-
1
-
-
84904439445
-
Targeting BCL2 for the treatment of lymphoid malignancies. Semin
-
[CrossRef][PubMed]
-
Anderson, M.A.; Huang, D.; Roberts, A. Targeting BCL2 for the treatment of lymphoid malignancies. Semin. Hematol. 2014, 51, 219–227. [CrossRef][PubMed]
-
(2014)
Hematol
, vol.51
, pp. 219-227
-
-
Anderson, M.A.1
Huang, D.2
Roberts, A.3
-
2
-
-
84959497243
-
ABT-199 (Venetoclax) and BCL-2 inhibitors in clinical development
-
[CrossRef][PubMed]
-
Cang, S.; Iragavarapu, C.; Savooji, J.; Song, Y.; Liu, D. ABT-199 (venetoclax) and BCL-2 inhibitors in clinical development. J. Hematol. Oncol. 2015, 8, 129. [CrossRef][PubMed]
-
(2015)
J. Hematol. Oncol
, vol.8
-
-
Cang, S.1
Iragavarapu, C.2
Savooji, J.3
Song, Y.4
Liu, D.5
-
3
-
-
84955491187
-
-
[CrossRef][PubMed]
-
Roberts, A.W.; Davids, M.S.; Pagel, J.M.; Kahl, B.S.; Puvvada, S.D.; Gerecitano, J.F.; Kipps, T.J.; Anderson, M.A.; Brown, J.R.; Gressick, L.; et al. Targeting BCL2 with Venetoclax in Relapsed Chronic Lymphocytic Leukemia. N. Engl. J. Med. 2016, 374, 311–322. [CrossRef][PubMed]
-
(2016)
Targeting BCL2 with Venetoclax in Relapsed Chronic Lymphocytic Leukemia. N. Engl. J. Med.
, vol.374
, pp. 311-322
-
-
Roberts, A.W.1
Davids, M.S.2
Pagel, J.M.3
Kahl, B.S.4
Puvvada, S.D.5
Gerecitano, J.F.6
Kipps, T.J.7
Anderson, M.A.8
Brown, J.R.9
Gressick, L.10
-
4
-
-
84873540049
-
ABT-199, a potent and selective BCL-2 inhibitor, achieves antitumor activity while sparing platelets
-
[CrossRef][PubMed]
-
Souers, A.J.; Leverson, J.D.; Boghaert, E.R.; Ackler, S.L.; Catron, N.D.; Chen, J.; Dayton, B.D.; Ding, H.; Enschede, S.H.; Fairbrother, W.J.; et al. ABT-199, a potent and selective BCL-2 inhibitor, achieves antitumor activity while sparing platelets. Nat. Med. 2013, 19, 202–208. [CrossRef][PubMed]
-
(2013)
Nat. Med
, vol.19
, pp. 202-208
-
-
Souers, A.J.1
Leverson, J.D.2
Boghaert, E.R.3
Ackler, S.L.4
Catron, N.D.5
Chen, J.6
Dayton, B.D.7
Ding, H.8
Enschede, S.H.9
Fairbrother, W.J.10
-
5
-
-
0028825399
-
Absence of the MDR1a P-glycoprotein in mice affects tissue distribution and pharmacokinetics of dexamethasone, digoxin, and cyclosporin A
-
[CrossRef][PubMed]
-
Schinkel, A.H.; Wagenaar, E.; van Deemter, L.; Mol, C.A.; Borst, P. Absence of the MDR1a P-glycoprotein in mice affects tissue distribution and pharmacokinetics of dexamethasone, digoxin, and cyclosporin A. J. Clin. Investig. 1995, 96, 1698–1705. [CrossRef][PubMed]
-
(1995)
J. Clin. Investig
, vol.96
, pp. 1698-1705
-
-
Schinkel, A.H.1
Wagenaar, E.2
Van Deemter, L.3
Mol, C.A.4
Borst, P.5
-
6
-
-
0001308329
-
Drug export activity of the human canalicular multispecific organic anion transporter in polarized kidney MDCK cells expressing cMOAT (MRP2) cDNA
-
[CrossRef][PubMed]
-
Evers, R.; Kool, M.; van Deemter, L.; Janssen, H.; Calafat, J.; Oomen, L.C.; Paulusma, C.C.; Oude Elferink, R.P.; Baas, F.; Schinkel, A.H.; et al. Drug export activity of the human canalicular multispecific organic anion transporter in polarized kidney MDCK cells expressing cMOAT (MRP2) cDNA. J. Clin. Investig. 1998, 101, 1310–1319. [CrossRef][PubMed]
-
(1998)
