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Volumn 20, Issue , 2010, Pages 63-79

Clinical and biochemical consequences of P450 oxidoreductase deficiency

Author keywords

[No Author keywords available]

Indexed keywords

ANDROGEN; ANDROSTANOLONE; ANDROSTENEDIONE; CYTOCHROME P450 REDUCTASE; DRUG METABOLIZING ENZYME; ESTRIOL; TESTOSTERONE; UNSPECIFIC MONOOXYGENASE;

EID: 78751537714     PISSN: 14217082     EISSN: 16622979     Source Type: Book Series    
DOI: 10.1159/000321221     Document Type: Article
Times cited : (44)

References (70)
  • 1
    • 0014670327 scopus 로고
    • Resolution of the cytochrome P-450-containing β-hydroxylation system of liver microsomes into three components
    • Lu AY, Junk KW, Coon MJ: Resolution of the cytochrome P-450-containing β-hydroxylation system of liver microsomes into three components. J Biol Chem 1969;244:3714-3721.
    • (1969) J Biol Chem , vol.244 , pp. 3714-3721
    • Lu, A.Y.1    Junk, K.W.2    Coon, M.J.3
  • 2
    • 0024397098 scopus 로고
    • Human NADPH-P450 oxidoreductase: Complementary DNA cloning, sequence and vaccinia virus-mediated expression and localization of the CYPOR gene to chromosome 7
    • Yamano S, Aoyama T, McBride OW, Hardwick JP, Gelboin HV, Gonzalez FJ: Human NADPH-P450 oxidoreductase: complementary DNA cloning, sequence and vaccinia virus-mediated expression and localization of the CYPOR gene to chromosome 7. Mol Pharmacol 1989;36:83-88.
    • (1989) Mol Pharmacol , vol.36 , pp. 83-88
    • Yamano, S.1    Aoyama, T.2    McBride, O.W.3    Hardwick, J.P.4    Gelboin, H.V.5    Gonzalez, F.J.6
  • 3
    • 34347219795 scopus 로고    scopus 로고
    • Apparent manifesting heterozygosity in P450 oxidoreductase deficiency and its effect on coexisting 21-hydroxylase deficiency
    • Scott RR, Gomes LG, Huang N, Van Vliet G, Miller WL: Apparent manifesting heterozygosity in P450 oxidoreductase deficiency and its effect on coexisting 21-hydroxylase deficiency. J Clin Endocrinol Metab 2007;92:2318-2322.
    • (2007) J Clin Endocrinol Metab , vol.92 , pp. 2318-2322
    • Scott, R.R.1    Gomes, L.G.2    Huang, N.3    Van Vliet, G.4    Miller, W.L.5
  • 4
    • 0030873316 scopus 로고    scopus 로고
    • Three-dimensional structure of NADPH-cytochrome P450 reductase: Prototype for FMN-and FAD-containing enzymes
    • Wang M, Roberts DL, Paschke R, Shea TM, Masters BSS, Kim JJ: Three-dimensional structure of NADPH-cytochrome P450 reductase: prototype for FMN-and FAD-containing enzymes. Proc Natl Acad Sci USA 1997;94:8411-8416.
    • (1997) Proc Natl Acad Sci USA , vol.94 , pp. 8411-8416
    • Wang, M.1    Roberts, D.L.2    Paschke, R.3    Shea, T.M.4    Bss, M.5    Kim, J.J.6
  • 5
    • 18844367746 scopus 로고    scopus 로고
    • Regulation of steroidogenesis by electron transfer
    • Miller WL: Regulation of steroidogenesis by electron transfer. Endocrinology 2005;146:2544-2550.
    • (2005) Endocrinology , vol.146 , pp. 2544-2550
    • Miller, W.L.1
  • 6
    • 0030781147 scopus 로고    scopus 로고
    • Kinetics of ferric cytochrome P450 reduction by NADPH-cytochrome P450 reductase: Rapid reduction in the absence of substrate and variations among cytochrome P450 systems
    • Guengerich FP, Johnson WW: Kinetics of ferric cytochrome P450 reduction by NADPH-cytochrome P450 reductase: rapid reduction in the absence of substrate and variations among cytochrome P450 systems. Biochemistry 1997;36:14741-14750.
