Dover GJ - Search Results

1

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.

Chang YC, Smith KD, Moore RD, Serjeant GR, Dover GJ. Chang YC, et al. Among authors: dover gj. Blood. 1995 Feb 15;85(4):1111-7. Blood. 1995. PMID: 7531513 Free article.

2

Hydroxyurea: effects on hemoglobin F production in patients with sickle cell anemia.

Charache S, Dover GJ, Moore RD, Eckert S, Ballas SK, Koshy M, Milner PF, Orringer EP, Phillips G Jr, Platt OS, et al. Charache S, et al. Among authors: dover gj. Blood. 1992 May 15;79(10):2555-65. Blood. 1992. PMID: 1375104 Free article. Clinical Trial.

3

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, Purvis S, Mays A, Meyers DA, Sheils C, Serjeant G. Dover GJ, et al. Blood. 1992 Aug 1;80(3):816-24. Blood. 1992. PMID: 1379090 Free article.

4

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

Economou EP, Antonarakis SE, Kazazian HH Jr, Serjeant GR, Dover GJ. Economou EP, et al. Among authors: dover gj. Blood. 1991 Jan 1;77(1):174-7. Blood. 1991. PMID: 1702028 Free article.

5

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

Dover GJ, Chang VT, Boyer SH, Serjeant GR, Antonarakis S, Higgs DR. Dover GJ, et al. Blood. 1987 Jan;69(1):341-4. Blood. 1987. PMID: 2431731 Free article.

6

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

Boyer SH, Dover GJ, Serjeant GR, Smith KD, Antonarakis SE, Embury SH, Margolet L, Noyes AN, Boyer ML, Bias WB. Boyer SH, et al. Among authors: dover gj. Blood. 1984 Nov;64(5):1053-8. Blood. 1984. PMID: 6207872 Free article.

7

The relative importance of the X-linked FCP locus and beta-globin haplotypes in determining haemoglobin F levels: a study of SS patients homozygous for beta S haplotypes.

Chang YP, Maier-Redelsperger M, Smith KD, Contu L, Ducroco R, de Montalembert M, Belloy M, Elion J, Dover GJ, Girot R. Chang YP, et al. Among authors: dover gj. Br J Haematol. 1997 Mar;96(4):806-14. doi: 10.1046/j.1365-2141.1997.d01-2094.x. Br J Haematol. 1997. PMID: 9074425 Free article.

8

Treatment of sickle cell anemia with 5-azacytidine results in increased fetal hemoglobin production and is associated with nonrandom hypomethylation of DNA around the gamma-delta-beta-globin gene complex.

Charache S, Dover G, Smith K, Talbot CC Jr, Moyer M, Boyer S. Charache S, et al. Proc Natl Acad Sci U S A. 1983 Aug;80(15):4842-6. doi: 10.1073/pnas.80.15.4842. Proc Natl Acad Sci U S A. 1983. PMID: 6192443 Free PMC article.

9

Are there clinical phenotypes of homozygous sickle cell disease?

Alexander N, Higgs D, Dover G, Serjeant GR. Alexander N, et al. Br J Haematol. 2004 Aug;126(4):606-11. doi: 10.1111/j.1365-2141.2004.05025.x. Br J Haematol. 2004. PMID: 15287956 Free article.

10

Factors affecting prepubertal growth in homozygous sickle cell disease.

Singhal A, Morris J, Thomas P, Dover G, Higgs D, Serjeant G. Singhal A, et al. Arch Dis Child. 1996 Jun;74(6):502-6. doi: 10.1136/adc.74.6.502. Arch Dis Child. 1996. PMID: 8758125 Free PMC article.

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