J. Clin. Investig.
, vol.101
, pp. 1310-1319
-
-
Evers, R.1
Kool, M.2
Van Deemter, L.3
Janssen, H.4
Calafat, J.5
Oomen, L.C.6
Paulusma, C.C.7
Oude Elferink, R.P.8
Baas, F.9
Schinkel, A.H.10
-
7
-
-
11844284860
-
Human breast cancer resistance protein: Interactions with steroid drugs, hormones, the dietary carcinogen 2-amino-1-methyl-6-phenylimidazo(4,5-b)pyridine, and transport of cimetidine
-
[CrossRef][PubMed]
-
Pavek, P.; Merino, G.; Wagenaar, E.; Bolscher, E.; Novotna, M.; Jonker, J.W.; Schinkel, A.H. Human breast cancer resistance protein: interactions with steroid drugs, hormones, the dietary carcinogen 2-amino-1-methyl-6-phenylimidazo(4,5-b)pyridine, and transport of cimetidine. J. Pharmacol. Exp. Ther. 2005, 312, 144–152. [CrossRef][PubMed]
-
(2005)
J. Pharmacol. Exp. Ther
, vol.312
, pp. 144-152
-
-
Pavek, P.1
Merino, G.2
Wagenaar, E.3
Bolscher, E.4
Novotna, M.5
Jonker, J.W.6
Schinkel, A.H.7
-
8
-
-
0029892497
-
L. P-glycoprotein in the blood-brain barrier of mice influences the brain penetration and pharmacological activity of many drugs
-
[CrossRef][PubMed]
-
Schinkel, A.H.; Wagenaar, E.; Mol, C.A.; van Deemter, L. P-glycoprotein in the blood-brain barrier of mice influences the brain penetration and pharmacological activity of many drugs. J. Clin. Investig. 1996, 97, 2517–2524. [CrossRef][PubMed]
-
(1996)
J. Clin. Investig
, vol.97
, pp. 2517-2524
-
-
Schinkel, A.H.1
Wagenaar, E.2
Mol, C.A.3
van Deemter4
-
9
-
-
0026014503
-
In vivo circumvention of P-glycoprotein-mediated multidrug resistance of tumor cells with SDZ PSC 833
-
[PubMed]
-
Boesch, D.; Gavériaux, C.; Jachez, B.; Pourtier-Manzanedo, A.; Bollinger, P.; Loor, F. In vivo circumvention of P-glycoprotein-mediated multidrug resistance of tumor cells with SDZ PSC 833. Cancer Res. 1991, 51, 4226–4233. [PubMed]
-
(1991)
Cancer Res
, vol.51
, pp. 4226-4233
-
-
Boesch, D.1
Gavériaux, C.2
Jachez, B.3
Pourtier-Manzanedo, A.4
Bollinger, P.5
Loor, F.6
-
10
-
-
0034725617
-
Localization and genomic organization of a new hepatocellular organic anion transporting polypeptide
-
[CrossRef][PubMed]
-
König, J.; Cui, Y.; Nies, A.T.; Keppler, D. Localization and genomic organization of a new hepatocellular organic anion transporting polypeptide. J. Biol. Chem. 2000, 275, 23161–23168. [CrossRef][PubMed]
-
(2000)
J. Biol. Chem
, vol.275
, pp. 23161-23168
-
-
König, J.1
Cui, Y.2
Nies, A.T.3
Keppler, D.4
-
11
-
-
0037733365
-
Novel human organic anion transporting polypeptide localized to the basolateral hepatocyte membrane
-
[PubMed]
-
König, J.; Cui, Y.; Nies, A.T.; Keppler, D. A novel human organic anion transporting polypeptide localized to the basolateral hepatocyte membrane. Am. J. Physiol. Gastrointest. Liver Physiol. 2000, 278, G156–G164. [PubMed]
