-
1
-
-
0011355386
-
Warfarin sodium derivative: (coumadin sodium); an intravenous hypoprothrombinemia-inducing agent
-
Shapiro S. Warfarin sodium derivative: (coumadin sodium); an intravenous hypoprothrombinemia-inducing agent. Angiology 1953; 4: 380-90.
-
(1953)
Angiology
, vol.4
, pp. 380-390
-
-
Shapiro, S.1
-
2
-
-
34249786697
-
Experience with a new intravenous coumarin anticoagulant (warfarin, sodium derivative)
-
Wolff JM, Barker NW, Gifford RW, Mann FD. Experience with a new intravenous coumarin anticoagulant (warfarin, sodium derivative). Proc Staff Meet Mayo Clin 1953; 28: 489-97.
-
(1953)
Proc Staff Meet Mayo Clin
, vol.28
, pp. 489-497
-
-
Wolff, J.M.1
Barker, N.W.2
Gifford, R.W.3
Mann, F.D.4
-
3
-
-
4644230820
-
The pharmacology and management of the vitamin K antagonists: the Seventh ACCP Conference on Antithrombotic and Thrombolytic Therapy
-
Ansell J, Hirsh J, Poller L, Bussey H, Jacobson A, Hylek E. The pharmacology and management of the vitamin K antagonists: the Seventh ACCP Conference on Antithrombotic and Thrombolytic Therapy. Chest 2004; 126: 204S-33S.
-
(2004)
Chest
, vol.126
-
-
Ansell, J.1
Hirsh, J.2
Poller, L.3
Bussey, H.4
Jacobson, A.5
Hylek, E.6
-
4
-
-
0015494743
-
Warfarin and the inhibition of vitamin K activity by an oxide metabolite
-
Bell RG, Matschiner JT. Warfarin and the inhibition of vitamin K activity by an oxide metabolite. Nature 1972; 237: 32-3.
-
(1972)
Nature
, vol.237
, pp. 32-33
-
-
Bell, R.G.1
Matschiner, J.T.2
-
5
-
-
10744228888
-
Mutations in VKORC1 cause warfarin resistance and multiple coagulation factor deficiency type 2
-
Rost S, Fregin A, Ivaskevicius V, Conzelmann E, Hortnagel K, Pelz HJ, Lappegard K, Seifried E, Scharrer I, Tuddenham EG, Muller CR, Strom TM, Oldenburg J. Mutations in VKORC1 cause warfarin resistance and multiple coagulation factor deficiency type 2. Nature 2004; 427: 537-41.
-
(2004)
Nature
, vol.427
, pp. 537-541
-
-
Rost, S.1
Fregin, A.2
Ivaskevicius, V.3
Conzelmann, E.4
Hortnagel, K.5
Pelz, H.J.6
Lappegard, K.7
Seifried, E.8
Scharrer, I.9
Tuddenham, E.G.10
Muller, C.R.11
Strom, T.M.12
Oldenburg, J.13
-
6
-
-
0018136725
-
Mechanism of coumarin action: significance of vitamin K epoxide reductase inhibition
-
Whitlon DS, Sadowski JA, Suttie JW. Mechanism of coumarin action: significance of vitamin K epoxide reductase inhibition. Biochemistry 1978; 17: 1371-7.
-
(1978)
Biochemistry
, vol.17
, pp. 1371-1377
-
-
Whitlon, D.S.1
Sadowski, J.A.2
Suttie, J.W.3
-
7
-
-
13244255512
-
The physiology of vitamin K nutriture and vitamin K-dependent protein function in atherosclerosis
-
Berkner KL, Runge KW. The physiology of vitamin K nutriture and vitamin K-dependent protein function in atherosclerosis. J Thromb Haemost 2004; 2: 2118-32.
-
(2004)
J Thromb Haemost
, vol.2
, pp. 2118-2132
-
-
Berkner, K.L.1
Runge, K.W.2
-
8
-
-
45849118924
-
Metabolism and cell biology of vitamin K
-
Shearer MJ, Newman P. Metabolism and cell biology of vitamin K. Thromb Haemost 2008; 100: 530-47.
-
(2008)
Thromb Haemost
, vol.100
, pp. 530-547
-
-
Shearer, M.J.1
Newman, P.2
-
9
-
-
0015790825
-
Plasma half-lives, plasma metabolites and anticoagulant efficacies of the enantiomers of warfarin in man
-
Hewick DS, McEwen J. Plasma half-lives, plasma metabolites and anticoagulant efficacies of the enantiomers of warfarin in man. J Pharm Pharmacol 1973; 25: 458-65.
