메뉴 건너뛰기




Volumn 12, Issue 1, 1996, Pages 58-64

Dissecting the loci controlling fetal haemoglobin production on chromosomes 11p and 6q by the regressive approach

Author keywords

[No Author keywords available]

Indexed keywords

HEMOGLOBIN F;

EID: 0030065604     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/ng0196-58     Document Type: Article
Times cited : (146)

References (44)
  • 1
    • 0002398438 scopus 로고
    • Hemoglobin switching
    • (eds Stamatoyannopoulos, G., Nienhuis, A.W., Majerus, P.W. & Varmus, H.) W.B. Saunders and Co., Philadelphia
    • Stamatoyannopoulos, G. & Nienhuis, A.W. Hemoglobin switching. in The molecular basis of blood diseases (2nd Edition) (eds Stamatoyannopoulos, G., Nienhuis, A.W., Majerus, P.W. & Varmus, H.) 107-155 (W.B. Saunders and Co., Philadelphia, 1994).
    • (1994) The Molecular Basis of Blood Diseases (2nd Edition) , pp. 107-155
    • Stamatoyannopoulos, G.1    Nienhuis, A.W.2
  • 2
    • 0023663887 scopus 로고
    • Position-independent, high-level expression of the human γ-globin gene in transgenic mice
    • Grosveld, F., van Assendelft, G.B., Breaves, D.R. & Kollias, G. Position-independent, high-level expression of the human γ-globin gene in transgenic mice. Cell 51, 975-985 (1987).
    • (1987) Cell , vol.51 , pp. 975-985
    • Grosveld, F.1    Van Assendelft, G.B.2    Breaves, D.R.3    Kollias, G.4
  • 3
    • 0026557081 scopus 로고
    • Variation of HbF and F-cell number with the G-γ Xmn I (C-T) polymorphism in normal individuals
    • Sampietro, M., Thein, S.L., Contreras, M. & Pazmany, L. Variation of HbF and F-cell number with the G-γ Xmn I (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
  • 4
    • 0018764371 scopus 로고
    • Genetic control of F cells in human adults
    • Zago, MA et al. Genetic control of F cells in human adults. Blood 53, 977-986 (1979).
    • (1979) Blood , vol.53 , pp. 977-986
    • Zago, M.A.1
  • 5
    • 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. et al. 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, K.1
  • 6
    • 0020985678 scopus 로고
    • A gene controlling fetal hemoglobin expression in adults is not linked to the non-α globin cluster
    • Gianni, A.M. et al. A gene controlling fetal hemoglobin expression in adults is not linked to the non-α globin cluster. EMBO J. 2, 921-925 (1983).
    • (1983) EMBO J. , vol.2 , pp. 921-925
    • Gianni, A.M.1
  • 7
    • 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
  • 8
    • 0024780661 scopus 로고
    • A non-deletion hereditary persistance of fetal hemoglobin (HPFH) determinant not linked to the β-globin gene complex
    • (eds Stamatoyannopoulos, G. & Nienhuis, A.W.) Alan R. Liss, Inc., New York
    • Thein, S.L. & Weatherall, D.J. A non-deletion hereditary persistance of fetal hemoglobin (HPFH) determinant not linked to the β-globin gene complex. in Hemoglobin Switching, Part B: Cellular and Molecular Mechanisms (eds Stamatoyannopoulos, G. & Nienhuis, A.W.) 97-111 (Alan R. Liss, Inc., New York, 1989).
    • (1989) Hemoglobin Switching, Part B: Cellular and Molecular Mechanisms , pp. 97-111
    • Thein, S.L.1    Weatherall, D.J.2
  • 9
    • 0021359892 scopus 로고
    • Heterocellular HPFH: Molecular mechanisms of abnormal γ gene expression in association with β thalassemia and linkage relationship with the β globin gene cluster
    • Giampaolo, A. et al. Heterocellular HPFH: molecular mechanisms of abnormal γ gene expression in association with β thalassemia and linkage relationship with the β globin gene cluster. Hum. Genet. 66, 151-156 (1984).
