-
2
-
-
10744232330
-
The conduct of in vitro and in vivo drug-drug interaction studies: A pharmaceutical research and manufactures of America (PhRMA) perspective
-
Bjornsson TD, Callaghan JT, Einolf HJ, Fisher V, Gan L, Grimm S, Kao J, King SP, Miwa G, Ni L, Kumar G, McLeod J, Obach RS, Roberts S, Roe A, Shah A, Snikeris F, Sullivan JT, Tweedie D, Vega JM, Walsh J, Wrighton SA. 2003. The conduct of in vitro and in vivo drug-drug interaction studies: A pharmaceutical research and manufactures of America (PhRMA) perspective. Drug Metabolism and Disposition 31:815-832.
-
(2003)
Drug Metabolism and Disposition
, vol.31
, pp. 815-832
-
-
Bjornsson, T.D.1
Callaghan, J.T.2
Einolf, H.J.3
Fisher, V.4
Gan, L.5
Grimm, S.6
Kao, J.7
King, S.P.8
Miwa, G.9
Ni, L.10
Kumar, G.11
McLeod, J.12
Obach, R.S.13
Roberts, S.14
Roe, A.15
Shah, A.16
Snikeris, F.17
Sullivan, J.T.18
Tweedie, D.19
Vega, J.M.20
Walsh, J.21
Wrighton, S.A.22
more..
-
3
-
-
0035523263
-
Strategies for absorption screening in drug discovery and development
-
Bohers H, Annaert P, Mannens G, Van Beijsterveldt L, Anciaux K, Verboven P, Meuldermans W, Lavrijsen K. 2001. Strategies for absorption screening in drug discovery and development. Current Topics in Medicinal Chemistry 1:367-383.
-
(2001)
Current Topics in Medicinal Chemistry
, vol.1
, pp. 367-383
-
-
Bohers, H.1
Annaert, P.2
Mannens, G.3
Van Beijsterveldt, L.4
Anciaux, K.5
Verboven, P.6
Meuldermans, W.7
Lavrijsen, K.8
-
4
-
-
0035192078
-
Hepatic and intestinal cytochrome P450 3A activity in cirrhosis: Effects of transjugular intrahepatic portosystemic shunts
-
Chalasani N, Gorski JV, Patel NH, Hall SD, Galinsky RE. 2001. Hepatic and intestinal cytochrome P450 3A activity in cirrhosis: Effects of transjugular intrahepatic portosystemic shunts. Hepatology 34:1103-1108.
-
(2001)
Hepatology
, vol.34
, pp. 1103-1108
-
-
Chalasani, N.1
Gorski, J.V.2
Patel, N.H.3
Hall, S.D.4
Galinsky, R.E.5
-
5
-
-
0036296060
-
Comparison of oral absorption and bioavailability of drugs between monkey and human
-
Chiou WL, Buehler PW. 2002. Comparison of oral absorption and bioavailability of drugs between monkey and human. Pharmaceutical Research 19:868-874.
-
(2002)
Pharmaceutical Research
, vol.19
, pp. 868-874
-
-
Chiou, W.L.1
Buehler, P.W.2
-
6
-
-
0017888789
-
Absorption of the β-adrenergic-blocking agent, nadolol, by mice, rats, hamsters, rabbits, dogs, monkeys and man: An unusual species difference
-
Dreyfuss J, Shaw JM, Ross JJ. 1978. Absorption of the β-adrenergic-blocking agent, nadolol, by mice, rats, hamsters, rabbits, dogs, monkeys and man: An unusual species difference. Xenobiotica 8:503-508.
-
(1978)
Xenobiotica
, vol.8
, pp. 503-508
-
-
Dreyfuss, J.1
Shaw, J.M.2
Ross, J.J.3
-
7
-
-
0028234586
-
Regioselective biotransformation of midazolam by members of the human cytochrome P450 3A (CYP3A) subfamily
-
Gorski JC, Hall SD, Jones DR, VandenBranden M, Wrighton SA. 1994. Regioselective biotransformation of midazolam by members of the human cytochrome P450 3A (CYP3A) subfamily. Biochemical Pharmacology 47:1643-1653.
-
(1994)
Biochemical Pharmacology
, vol.47
, pp. 1643-1653
-
-
Gorski, J.C.1
Hall, S.D.2
Jones, D.R.3
VandenBranden, M.4
Wrighton, S.A.5
-
8
-
-
0015016365
-
Studies on the absorption, distribution and excretion of propranolol in rat, dog and monkey
-
Hayes A, Cooper RG. 1971. Studies on the absorption, distribution and excretion of propranolol in rat, dog and monkey. Journal of Pharmacology and Experimental Therapeutics 176:302-311.
-
(1971)
Journal of Pharmacology and Experimental Therapeutics
, vol.176
, pp. 302-311
-
-
Hayes, A.1
Cooper, R.G.2
-
11
-
-
0023733931
-
The non-human primate: A possible model for human genetically determined polymorphisms in oxidative drug metabolism
-
Jacqz E, Billante C, Moysan F, Mathieu H. 1988. The non-human primate: A possible model for human genetically determined polymorphisms in oxidative drug metabolism. Molecular Pharmacology 34:215-217.