    • (1997) Biochemistry , vol.36 , pp. 14741-14750
    • Guengerich, F.P.1    Johnson, W.W.2
  • 7
    • 0032488666 scopus 로고    scopus 로고
    • Cytochrome b5 augments the 17,20-lyase activity of human P450c17 without direct electron transfer
    • Auchus RJ, Lee TC, Miller WL: Cytochrome b5 augments the 17,20-lyase activity of human P450c17 without direct electron transfer. J Biol Chem 1998; 273:3158-3165.
    • (1998) J Biol Chem , vol.273 , pp. 3158-3165
    • Auchus, R.J.1    Lee, T.C.2    Miller, W.L.3
  • 8
    • 0029671251 scopus 로고    scopus 로고
    • Roles of cytochrome b5 in the oxidation of testosterone and nifedipine by recombinant cytochrome P450 3A4 and by human liver microsomes
    • Yamazaki H, Nakano M, Imai Y, Ueng YF, Guengerich FP, Shimada T: Roles of cytochrome b5 in the oxidation of testosterone and nifedipine by recombinant cytochrome P450 3A4 and by human liver microsomes. Arch Biochem Biophys 1996;325: 174-182.
    • (1996) Arch Biochem Biophys , vol.325 , pp. 174-182
    • Yamazaki, H.1    Nakano, M.2    Imai, Y.3    Ueng, Y.F.4    Guengerich, F.P.5    Shimada, T.6
  • 9
    • 0035862176 scopus 로고    scopus 로고
    • The kinetic and spectral characterization of the E. coli-expressed mammalian CYP4A7: Cytochrome b5 effects vary with substrate
    • Loughran PA, Roman LJ, Miller RT, Masters BS: The kinetic and spectral characterization of the E. coli-expressed mammalian CYP4A7: cytochrome b5 effects vary with substrate. Arch Biochem Biophys 2001;385:311-321.
    • (2001) Arch Biochem Biophys , vol.385 , pp. 311-321
    • Loughran, P.A.1    Roman, L.J.2    Miller, R.T.3    Masters, B.S.4
  • 10
    • 0022997597 scopus 로고
    • Role of electron transport in the regulation of the lyase activity of C21 sidechain cleavage P-450 from porcine adrenal and testicular microsomes
    • Yanagibashi K, Hall PF: Role of electron transport in the regulation of the lyase activity of C21 sidechain cleavage P-450 from porcine adrenal and testicular microsomes. J Biol Chem 1986;261: 8429-8433.
    • (1986) J Biol Chem , vol.261 , pp. 8429-8433
    • Yanagibashi, K.1    Hall, P.F.2
  • 11
    • 0027230967 scopus 로고
    • Steroid 17α-hydroxylase and 17,20-lyase activities of P450c17: Contributions of serine-106 and P450 reductase
    • Lin D, Black SM, Nagahama Y, Miller WL: Steroid 17α-hydroxylase and 17,20-lyase activities of P450c17: contributions of serine-106 and P450 reductase. Endocrinology 1993;132:2498-2506.
    • (1993) Endocrinology , vol.132 , pp. 2498-2506
    • Lin, D.1    Black, S.M.2    Nagahama, Y.3    Miller, W.L.4
  • 12
    • 0033305733 scopus 로고    scopus 로고
    • Estrogen: Consequences and implications of human mutations in synthesis and action
    • Grumbach MM, Auchus RJ: Estrogen: consequences and implications of human mutations in synthesis and action. J Clin Endocrinol Metab 1999;84:4677-4694.
    • (1999) J Clin Endocrinol Metab , vol.84 , pp. 4677-4694
    • Grumbach, M.M.1    Auchus, R.J.2
  • 13
    • 7444233759 scopus 로고    scopus 로고
    • The backdoor pathway to dihydrotestosterone
    • Auchus RJ: The backdoor pathway to dihydrotestosterone. Trends Endocrinol Metab 2004;15:432-438.
