Smith KD - 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: smith kd. Blood. 1995 Feb 15;85(4):1111-7. Blood. 1995. PMID: 7531513 Free article.

2

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: smith kd. Blood. 1984 Nov;64(5):1053-8. Blood. 1984. PMID: 6207872 Free article.

3

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: smith kd. 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.

4

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. Among authors: smith kd. Blood. 1992 Aug 1;80(3):816-24. Blood. 1992. PMID: 1379090 Free article.

5

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.

6

5-Azacytidine increases fetal hemoglobin production in a patient with sickle cell disease.

Dover GJ, Charache SH, Boyer SH, Talbot CC Jr, Smith KD. Dover GJ, et al. Among authors: smith kd. Prog Clin Biol Res. 1983;134:475-88. Prog Clin Biol Res. 1983. PMID: 6198661

7

Dinucleotide repeat polymorphisms at the DXS85, DXS16 and DXS43 loci.

Chang YP, Smith KD, Dover GJ. Chang YP, et al. Among authors: smith kd. Hum Mol Genet. 1994 Jun;3(6):1029. doi: 10.1093/hmg/3.6.1029. Hum Mol Genet. 1994. PMID: 7951221 No abstract available.

8

The evolution of two west African populations.

Stine OC, Dover GJ, Zhu D, Smith KD. Stine OC, et al. Among authors: smith kd. J Mol Evol. 1992 Apr;34(4):336-44. doi: 10.1007/BF00160241. J Mol Evol. 1992. PMID: 1569586

9

Role of cyclic nucleotides in fetal hemoglobin induction in cultured CD34+ cells.

Keefer JR, Schneidereith TA, Mays A, Purvis SH, Dover GJ, Smith KD. Keefer JR, et al. Among authors: smith kd. Exp Hematol. 2006 Sep;34(9):1151-61. doi: 10.1016/j.exphem.2006.03.018. Exp Hematol. 2006. PMID: 16939808 Free article.

10

The role of heterocellular hereditary persistence of fetal haemoglobin in beta(0)-thalassaemia intermedia.

Chang YP, Littera R, Garau R, Smith KD, Dover GJ, Iannelli S, Cacace E, Contu L. Chang YP, et al. Among authors: smith kd. Br J Haematol. 2001 Sep;114(4):899-906. doi: 10.1046/j.1365-2141.2001.03042.x. Br J Haematol. 2001. PMID: 11564083 Free article.

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