-
(2000)
Am. J. Physiol. Gastrointest. Liver Physiol
, vol.278
, pp. G156-G164
-
-
König, J.1
Cui, Y.2
Nies, A.T.3
Keppler, D.A.4
-
12
-
-
84872009154
-
Influence of sildenafil and tadalafil on the enzyme- and transporter-inducing effects of bosentan and ambrisentan in LS180 cells. Biochem
-
[CrossRef][PubMed]
-
Weiss, J.; Theile, D.; Spalwisz, A.; Burhenne, J.; Riedel, K.D.; Haefeli, W.E. Influence of sildenafil and tadalafil on the enzyme- and transporter-inducing effects of bosentan and ambrisentan in LS180 cells. Biochem. Pharmacol. 2013, 85, 265–273. [CrossRef][PubMed]
-
(2013)
Pharmacol
, vol.85
, pp. 265-273
-
-
Weiss, J.1
Theile, D.2
Spalwisz, A.3
Burhenne, J.4
Riedel, K.D.5
Haefeli, W.E.6
-
13
-
-
44149123590
-
Comparison of two immortalized human cell lines to study nuclear receptor-mediated CYP3A4 induction
-
[CrossRef][PubMed]
-
Harmsen, S.; Koster, A.S.; Beijnen, J.H.; Schellens, J.H.; Meijerman, I. Comparison of two immortalized human cell lines to study nuclear receptor-mediated CYP3A4 induction. Drug Metab. Dispos. 2008, 36, 1166–1171. [CrossRef][PubMed]
-
(2008)
Drug Metab. Dispos
, vol.36
, pp. 1166-1171
-
-
Harmsen, S.1
Koster, A.S.2
Beijnen, J.H.3
Schellens, J.H.4
Meijerman, I.5
-
14
-
-
44149109915
-
Intestinal human colon adenocarcinoma cell line LS180 is an excellent model to study pregnane X receptor; but not constitutive androstane receptor; mediated CYP3A4 and multidrug resistance transporter 1 induction: Studies with anti-human immunodeficiency virus protease inhibitors
-
[PubMed]
-
Gupta, A.; Mugundu, G.M.; Desai, P.B.; Thummel, K.E.; Unadkat, J.D. Intestinal human colon adenocarcinoma cell line LS180 is an excellent model to study pregnane X receptor; but not constitutive androstane receptor; mediated CYP3A4 and multidrug resistance transporter 1 induction: Studies with anti-human immunodeficiency virus protease inhibitors. Drug Metab. Dispos. 2008, 36, 1172–1180. [PubMed]
-
(2008)
Drug Metab. Dispos
, vol.36
, pp. 1172-1180
-
-
Gupta, A.1
Mugundu, G.M.2
Desai, P.B.3
Thummel, K.E.4
Unadkat, J.D.5
-
15
-
-
79956096972
-
Differential modulation of the expression of important drug metabolising enzymes and transporters by endothelin-1 receptor antagonists ambrisentan and bosentan in vitro
-
[CrossRef][PubMed]
-
Weiss, J.; Herzog, M.; Haefeli, W.E. Differential modulation of the expression of important drug metabolising enzymes and transporters by endothelin-1 receptor antagonists ambrisentan and bosentan in vitro. Eur. J. Pharmacol. 2011, 660, 298–304. [CrossRef][PubMed]
-
(2011)
Eur. J. Pharmacol.