    • (2004) Trends Endocrinol Metab , vol.15 , pp. 432-438
    • Auchus, R.J.1
  • 15
    • 4344591415 scopus 로고    scopus 로고
    • Prenatal diagnosis of P450 oxidoreductase deficiency (ORD): A disorder causing low pregnancy estriol, maternal and fetal virilization, and the Antley-Bixler syndrome phenotype
    • Shackleton C, Marcos J, Arlt W, Hauffa BP: Prenatal diagnosis of P450 oxidoreductase deficiency (ORD): a disorder causing low pregnancy estriol, maternal and fetal virilization, and the Antley-Bixler syndrome phenotype. Am J Med Genet 2004;129A:105-112.
    • (2004) Am J Med Genet , vol.129 A , pp. 105-112
    • Shackleton, C.1    Marcos, J.2    Arlt, W.3    Hauffa, B.P.4
  • 16
  • 17
    • 0022374725 scopus 로고
    • Male pseudohermaphroditism due to multiple defects in steroid-biosynthetic microsomal mixed-function oxidases. A new variant of congenital adrenal hyperplasia
    • Peterson RE, Imperato-McGinley J, Gautier T, Shackleton CH: Male pseudohermaphroditism due to multiple defects in steroid-biosynthetic microsomal mixed-function oxidases. A new variant of congenital adrenal hyperplasia. N Engl J Med 1985; 313:1182-1191.
    • (1985) N Engl J Med , vol.313 , pp. 1182-1191
    • Peterson, R.E.1    Imperato-Mcginley, J.2    Gautier, T.3    Shackleton, C.H.4
  • 21
    • 0032996258 scopus 로고    scopus 로고
    • A male patient presenting with major clinical symptoms of glucocorticoid deficiency and skeletal dysplasia, showing a steroid pattern compatible with 17α-hydroxylase/17,20-lyase deficiency, but without obvious CYP17 gene mutations
    • Adachi M, Tachibana K, Asakura Y, Suwa S, Nishimura G: A male patient presenting with major clinical symptoms of glucocorticoid deficiency and skeletal dysplasia, showing a steroid pattern compatible with 17α-hydroxylase/17,20-lyase deficiency, but without obvious CYP17 gene mutations. Endocr J 1999;46:285-292.
    • (1999) Endocr J , vol.46 , pp. 285-292
    • Adachi, M.1    Tachibana, K.2    Asakura, Y.3    Suwa, S.4    Nishimura, G.5
  • 23
    • 0031454319 scopus 로고    scopus 로고
    • Congenital lipoid adrenal hyperplasia: The human gene knockout for the steroidogenic acute regulatory protein
    • Miller WL: Congenital lipoid adrenal hyperplasia: the human gene knockout for the steroidogenic acute regulatory protein. J Mol Endocrinol 1997;19: 227-240.
    • (1997) J Mol Endocrinol , vol.19 , pp. 227-240
    • Miller, W.L.1
  • 26
    • 0022590907 scopus 로고
    • Congenital adrenal hyperplasia
    • Miller WL: Congenital adrenal hyperplasia. N Engl J Med 1986;314:1321-1322.
    • (1986) N Engl J Med , vol.314 , pp. 1321-1322
    • Miller, W.L.1
  • 27
    • 0037155271 scopus 로고    scopus 로고
    • Association of multiple developmental defects and embryonic lethality with loss of microsomal NADPHcytochrome P450 oxidoreductase
    • Shen AL, OLeary KA, Kasper CB: Association of multiple developmental defects and embryonic lethality with loss of microsomal NADPHcytochrome P450 oxidoreductase. J Biol Chem 2002;277:6536-6541.
    • (2002) J Biol Chem , vol.277 , pp. 6536-6541
    • Shen, A.L.1    Oleary, K.A.2    Kasper, C.B.3
  • 28
    • 0041468898 scopus 로고    scopus 로고
    • Identification of novel roles of the cytochrome P450 system in early embryogenesis: Effects on vasculogenesis and retinoic acid homeostasis
    • Otto DM, Henderson CJ, Carrie D, Davey M, Gundersen TE, Blomhoff R, Adams RH, Tickle C, Wolf CR: Identification of novel roles of the cytochrome P450 system in early embryogenesis: effects on vasculogenesis and retinoic acid homeostasis. Mol Cell Biol 2003;23:6103-6116.
