-
1
-
-
0028044085
-
Identification of a new genetic defect responsible for the polymorphism of (S)-mephenytoin metabolism in Japanese
-
7969038
-
De Morais SM, Wilkinson GR, Blaisdell J, Meyer UA, Nakamura K, Goldstein JA (1994) Identification of a new genetic defect responsible for the polymorphism of (S)-mephenytoin metabolism in Japanese. Mol Pharmacol 46:594-598
-
(1994)
Mol Pharmacol
, vol.46
, pp. 594-598
-
-
De Morais, S.M.1
Wilkinson, G.R.2
Blaisdell, J.3
Meyer, U.A.4
Nakamura, K.5
Goldstein, J.A.6
-
2
-
-
42049085520
-
Stereoselective disposition of proton pump inhibitors
-
18407713 10.2165/00044011-200828050-00001 1:CAS:528:DC%2BD1cXntVSru7k%3D
-
Andersson T, Weidolf L (2008) Stereoselective disposition of proton pump inhibitors. Clin Drug Investig 28:263-279
-
(2008)
Clin Drug Investig
, vol.28
, pp. 263-279
-
-
Andersson, T.1
Weidolf, L.2
-
3
-
-
0034935013
-
Pharmacokinetic studies with esomeprazole, the (S)-isomer of omeprazole
-
11475467 10.2165/00003088-200140060-00003 1:CAS:528:DC%2BD3MXlvFajsbo%3D
-
Andersson T, Hassan-Alin M, Hasselgren G, Röhss K, Weidolf L (2001) Pharmacokinetic studies with esomeprazole, the (S)-isomer of omeprazole. Clin Pharmacokinet 40:411-426
-
(2001)
Clin Pharmacokinet
, vol.40
, pp. 411-426
-
-
Andersson, T.1
Hassan-Alin, M.2
Hasselgren, G.3
Röhss, K.4
Weidolf, L.5
-
4
-
-
33745524102
-
The effect of CYP2C19 polymorphisms on H. pylori eradication rate in dual and triple first-line PPI therapies: A meta- analysis
-
16863547 10.1111/j.1572-0241.2006.00717.x 1:CAS:528:DC%2BD28XotFKitLk%3D
-
Padol S, Yuan Y, Thabane M, Padol IT, Hunt RH (2006) The effect of CYP2C19 polymorphisms on H. pylori eradication rate in dual and triple first-line PPI therapies: a meta- analysis. Am J Gastroenterol 101:1467-1475
-
(2006)
Am J Gastroenterol
, vol.101
, pp. 1467-1475
-
-
Padol, S.1
Yuan, Y.2
Thabane, M.3
Padol, I.T.4
Hunt, R.H.5
-
5
-
-
33947375710
-
Pharmacogenomics-based tailored versus standard therapeutic regimen for eradication of H. pylori
-
17215846 10.1038/sj.clpt.6100043 1:CAS:528:DC%2BD2sXkvFymu7o%3D
-
Furuta T, Shirai N, Kodaira M, Sugimoto M, Nogaki A, Kuriyama S, Iwaizumi M, Yamade M, Terakawa I, Ohashi K, Ishizaki T, Hishida A (2007) Pharmacogenomics-based tailored versus standard therapeutic regimen for eradication of H. pylori. Clin Pharmacol Ther 81:521-528
-
(2007)
Clin Pharmacol Ther
, vol.81
, pp. 521-528
-
-
Furuta, T.1
Shirai, N.2
Kodaira, M.3
Sugimoto, M.4
Nogaki, A.5
Kuriyama, S.6
Iwaizumi, M.7
Yamade, M.8
Terakawa, I.9
Ohashi, K.10
Ishizaki, T.11
Hishida, A.12
-
6
-
-
0035103705
-
Effect of genotypic differences in CYP2C19 on cure rates for Helicobacter pylori infection by triple therapy with a proton pump inhibitor, amoxicillin, and clarithromycin
-
11240980 10.1067/mcp.2001.113959 1:CAS:528:DC%2BD3MXislylsbw%3D
-