-
(1973)
J Pharm Pharmacol
, vol.25
, pp. 458-465
-
-
Hewick, D.S.1
McEwen, J.2
-
10
-
-
0031015345
-
Human P450 metabolism of warfarin
-
Kaminsky LS, Zhang ZY. Human P450 metabolism of warfarin. Pharmacol Ther 1997; 73: 67-74.
-
(1997)
Pharmacol Ther
, vol.73
, pp. 67-74
-
-
Kaminsky, L.S.1
Zhang, Z.Y.2
-
11
-
-
0024403279
-
Characteristics of warfarin hydroxylation catalyzed by human liver microsomes
-
Rettie AE, Eddy AC, Heimark LD, Gibaldi M, Trager WF. Characteristics of warfarin hydroxylation catalyzed by human liver microsomes. Drug Metab Dispos 1989; 17: 265-70.
-
(1989)
Drug Metab Dispos
, vol.17
, pp. 265-270
-
-
Rettie, A.E.1
Eddy, A.C.2
Heimark, L.D.3
Gibaldi, M.4
Trager, W.F.5
-
12
-
-
67651006101
-
Assessing cytochrome P450 and UDP-glucuronosyltransferase contributions to warfarin metabolism in humans
-
Miller GP, Jones DR, Sullivan SZ, Mazur A, Owen SN, Mitchell NC, Radominska-Pandya A, Moran JH. Assessing cytochrome P450 and UDP-glucuronosyltransferase contributions to warfarin metabolism in humans. Chem Res Toxicol 2009; 22: 1239-45.
-
(2009)
Chem Res Toxicol
, vol.22
, pp. 1239-1245
-
-
Miller, G.P.1
Jones, D.R.2
Sullivan, S.Z.3
Mazur, A.4
Owen, S.N.5
Mitchell, N.C.6
Radominska-Pandya, A.7
Moran, J.H.8
-
13
-
-
0026519541
-
Hydroxylation of warfarin by human cDNA-expressed cytochrome P-450: a role for P-4502C9 in the etiology of (S)-warfarin-drug interactions
-
Rettie AE, Korzekwa KR, Kunze KL, Lawrence RF, Eddy AC, Aoyama T, Gelboin HV, Gonzalez FJ, Trager WF. Hydroxylation of warfarin by human cDNA-expressed cytochrome P-450: a role for P-4502C9 in the etiology of (S)-warfarin-drug interactions. Chem Res Toxicol 1992; 5: 54-9.
-
(1992)
Chem Res Toxicol
, vol.5
, pp. 54-59
-
-
Rettie, A.E.1
Korzekwa, K.R.2
Kunze, K.L.3
Lawrence, R.F.4
Eddy, A.C.5
Aoyama, T.6
Gelboin, H.V.7
Gonzalez, F.J.8
Trager, W.F.9
-
14
-
-
33846919393
-
Synthesis and structure-activity relationships of novel warfarin derivatives
-
Gebauer M. Synthesis and structure-activity relationships of novel warfarin derivatives. Bioorg Med Chem 2007; 15: 2414-20.
-
(2007)
Bioorg Med Chem
, vol.15
, pp. 2414-2420
-
-
Gebauer, M.1
-
15
-
-
0023103840
-
The anticoagulant activity of some selected warfarin analogues
-
Obaseki AO, Coker HB. The anticoagulant activity of some selected warfarin analogues. J Pharm Pharmacol 1987; 39: 142-4.
-
(1987)
J Pharm Pharmacol
, vol.39
, pp. 142-144
-
-
Obaseki, A.O.1
Coker, H.B.2
-
16
-
-
0029559028
-
Human cytochromes P4501A1 and P4501A2: R-warfarin metabolism as a probe
-
Zhang Z, Fasco MJ, Huang Z, Guengerich FP, Kaminsky LS. Human cytochromes P4501A1 and P4501A2: R-warfarin metabolism as a probe. Drug Metab Dispos 1995; 23: 1339-46.
-
(1995)
Drug Metab Dispos
, vol.23
, pp. 1339-1346
-
-
Zhang, Z.1
Fasco, M.J.2
Huang, Z.3
Guengerich, F.P.4
Kaminsky, L.S.5
-
17
-
-
0024422827
-
The in vitro ketone reduction of warfarin and analogues. Substrate stereoselectivity, product stereoselectivity and species differences
-
Hermans JJ, Thijssen HH. The in vitro ketone reduction of warfarin and analogues. Substrate stereoselectivity, product stereoselectivity and species differences. Biochem Pharmacol 1989; 38: 3365-70.
