-
1
-
-
0035977882
-
Molecular biology of the Ah receptor and its role in carcinogenesis
-
Safe S. Molecular biology of the Ah receptor and its role in carcinogenesis. Toxicol Lett 2001;120:1-7.
-
(2001)
Toxicol Lett
, vol.120
, pp. 1-7
-
-
Safe, S.1
-
2
-
-
0032420358
-
Ah receptor agonists as endocrine disruptors: Antiestrogenic activity and mechanisms
-
Safe S, Wang F, Porter W, Duan R, McDougal A. Ah receptor agonists as endocrine disruptors: antiestrogenic activity and mechanisms. Toxicol Lett 1998;102-3:343-7.
-
(1998)
Toxicol Lett
, vol.102-103
, pp. 343-347
-
-
Safe, S.1
Wang, F.2
Porter, W.3
Duan, R.4
McDougal, A.5
-
3
-
-
0025719532
-
2,3,7,8-Tetrachlorodibenzo-p-dioxin (TCDD) and related compounds as antioestrogens: Characterization and mechanism of action
-
Safe S, Astroff B, Harris M, et al. 2,3,7,8-Tetrachlorodibenzo-p-dioxin (TCDD) and related compounds as antioestrogens: characterization and mechanism of action. Pharmacol Toxicol 1991;69:400-9.
-
(1991)
Pharmacol Toxicol
, vol.69
, pp. 400-409
-
-
Safe, S.1
Astroff, B.2
Harris, M.3
-
4
-
-
0035421182
-
Selective estrogen receptor modulation: A personal perspective
-
Jordan VC. Selective estrogen receptor modulation: a personal perspective. Cancer Res 2001;61:5683-7.
-
(2001)
Cancer Res
, vol.61
, pp. 5683-5687
-
-
Jordan, V.C.1
-
5
-
-
0035802285
-
Selective estrogen receptor modulation and reduction in risk of breast cancer, osteoporosis, and coronary heart disease
-
Jordan VC, Gapstur S, Morrow M. Selective estrogen receptor modulation and reduction in risk of breast cancer, osteoporosis, and coronary heart disease. J Natl Cancer Inst (Bethesda) 2001;93:1449-57.
-
(2001)
J Natl Cancer Inst (Bethesda)
, vol.93
, pp. 1449-1457
-
-
Jordan, V.C.1
Gapstur, S.2
Morrow, M.3
-
6
-
-
0032537990
-
Tamoxifen for prevention of breast cancer: Report of the National Surgical Adjuvant Breast and Bowel Project P-1 Study
-
Fisher B, Costantino JP, Wickerham DL, et al. Tamoxifen for prevention of breast cancer: report of the National Surgical Adjuvant Breast and Bowel Project P-1 Study. J Natl Cancer Inst (Bethesda) 1998;90:1371-88.
-
(1998)
J Natl Cancer Inst (Bethesda)
, vol.90
, pp. 1371-1388
-
-
Fisher, B.1
Costantino, J.P.2
Wickerham, D.L.3
-
7
-
-
0033372865
-
Selective oestrogen receptor modulation: Molecular pharmacology for the millennium
-
Levenson AS, Jordan VC. Selective oestrogen receptor modulation: molecular pharmacology for the millennium. Eur J Cancer 1999;35:1974-85.
-
(1999)
Eur J Cancer
, vol.35
, pp. 1974-1985
-
-
Levenson, A.S.1
Jordan, V.C.2
-
8
-
-
0026560435
-
Antiestrogen ICI 164,384 reduces cellular estrogen receptor content by increasing its turnover
-
Dauvois S, Danielian PS, White R, Parker MG. Antiestrogen ICI 164,384 reduces cellular estrogen receptor content by increasing its turnover. Proc Natl Acad Sci USA 1992;89:4037-41.
-
(1992)
Proc Natl Acad Sci USA
, vol.89
, pp. 4037-4041
-
-
Dauvois, S.1
Danielian, P.S.2
White, R.3
Parker, M.G.4
-
9
-
-
0037102121
-
Fulvestrant, formerly ICI 182,780, is as effective as anastrozole in postmenopausal women with advanced breast cancer progressing after prior endocrine treatment
-
Howell A, Robertson IF, Quaresma Albano J, et al. Fulvestrant, formerly ICI 182,780, is as effective as anastrozole in postmenopausal women with advanced breast cancer progressing after prior endocrine treatment. J Clin Oncol 2002;20: 3396-403.