Furuta T, Shirai N, Takashima M, Xiao F, Hanai H, Sugimura H, Ohashi K, Ishizaki T, Kaneko E (2001) Effect of genotypic differences in CYP2C19 on cure rates for Helicobacter pylori infection by triple therapy with a proton pump inhibitor, amoxicillin, and clarithromycin. Clin Pharmacol Ther 69:158-168
-
(2001)
Clin Pharmacol Ther
, vol.69
, pp. 158-168
-
-
Furuta, T.1
Shirai, N.2
Takashima, M.3
Xiao, F.4
Hanai, H.5
Sugimura, H.6
Ohashi, K.7
Ishizaki, T.8
Kaneko, E.9
-
7
-
-
3342997410
-
CYP2C19 polymorphism is a major predictor of treatment failure in white patients by use of lansoprazole-based quadruple therapy for eradication of Helicobacter pylori
-
15371981 10.1016/j.clpt.2004.05.002 1:CAS:528:DC%2BD2cXnslKks7w%3D
-
Schwab M, Schaeffeler E, Klotz U, Treiber G (2004) CYP2C19 polymorphism is a major predictor of treatment failure in white patients by use of lansoprazole-based quadruple therapy for eradication of Helicobacter pylori. Clin Pharmacol Ther 76:201-209
-
(2004)
Clin Pharmacol Ther
, vol.76
, pp. 201-209
-
-
Schwab, M.1
Schaeffeler, E.2
Klotz, U.3
Treiber, G.4
-
8
-
-
0037313425
-
A proton-pump inhibitor expedition: The case histories of omeprazole and esomeprazole
-
12563304 10.1038/nrd1010 1:CAS:528:DC%2BD3sXot12lsA%3D%3D
-
Olbe L, Carlsson E, Lindberg P (2003) A proton-pump inhibitor expedition: The case histories of omeprazole and esomeprazole. Nat Rev Drug Discov 2:132-139
-
(2003)
Nat Rev Drug Discov
, vol.2
, pp. 132-139
-
-
Olbe, L.1
Carlsson, E.2
Lindberg, P.3
-
9
-
-
77749233911
-
A randomized controlled trial: Efficacy and safety of azathromycin, ofloxacin, bismutu and omeprazole compared with amoxicillin, clarithromycin, bismuth, and omeprazole as second-line therapy in patients with Helicobacter pylori infection
-
10.1111/j.1523-5378.2009.00739.x
-
Mohammad M, Amir HDJ, Ahmad S, Neda M, Farinaz T (2010) A randomized controlled trial: Efficacy and safety of azathromycin, ofloxacin, bismutu and omeprazole compared with amoxicillin, clarithromycin, bismuth, and omeprazole as second-line therapy in patients with Helicobacter pylori infection. Helicobacter 15:154-159
-
(2010)
Helicobacter
, vol.15
, pp. 154-159
-
-
Mohammad, M.1
Amir, H.D.J.2
Ahmad, S.3
Neda, M.4
Farinaz, T.5
-
10
-
-
77954529126
-
Drug-drug interaction profiles of proton pump inhibitors
-
10.2165/11531320-000000000-00000
-
Ogawa R, Echizen H (2010) Drug-drug interaction profiles of proton pump inhibitors. Clin Pharmacokinet 1:509-533
-
(2010)
Clin Pharmacokinet
, vol.1
, pp. 509-533
-
-
Ogawa, R.1
Echizen, H.2
-
11
-
-
0027366623
-
Oxidative metabolism of omeprazole in human liver microsomes: Cosegregation with S-mephenytoin 4′-hydroxylation
-
8331574 1:CAS:528:DyaK3sXlvFGjtLc%3D
-
Chiba K, Kobayashi K, Manabe K, Tani M, Kamataki T, Ishizaki T (1993) Oxidative metabolism of omeprazole in human liver microsomes: Cosegregation with S-mephenytoin 4′-hydroxylation. J Pharmacol Exp Ther 266:52-59