-
(1988)
Molecular Pharmacology
, vol.34
, pp. 215-217
-
-
Jacqz, E.1
Billante, C.2
Moysan, F.3
Mathieu, H.4
-
12
-
-
20944439414
-
The intestinal first-pass metabolism of substrates of CYP3A4 and P-glycoprotein - Quantitative analysis based on information from the literature
-
Kato M, Chiba K, Hisaka A, Ishigami M, Kayama M, Mizuno N, Nagata Y, Takakuwa S, Tsukamoto Y, Ueda K, Kusuhara H, Ito K, Sugiyama Y. 2003. The intestinal first-pass metabolism of substrates of CYP3A4 and P-glycoprotein - quantitative analysis based on information from the literature. Drug Metabolism and Pharmacokinetics 18:365-372.
-
(2003)
Drug Metabolism and Pharmacokinetics
, vol.18
, pp. 365-372
-
-
Kato, M.1
Chiba, K.2
Hisaka, A.3
Ishigami, M.4
Kayama, M.5
Mizuno, N.6
Nagata, Y.7
Takakuwa, S.8
Tsukamoto, Y.9
Ueda, K.10
Kusuhara, H.11
Ito, K.12
Sugiyama, Y.13
-
14
-
-
0027050579
-
Molecular cloning of monkey liver cytochrome P-450 cDNAs: Similarity of the primary sequences to human cytochromes P-450
-
Komori M, Kikuchi O, Sakuma T, Funai J, Kitada M, Kamataki T. 1992b. Molecular cloning of monkey liver cytochrome P-450 cDNAs: Similarity of the primary sequences to human cytochromes P-450. Biochimica et Biophysica Acta 1171:141-146.
-
(1992)
Biochimica et Biophysica Acta
, vol.1171
, pp. 141-146
-
-
Komori, M.1
Kikuchi, O.2
Sakuma, T.3
Funai, J.4
Kitada, M.5
Kamataki, T.6
-
15
-
-
0024373348
-
Oxidation of midazolam and triazolam by human liver cytochrome P450IIIA4
-
Kronbach T, Mathys D, Umeno M, Gonzalez FJ, Meyer UA. 1989. Oxidation of midazolam and triazolam by human liver cytochrome P450IIIA4. Molecular Pharmacology 36:89-96.
-
(1989)
Molecular Pharmacology
, vol.36
, pp. 89-96
-
-
Kronbach, T.1
Mathys, D.2
Umeno, M.3
Gonzalez, F.J.4
Meyer, U.A.5
-
16
-
-
0026611310
-
Pharmacokinetic-pharmacodynamic modeling of the central nervous system effects of midazolam and its main metabolite α-hydroxymidazolam in healthy volunteers
-
Mandema JW, Tuk B, Van Steveninck AL, Breimer DD, Cohen AF, Danhof M. 1992. Pharmacokinetic-pharmacodynamic modeling of the central nervous system effects of midazolam and its main metabolite α-hydroxymidazolam in healthy volunteers. Clinical Pharmacology and Therapeutics 51:715-728.
-
(1992)
Clinical Pharmacology and Therapeutics
, vol.51
, pp. 715-728
-
-
Mandema, J.W.1
Tuk, B.2
Van Steveninck, A.L.3
Breimer, D.D.4
Cohen, A.F.5
Danhof, M.6
-
17
-
-
0033485965
-
Molecular cloning, expression, and characterization of CYP2D17 from cynomolgus monkey liver
-
Mankowski DC, Laddison KJ, Christopherson PA, Ekins S, Tweedie DJ, Lawton MP. 1999. Molecular cloning, expression, and characterization of CYP2D17 from cynomolgus monkey liver. Archives of Biochemistry and Biophysics 372:189-196.
-
(1999)
Archives of Biochemistry and Biophysics
, vol.372
, pp. 189-196
-
-
Mankowski, D.C.1
Laddison, K.J.2
Christopherson, P.A.3
Ekins, S.4
Tweedie, D.J.5
Lawton, M.P.6
-
18
-
-
0028801964
-
Characterisation of CYP3A gene subfamily expression in human gastrointestinal tissues
-
McKinnon RA, Burgess WM, Hall PM, Roberts-Thomson SJ, Gonzalez FJ, McManus ME. 1995. Characterisation of CYP3A gene subfamily expression in human gastrointestinal tissues. Gut 36:259-267.
-
(1995)
Gut
, vol.36
, pp. 259-267
-
-
McKinnon, R.A.1
Burgess, W.M.2
Hall, P.M.3
Roberts-Thomson, S.J.4
Gonzalez, F.J.5
McManus, M.E.6
-
19
-
-
0017841489
-
Disposition and metabolism of atenolol in animals
-
Reeves PR, Barnfield DJ, Longshaw S, McIntosh DAD, Winrow MJ. 1978. Disposition and metabolism of atenolol in animals. Xenobiotica 8:305-311.