    • (1984) Hum. Genet. , vol.66 , pp. 151-156
    • Giampaolo, A.1
  • 10
    • 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, G. J. et al. Fetal hemoglobin levels in sickle cell disease and normal individuals are partially controlled by an X-linked gene located at Xp22.2. Blood 80, 816-824 (1992).
    • (1992) Blood , vol.80 , pp. 816-824
    • Dover, G.J.1
  • 11
    • 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, Y.C., Smith, K.D., Moore, R.D., Serjeant, G.R. & Dover, G.J. 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, 1111-1117 (1995).
    • (1995) 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
  • 12
    • 0019518167 scopus 로고
    • Interaction between homozygous β° thalassaemia and the Swiss type of hereditary persistence of fetal haemoglobin
    • Cappellini, M.D., Fiorelli, G. & Bernini, L.F. Interaction between homozygous β° thalassaemia and the Swiss type of hereditary persistence of fetal haemoglobin. Br. J. Haem. 48, 561-572 (1981).
    • (1981) Br. J. Haem. , vol.48 , pp. 561-572
    • Cappellini, M.D.1    Fiorelli, G.2    Bernini, L.F.3
  • 14
    • 0020560380 scopus 로고
    • The estimation of fetal haemoglobin in healthy adults by radioimmunoassay
    • Rutland, P.C., Pembrey, M.E. & Davies, T. The estimation of fetal haemoglobin in healthy adults by radioimmunoassay. Br. J. Haem. 53, 673-682 (1983).
    • (1983) Br. J. Haem. , vol.53 , pp. 673-682
    • Rutland, P.C.1    Pembrey, M.E.2    Davies, T.3
  • 15
    • 0016760198 scopus 로고
    • A new form of hereditary persistence of fetal hemoglobin in blacks and its association with sickle cell trait
    • Stamatoyannopoulos, G., Wood, W.G. & Papayannopoulou, T. A new form of hereditary persistence of fetal hemoglobin in blacks and its association with sickle cell trait. Blood 46, 683-692 (1975).
    • (1975) Blood , vol.46 , pp. 683-692
    • Stamatoyannopoulos, G.1    Wood, W.G.2    Papayannopoulou, T.3
  • 16
    • 0025288473 scopus 로고
    • Level and composition of fetal hemoglobin expression in normal newborn babies are not dependent on β cluster DNA haplotype
    • Pochette, J., Dode, C., Leturcq, F. & Krishnamoorthy, R. Level and composition of fetal hemoglobin expression in normal newborn babies are not dependent on β cluster DNA haplotype. Am. J. Hem. 34, 223-224 (1990).
    • (1990) Am. J. Hem. , vol.34 , pp. 223-224
    • Pochette, J.1    Dode, C.2    Leturcq, F.3    Krishnamoorthy, R.4
  • 18
    • 0021281699 scopus 로고
    • On the statistical determination of major gene mechanisms in continuous human traits: Regressive models
    • Bonney, G.E. On the statistical determination of major gene mechanisms in continuous human traits: regressive models. Am. J. Med. Genet. 18, 731-749 (1984).
    • (1984) Am. J. Med. Genet. , vol.18 , pp. 731-749
    • Bonney, G.E.1
  • 19
    • 0023694035 scopus 로고
    • Combined linkage and segregation analysis using regressive models
    • Bonney, G.E., Lathrop, G.M. & Lalouel, J.-M. Combined linkage and segregation analysis using regressive models. Am. J. Hum. Genet. 43, 29-37 (1988).
    • (1988) Am. J. Hum. Genet. , vol.43 , pp. 29-37
    • Bonney, G.E.1    Lathrop, G.M.2    Lalouel, J.-M.3
  • 20
    • 0028012604 scopus 로고
    • Detection of a major gene for heterocellular hereditary persistence of fetal hemoglobin after accounting for genetic modifiers
    • Thein, S.L. et al. 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
  • 21
    • 0025123664 scopus 로고
    • Search for faster methods of fitting the regressive models to quantitative traits