, vol.660
, pp. 298-304
-
-
Weiss, J.1
Herzog, M.2
Haefeli, W.E.3
-
16
-
-
33947585786
-
Effects of herbal medicinal products and food supplements on induction of CYP1A2; CYP3A4 and MDR1 in the human colon carcinoma cell line LS180
-
[CrossRef][PubMed]
-
Brandin, H.; Viitanen, E.; Myrberg, O.; Arvidsson, A.K. Effects of herbal medicinal products and food supplements on induction of CYP1A2; CYP3A4 and MDR1 in the human colon carcinoma cell line LS180. Phytother. Res. 2007, 21, 239–244. [CrossRef][PubMed]
-
(2007)
Phytother. Res
, vol.21
, pp. 239-244
-
-
Brandin, H.1
Viitanen, E.2
Myrberg, O.3
Arvidsson, A.K.4
-
17
-
-
62649141791
-
Effects of acid and lactone forms of 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitors on the induction of MDR1 expression and function in LS180 cells
-
[CrossRef][PubMed]
-
Yamasaki, D.; Nakamura, T.; Okamura, N.; Kokudai, M.; Inui, N.; Takeuchi, K.; Watanabe, H.; Hirai, M.; Okumura, K.; Sakaeda, T. Effects of acid and lactone forms of 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitors on the induction of MDR1 expression and function in LS180 cells. Eur. J. Pharm. Sci. 2009, 37, 126–132. [CrossRef][PubMed]
-
(2009)
Eur. J. Pharm. Sci
, vol.37
, pp. 126-132
-
-
Yamasaki, D.1
Nakamura, T.2
Okamura, N.3
Kokudai, M.4
Inui, N.5
Takeuchi, K.6
Watanabe, H.7
Hirai, M.8
Okumura, K.9
Sakaeda, T.10
-
18
-
-
0032169826
-
Regulation of cytochrome P450 enzymes by aryl hydrocarbon receptor in human cells: CYP1A2 expression in the LS180 colon carcinoma cell line after treatment with 2,3,7,8-tetrachlorodibenzo-p-dioxin or 3-methylcholanthrene
-
[CrossRef]
-
Li, W.; Harper, P.A.; Tang, B.K.; Okey, A.B. Regulation of cytochrome P450 enzymes by aryl hydrocarbon receptor in human cells: CYP1A2 expression in the LS180 colon carcinoma cell line after treatment with 2,3,7,8-tetrachlorodibenzo-p-dioxin or 3-methylcholanthrene. Biochem. Pharmacol. 1998, 56, 599–612. [CrossRef]
-
(1998)
Biochem. Pharmacol.
, vol.56
, pp. 599-612
-
-
Li, W.1
Harper, P.A.2
Tang, B.K.3
Okey, A.B.4
-
19
-
-
0025951740
-
Detection and characterization of the Ah receptor for 2,3,7,8-tetrachlorodibenzo-p-dioxin in the human colon adenocarcinoma cell line LS180
-
[CrossRef]
-
Harper, P.A.; Prokipcak, R.D.; Bush, L.E.; Golas, C.L.; Okey, A.B. Detection and characterization of the Ah receptor for 2,3,7,8-tetrachlorodibenzo-p-dioxin in the human colon adenocarcinoma cell line LS180. Arch. Biochem. Biophys. 1991, 290, 27–36. [CrossRef]
-
(1991)
Arch. Biochem. Biophys
, vol.290
, pp. 27-36
-
-
Harper, P.A.1
Prokipcak, R.D.2
Bush, L.E.3
Golas, C.L.4
Okey, A.B.5
-
20
-
-
82355163506
-
Novel stably transfected gene reporter human hepatoma cell line for assessment of aryl hydrocarbon receptor transcriptional activity
-
[CrossRef][PubMed]
-
Novotna, A.; Pavek, P.; Dvorak, Z. Novel stably transfected gene reporter human hepatoma cell line for assessment of aryl hydrocarbon receptor transcriptional activity: Construction and characterization. Environ. Sci. Technol. 2011, 45, 10133–10139. [CrossRef][PubMed]
-
(2011)
Construction and Characterization. Environ. Sci. Technol.
