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Volumn 89, Issue 3, 1997, Pages 1078-1088

Fetal hemoglobin in sickle cell anemia: Determinants of response to hydroxyurea

Author keywords

[No Author keywords available]

Indexed keywords

HEMOGLOBIN F; HYDROXYUREA;

EID: 0030893396     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood.v89.3.1078     Document Type: Article
Times cited : (328)

References (49)
  • 7
    • 0022001839 scopus 로고
    • Hematologically and genetically distinct forms of sickle cell anemia in Africa. The Senegal type and the Benin type
    • Nagel RL, Fabry ME, Pagnier J, Zohoun I, Wajcman H, Baudin V, Labie D: Hematologically and genetically distinct forms of sickle cell anemia in Africa. The Senegal type and the Benin type. N Engl J Med 312:880, 1984
    • (1984) N Engl J Med , vol.312 , pp. 880
    • Nagel, R.L.1    Fabry, M.E.2    Pagnier, J.3    Zohoun, I.4    Wajcman, H.5    Baudin, V.6    Labie, D.7
  • 10
    • 0028012604 scopus 로고
    • 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, 1994
    • (1994) Am J Hum Genet , vol.54 , pp. 214
    • Thein, S.L.1    Sampietro, M.2    Rohde, K.3    Rochette, J.4    Weatherall, D.J.5    Lathrop, G.M.6    Demenais, F.7
  • 11
    • 0001379740 scopus 로고
    • The X-linked F cell production locus: Genetic mapping and role in fetal hemoglobin production
    • abstr
    • Chang YC, Smith KD, Serjeant G, Dover G: The X-linked F cell production locus: Genetic mapping and role in fetal hemoglobin production. Clin Res 42:237A, 1994 (abstr)
    • (1994) Clin Res , vol.42
    • Chang, Y.C.1    Smith, K.D.2    Serjeant, G.3    Dover, G.4
  • 12
    • 0024209310 scopus 로고
    • 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, 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, 1988
    • (1988) Blood , vol.72 , pp. 1854
    • Miyoshi, K.1    Kaneto, Y.2    Kawai, H.3    Ohchi, H.4    Niki, S.5    Hasegawa, K.6    Shirakami, A.7    Yamano, T.8
  • 13
    • 0026708201 scopus 로고
    • 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: Fetal hemoglobin levels in sickle cell disease and normal individuals are partially controlled by an X-linked gene located at Xp22.2. Blood 80:816, 1992
    • (1992) Blood , vol.80 , pp. 816
    • Dover, G.J.1    Smith, K.D.2    Chang, Y.C.3    Purvis, S.4    Mays, A.5    Meyers, D.A.6    Sheils, C.7    Serjeant, G.8
  • 14
    • 0028897283 scopus 로고
    • An analysis of fetal hemoglobin variation in sickle cell disease: The relative contributions of the 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 the X-linked factor, β-globin haplotypes, α-globin gene number, gender, and age. Blood 85:1111, 1995
    • (1995) Blood , vol.85 , pp. 1111
    • Chang, Y.C.1    Smith, K.D.2    Moore, R.D.3    Serjeant, G.R.4    Dover, G.J.5
  • 15
    • 0029129942 scopus 로고
    • Hydroxyurea: An alternative to transfusion therapy for stroke in sickle cell anemia
    • Ware RE, Steinberg MH, Kinney TR: Hydroxyurea: An alternative to transfusion therapy for stroke in sickle cell anemia. Am J Hematol 50:140, 1995
    • (1995) Am J Hematol , vol.50 , pp. 140
    • Ware, R.E.1    Steinberg, M.H.2    Kinney, T.R.3
  • 16
    • 0023130331 scopus 로고
    • Hydroxyurea-induced augmentation of fetal hemoglobin production in patients with sickle cell anemia
    • Charache S, Dover GJ, Moyer MA, Moore JW: Hydroxyurea-induced augmentation of fetal hemoglobin production in patients with sickle cell anemia. Blood 69:109, 1987
    • (1987) Blood , vol.69 , pp. 109
    • Charache, S.1    Dover, G.J.2    Moyer, M.A.3    Moore, J.W.4
  • 18
    • 0029294082 scopus 로고
    • The β- and δ-thalassemia repository (eighth edition)
    • Baysal E, Carver MFH: The β-and δ-thalassemia repository (eighth edition). Hemoglobin 19:213, 1995
    • (1995) Hemoglobin , vol.19 , pp. 213
    • Baysal, E.1    Carver, M.F.H.2
  • 19
    • 0023192454 scopus 로고
    • Flow cytometric reticulocyte counting with thioflavin T in a clinical hematology laboratory
    • Metzger DK, Charache S: Flow cytometric reticulocyte counting with thioflavin T in a clinical hematology laboratory. Arch Pathol Lab Med 111:540, 1987