    • Demenais, F.M., Murigande, C. & Bonney, G.E. Search for faster methods of fitting the regressive models to quantitative traits. Genet. Epidemiol. 7, 319-334 (1990).
    • (1990) Genet. Epidemiol. , vol.7 , pp. 319-334
    • Demenais, F.M.1    Murigande, C.2    Bonney, G.E.3
  • 22
    • 0026446099 scopus 로고
    • A second-generation linkage map of the human genome
    • Weissenbach, J. et al. A second-generation linkage map of the human genome. Nature 359, 794-801 (1992).
    • (1992) Nature , vol.359 , pp. 794-801
    • Weissenbach, J.1
  • 23
    • 0028231090 scopus 로고
    • The 1993-94 Généthon human genetic linkage map
    • Gyapay, G. et al. The 1993-94 Généthon human genetic linkage map. Nature Genetics 7, 246-339 (1994).
    • (1994) Nature Genetics , vol.7 , pp. 246-339
    • Gyapay, G.1
  • 24
    • 77049298733 scopus 로고
    • The detection and estimation of linkage between the genes for elliptocytes and Rh phenotype
    • Morton, I.N. The detection and estimation of linkage between the genes for elliptocytes and Rh phenotype. Am. J. Hum. Genet. 8, 80-96 (1956).
    • (1956) Am. J. Hum. Genet. , vol.8 , pp. 80-96
    • Morton, I.N.1
  • 26
    • 0028090414 scopus 로고
    • Genetic dissection of complex traits
    • Lander, E.S. & Schork, N.J. Genetic dissection of complex traits. Science 265, 2037-2048 (1994).
    • (1994) Science , vol.265 , pp. 2037-2048
    • Lander, E.S.1    Schork, N.J.2
  • 27
    • 0028070552 scopus 로고
    • Genetic mapping of a susceptibility locus for insulin-dependent diabetes mellitus on chromosome 11q
    • Hashimoto, L. et al. Genetic mapping of a susceptibility locus for insulin-dependent diabetes mellitus on chromosome 11q. Nature 371, 161-164 (1994).
    • (1994) Nature , vol.371 , pp. 161-164
    • Hashimoto, L.1
  • 28
    • 0027933734 scopus 로고
    • A genome-wide search for human type 1 diabetes susceptibility genes
    • Davies, J.L. et al. A genome-wide search for human type 1 diabetes susceptibility genes. Nature 371, 130-136 (1994).
    • (1994) Nature , vol.371 , pp. 130-136
    • Davies, J.L.1
  • 29
    • 0028230946 scopus 로고
    • Linkage analysis of IL4 and other chromosomes 5q31.1 markers and total serum immunoglobulin e concentrations
    • Marsh, D.G. et al. Linkage analysis of IL4 and other chromosomes 5q31.1 markers and total serum immunoglobulin E concentrations. Science 264, 1152-1156 (1994).
    • (1994) Science , vol.264 , pp. 1152-1156
    • Marsh, D.G.1
  • 31
    • 9044225798 scopus 로고    scopus 로고
    • How can maximum likelihood methods reveal candidate genes in a quantitative trait? Genet
    • in the press
    • Martinez, M., Abel, L. & Demenais, F. How can maximum likelihood methods reveal candidate genes in a quantitative trait? Genet. Epidemiol. (in the press).
    • Epidemiol.
    • Martinez, M.1    Abel, L.2    Demenais, F.3
  • 33
    • 0027266979 scopus 로고
    • The regulation of human globin gene expression. in Baillière's
    • eds Higgs, D.R. & Weatherall, D.J. Baillière Tindall, London
    • Grosveld, F., Dillon, N. & Higgs, D. The regulation of human globin gene expression. in Baillière's Clinical Haematology (eds Higgs, D.R. & Weatherall, D.J.) p. 31-55 (Baillière Tindall, London, 1993).
    • (1993) Clinical Haematology , pp. 31-55
    • Grosveld, F.1    Dillon, N.2    Higgs, D.3
  • 34
    • 0026849567 scopus 로고
    • Positional cloning: Let's not call it reverse anymore
    • Collins, F.S. Positional cloning: Let's not call it reverse anymore. Nature Genet. 1, 3-6 (1992).
    • (1992) Nature Genet. , vol.1 , pp. 3-6