, vol.45
, pp. 10133-10139
-
-
Novotna, A.1
Pavek, P.2
Dvorak, Z.3
-
21
-
-
8844275880
-
In vitro and ex vivo evidence for modulation of P-glycoprotein activity by progestins
-
[CrossRef][PubMed]
-
Fröhlich, M.; Albermann, N.; Sauer, A.; Walter-Sack, I.; Haefel, W.E.; Weiss, J. In vitro and ex vivo evidence for modulation of P-glycoprotein activity by progestins. Biochem. Pharmacol. 2004, 68, 2409–2416. [CrossRef][PubMed]
-
(2004)
Biochem. Pharmacol
, vol.68
, pp. 2409-2416
-
-
Fröhlich, M.1
Albermann, N.2
Sauer, A.3
Walter-Sack, I.4
Haefel, W.E.5
Weiss, J.6
-
22
-
-
33947498515
-
Modulation of human BCRP (ABCG2) activity by anti-HIV drugs
-
[CrossRef][PubMed]
-
Weiss, J.; Rose, J.; Storch, C.H.; Ketabi-Kiyanvash, N.; Sauer, A.; Haefeli, W.E.; Efferth, T. Modulation of human BCRP (ABCG2) activity by anti-HIV drugs. J. Antimicrob. Chemother. 2007, 59, 238–245. [CrossRef][PubMed]
-
(2007)
J. Antimicrob. Chemother
, vol.59
, pp. 238-245
-
-
Weiss, J.1
Rose, J.2
Storch, C.H.3
Ketabi-Kiyanvash, N.4
Sauer, A.5
Haefeli, W.E.6
Efferth, T.7
-
23
-
-
31044439774
-
Interaction of the mitotic kinesin Eg5 inhibitor monastrol with P-glycoprotein. Naunyn Schmiedebergs Arch
-
[CrossRef][PubMed]
-
Peters, T.; Lindenmaier, H.; Haefeli, W.E.; Weiss, J. Interaction of the mitotic kinesin Eg5 inhibitor monastrol with P-glycoprotein. Naunyn Schmiedebergs Arch. Pharmacol. 2006, 372, 291–299. [CrossRef][PubMed]
-
(2006)
Pharmacol
, vol.372
, pp. 291-299
-
-
Peters, T.1
Lindenmaier, H.2
Haefeli, W.E.3
Weiss, J.4
-
24
-
-
23744464363
-
Expression of the drug transporters MDR1/ABCB1; MRP1/ABCC1; MRP2/ABCC2; BCRP/ABCG2; and PXR in peripheral blood mononuclear cells and their relationship with the expression in intestine and liver
-
[CrossRef][PubMed]
-
Albermann, N.; Schmitz-Winnenthal, F.H.; Z’graggen, K.; Volk, C.; Hoffmann, M.M.; Haefeli, W.E.; Weiss, J. Expression of the drug transporters MDR1/ABCB1; MRP1/ABCC1; MRP2/ABCC2; BCRP/ABCG2; and PXR in peripheral blood mononuclear cells and their relationship with the expression in intestine and liver. Biochem. Pharmacol. 2005, 70, 949–958. [CrossRef][PubMed]
-
(2005)
Biochem. Pharmacol
, vol.70
, pp. 949-958
-
-
Albermann, N.1
Schmitz-Winnenthal, F.H.2
Z’Graggen, K.3
Volk, C.4
Hoffmann, M.M.5
Haefeli, W.E.6
Weiss, J.7
-
25
-
-
77957886065
-
Impact of drug transporters for the cellular resistance towards saquinavir and darunavir
-
[CrossRef][PubMed]
-
König, S.J.; Herzog, M.; Theile, D.; Zembruski, N.; Haefeli, W.E.; Weiss, J. Impact of drug transporters for the cellular resistance towards saquinavir and darunavir. J. Antimicrob. Chemother. 2010, 65, 2319–2328. [CrossRef][PubMed]
-
(2010)