    • (2003) Mol Cell Biol , vol.23 , pp. 6103-6116
    • Otto, D.M.1    Henderson, C.J.2    Carrie, D.3    Davey, M.4    Gundersen, T.E.5    Blomhoff, R.6    Adams, R.H.7    Tickle, C.8    Wolf, C.R.9
  • 31
    • 3342918965 scopus 로고    scopus 로고
    • Compound heterozygous mutations of cytochrome P450 oxidoreductase gene (POR) in two patients with Antley-Bixler syndrome
    • Adachi M, Tachibana K, Asakura Y, Yamamoto T, Hanaki K, Oka A: Compound heterozygous mutations of cytochrome P450 oxidoreductase gene (POR) in two patients with Antley-Bixler syndrome. Am J Med Genet 2004;128A:333-339.
    • (2004) Am J Med Genet , vol.128 A , pp. 333-339
    • Adachi, M.1    Tachibana, K.2    Asakura, Y.3    Yamamoto, T.4    Hanaki, K.5    Oka, A.6
  • 34
    • 33646691530 scopus 로고    scopus 로고
    • Cytochrome P450 oxidoreductase deficiency in three patients initially regarded as having 21-hydroxylase deficiency and/or aromatase deficiency: Diagnostic value of urine steroid hormone analysis
    • Fukami M, Hasegawa T, Horikawa R, Ohashi T, Nishimura G, Homma K, Ogata T: Cytochrome P450 oxidoreductase deficiency in three patients initially regarded as having 21-hydroxylase deficiency and/or aromatase deficiency: diagnostic value of urine steroid hormone analysis. Pediatr Res 2006;59:276-280.
    • (2006) Pediatr Res , vol.59 , pp. 276-280
    • Fukami, M.1    Hasegawa, T.2    Horikawa, R.3    Ohashi, T.4    Nishimura, G.5    Homma, K.6    Ogata, T.7
  • 37
    • 40349092943 scopus 로고    scopus 로고
    • Genetics of P450 oxidoreductase: Sequence variation in 842 individuals of four ethnicities and activities of 15 missense mutations
    • Huang N, Agrawal V, Giacomini KM, Miller WL: Genetics of P450 oxidoreductase: sequence variation in 842 individuals of four ethnicities and activities of 15 missense mutations. Proc Natl Acad Sci USA 2008;105:1733-1738.
    • (2008) Proc Natl Acad Sci USA , vol.105 , pp. 1733-1738
    • Huang, N.1    Agrawal, V.2    Giacomini, K.M.3    Miller, W.L.4
  • 38
    • 34948830894 scopus 로고    scopus 로고
    • Modulation of human CYP19A1 activity by mutant NADPH P450 oxidoreductase
    • Pandey AV, Kempna P, Hofer G, Mullis PE, Fluck CE: Modulation of human CYP19A1 activity by mutant NADPH P450 oxidoreductase. Mol Endocrinol 2007;21:2579-2595.
    • (2007) Mol Endocrinol , vol.21 , pp. 2579-2595
    • Pandey, A.V.1    Kempna, P.2    Hofer, G.3    Mullis, P.E.4    Fluck, C.E.5
  • 39
    • 34547465321 scopus 로고    scopus 로고
    • Differential inhibition of CYP17A1 and CYP21A2 activities by the P450 oxidoreductase mutant A287P
    • Dhir V, Ivison HE, Krone N, Shackleton CHL, Doherty AJ, Stewart PM, Arlt W: Differential inhibition of CYP17A1 and CYP21A2 activities by the P450 oxidoreductase mutant A287P. Mol Endocrinol 2007;21:1958-1968.
