dependence of high Gγ-globin gene expression and high Hb F levels in β-thalassemia and sickle cell anemia patients
-
Labie D, Pagnier J, Lapoumeroulie C, Rouahbi F, Dunda-Belkhodja O, Chardin P, Beldjord C, Wacjman H, Fabry ME, and Nagel RL: Common haplotype dependence of high Gγ-globin gene expression and high Hb F levels in β-thalassemia and sickle cell anemia patients. Proc Natl Acad Sci USA 82:2111-2114, 1985.
-
(1985)
Proc Natl Acad Sci USA
, vol.82
, pp. 2111-2114
-
-
Labie, D.1
Pagnier, J.2
Lapoumeroulie, C.3
Rouahbi, F.4
Dunda-Belkhodja, O.5
Chardin, P.6
Beldjord, C.7
Wacjman, H.8
Fabry, M.E.9
Nagel, R.L.10
-
23
-
-
0028113849
-
Variation in fetal hemoglobin parameters and predicted hemoglobin S polymerization in sickle cell children in the first two years of life: Parisian prospective study on sickle cell disease
-
Maier-Redelsperger M, Noguchi CT, de Montalembert M, Rodgers GP, Schechter AN, Gourbil A, Blanchard D, Jais JP, Ducrocq R, Peltier JY, Cottat MC, Lacaille F, Belloy M, Elion J, Labie D, Girat R: Variation in fetal hemoglobin parameters and predicted hemoglobin S polymerization in sickle cell children in the first two years of life: Parisian prospective study on sickle cell disease. Blood 84:3182-3188, 1994.
-
(1994)
Blood
, vol.84
, pp. 3182-3188
-
-
Maier-Redelsperger, M.1
Noguchi, C.T.2
De Montalembert, M.3
Rodgers, G.P.4
Schechter, A.N.5
Gourbil, A.6
Blanchard, D.7
Jais, J.P.8
Ducrocq, R.9
Peltier, J.Y.10
Cottat, M.C.11
Lacaille, F.12
Belloy, M.13
Elion, J.14
Labie, D.15
Girat, R.16
-
24
-
-
0024376665
-
Polymerase chain reaction amplification applied to the determination of β-like globin gene cluster haplotypes
-
Sutton M, Bouhassira EE, Nagel RL: Polymerase chain reaction amplification applied to the determination of β-like globin gene cluster haplotypes. Am J Hematol 33:66-69, 1989.
-
(1989)
Am J Hematol
, vol.33
, pp. 66-69
-
-
Sutton, M.1
Bouhassira, E.E.2
Nagel, R.L.3
-
25
-
-
0027305601
-
Inter-ethnic polymorphism of the β-globin gene locus control region (LCR) in sickle cell anemia patients
-
Périchon B, Ragusa A, Lapouméroulie C, Romand A, Moi P, Ikuta T, Labie D, Elion J, Krishnamoorthy R: Inter-ethnic polymorphism of the β-globin gene locus control region (LCR) in sickle cell anemia patients. Hum Genet 91:464-468, 1993.
-
(1993)
Hum Genet
, vol.91
, pp. 464-468
-
-
Périchon, B.1
Ragusa, A.2
Lapouméroulie, C.3
Romand, A.4
Moi, P.5
Ikuta, T.6
Labie, D.7
Elion, J.8
Krishnamoorthy, R.9
-
26
-
-
0026655070
-
Presence of African beta-globin gene cluster haplotype in normal chromosomes in Sicily
-
Ragusa A, Frontini V, Lombardo M, Amata S, Lombardo T, Labie D, Krishnamoorthy R, Nagel RL: Presence of African beta-globin gene cluster haplotype in normal chromosomes in Sicily. Am J Hematol 40:313-315, 1992.
-
(1992)
Am J Hematol
, vol.40
, pp. 313-315
-
-
Ragusa, A.1
Frontini, V.2
Lombardo, M.3
Amata, S.4
Lombardo, T.5
Labie, D.6
Krishnamoorthy, R.7
Nagel, R.L.8
-
27
-
-
0022746471
-
A transcriptional enhancer with specificity for erythroid cells is located in the long terminal repeat of the Friend's murine leukemia virus
-
Bosze Z, Hans-Jurgen T, Charnay P: A transcriptional enhancer with specificity for erythroid cells is located in the long terminal repeat of the Friend's murine leukemia virus. EMBO J 5:1615-1623, 1986.
-
(1986)
EMBO J
, vol.5
, pp. 1615-1623
-
-
Bosze, Z.1
Hans-Jurgen, T.2
Charnay, P.3
-
28
-
-
0023663884
-
Isolation of cDNA encoding transcription factor Sp1 and functional analysis of the DNA binding domain
-
Kadonaga JT, Carner KR, Masiarz FR, Tijan R: Isolation of cDNA encoding transcription factor Sp1 and functional analysis of the DNA binding domain. Cell 51:1079-1090, 1987.
-
(1987)
Cell
, vol.51
, pp. 1079-1090
-
-
Kadonaga, J.T.1
Carner, K.R.2
Masiarz, F.R.3
Tijan, R.4
-
29
-
-
0025365230
-
Detailed analysis of the site 3 region of the human β-globin dominant control region
-
Talbot D, Philipsen S, Fraser P, Grosveld F. Detailed analysis of the site 3 region of the human β-globin dominant control region. EMBO J 9:2169-2178, 1990.
-
(1990)
EMBO J
, vol.9
, pp. 2169-2178
-
-
Talbot, D.1
Philipsen, S.2
Fraser, P.3
Grosveld, F.4
-
30
-
-
0026570768
-
s mutation
-
s mutation. Blood 79:787-792, 1992.
-
(1992)
Blood
, vol.79
, pp. 787-792
-
-
Elion, J.1
Berg, P.E.2
Lapouméroulie, C.3
Trabuchet, G.4
Mittelman, M.5
Krishnamoorthy, R.6
Schechter, A.N.7
Labie, D.8
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