    • (1987) Arch Pathol Lab Med , vol.111 , pp. 540
    • Metzger, D.K.1    Charache, S.2
  • 20
    • 0017148259 scopus 로고
    • A general method for isolation of high molecular weight DNA from eukaryotes
    • Blin N, Stafford DW: A general method for isolation of high molecular weight DNA from eukaryotes. Nucleic Acids Res 3:2303, 1976
    • (1976) Nucleic Acids Res , vol.3 , pp. 2303
    • Blin, N.1    Stafford, D.W.2
  • 21
    • 0022648392 scopus 로고
    • A new gene deletion in the alpha-like globin gene cluster as the molecular basis for the rare alpha-thalassemia-1(-/ αα) in blacks: HbH disease in sickle cell trait
    • Steinberg MH, Coleman MB, Adams JG, Hartmann RC, Saba H, Anagnou NP: A new gene deletion in the alpha-like globin gene cluster as the molecular basis for the rare alpha-thalassemia-1(-/ αα) in blacks: HbH disease in sickle cell trait. Blood 67:469, 1986
    • (1986) Blood , vol.67 , pp. 469
    • Steinberg, M.H.1    Coleman, M.B.2    Adams, J.G.3    Hartmann, R.C.4    Saba, H.5    Anagnou, N.P.6
  • 23
    • 36949068851 scopus 로고
    • Estimation of small percentages of foetal haemoglobin
    • Betke K, Marti HR, Schlicht I: Estimation of small percentages of foetal haemoglobin. Nature 184:1887, 1959
    • (1959) Nature , vol.184 , pp. 1887
    • Betke, K.1    Marti, H.R.2    Schlicht, I.3
  • 24
    • 0023275919 scopus 로고
    • Fetal hemoglobin-containing cells have the same mean corpuscular hemoglobin as cells without fetal hemoglobin: A reciprocal relationship between γ- and-β-globin gene expression in normal subjects and those with high fetal hemoglobin production
    • Dover GJ, Boyer SH: Fetal hemoglobin-containing cells have the same mean corpuscular hemoglobin as cells without fetal hemoglobin: A reciprocal relationship between γ-and-β-globin gene expression in normal subjects and those with high fetal hemoglobin production. Blood 69:1109, 1987
    • (1987) Blood , vol.69 , pp. 1109
    • Dover, G.J.1    Boyer, S.H.2
  • 25
    • 0018078193 scopus 로고
    • Microscopic method for assaying F cell production: Illustrative changes during infancy and in aplastic anemia
    • Dover GJ, Boyer SH, Bell WR: Microscopic method for assaying F cell production: Illustrative changes during infancy and in aplastic anemia. Blood 52:664, 1978
    • (1978) Blood , vol.52 , pp. 664
    • Dover, G.J.1    Boyer, S.H.2    Bell, W.R.3
  • 26
    • 0018227087 scopus 로고
    • Individual variation in the production and survival of F cells in sickle-cell disease
    • Dover GJ, Boyer SH, Charache S, Heintzelman K: Individual variation in the production and survival of F cells in sickle-cell disease. N Engl J Med 299:1428, 1978
    • (1978) N Engl J Med , vol.299 , pp. 1428
    • Dover, G.J.1    Boyer, S.H.2    Charache, S.3    Heintzelman, K.4
  • 27
    • 0015104003 scopus 로고
    • Determination of hydroxyurea in mammalian tissues und blood
    • Fabricius E, Rajewsky MF: Determination of hydroxyurea in mammalian tissues und blood. Rev Eur Etudes Clin Biol 16:679, 1971
    • (1971) Rev Eur Etudes Clin Biol , vol.16 , pp. 679
    • Fabricius, E.1    Rajewsky, M.F.2
  • 30
    • 77649173768 scopus 로고
    • Longitudinal data analysis using generalized linear models
    • Liang KY, Zeger SL: Longitudinal data analysis using generalized linear models. Biometrika 73:13, 1986
    • (1986) Biometrika , vol.73 , pp. 13
    • Liang, K.Y.1    Zeger, S.L.2
  • 33
    • 0024360719 scopus 로고
    • β-Cluster haplotypes α-gene status and hematological data from SS SC and S-β-thalassemia patients in southern California
    • Schroeder WA, Powars DR, Kay LM, Chan LS, Huynh V, Shelton JB, Shelton JR: β-Cluster haplotypes α-gene status and hematological data from SS SC and S-β-thalassemia patients in southern California. Hemoglobin 13:325, 1989
    • (1989) Hemoglobin , vol.13 , pp. 325
    • Schroeder, W.A.1    Powars, D.R.2    Kay, L.M.3    Chan, L.S.4    Huynh, V.5    Shelton, J.B.6    Shelton, J.R.7
  • 38
    • 0025756644 scopus 로고
    • S Gene-cluster haplotypes in sickle cell anemia: Clinical and hematologie features