-
(1993)
J Pharmacol Exp Ther
, vol.266
, pp. 52-59
-
-
Chiba, K.1
Kobayashi, K.2
Manabe, K.3
Tani, M.4
Kamataki, T.5
Ishizaki, T.6
-
12
-
-
0028276695
-
Identification of human liver cytochrome P450 isoform mediating secondary omeprazole metabolism
-
10.1111/j.1365-2125.1994.tb04310.x
-
Andersson T, Miners JO, Veronese ME, Birkett DJ (1994) Identification of human liver cytochrome P450 isoform mediating secondary omeprazole metabolism. Br J Clin Pharmacol 35:597-604
-
(1994)
Br J Clin Pharmacol
, vol.35
, pp. 597-604
-
-
Andersson, T.1
Miners, J.O.2
Veronese, M.E.3
Birkett, D.J.4
-
13
-
-
0033856082
-
Stereoselective metabolism of omeprazole by human cytochrome P450 enzyme
-
10901708
-
Äbelö A, Andersson T, Antonsson M, Naudot AK, Skanberg I, Weidolf L (2000) Stereoselective metabolism of omeprazole by human cytochrome P450 enzyme. Drug Metab Dispos 28:966-972
-
(2000)
Drug Metab Dispos
, vol.28
, pp. 966-972
-
-
Äbelö, A.1
Andersson, T.2
Antonsson, M.3
Naudot, A.K.4
Skanberg, I.5
Weidolf, L.6
-
14
-
-
33846453309
-
Absolute bioavailability and metabolism of omeprazole in relation to CYP2C19 genotypes following single intravenous and oral administrations
-
17203292 10.1007/s00228-006-0251-7 1:CAS:528:DC%2BD2sXnsFyrtw%3D%3D
-
Uno T, Niioka T, Hayakari M, Yasui-Furukori N, Sugawara K, Tateishi T (2007) Absolute bioavailability and metabolism of omeprazole in relation to CYP2C19 genotypes following single intravenous and oral administrations. Eur J Clin Pharmacol 63:143-149
-
(2007)
Eur J Clin Pharmacol
, vol.63
, pp. 143-149
-
-
Uno, T.1
Niioka, T.2
Hayakari, M.3
Yasui-Furukori, N.4
Sugawara, K.5
Tateishi, T.6
-
15
-
-
33644777564
-
Sensitive determination of omeprazole and its two main metabolites in human plasma by column-switching high-performance liquid chromatography: Application to pharmacokinetic study in relation to CYP2C19 genotypes
-
16497565 10.1016/j.jchromb.2006.01.022 1:CAS:528:DC%2BD28XitVeiu7g%3D
-
Shimizu M, Uno T, Niioka T, Yasui-Furukori N, Takahata T, Sugawara K, Tateishi T (2006) Sensitive determination of omeprazole and its two main metabolites in human plasma by column-switching high-performance liquid chromatography: application to pharmacokinetic study in relation to CYP2C19 genotypes. J Chromatogr B Analyt Technol Biomed Life Sci 832:241-248
-
(2006)
J Chromatogr B Analyt Technol Biomed Life Sci
, vol.832
, pp. 241-248
-
-
Shimizu, M.1
Uno, T.2
Niioka, T.3
Yasui-Furukori, N.4
Takahata, T.5
Sugawara, K.6
Tateishi, T.7
-
16
-
-
12644315063
-
Pharmacokinetics of omeprazole (a substrate of CYP2C19) and comparison with two mutant alleles, C gamma P2C19m1 in exon 5 and C gamma P2C19m2 in exon 4, in Japanese subjects
-
8681489 10.1016/S0009-9236(96)90004-1 1:CAS:528:DyaK28XksFemurc%3D
-