-
(1989)
Biochem Pharmacol
, vol.38
, pp. 3365-3370
-
-
Hermans, J.J.1
Thijssen, H.H.2
-
18
-
-
0026558921
-
Phase II metabolism of warfarin in primary culture of adult rat hepatocytes
-
Jansing RL, Chao ES, Kaminsky LS. Phase II metabolism of warfarin in primary culture of adult rat hepatocytes. Mol Pharmacol 1992; 41: 209-15.
-
(1992)
Mol Pharmacol
, vol.41
, pp. 209-215
-
-
Jansing, R.L.1
Chao, E.S.2
Kaminsky, L.S.3
-
19
-
-
41549114526
-
Xenobiotic-induced transcriptional regulation of xenobiotic metabolizing enzymes of the cytochrome P450 superfamily in human extrahepatic tissues
-
Pavek P, Dvorak Z. Xenobiotic-induced transcriptional regulation of xenobiotic metabolizing enzymes of the cytochrome P450 superfamily in human extrahepatic tissues. Curr Drug Metab 2008; 9: 129-43.
-
(2008)
Curr Drug Metab
, vol.9
, pp. 129-143
-
-
Pavek, P.1
Dvorak, Z.2
-
20
-
-
65349091444
-
The steroid and xenobiotic receptor (SXR), beyond xenobiotic metabolism
-
Zhou C, Verma S, Blumberg B. The steroid and xenobiotic receptor (SXR), beyond xenobiotic metabolism. Nucl Recept Signal 2009; 7: e001.
-
(2009)
Nucl Recept Signal
, vol.7
-
-
Zhou, C.1
Verma, S.2
Blumberg, B.3
-
21
-
-
33846864449
-
Transcriptional regulation and expression of CYP3A4 in hepatocytes
-
Martinez-Jimenez CP, Jover R, Donato MT, Castell JV, Gomez-Lechon MJ. Transcriptional regulation and expression of CYP3A4 in hepatocytes. Curr Drug Metab 2007; 8: 185-94.
-
(2007)
Curr Drug Metab
, vol.8
, pp. 185-194
-
-
Martinez-Jimenez, C.P.1
Jover, R.2
Donato, M.T.3
Castell, J.V.4
Gomez-Lechon, M.J.5
-
22
-
-
21344439074
-
Nuclear receptors and drug disposition gene regulation
-
Tirona RG, Kim RB. Nuclear receptors and drug disposition gene regulation. J Pharm Sci 2005; 94: 1169-86.
-
(2005)
J Pharm Sci
, vol.94
, pp. 1169-1186
-
-
Tirona, R.G.1
Kim, R.B.2
-
23
-
-
28144459680
-
The nuclear xenobiotic receptor pregnane X receptor: recent insights and new challenges
-
Orans J, Teotico DG, Redinbo MR. The nuclear xenobiotic receptor pregnane X receptor: recent insights and new challenges. Mol Endocrinol 2005; 19: 2891-900.
-
(2005)
Mol Endocrinol
, vol.19
, pp. 2891-2900
-
-
Orans, J.1
Teotico, D.G.2
Redinbo, M.R.3
-
24
-
-
0242498469
-
Vitamin K2 regulation of bone homeostasis is mediated by the steroid and xenobiotic receptor SXR
-
Tabb MM, Sun A, Zhou C, Grun F, Errandi J, Romero K, Pham H, Inoue S, Mallick S, Lin M, Forman BM, Blumberg B. Vitamin K2 regulation of bone homeostasis is mediated by the steroid and xenobiotic receptor SXR. J Biol Chem 2003; 278: 43919-27.
-
(2003)
J Biol Chem
, vol.278
, pp. 43919-43927
-
-
Tabb, M.M.1
Sun, A.2
Zhou, C.3
Grun, F.4
Errandi, J.5
Romero, K.6
Pham, H.7
Inoue, S.8
Mallick, S.9
Lin, M.10
Forman, B.M.11
Blumberg, B.12
-
25
-
-
36048965821
-
Vitamin K induces osteoblast differentiation through pregnane X receptor-mediated transcriptional control of the Msx2 gene
-
Igarashi M, Yogiashi Y, Mihara M, Takada I, Kitagawa H, Kato S. Vitamin K induces osteoblast differentiation through pregnane X receptor-mediated transcriptional control of the Msx2 gene. Mol Cell Biol 2007; 27: 7947-54.