    • Collins, F.S.1
  • 35
    • 0019512161 scopus 로고
    • Genetic relationship between fetal Hb levels in normal and erythropoietically stressed baboons
    • DeSimone, J., Heller, P., Biel, M. & Zwiers, D. Genetic relationship between fetal Hb levels in normal and erythropoietically stressed baboons. Br. J. Haem. 49, 175-183 (1981).
    • (1981) Br. J. Haem. , vol.49 , pp. 175-183
    • Desimone, J.1    Heller, P.2    Biel, M.3    Zwiers, D.4
  • 36
    • 0028154746 scopus 로고
    • Report of the Second International Workshop on Human Chromosome 6
    • Volz, A. et al. Report of the Second International Workshop on Human Chromosome 6. Genomes 21, 464-472 (1994).
    • (1994) Genomes , vol.21 , pp. 464-472
    • Volz, A.1
  • 37
    • 0022547276 scopus 로고
    • The gene for human liver arginase (ARG1) is assigned to chromosome band 6q23
    • Sparkes, R.S. et al. The gene for human liver arginase (ARG1) is assigned to chromosome band 6q23. Am. J. hum. Genet. 39, 186-193 (1986).
    • (1986) Am. J. Hum. Genet. , vol.39 , pp. 186-193
    • Sparkes, R.S.1
  • 38
    • 0027117567 scopus 로고
    • Dinucleotide repeat polymorphism at the human liver arginase gene (ARG1)
    • Meloni, R., Fougerousse, F., Roudaut, C. & Beckmann, J.S. Dinucleotide repeat polymorphism at the human liver arginase gene (ARG1). Nucl. Acids Res. 20, 1166 (1993).
    • (1993) Nucl. Acids Res. , vol.20 , pp. 1166
    • Meloni, R.1    Fougerousse, F.2    Roudaut, C.3    Beckmann, J.S.4
  • 40
    • 0028939603 scopus 로고
    • X-linked mental retardation associated with a thalassaemia (ATR-X syndrome) results from mutations in a putative global transcriptional regulator
    • Gibbons, R.J., Picketts, D.J., Villard, L. & Higgs, D.R. X-linked mental retardation associated with a thalassaemia (ATR-X syndrome) results from mutations in a putative global transcriptional regulator. Cell 80, 837-845 (1995).
    • (1995) Cell , vol.80 , pp. 837-845
    • Gibbons, R.J.1    Picketts, D.J.2    Villard, L.3    Higgs, D.R.4
  • 41
    • 0027202405 scopus 로고
    • β-thalassemia unlinked to the β-globin gene in an English family
    • Thein, S.L., Wood, W.G., Wickramasinghe, S.N. & Galvin, M.C. β-thalassemia unlinked to the β-globin gene in an English family. Blood 82, 961-967 (1993).
    • (1993) Blood , vol.82 , pp. 961-967
    • Thein, S.L.1    Wood, W.G.2    Wickramasinghe, S.N.3    Galvin, M.C.4
  • 42
    • 0021850103 scopus 로고
    • Multilocus linkage analysis in humans: Detection of linkage and estimation of recombination
    • Lathrop, G.M., Lalouel, J.M., Julier, C. & Ott, J. Multilocus linkage analysis in humans: detection of linkage and estimation of recombination. Am. J. Hum. Genet. 37, 482-498 (1985).
    • (1985) Am. J. Hum. Genet. , vol.37 , pp. 482-498
    • Lathrop, G.M.1    Lalouel, J.M.2    Julier, C.3    Ott, J.4
  • 43
    • 0015183542 scopus 로고
    • A general model for the genetic anlaysis of pedigree data
    • Elston, R.C. & Stewart, J. A general model for the genetic anlaysis of pedigree data. Hum. Hered. 21, 523-542 (1971).
    • (1971) Hum. Hered. , vol.21 , pp. 523-542
    • Elston, R.C.1    Stewart, J.2
  • 44
    • 0000814464 scopus 로고
    • REGRESS: A computer program including the regression approach into the linkage package
    • Demenais, F. & Lathrop, G.M. REGRESS: A computer program including the regression approach into the linkage package. Genet. Epidemiol. 11, 291 (1994).
    • (1994) Genet. Epidemiol. , vol.11 , pp. 291
    • Demenais, F.1    Lathrop, G.M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.