Ieiri I, Kubota T, Urae A, Kimura M, Wada Y, Mamiya K, Yoshioka S, Irie S, Amamoto T, Nakamura K, Nakano S, Higuchi S (1996) Pharmacokinetics of omeprazole (a substrate of CYP2C19) and comparison with two mutant alleles, C gamma P2C19m1 in exon 5 and C gamma P2C19m2 in exon 4, in Japanese subjects. Clin Pharmacol Ther 59:647-653
-
(1996)
Clin Pharmacol Ther
, vol.59
, pp. 647-653
-
-
Ieiri, I.1
Kubota, T.2
Urae, A.3
Kimura, M.4
Wada, Y.5
Mamiya, K.6
Yoshioka, S.7
Irie, S.8
Amamoto, T.9
Nakamura, K.10
Nakano, S.11
Higuchi, S.12
-
17
-
-
0013389471
-
Reliability of the omeprazole hydroxylation index for CYP2C19 phenotyping: Possible effect of age, liver disease and length of therapy
-
10073749 10.1046/j.1365-2125.1999.00858.x 1:CAS:528:DyaK1MXht12isr4%3D
-
Kimura M, Ieiri I, Wada Y, Mamiya K, Urae A, Iimori E, Sakai T, Otsubo K, Higuchi S (1999) Reliability of the omeprazole hydroxylation index for CYP2C19 phenotyping: possible effect of age, liver disease and length of therapy. Br J Clin Pharmacol 47:115-119
-
(1999)
Br J Clin Pharmacol
, vol.47
, pp. 115-119
-
-
Kimura, M.1
Ieiri, I.2
Wada, Y.3
Mamiya, K.4
Urae, A.5
Iimori, E.6
Sakai, T.7
Otsubo, K.8
Higuchi, S.9
-
18
-
-
35248859765
-
Estimation of CYP2C19 activity by the omeprazole hydroxylation index at a single point in time after intravenous and oral administration
-
17701405 10.1007/s00228-007-0331-3 1:CAS:528:DC%2BD2sXhtFGgsLjN
-
Niioka T, Uno T, Sugimoto K, Sugawara K, Hayakari M, Tateishi T (2007) Estimation of CYP2C19 activity by the omeprazole hydroxylation index at a single point in time after intravenous and oral administration. Eur J Clin Pharmacol 63:1031-1038
-
(2007)
Eur J Clin Pharmacol
, vol.63
, pp. 1031-1038
-
-
Niioka, T.1
Uno, T.2
Sugimoto, K.3
Sugawara, K.4
Hayakari, M.5
Tateishi, T.6
-
19
-
-
17644379067
-
The effect of the CYP2C19 genotype on the hydroxylation index of omeprazole in South Indians
-
15662508 10.1007/s00228-004-0833-1 1:CAS:528:DC%2BD2MXisV2hsrg%3D
-
Rosemary J, Adithan C, Padmaja N, Shashindran CH, Gerard N, Krishnamoorthy R (2005) The effect of the CYP2C19 genotype on the hydroxylation index of omeprazole in South Indians. Eur J Clin Pharmacol 61:19-23
-
(2005)
Eur J Clin Pharmacol
, vol.61
, pp. 19-23
-
-
Rosemary, J.1
Adithan, C.2
Padmaja, N.3
Shashindran, C.H.4
Gerard, N.5
Krishnamoorthy, R.6
-
20
-
-
2442694261
-
Omeprazole as a CYP2C19 marker in Chinese subjects: Assessment of its gene-dose effect and intrasubject variability
-
15145965 10.1177/0091270004265702 1:CAS:528:DC%2BD2cXltV2ltLs%3D
-
Yin OQ, Tomlinson B, Chow AH, Waye MM, Chow MS (2004) Omeprazole as a CYP2C19 marker in Chinese subjects: assessment of its gene-dose effect and intrasubject variability. J Clin Pharmacol 44:582-589
-
(2004)
J Clin Pharmacol
, vol.44
, pp. 582-589
-
-
Yin, O.Q.1
Tomlinson, B.2
Chow, A.H.3
Waye, M.M.4
Chow, M.S.5
-