-
(2007)
Mol Cell Biol
, vol.27
, pp. 7947-7954
-
-
Igarashi, M.1
Yogiashi, Y.2
Mihara, M.3
Takada, I.4
Kitagawa, H.5
Kato, S.6
-
26
-
-
33745210139
-
Steroid and xenobiotic receptor SXR mediates vitamin K2-activated transcription of extracellular matrix-related genes and collagen accumulation in osteoblastic cells
-
Ichikawa T, Horie-Inoue K, Ikeda K, Blumberg B, Inoue S. Steroid and xenobiotic receptor SXR mediates vitamin K2-activated transcription of extracellular matrix-related genes and collagen accumulation in osteoblastic cells. J Biol Chem 2006; 281: 16927-34.
-
(2006)
J Biol Chem
, vol.281
, pp. 16927-16934
-
-
Ichikawa, T.1
Horie-Inoue, K.2
Ikeda, K.3
Blumberg, B.4
Inoue, S.5
-
27
-
-
45249121177
-
Drugs behave as substrates, inhibitors and inducers of human cytochrome P450 3A4
-
Zhou SF. Drugs behave as substrates, inhibitors and inducers of human cytochrome P450 3A4. Curr Drug Metab 2008; 9: 310-22.
-
(2008)
Curr Drug Metab
, vol.9
, pp. 310-322
-
-
Zhou, S.F.1
-
28
-
-
34250758597
-
Valproic acid induces CYP3A4 and MDR1 gene expression by activation of constitutive androstane receptor and pregnane X receptor pathways
-
Cerveny L, Svecova L, Anzenbacherova E, Vrzal R, Staud F, Dvorak Z, Ulrichova J, Anzenbacher P, Pavek P. Valproic acid induces CYP3A4 and MDR1 gene expression by activation of constitutive androstane receptor and pregnane X receptor pathways. Drug Metab Dispos 2007; 35: 1032-41.
-
(2007)
Drug Metab Dispos
, vol.35
, pp. 1032-1041
-
-
Cerveny, L.1
Svecova, L.2
Anzenbacherova, E.3
Vrzal, R.4
Staud, F.5
Dvorak, Z.6
Ulrichova, J.7
Anzenbacher, P.8
Pavek, P.9
-
29
-
-
71749099966
-
Intestinal cell-specific vitamin D receptor (VDR)-mediated transcriptional regulation of CYP3A4 gene
-
Pavek P, Pospechova K, Svecova L, Syrova Z, Stejskalova L, Blazkova J, Dvorak Z, Blahos J. Intestinal cell-specific vitamin D receptor (VDR)-mediated transcriptional regulation of CYP3A4 gene. Biochem Pharmacol 2010; 79: 277-87.
-
(2010)
Biochem Pharmacol
, vol.79
, pp. 277-287
-
-
Pavek, P.1
Pospechova, K.2
Svecova, L.3
Syrova, Z.4
Stejskalova, L.5
Blazkova, J.6
Dvorak, Z.7
Blahos, J.8
-
30
-
-
38749114272
-
Azole antimycotics differentially affect rifampicin-induced pregnane X receptor-mediated CYP3A4 gene expression
-
Svecova L, Vrzal R, Burysek L, Anzenbacherova E, Cerveny L, Grim J, Trejtnar F, Kunes J, Pour M, Staud F, Anzenbacher P, Dvorak Z, Pavek P. Azole antimycotics differentially affect rifampicin-induced pregnane X receptor-mediated CYP3A4 gene expression. Drug Metab Dispos 2008; 36: 339-48.
-
(2008)
Drug Metab Dispos
, vol.36
, pp. 339-348
-
-
Svecova, L.1
Vrzal, R.2
Burysek, L.3
Anzenbacherova, E.4
Cerveny, L.5
Grim, J.6
Trejtnar, F.7
Kunes, J.8
Pour, M.9
Staud, F.10
Anzenbacher, P.11
Dvorak, Z.12
Pavek, P.13
-
31
-
-
41649100943
-
The phytoestrogen coumestrol is a naturally occurring antagonist of the human pregnane X receptor
-
Wang H, Li H, Moore LB, Johnson MD, Maglich JM, Goodwin B, Ittoop OR, Wisely B, Creech K, Parks DJ, Collins JL, Willson TM, Kalpana GV, Venkatesh M, Xie W, Cho SY, Roboz J, Redinbo M, Moore JT, Mani S. The phytoestrogen coumestrol is a naturally occurring antagonist of the human pregnane X receptor. Mol Endocrinol 2008; 22: 838-57.
-
(2008)
Mol Endocrinol
, vol.22
, pp. 838-857
-
-
Wang, H.1
Li, H.2
Moore, L.B.3
Johnson, M.D.4
Maglich, J.M.5
Goodwin, B.6
Ittoop, O.R.7
Wisely, B.8
Creech, K.9
Parks, D.J.10
Collins, J.L.11
Willson, T.M.12
Kalpana, G.V.13
Venkatesh, M.14
Xie, W.15
Cho, S.Y.16
Roboz, J.17
Redinbo, M.18
Moore, J.T.19
Mani, S.20
more..