J. Antimicrob. Chemother.
, vol.65
, pp. 2319-2328
-
-
König, S.J.1
Herzog, M.2
Theile, D.3
Zembruski, N.4
Haefeli, W.E.5
Weiss, J.6
-
26
-
-
37349124686
-
JNK inhibitor SP600125 is a partial agonist of human aryl hydrocarbon receptor and induces CYP1A1 and CYP1A2 genes in primary human hepatocytes
-
[CrossRef][PubMed]
-
Dvorak, Z.; Vrzal, R.; Henklova, P.; Jancova, P.; Anzenbacherova, E.; Maurel, P.; Svecova, L.; Pavek, P.; Ehrmann, J.; Havlik, R.; et al. JNK inhibitor SP600125 is a partial agonist of human aryl hydrocarbon receptor and induces CYP1A1 and CYP1A2 genes in primary human hepatocytes. Biochem. Pharmacol. 2008, 5, 580–588. [CrossRef][PubMed]
-
(2008)
Biochem. Pharmacol
, vol.5
, pp. 580-588
-
-
Dvorak, Z.1
Vrzal, R.2
Henklova, P.3
Jancova, P.4
Anzenbacherova, E.5
Maurel, P.6
Svecova, L.7
Pavek, P.8
Ehrmann, J.9
Havlik, R.10
-
27
-
-
78650210958
-
Zearalenone activates pregnane X receptor; constitutive androstane receptor and aryl hydrocarbon receptor and corresponding phase I target genes mRNA in primary cultures of human hepatocytes
-
[CrossRef][PubMed]
-
Ayed-Boussema, I.; Pascussi, J.M.; Maurel, P.; Bacha, H.; Hassen, W. Zearalenone activates pregnane X receptor; constitutive androstane receptor and aryl hydrocarbon receptor and corresponding phase I target genes mRNA in primary cultures of human hepatocytes. Environ. Toxicol. Pharmacol. 2011, 31, 79–87. [CrossRef][PubMed]
-
(2011)
Environ. Toxicol. Pharmacol
, vol.31
, pp. 79-87
-
-
Ayed-Boussema, I.1
Pascussi, J.M.2
Maurel, P.3
Bacha, H.4
Hassen, W.5
-
28
-
-
0037129827
-
Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes
-
RESEARCH0034[CrossRef][PubMed]
-
Vandesompele, J.; De Preter, K.; Pattyn, F.; Poppe, B.; Van Roy, N.; De Paepe, A.; Speleman, F. Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes. Genome Biol. 2002, 3, RESEARCH0034. [CrossRef][PubMed]
-
(2002)
Genome Biol
, vol.3
-
-
Vandesompele, J.1
De Preter, K.2
Pattyn, F.3
Poppe, B.4
Van Roy, N.5
De Paepe, A.6
Speleman, F.7
-
29
-
-
31044448805
-
Evaluation of inhibitory potencies for compounds inhibiting P-glycoprotein but without maximum effects: F2 values. Drug Metab
-
[CrossRef][PubMed]
-
Weiss, J.; Haefeli, W.E. Evaluation of inhibitory potencies for compounds inhibiting P-glycoprotein but without maximum effects: f2 values. Drug Metab. Dispos. 2006, 34, 203–207. [CrossRef][PubMed]
-
(2006)
Dispos
, vol.34
, pp. 203-207
-
-
Weiss, J.1
Haefeli, W.E.2
-
30
-
-
77951031222
-
Interaction of angiotensin receptor type 1 blockers with ATP-binding cassette transporters. Biopharm
-
[CrossRef][PubMed]
-
Weiss, J.; Sauer, A.; Divac, N.; Herzog, M.; Schwedhelm, E.; Böger, R.H.; Haefeli, W.E.; Benndorf, R.A. Interaction of angiotensin receptor type 1 blockers with ATP-binding cassette transporters. Biopharm. Drug Dispos. 2010, 31, 150–161. [CrossRef][PubMed]
-
(2010)
Drug Dispos
, vol.31
, pp. 150-161
-
-
Weiss, J.1
Sauer, A.2
