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Journal Articles

An analysis of fetal hemoglobin variation in sickle cell disease: the relative contributions of the X-linked factor, beta-globin haplotypes, alpha-globin gene number, gender, and age

YC Chang, KD Smith, RD Moore, GR Serjeant, GJ Dover

Blood (1995) 85 (4): 1111–1117.

https://doi.org/10.1182/blood.V85.4.1111.bloodjournal8541111

Published: 1995

Journal Articles

Oral sodium phenylbutyrate therapy in homozygous beta thalassemia: a clinical trial

AF Collins, HA Pearson, P Giardina, KT McDonagh, SW Brusilow, GJ Dover

Blood (1995) 85 (1): 43–49.

https://doi.org/10.1182/blood.V85.1.43.bloodjournal85143

Published: 1995

Journal Articles

Increased fetal hemoglobin production in patients receiving valproic acid for epilepsy [letter]

AF Collins, GJ Dover, NL Luban

Blood (1994) 84 (5): 1690–1691.

https://doi.org/10.1182/blood.V84.5.1690.1690

Published: 1994

Journal Articles

Induction of fetal hemoglobin production in subjects with sickle cell anemia by oral sodium phenylbutyrate

GJ Dover, S Brusilow, S Charache

Blood (1994) 84 (1): 339–343.

https://doi.org/10.1182/blood.V84.1.339.339

Published: 1994

Journal Articles

Trial of recombinant human erythropoietin: three patients with thalassemia intermedia [letter]

NF Olivieri, MH Freedman, SP Perrine, GJ Dover, B Sheridan, DL Essentine, RL Nagel

Blood (1992) 80 (12): 3258–3260.

https://doi.org/10.1182/blood.V80.12.3258.3258

Published: 1992

Journal Articles

Fetal hemoglobin levels in sickle cell disease and normal individuals are partially controlled by an X-linked gene located at Xp22.2

GJ Dover, KD Smith, YC Chang, S Purvis, A Mays, DA Meyers, C Sheils, G Serjeant

Blood (1992) 80 (3): 816–824.

https://doi.org/10.1182/blood.V80.3.816.816

Published: 1992

Journal Articles

Hydroxyurea: effects on hemoglobin F production in patients with sickle cell anemia [see comments]

S Charache, GJ Dover, RD Moore, S Eckert, SK Ballas, M Koshy, PF Milner, EP Orringer, G Jr Phillips, OS Platt

Blood (1992) 79 (10): 2555–2565.

https://doi.org/10.1182/blood.V79.10.2555.2555

Published: 1992

Journal Articles

Effects of hydroxyurea on hemoglobin F and water content in the red blood cells of dogs and of patients with sickle cell anemia

EP Orringer, DS Blythe, AE Johnson, G Jr Phillips, GJ Dover, JC Parker

Blood (1991) 78 (1): 212–216.

https://doi.org/10.1182/blood.V78.1.212.212

Published: 1991

Journal Articles

Variation in hemoglobin F production among normal and sickle cell adults is not related to nucleotide substitutions in the gamma promoter regions

EP Economou, SE Antonarakis, HH Jr Kazazian, GR Serjeant, GJ Dover

Blood (1991) 77 (1): 174–177.

https://doi.org/10.1182/blood.V77.1.174.174

Published: 1991

Journal Articles

Serum-free culture of enriched hematopoietic progenitors reflects physiologic levels of fetal hemoglobin biosynthesis

Y Fujimori, M Ogawa, SC Clark, GJ Dover

Blood (1990) 75 (8): 1718–1722.

https://doi.org/10.1182/blood.V75.8.1718.1718

Published: 1990

Journal Articles

Fetal hemoglobin-containing cells have the same mean corpuscular hemoglobin as cells without fetal hemoglobin: a reciprocal relationship between gamma- and beta-globin gene expression in normal subjects and in those with high fetal hemoglobin production

GJ Dover, SH Boyer

Blood (1987) 69 (4): 1109–1113.

https://doi.org/10.1182/blood.V69.4.1109.1109

Published: 1987

Journal Articles

The cellular basis for different fetal hemoglobin levels among sickle cell individuals with two, three, and four alpha-globin genes

GJ Dover, VT Chang, SH Boyer, GR Serjeant, S Antonarakis, DR Higgs

Blood (1987) 69 (1): 341–344.

https://doi.org/10.1182/blood.V69.1.341.341

Published: 1987

Journal Articles

Hydroxyurea-induced augmentation of fetal hemoglobin production in patients with sickle cell anemia

S Charache, GJ Dover, MA Moyer, JW Moore

Blood (1987) 69 (1): 109–116.

https://doi.org/10.1182/blood.V69.1.109.109

Published: 1987

Journal Articles

Hydroxyurea induction of hemoglobin F production in sickle cell disease: relationship between cytotoxicity and F cell production

GJ Dover, RK Humphries, JG Moore, TJ Ley, NS Young, S Charache, AW Nienhuis

Blood (1986) 67 (3): 735–738.

