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Volumn 56, Issue 4, 1997, Pages 239-243

Dissection of the Association Status of Two Polymorphisms in the β-Globin Gene Cluster with Variations in F-Cell Number in Non-Anemic Individuals

Author keywords

F cells; Fetal hemoglobin; Locus control region; Polymorphism

Indexed keywords

DNA; DNA MODIFICATION METHYLASE XMNI; GLOBIN; HEMOGLOBIN F; SITE SPECIFIC DNA METHYLTRANSFERASE (ADENINE SPECIFIC);

EID: 0031451825     PISSN: 03618609     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8652(199712)56:4<239::AID-AJH7>3.0.CO;2-Y     Document Type: Article
Times cited : (17)

References (30)
  • 1
    • 0016793039 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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
  • 8
    • 0020064422 scopus 로고
    • 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
  • 10
    • 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 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 scopus 로고
    • 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 scopus 로고
    • 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 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 54:214-228, 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
  • 15
    • 0022006714 scopus 로고
    • 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
  • 17
    • 0026557081 scopus 로고
    • 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
  • 19
    • 0026665430 scopus 로고
    • 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
  • 24
    • 0024376665 scopus 로고
    • 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
  • 27
    • 0022746471 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.