    • S Gene-cluster haplotypes in sickle cell anemia: Clinical and hematologie features. Hematol Oncol Clin North Am 5:475, 1991
    • (1991) Hematol Oncol Clin North Am , vol.5 , pp. 475
    • Powars, D.R.1
  • 39
    • 0025797296 scopus 로고
    • S-Gene-cluster haplotypes as prognostic indicators of vital organ failure
    • S-Gene-cluster haplotypes as prognostic indicators of vital organ failure. Semin Hematol 28:202, 1991
    • (1991) Semin Hematol , vol.28 , pp. 202
    • Powars, D.R.1
  • 40
    • 0027452375 scopus 로고
    • S gene cluster haplotypes as genetic markers for severe disease expression
    • S gene cluster haplotypes as genetic markers for severe disease expression. Am J Dis Child 147:1197, 1993
    • (1993) Am J Dis Child , vol.147 , pp. 1197
    • Powars, D.1    Hiti, A.2
  • 41
    • 0025939624 scopus 로고
    • Chronic renal failure in sickle cell disease: Risk factors, clinical course, and mortality
    • Powars DR, Elliott Mills DD, Chan L: Chronic renal failure in sickle cell disease: Risk factors, clinical course, and mortality. Ann Intern Med 115:614, 1991
    • (1991) Ann Intern Med , vol.115 , pp. 614
    • Powars, D.R.1    Elliott Mills, D.D.2    Chan, L.3
  • 42
    • 0021911330 scopus 로고
    • The haematology of steady state homozygous sickle cell disease: Frequency distributions variation with age and sex, longitudinal observations
    • Hayes RJ, Beckford M, Grandison Y, Mason K, Serjeant BE, Serjeant GR: The haematology of steady state homozygous sickle cell disease: Frequency distributions variation with age and sex, longitudinal observations. Br J Haematol 59:369, 1985
    • (1985) Br J Haematol , vol.59 , pp. 369
    • Hayes, R.J.1    Beckford, M.2    Grandison, Y.3    Mason, K.4    Serjeant, B.E.5    Serjeant, G.R.6
  • 43
    • 0026767491 scopus 로고
    • Laboratory profile of sickle cell disease: A cross-sectional analysis
    • West MS, Wethers D, Smith J, Steinberg MH, Coop Study of Sickle Cell Diseuse: Laboratory profile of sickle cell disease: A cross-sectional analysis. J Clin Epidemiol 45:893, 1992
    • (1992) J Clin Epidemiol , vol.45 , pp. 893
    • West, M.S.1    Wethers, D.2    Smith, J.3    Steinberg, M.H.4
  • 45
    • 0025821277 scopus 로고
    • Effects of hydroxyurea on hemoglobin F and water content in the red blood cells of dogs and of patients with sickle cell anemia
    • Orringer EP, Blythe DSB, Johnson AE, Phillips G, Jr., Dover GJ, Parker JC: Effects of hydroxyurea on hemoglobin F and water content in the red blood cells of dogs and of patients with sickle cell anemia. Blood 78:212, 1991
    • (1991) Blood , vol.78 , pp. 212
    • Orringer, E.P.1    Blythe, D.S.B.2    Johnson, A.E.3    Phillips Jr., G.4    Dover, G.J.5    Parker, J.C.6
  • 46
    • 0028038985 scopus 로고
    • Hydroxyurea affects cell morphology cation transport and red blood cell adhesion in cultured vascular endothelial cells
    • Adragna NC, Fonseca P, Lauf PK: Hydroxyurea affects cell morphology cation transport and red blood cell adhesion in cultured vascular endothelial cells. Blood 83:553, 1994
    • (1994) Blood , vol.83 , pp. 553
    • Adragna, N.C.1    Fonseca, P.2    Lauf, P.K.3
  • 47
    • 0005655772 scopus 로고    scopus 로고
    • Hydroxyurea independent of HbF alters the erythrocytes of Hb SC disease
    • Steinberg MH, Nagel RL, Brugnara C: Hydroxyurea independent of HbF alters the erythrocytes of Hb SC disease. J Invest Med 44:233A, 1996
    • (1996) J Invest Med , vol.44
    • Steinberg, M.H.1    Nagel, R.L.2    Brugnara, C.3
  • 48
    • 0022568850 scopus 로고
    • Hydroxyurea induction of hemoglobin F production in sickle cell disease: Relationship between cytotoxicity and F cell production
    • Dover GJ, Humphries RK, Moore JG, Ley TJ, Young NS, Charache S, Nienhuis AW: Hydroxyurea induction of hemoglobin F production in sickle cell disease: Relationship between cytotoxicity and F cell production. Blood 67:735, 1986
    • (1986) Blood , vol.67 , pp. 735
    • Dover, G.J.1    Humphries, R.K.2    Moore, J.G.3    Ley, T.J.4    Young, N.S.5    Charache, S.6    Nienhuis, A.W.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.