21
-
-
84864442361
-
Hydroxylation of R(+)- and S(-)-Omeprazole after Racemic Dosing are Different among the CYP2C19 Genotypes
-
22549736 10.1007/s11095-012-0757-x 1:CAS:528:DC%2BC38XmtlGru78%3D
-
Shiohira H, Yasui-Furukori N, Yamada S, Tateishi T, Akamine Y, Uno T (2012) Hydroxylation of R(+)- and S(-)-Omeprazole after Racemic Dosing are Different among the CYP2C19 Genotypes. Pharm Res 29:2310-2316
-
(2012)
Pharm Res
, vol.29
, pp. 2310-2316
-
-
Shiohira, H.1
Yasui-Furukori, N.2
Yamada, S.3
Tateishi, T.4
Akamine, Y.5
Uno, T.6
-
22
-
-
0025005022
-
Induction of polymorphic 4′-hydroxylation of S-mephenytoin by rifampicin
-
2223426 10.1111/j.1365-2125.1990.tb03799.x 1:CAS:528:DyaK3MXitVI%3D
-
Zhou HH, Anthony LB, Wood AJ, Wilkinson GR (1990) Induction of polymorphic 4′-hydroxylation of S-mephenytoin by rifampicin. Br J Clin Pharmacol 30:471-475
-
(1990)
Br J Clin Pharmacol
, vol.30
, pp. 471-475
-
-
Zhou, H.H.1
Anthony, L.B.2
Wood, A.J.3
Wilkinson, G.R.4
-
23
-
-
0031931510
-
The induction effect of rifampicin on activity of mephenytoin 4′-hydroxylase related to M1 mutation of CYP2C19 and gene dose
-
9489590 10.1046/j.1365-2125.1998.00643.x 1:CAS:528:DyaK1cXpslehuw%3D%3D
-
Feng HJ, Huang SL, Wang W, Zhou HH (1998) The induction effect of rifampicin on activity of mephenytoin 4′-hydroxylase related to M1 mutation of CYP2C19 and gene dose. Br J Clin Pharmacol 45:27-29
-
(1998)
Br J Clin Pharmacol
, vol.45
, pp. 27-29
-
-
Feng, H.J.1
Huang, S.L.2
Wang, W.3
Zhou, H.H.4
-
24
-
-
0034752109
-
CYP2C19 genotype determines enzyme activity and inducibility of S-mephenytoin hydroxylase
-
11694260 10.1016/S0009-8981(01)00696-9 1:CAS:528:DC%2BD3MXnvFGqu74%3D
-
Zhou HH (2001) CYP2C19 genotype determines enzyme activity and inducibility of S-mephenytoin hydroxylase. Clin Chim Acta 313:203-208
-
(2001)
Clin Chim Acta
, vol.313
, pp. 203-208
-
-
Zhou, H.H.1
-
25
-
-
0021927630
-
Phenotypic differences in mephenytoin pharmacokinetics in normal subjects
-
4032286 1:CAS:528:DyaL2MXlslWnsLk%3D
-
Wedlund PJ, Aslanian WS, Jacqz E, McAllister CB, Branch RA, Wilkinson GR (1985) Phenotypic differences in mephenytoin pharmacokinetics in normal subjects. J Pharmacol Exp Ther 234:662-669
-
(1985)
J Pharmacol Exp Ther
, vol.234
, pp. 662-669
-
-
Wedlund, P.J.1
Aslanian, W.S.2
Jacqz, E.3
McAllister, C.B.4
Branch, R.A.5
Wilkinson, G.R.6
-
26
-
-
39849088722
-
Limited frequency of the CYP2C19*17 allele and its minor role in a Japanese population
-
18241287 10.1111/j.1365-2125.2007.03057.x 1:CAS:528:DC%2BD1cXkvFOrsbg%3D
-
Sugimoto K, Uno T, Yamazaki H, Tateishi T (2008) Limited frequency of the CYP2C19*17 allele and its minor role in a Japanese population. Br J Clin Pharmacol 65:437-439
-
(2008)
Br J Clin Pharmacol
, vol.65
, pp. 437-439
-
-
Sugimoto, K.1
Uno, T.2
Yamazaki, H.3
Tateishi, T.4
-
27
-
-
30344457586
-