Divac, N.3
Herzog, M.4
Schwedhelm, E.5
Böger, R.H.6
Haefeli, W.E.7
Benndorf, R.A.8
-
31
-
-
84959357267
-
Interaction potential of the multitargeted receptor tyrosine kinase inhibitor dovitinib with drug transporters and drug metabolizing enzymes assessed in vitro
-
[CrossRef][PubMed]
-
Weiss, J.; Theile, D.; Dvorak, Z.; Haefeli, W.E. Interaction potential of the multitargeted receptor tyrosine kinase inhibitor dovitinib with drug transporters and drug metabolizing enzymes assessed in vitro. Pharmaceutics 2014, 6, 632–650. [CrossRef][PubMed]
-
(2014)
Pharmaceutics
, vol.6
, pp. 632-650
-
-
Weiss, J.1
Theile, D.2
Dvorak, Z.3
Haefeli, W.E.4
-
32
-
-
84907859379
-
A multicenter phase I/II study of obatoclax mesylate administered as a 3- or 24-hour infusion in older patients with previously untreated acute myeloid leukemia
-
[CrossRef][PubMed]
-
Schimmer, A.D.; Raza, A.; Carter, T.H.; Claxton, D.; Erba, H.; DeAngelo, D.J.; Tallman, M.S.; Goard, C.; Borthakur, G. A multicenter phase I/II study of obatoclax mesylate administered as a 3- or 24-hour infusion in older patients with previously untreated acute myeloid leukemia. PLoS ONE 2014, 9, e108694. [CrossRef][PubMed]
-
(2014)
Plos ONE
, vol.9
-
-
Schimmer, A.D.1
Raza, A.2
Carter, T.H.3
Claxton, D.4
Erba, H.5
Deangelo, D.J.6
Tallman, M.S.7
Goard, C.8
Borthakur, G.9
-
33
-
-
84937394274
-
Polypharmacy in patients with advanced cancer and the role of medication discontinuation
-
[CrossRef]
-
LeBlanc, T.W.; McNeil, M.J.; Kamal, A.H.; Currow, D.C.; Abernethy, A.P. Polypharmacy in patients with advanced cancer and the role of medication discontinuation. Lancet Oncol. 2015, 16, e333–e341. [CrossRef]
-
(2015)
Lancet Oncol
, vol.16
, pp. e333-e341
-
-
Leblanc, T.W.1
McNeil, M.J.2
Kamal, A.H.3
Currow, D.C.4
Abernethy, A.P.5
-
34
-
-
84863116430
-
Substantial susceptibility of chronic lymphocytic leukemia to BCL2 inhibition
-
[CrossRef][PubMed]
-
Roberts, A.W.; Seymour, J.F.; Brown, J.R.; Wierda, W.G.; Kipps, T.J.; Khaw, S.L.; Carney, D.A.; He, S.Z.; Huang, D.C.; Xiong, H.; et al. Substantial susceptibility of chronic lymphocytic leukemia to BCL2 inhibition: results of a phase I study of navitoclax in patients with relapsed or refractory disease. J. Clin. Oncol. 2012, 30, 488–496. [CrossRef][PubMed]
-
(2012)
Results of a phase I study of navitoclax in patients with relapsed or refractory disease
, vol.30
, pp. 488-496
-
-
Roberts, A.W.1
Seymour, J.F.2
Brown, J.R.3
Wierda, W.G.4
Kipps, T.J.5
Khaw, S.L.6
Carney, D.A.7
He, S.Z.8
Huang, D.C.9
Xiong, H.10
-
35
-
-
84928333417
-
A phase 2 study of venetoclax (ABT-199/GDC-0199) in patients with acute myelogenous leukemia (AML)
-
Konopleva, M.; Pollyea, D.A.; Potluri, J.; Chyla, B.J.; Busman, T.; McKeegan, E.; Salem, A.; Zhu, M.; Ricker, J.L.; Blum, W.; et al. A phase 2 study of venetoclax (ABT-199/GDC-0199) in patients with acute myelogenous leukemia (AML). Blood 2014, 124, 118.