-
(1978)
Xenobiotica
, vol.8
, pp. 305-311
-
-
Reeves, P.R.1
Barnfield, D.J.2
Longshaw, S.3
McIntosh, D.A.D.4
Winrow, M.J.5
-
20
-
-
85031333293
-
The effects of portal shunts on intestinal cytochrome P450 3A activity
-
Rostami-Hodjegan A, Tucker GT. 2002. The effects of portal shunts on intestinal cytochrome P450 3A activity. Hepatology 35:1549-1551.
-
(2002)
Hepatology
, vol.35
, pp. 1549-1551
-
-
Rostami-Hodjegan, A.1
Tucker, G.T.2
-
22
-
-
0034932521
-
Evaluation of a single-pass intestinal-perfusion method in rat for the prediction of absorption in man
-
Salphati L, Childers K, Pan L, Tsutsui K, Takahashi L. 2001. Evaluation of a single-pass intestinal-perfusion method in rat for the prediction of absorption in man. Journal of Pharmacy and Pharmacology 53:1007-1013.
-
(2001)
Journal of Pharmacy and Pharmacology
, vol.53
, pp. 1007-1013
-
-
Salphati, L.1
Childers, K.2
Pan, L.3
Tsutsui, K.4
Takahashi, L.5
-
23
-
-
0028237729
-
Interindividual variations in human liver cytochrome P-450 enzymes involved in the oxidation of drugs, carcinogens and toxic chemicals: Studies with liver microsomes of 30 Japanese and 30 Caucasians
-
Shimada T, Yamazaki H, Mimura M, Inui Y, Guengerich FP. 1994. Interindividual variations in human liver cytochrome P-450 enzymes involved in the oxidation of drugs, carcinogens and toxic chemicals: Studies with liver microsomes of 30 Japanese and 30 Caucasians. Journal of Pharmacology and Experimental Therapeutics 270:414-423.
-
(1994)
Journal of Pharmacology and Experimental Therapeutics
, vol.270
, pp. 414-423
-
-
Shimada, T.1
Yamazaki, H.2
Mimura, M.3
Inui, Y.4
Guengerich, F.P.5
-
25
-
-
0030015297
-
Oral first-pass elimination of midazolam involves both gastrointestinal and hepatic CYP3A-mediated metabolism
-
Thummel KE, O'Shea D, Paine MF, Shen DD, Kunze KL, Perkins JD, Wilkinson GR. 1996. Oral first-pass elimination of midazolam involves both gastrointestinal and hepatic CYP3A-mediated metabolism. Clinical Pharmacology and Therapeutics 59:491-502.
-
(1996)
Clinical Pharmacology and Therapeutics
, vol.59
, pp. 491-502
-
-
Thummel, K.E.1
O'Shea, D.2
Paine, M.F.3
Shen, D.D.4
Kunze, K.L.5
Perkins, J.D.6
Wilkinson, G.R.7
-
26
-
-
0028114619
-
Use of midazolam as a human cytochrome P450 3A probe: I. in vitro-in vivo correlations in liver transplant patients
-
Thummel KE, Shen DD, Podoll TD, Kunze KL, Trager WF, Hartwell PS, Raisys VA, Marsh CL, McVicar JP, Barr DM, Perkins JD, Carithers RL. 1994. Use of midazolam as a human cytochrome P450 3A probe: I. In vitro-in vivo correlations in liver transplant patients. Journal of Pharmacology and Experimental Therapeutics 271:549-556.
-
(1994)
Journal of Pharmacology and Experimental Therapeutics
, vol.271
, pp. 549-556
-
-
Thummel, K.E.1
Shen, D.D.2
Podoll, T.D.3
Kunze, K.L.4
Trager, W.F.5
Hartwell, P.S.6
Raisys, V.A.7
Marsh, C.L.8
McVicar, J.P.9
Barr, D.M.10
Perkins, J.D.11
Carithers, R.L.12
-
27
-
-
0032700543
-
Differentiation of intestinal and hepatic cytochrome P450 3A activity with use of midazolam as an in vivo probe: Effect of ketoconazole
-
Tsunoda SM, Velez RL, Von Moltke LL, Greenblatt DJ. 1999. Differentiation of intestinal and hepatic cytochrome P450 3A activity with use of midazolam as an in vivo probe: Effect of ketoconazole. Clinical Pharmacology and Therapeutics 66:461-471.
-
(1999)
Clinical Pharmacology and Therapeutics
, vol.66
, pp. 461-471
-
-
Tsunoda, S.M.1
Velez, R.L.2
Von Moltke, L.L.3
Greenblatt, D.J.4
-
28
-
-
0033005086
-
Predicting drug interactions and pharmacokinetic variability with in vitro methods: The olanzapine experience
-
Wrighton SA, Ring BJ. 1999. Predicting drug interactions and pharmacokinetic variability with in vitro methods: The olanzapine experience. Drug Metabolism Reviews 31:15-28.
-
(1999)
Drug Metabolism Reviews
, vol.31
, pp. 15-28
-
-
Wrighton, S.A.1
Ring, B.J.2
|