A common novel CYP2C19 gene variant causes ultrarapid drug metabolism relevant for the drug response to proton pump inhibitors and antidepressants
-
16413245 10.1016/j.clpt.2005.10.002 1:CAS:528:DC%2BD28XksVGltw%3D%3D
-
Sim SC, Risinger C, Dahl ML, Aklillu E, Christensen M, Bertilsson L, Ingelman-Sundberg M (2006) A common novel CYP2C19 gene variant causes ultrarapid drug metabolism relevant for the drug response to proton pump inhibitors and antidepressants. Clin Pharmacol Ther 79:103-113
-
(2006)
Clin Pharmacol Ther
, vol.79
, pp. 103-113
-
-
Sim, S.C.1
Risinger, C.2
Dahl, M.L.3
Aklillu, E.4
Christensen, M.5
Bertilsson, L.6
Ingelman-Sundberg, M.7
-
28
-
-
79960980893
-
Chiral assay of omeprazole and metabolites and its application to a pharmacokinetics related to CYP2C19 genotypes
-
21783435 10.1016/j.jchromb.2011.06.046 1:CAS:528:DC%2BC3MXpvFSru7k%3D
-
Shiohira H, Yasui-Furukori N, Tateishi T, Uno T (2011) Chiral assay of omeprazole and metabolites and its application to a pharmacokinetics related to CYP2C19 genotypes. J Chromatogr B Analyt Technol Biomed Life Sci 879:2465-2470
-
(2011)
J Chromatogr B Analyt Technol Biomed Life Sci
, vol.879
, pp. 2465-2470
-
-
Shiohira, H.1
Yasui-Furukori, N.2
Tateishi, T.3
Uno, T.4
-
29
-
-
0030803665
-
Enantioselective hydroxylation of omeprazole catalyzed by CYP2C19 in Swedish white subjects
-
9284848 10.1016/S0009-9236(97)90060-6 1:CAS:528:DyaK2sXmtVGju7g%3D
-
Tybring G, Böttiger Y, Widén J, Bertilsson L (1997) Enantioselective hydroxylation of omeprazole catalyzed by CYP2C19 in Swedish white subjects. Clin Pharmacol Ther 62:129-137
-
(1997)
Clin Pharmacol Ther
, vol.62
, pp. 129-137
-
-
Tybring, G.1
Böttiger, Y.2
Widén, J.3
Bertilsson, L.4
-
30
-
-
1942423665
-
Different inhibitory effect of fluvoxamine on omeprazole metabolism between CYP2C19 genotypes
-
15025747 10.1111/j.1365-2125.2003.02047.x 1:CAS:528:DC%2BD2cXjslGmsbw%3D
-
Yasui-Furukori N, Takahata T, Nakagami T, Yoshiya G, Inoue Y, Kaneko S, Tateishi T (2004) Different inhibitory effect of fluvoxamine on omeprazole metabolism between CYP2C19 genotypes. Br J Clin Pharmacol 57:487-494
-
(2004)
Br J Clin Pharmacol
, vol.57
, pp. 487-494
-
-
Yasui-Furukori, N.1
Takahata, T.2
Nakagami, T.3
Yoshiya, G.4
Inoue, Y.5
Kaneko, S.6
Tateishi, T.7
-
31
-
-
27144526218
-
Enantiomer/Enantiomer interaction between the S- and R-isomers of omeprazole in human cytochrome P450 enzymes: Major role of CYP2C19 and CYP3A4
-
16093273 10.1124/jpet.105.090928 1:CAS:528:DC%2BD2MXhtFyhtr%2FK
-
Li X, Weidolf L, Simonsson R, Andersson TB (2005) Enantiomer/Enantiomer interaction between the S- and R-isomers of omeprazole in human cytochrome P450 enzymes: major role of CYP2C19 and CYP3A4. J Pharmacol Exp Ther 315:777-787
-
(2005)
J Pharmacol Exp Ther
, vol.315
, pp. 777-787
-
-
Li, X.1
Weidolf, L.2
Simonsson, R.3
Andersson, T.B.4
|