-
(2014)
Blood
, vol.124
-
-
Konopleva, M.1
Pollyea, D.A.2
Potluri, J.3
Chyla, B.J.4
Busman, T.5
McKeegan, E.6
Salem, A.7
Zhu, M.8
Ricker, J.L.9
Blum, W.10
-
36
-
-
48749084803
-
A regulatory viewpoint on transporter-based drug interactions
-
[CrossRef][PubMed]
-
Zhang, L.; Zhang, Y.D.; Strong, J.M.; Reynolds, K.S.; Huang, S.M. A regulatory viewpoint on transporter-based drug interactions. Xenobiotica 2008, 38, 709–724. [CrossRef][PubMed]
-
(2008)
Xenobiotica
, vol.38
, pp. 709-724
-
-
Zhang, L.1
Zhang, Y.D.2
Strong, J.M.3
Reynolds, K.S.4
Huang, S.M.5
-
37
-
-
0141831861
-
Differential expression and function of CYP2C isoforms in human intestine and liver
-
[CrossRef][PubMed]
-
Läpple, F.; von Richter, O.; Fromm, M.F.; Richter, T.; Thon, K.P.; Wisser, H.; Griese, E.U.; Eichelbaum, M.; Kivistö, K.T. Differential expression and function of CYP2C isoforms in human intestine and liver. Pharmacogenetics 2003, 13, 565–575. [CrossRef][PubMed]
-
(2003)
Pharmacogenetics
, vol.13
, pp. 565-575
-
-
Läpple, F.1
Von Richter, O.2
Fromm, M.F.3
Richter, T.4
Thon, K.P.5
Wisser, H.6
Griese, E.U.7
Eichelbaum, M.8
Kivistö, K.T.9
-
38
-
-
0028006520
-
The Ah receptor: Mediator of the toxicity of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) and related compounds
-
[CrossRef]
-
Okey, A.B.; Riddick, D.S.; Harper, P.A. The Ah receptor: Mediator of the toxicity of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) and related compounds. Toxicol. Lett. 1994, 70, 1–22. [CrossRef]
-
(1994)
Toxicol. Lett
, vol.70
, pp. 1-22
-
-
Okey, A.B.1
Riddick, D.S.2
Harper, P.A.3
-
39
-
-
50649102122
-
Aryl hydrocarbon receptor-mediated regulation of the human estrogen and bile acid UDP-glucuronosyltransferase 1A3 gene
-
[CrossRef][PubMed]
-
Lankisch, T.O.; Gillman, T.C.; Erichsen, T.J.; Ehmer, U.; Kalthoff, S.; Freiberg, N.; Munzel, P.A.; Manns, M.P.; Strassburg, C.P. Aryl hydrocarbon receptor-mediated regulation of the human estrogen and bile acid UDP-glucuronosyltransferase 1A3 gene. Arch. Toxicol. 2008, 82, 573–582. [CrossRef][PubMed]
-
(2008)
Arch. Toxicol
, vol.82
, pp. 573-582
-
-
Lankisch, T.O.1
Gillman, T.C.2
Erichsen, T.J.3
Ehmer, U.4
Kalthoff, S.5
Freiberg, N.6
Munzel, P.A.7
Manns, M.P.8
Strassburg, C.P.9
-
40
-
-
77958093867
-
Coffee induces expression of glucuronosyltransferases by the aryl hydrocarbon receptor and Nrf2 in liver and stomach
-
[CrossRef][PubMed]
-
Kalthoff, S.; Ehmer, U.; Freiberg, N.; Manns, M.P.; Strassburg, C.P. Coffee induces expression of glucuronosyltransferases by the aryl hydrocarbon receptor and Nrf2 in liver and stomach. Gastroenterology 2010, 139, 1699–1710. [CrossRef][PubMed]
-
(2010)
Gastroenterology
, vol.139
, pp. 1699-1710
-
-
Kalthoff, S.1
Ehmer, U.2
Freiberg, N.3
Manns, M.P.4
Strassburg, C.P.5
-
41
-
-
0036364467
-
Multidrug resistance in cancer: Role of ATP-dependent transporters
-
[CrossRef][PubMed]
-
Gottesman, M.M.; Fojo, T.; Bates, S.E. Multidrug resistance in cancer: Role of ATP-dependent transporters. Nat. Rev. Cancer. 2002, 2, 48–58. [CrossRef][PubMed]
-
(2002)
Nat. Rev. Cancer
, vol.2
, pp. 48-58
-
-
Gottesman, M.M.1
Fojo, T.2
Bates, S.E.3
|