-
32
-
-
0035883992
-
Cytochrome P-450 mRNA expression in human liver and its relationship with enzyme activity
-
Rodriguez-Antona C, Donato MT, Pareja E, Gomez-Lechon MJ, Castell JV. Cytochrome P-450 mRNA expression in human liver and its relationship with enzyme activity. Arch Biochem Biophys 2001; 393: 308-15.
-
(2001)
Arch Biochem Biophys
, vol.393
, pp. 308-315
-
-
Rodriguez-Antona, C.1
Donato, M.T.2
Pareja, E.3
Gomez-Lechon, M.J.4
Castell, J.V.5
-
33
-
-
17344392308
-
A new mathematical model for relative quantification in real-time RT-PCR
-
Pfaffl MW. A new mathematical model for relative quantification in real-time RT-PCR. Nucleic Acids Res 2001; 29: e45.
-
(2001)
Nucleic Acids Res
, vol.29
-
-
Pfaffl, M.W.1
-
34
-
-
69749107295
-
New high-performance liquid chromatography method for the determination of (R)-warfarin and (S)-warfarin using chiral separation on a glycopeptide-based stationary phase
-
Malakova J, Pavek P, Svecova L, Jokesova I, Zivny P, Palicka V. New high-performance liquid chromatography method for the determination of (R)-warfarin and (S)-warfarin using chiral separation on a glycopeptide-based stationary phase. J Chromatogr B Analyt Technol Biomed Life Sci 2009; 877: 3226-30.
-
(2009)
J Chromatogr B Analyt Technol Biomed Life Sci
, vol.877
, pp. 3226-3230
-
-
Malakova, J.1
Pavek, P.2
Svecova, L.3
Jokesova, I.4
Zivny, P.5
Palicka, V.6
-
35
-
-
77952389622
-
Hydroxywarfarin metabolites potently inhibit CYP2C9 Metabolism of S-Warfarin
-
Jones DR, Kim SY, Guderyon M, Yun CH, Moran JH, Miller GP. Hydroxywarfarin metabolites potently inhibit CYP2C9 Metabolism of S-Warfarin. Chem Res Toxicol 2010; 23: 939-45.
-
(2010)
Chem Res Toxicol
, vol.23
, pp. 939-945
-
-
Jones, D.R.1
Kim, S.Y.2
Guderyon, M.3
Yun, C.H.4
Moran, J.H.5
Miller, G.P.6
-
36
-
-
14744305072
-
Determination of warfarin enantiomers and hydroxylated metabolites in human blood plasma by liquid chromatography with achiral and chiral separation
-
Locatelli I, Kmetec V, Mrhar A, Grabnar I. Determination of warfarin enantiomers and hydroxylated metabolites in human blood plasma by liquid chromatography with achiral and chiral separation. J Chromatogr B Analyt Technol Biomed Life Sci 2005; 818: 191-8.
-
(2005)
J Chromatogr B Analyt Technol Biomed Life Sci
, vol.818
, pp. 191-198
-
-
Locatelli, I.1
Kmetec, V.2
Mrhar, A.3
Grabnar, I.4
-
37
-
-
33747352798
-
MDR- and CYP3A4-mediated drug-drug interactions
-
Pal D, Mitra AK. MDR- and CYP3A4-mediated drug-drug interactions. J Neuroimmune Pharmacol 2006; 1: 323-39.
-
(2006)
J Neuroimmune Pharmacol
, vol.1
, pp. 323-339
-
-
Pal, D.1
Mitra, A.K.2
-
39
-
-
0030888416
-
Steady-state clearance rates of warfarin and its enantiomers in therapeutically dosed patients
-
McAleer SD, Foondun AS, Feely M, Chrystyn H. Steady-state clearance rates of warfarin and its enantiomers in therapeutically dosed patients. Chirality 1997; 9: 13-6.
-
(1997)
Chirality
, vol.9
, pp. 13-16
-
-
McAleer, S.D.1
Foondun, A.S.2
Feely, M.3
Chrystyn, H.4
-
40
-
-
0031452488
-
Oral bioavailability and first-pass effects
-
Kwan KC. Oral bioavailability and first-pass effects. Drug Metab Dispos 1997; 25: 1329-36.
-
(1997)
Drug Metab Dispos
, vol.25
, pp. 1329-1336
-
-
Kwan, K.C.1
|