https://doi.org/10.1182/blood.V67.3.735.735

Published: 1986

Journal Articles

5-Azacytidine increases HbF production and reduces anemia in sickle cell disease: dose-response analysis of subcutaneous and oral dosage regimens

GJ Dover, S Charache, SH Boyer, G Vogelsang, M Moyer

Blood (1985) 66 (3): 527–532.

https://doi.org/10.1182/blood.V66.3.527.527

Published: 1985

Journal Articles

Production of F cells in sickle cell anemia: regulation by a genetic locus or loci separate from the beta-globin gene cluster

SH Boyer, GJ Dover, GR Serjeant, KD Smith, SE Antonarakis, SH Embury, L Margolet, AN Noyes, ML Boyer, WB Bias

Blood (1984) 64 (5): 1053–1058.

https://doi.org/10.1182/blood.V64.5.1053.1053

Published: 1984

Journal Articles

Fetal hemoglobin synthesis in erythroid cultures in hereditary persistence of fetal hemoglobin and beta o-thalassemia

RS Weinberg, SE Antonarakis, HH Jr Kazazian, GJ Dover, SH Orkin, AL Lenes, JM Schofield, BP Alter

Blood (1984) 63 (6): 1278–1284.

https://doi.org/10.1182/blood.V63.6.1278.1278

Published: 1984

Journal Articles

Fetal hemoglobin production in cultures of primitive and mature human erythroid progenitors: differentiation affects the quantity of fetal hemoglobin produced per fetal-hemoglobin-containing cell

GJ Dover, T Chan, F Sieber

Blood (1983) 61 (6): 1242–1246.

https://doi.org/10.1182/blood.V61.6.1242.1242

Published: 1983

Journal Articles

Quantitation of hemoglobins within individual red cells: asynchronous biosynthesis of fetal and adult hemoglobin during erythroid maturation in normal subjects

GJ Dover, SH Boyer

Blood (1980) 56 (6): 1082–1091.

https://doi.org/10.1182/blood.V56.6.1082.1082

Published: 1980

Journal Articles

Selective hemolysis of adult red blood cells: an aid to prenatal diagnosis of hemoglobinopathies

BP Alter, JB Metzger, PG Yock, SB Rothchild, GJ Dover

Blood (1979) 53 (2): 279–287.

https://doi.org/10.1182/blood.V53.2.279.279

Published: 1979

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An analysis of fetal hemoglobin variation in sickle cell disease: the relative contributions of the X-linked factor, beta-globin haplotypes, alpha-globin gene number, gender, and age

Oral sodium phenylbutyrate therapy in homozygous beta thalassemia: a clinical trial

Increased fetal hemoglobin production in patients receiving valproic acid for epilepsy [letter]

Induction of fetal hemoglobin production in subjects with sickle cell anemia by oral sodium phenylbutyrate

Trial of recombinant human erythropoietin: three patients with thalassemia intermedia [letter]

Fetal hemoglobin levels in sickle cell disease and normal individuals are partially controlled by an X-linked gene located at Xp22.2

Hydroxyurea: effects on hemoglobin F production in patients with sickle cell anemia [see comments]

Effects of hydroxyurea on hemoglobin F and water content in the red blood cells of dogs and of patients with sickle cell anemia

Variation in hemoglobin F production among normal and sickle cell adults is not related to nucleotide substitutions in the gamma promoter regions

Serum-free culture of enriched hematopoietic progenitors reflects physiologic levels of fetal hemoglobin biosynthesis

Fetal hemoglobin-containing cells have the same mean corpuscular hemoglobin as cells without fetal hemoglobin: a reciprocal relationship between gamma- and beta-globin gene expression in normal subjects and in those with high fetal hemoglobin production

The cellular basis for different fetal hemoglobin levels among sickle cell individuals with two, three, and four alpha-globin genes

Hydroxyurea-induced augmentation of fetal hemoglobin production in patients with sickle cell anemia

Hydroxyurea induction of hemoglobin F production in sickle cell disease: relationship between cytotoxicity and F cell production

5-Azacytidine increases HbF production and reduces anemia in sickle cell disease: dose-response analysis of subcutaneous and oral dosage regimens

Production of F cells in sickle cell anemia: regulation by a genetic locus or loci separate from the beta-globin gene cluster

Fetal hemoglobin synthesis in erythroid cultures in hereditary persistence of fetal hemoglobin and beta o-thalassemia

Fetal hemoglobin production in cultures of primitive and mature human erythroid progenitors: differentiation affects the quantity of fetal hemoglobin produced per fetal-hemoglobin-containing cell

Quantitation of hemoglobins within individual red cells: asynchronous biosynthesis of fetal and adult hemoglobin during erythroid maturation in normal subjects

Selective hemolysis of adult red blood cells: an aid to prenatal diagnosis of hemoglobinopathies

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American Society of Hematology

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