    • (2007) Mol Endocrinol , vol.21 , pp. 1958-1968
    • Dhir, V.1    Ivison, H.E.2    Krone, N.3    Chl, S.4    Doherty, A.J.5    Stewart, P.M.6    Arlt, W.7
  • 40
    • 0016736856 scopus 로고
    • Trapezoidocephaly, midfacial hypoplasia and cartilage abnormalities with multiple synostoses and skeletal fractures
    • Antley R, Bixler D: Trapezoidocephaly, midfacial hypoplasia and cartilage abnormalities with multiple synostoses and skeletal fractures. Birth Defects Orig Artic Ser 1975;11:397-401.
    • (1975) Birth Defects Orig Artic ser , vol.11 , pp. 397-401
    • Antley, R.1    Bixler, D.2
  • 42
    • 0028073158 scopus 로고
    • Antley-Bixler syndrome: Report of a patient and review of literature
    • Hassell S, Butler MG: Antley-Bixler syndrome: report of a patient and review of literature. Clin Genet 1994;46:372-376.
    • (1994) Clin Genet , vol.46 , pp. 372-376
    • Hassell, S.1    Butler, M.G.2
  • 43
    • 0031029098 scopus 로고    scopus 로고
    • Antley-Bixler syndrome: Case report and review of the literature
    • Crisponi G, Porcu C, Piu ME: Antley-Bixler syndrome: case report and review of the literature. Clin Dysmorphol 1997;6:61-68.
    • (1997) Clin Dysmorphol , vol.6 , pp. 61-68
    • Crisponi, G.1    Porcu, C.2    Piu, M.E.3
  • 44
    • 0032543288 scopus 로고    scopus 로고
    • FGFR2 mutation associated with clinical manifestations consistent with Antley-Bixler syndrome
    • Chun K, Siegel-Bartelt J, Chitayat D, Phillips J, Ray PN: FGFR2 mutation associated with clinical manifestations consistent with Antley-Bixler syndrome. Am J Med Genet 1998;77:219-224.
    • (1998) Am J Med Genet , vol.77 , pp. 219-224
    • Chun, K.1    Siegel-Bartelt, J.2    Chitayat, D.3    Phillips, J.4    Ray, P.N.5
  • 47
    • 0032559318 scopus 로고    scopus 로고
    • Novel mutation in the FGFR2 gene at the same codon as the Crouzon syndrome mutations in a severe Pfeiffer syndrome type 2 case
    • Schaefer F, Anderson C, Can B, Say B: Novel mutation in the FGFR2 gene at the same codon as the Crouzon syndrome mutations in a severe Pfeiffer syndrome type 2 case. Am J Med Genet 1998;75:252-255.
    • (1998) Am J Med Genet , vol.75 , pp. 252-255
    • Schaefer, F.1    Anderson, C.2    Can, B.3    Say, B.4
  • 48
    • 33644872519 scopus 로고    scopus 로고
    • The new bone biology: Pathologic, molecular, and clinical correlates
    • Cohen MM Jr: The new bone biology: pathologic, molecular, and clinical correlates. Am J Med Genet A 2006;140:2646-2706.
    • (2006) Am J Med Genet A , vol.140 , pp. 2646-2706
    • Cohen Jr., M.M.1
  • 52
    • 0029004086 scopus 로고
    • Novel FGFR2 mutations in Crouzon and Jackson-Weiss syndromes show allelic heterogeneity and phenotypic variability
    • Park WJ, Meyers GA, Li X, Theda C, Day D, Orlow SJ, Jones MC, Jabs EW: Novel FGFR2 mutations in Crouzon and Jackson-Weiss syndromes show allelic heterogeneity and phenotypic variability. Hum Mol Genet 1995;4:1229-1233.
    • (1995) Hum Mol Genet , vol.4 , pp. 1229-1233
    • Park, W.J.1    Meyers, G.A.2    Li, X.3    Theda, C.4    Day, D.5    Orlow, S.J.6    Jones, M.C.7    Jabs, E.W.8
  • 53
    • 58549083341 scopus 로고    scopus 로고
    • Characterization of the first FGFRL1 mutation identified in a craniosynostosis patient
    • Rieckmann T, Zhuang L, Fluck CE, Trueb B: Characterization of the first FGFRL1 mutation identified in a craniosynostosis patient. Biochim Biophys Acta 2009;1792:112-121.
    • (2009) Biochim Biophys Acta , vol.1792 , pp. 112-121
    • Rieckmann, T.1    Zhuang, L.2    Fluck, C.E.3    Trueb, B.4
  • 54
    • 0016641043 scopus 로고
    • Solubilization and partial characterization of rat liver squalene epoxidase
    • Ono T, Bloch K: Solubilization and partial characterization of rat liver squalene epoxidase. J Biol Chem 1975;250:1571-1579.
    • (1975) J Biol Chem , vol.250 , pp. 1571-1579
    • Ono, T.1    Bloch, K.2
  • 55
    • 0037223886 scopus 로고    scopus 로고
    • Many facets of mammalian lanosterol 14β-demethylase from the evolutionarily conserved cytochrome P450 family CYP51
    • Debeljak N, Fink M, Rozman D: Many facets of mammalian lanosterol 14β-demethylase from the evolutionarily conserved cytochrome P450 family CYP51. Arch Biochem Biophys 2003;409:159-171.
    • (2003) Arch Biochem Biophys , vol.409 , pp. 159-171
    • Debeljak, N.1    Fink, M.2    Rozman, D.3
  • 56
    • 0038778353 scopus 로고    scopus 로고
    • Molecular mechanisms underlying limb anomalies associated with cholesterol deficiency during gestation: Implications of hedgehog signaling
    • Gofflot F, Hars C, Illien F, Chevy F, Wolf C, Picard JJ, Roux C: Molecular mechanisms underlying limb anomalies associated with cholesterol deficiency during gestation: implications of hedgehog signaling. Hum Mol Genet 2003;12:1187-1198.
    • (2003) Hum Mol Genet , vol.12 , pp. 1187-1198
    • Gofflot, F.1    Hars, C.2    Illien, F.3    Chevy, F.4    Wolf, C.5    Picard, J.J.6    Roux, C.7
  • 59
    • 1942421701 scopus 로고    scopus 로고
    • Pharmacogenetics of cytochrome P450 and its applications in drug therapy: The past, present and future
    • Ingelman-Sundberg M: Pharmacogenetics of cytochrome P450 and its applications in drug therapy: the past, present and future. Trends Pharmacol Sci 2004;25:193-200.
    • (2004) Trends Pharmacol Sci , vol.25 , pp. 193-200
    • Ingelman-Sundberg, M.1
  • 60
    • 0026471292 scopus 로고
    • Congenital malformations in an infant born to a woman treated with fluconazole
    • Lee BE, Feinberg M, Abraham JJ, Murthy AR: Congenital malformations in an infant born to a woman treated with fluconazole. Pediatr Infect Dis J 1992;11:1062-1064.
    • (1992) Pediatr Infect Dis J , vol.11 , pp. 1062-1064
    • Lee, B.E.1    Feinberg, M.2    Abraham, J.J.3    Murthy, A.R.4
  • 62
    • 0030770714 scopus 로고    scopus 로고
    • Multiple malformation syndrome following fluconazole use in pregnancy: Report of an additional patient
    • Aleck KA, Bartley DL: Multiple malformation syndrome following fluconazole use in pregnancy: report of an additional patient. Am J Med Genet 1997;72:253-256.
    • (1997) Am J Med Genet , vol.72 , pp. 253-256
    • Aleck, K.A.1    Bartley, D.L.2
  • 64
    • 24944576037 scopus 로고    scopus 로고
    • Effect of antifungal drugs on cytochrome P450 (CYP) 2C9, CYP2C19, and CYP3A4 activities in human liver microsomes
    • Niwa T, Shiraga T, Takagi A: Effect of antifungal drugs on cytochrome P450 (CYP) 2C9, CYP2C19, and CYP3A4 activities in human liver microsomes. Biol Pharm Bull 2005;28:1805-1808.
    • (2005) Biol Pharm Bull , vol.28 , pp. 1805-1808
    • Niwa, T.1    Shiraga, T.2    Takagi, A.3
  • 65
    • 0038507099 scopus 로고    scopus 로고
    • Liver-specific deletion of the NADPH-cytochrome P450 reductase gene: Impact on plasma cholesterol homeostasis and the function and regulation of microsomal cytochrome P450 and heme oxygenase
    • Gu J, Weng Y, Zhang QY, Cui H, Behr M, Wu L, Yang W, Zhang L, Ding X: Liver-specific deletion of the NADPH-cytochrome P450 reductase gene: impact on plasma cholesterol homeostasis and the function and regulation of microsomal cytochrome P450 and heme oxygenase. J Biol Chem 2003;278: 25895-25901.
    • (2003) J Biol Chem , vol.278 , pp. 25895-25901
    • Gu, J.1    Weng, Y.2    Zhang, Q.Y.3    Cui, H.4    Behr, M.5    Wu, L.6    Yang, W.7    Zhang, L.8    Ding, X.9
  • 66
    • 38549085263 scopus 로고    scopus 로고
    • Genetic polymorphisms in cytochrome P450 oxidoreductase influence microsomal P450-catalyzed drug metabolism
    • Hart SN, Wang S, Nakamoto K, Wesselman C, Li Y, Zhong XB: Genetic polymorphisms in cytochrome P450 oxidoreductase influence microsomal P450-catalyzed drug metabolism. Pharmacogenet Genomics 2008;18:11-24.
    • (2008) Pharmacogenet Genomics , vol.18 , pp. 11-24
    • Hart, S.N.1    Wang, S.2    Nakamoto, K.3    Wesselman, C.4    Li, Y.5    Zhong, X.B.6
  • 67
    • 53049088208 scopus 로고    scopus 로고
    • Pharmacogenetics of P450 oxidoreductase. Effect of sequence variants on activities of CYP1A2 and CYP2C19
    • Agrawal V, Huang N, Miller WL: Pharmacogenetics of P450 oxidoreductase. Effect of sequence variants on activities of CYP1A2 and CYP2C19. Pharmacogenet Genomics 2008;18:569-576.
    • (2008) Pharmacogenet Genomics , vol.18 , pp. 569-576
    • Agrawal, V.1    Huang, N.2    Miller, W.L.3
  • 68
    • 77951254975 scopus 로고    scopus 로고
    • Restoration of mutant cytochrome P450 reductase activity by external flavin
    • Nicolo C, Fluck CE, Mullis PE, Pandey AV: Restoration of mutant cytochrome P450 reductase activity by external flavin. Mol Cell Endocrinol 2010;321:245-252.
    • (2010) Mol Cell Endocrinol , vol.321 , pp. 245-252
    • Nicolo, C.1    Fluck, C.E.2    Mullis, P.E.3    Pandey, A.V.4
  • 69
    • 77956907216 scopus 로고    scopus 로고
    • Altered heme catabolism by heme oxygenase-1 caused by mutations in human NADPH cytochrome P450 reductase
    • Pandey AV, Fluck CE, Mullis PE: Altered heme catabolism by heme oxygenase-1 caused by mutations in human NADPH cytochrome P450 reductase. Biochem Biophys Res Commun 2010;400: 374-378.
    • (2010) Biochem Biophys Res Commun , vol.400 , pp. 374-378
    • Pandey, A.V.1    Fluck, C.E.2    Mullis, P.E.3
  • 70
    • 77957687453 scopus 로고    scopus 로고
    • Reduction in hepatic drug metabolising CYP3A4 activities caused by P450 oxidoreductase mutations identified in patients with disordered steroid metabolism
    • Fluck CE, Mullis PE, Pandey AV: Reduction in hepatic drug metabolising CYP3A4 activities caused by P450 oxidoreductase mutations identified in patients with disordered steroid metabolism. Biochem Biophys Res Commun 2010;401:149-153.
    • (2010) Biochem Biophys Res Commun , vol.401 , pp. 149-153
    • Fluck, C.E.1    Mullis, P.E.2    Pandey, A.V.3


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