-
(2002)
J Clin Oncol
, vol.20
, pp. 3396-3403
-
-
Howell, A.1
Robertson, I.F.2
Quaresma Albano, J.3
-
10
-
-
0037102126
-
Double-blind, randomized trial comparing the efficacy and tolerability of fulvestrant versus anastrozole in postmenopausal women with advanced breast cancer progressing on prior endocrine therapy: Results of a North American trial
-
Osborne CK, Pippen J, Jones SE, et al. Double-blind, randomized trial comparing the efficacy and tolerability of fulvestrant versus anastrozole in postmenopausal women with advanced breast cancer progressing on prior endocrine therapy: results of a North American trial. J Clin Oncol 2002;20:3386-95.
-
(2002)
J Clin Oncol
, vol.20
, pp. 3386-3395
-
-
Osborne, C.K.1
Pippen, J.2
Jones, S.E.3
-
11
-
-
0036615860
-
Mechanism of action and development of selective aryl hydrocarbon receptor modulators for treatment of hormone-dependent cancers (review)
-
Safe S, McDougal A. Mechanism of action and development of selective aryl hydrocarbon receptor modulators for treatment of hormone-dependent cancers (review). Int J Oncol 2002;20:1123-8.
-
(2002)
Int J Oncol
, vol.20
, pp. 1123-1128
-
-
Safe, S.1
McDougal, A.2
-
12
-
-
0026691255
-
6-Methyl-1,3,8-trichlorodibenzofuran (MCDF) as an antiestrogen in human and rodent cancer cell lines: Evidence for the role of the Ah receptor
-
Zacharewski T, Harris M, Biegel L, et al. 6-Methyl-1,3,8-trichlorodibenzofuran (MCDF) as an antiestrogen in human and rodent cancer cell lines: evidence for the role of the Ah receptor. Toxicol Appl Pharmacol 1992;113:311-8.
-
(1992)
Toxicol Appl Pharmacol
, vol.113
, pp. 311-318
-
-
Zacharewski, T.1
Harris, M.2
Biegel, L.3
-
13
-
-
0030610471
-
Antiestrogenic activities of alternate-substituted polychlorinated dibenzofurans in MCF-7 human breast cancer cells
-
Sun G, Safe S. Antiestrogenic activities of alternate-substituted polychlorinated dibenzofurans in MCF-7 human breast cancer cells. Cancer Chemother Pharmacol 1997;40:239-44.
-
(1997)
Cancer Chemother Pharmacol
, vol.40
, pp. 239-244
-
-
Sun, G.1
Safe, S.2
-
14
-
-
0023816418
-
Comparative antiestrogenic activities of 2,3,7,8-tetrachlorodibenzo-p-dioxin and 6-methyl-1,3,8-trichlorodibenzofuran in the female rat
-
Astroff B, Safe S. Comparative antiestrogenic activities of 2,3,7,8-tetrachlorodibenzo-p-dioxin and 6-methyl-1,3,8-trichlorodibenzofuran in the female rat. Toxicol Appl Pharmacol 1988;95:435-43.
-
(1988)
Toxicol Appl Pharmacol
, vol.95
, pp. 435-443
-
-
Astroff, B.1
Safe, S.2
-
15
-
-
0030731436
-
Inhibition of 7,12-dimethylbenz[a]anthracene-induced rat mammary tumor growth by aryl hydrocarbon receptor agonists
-
McDougal A, Wilson C, Safe S. Inhibition of 7,12-dimethylbenz[a]anthracene-induced rat mammary tumor growth by aryl hydrocarbon receptor agonists. Cancer Lett 1997;120:53-63.
-
(1997)
Cancer Lett
, vol.120
, pp. 53-63
-
-
McDougal, A.1
Wilson, C.2
Safe, S.3
-
16
-
-
0034726057
-
Crosstalk between estrogen receptor α and the aryl hydrocarbon receptor in breast cancer cells involves unidirectional activation of proteasomes
-
Wormke M, Stoner M, Saville B, Safe S. Crosstalk between estrogen receptor α and the aryl hydrocarbon receptor in breast cancer cells involves unidirectional activation of proteasomes. FEBS Lett 2000;478:109-12.
-
(2000)
FEBS Lett
, vol.478
, pp. 109-112
-
-
Wormke, M.1
Stoner, M.2
Saville, B.3
Safe, S.4
-
17
-
-
0035872466
-
Tamoxifen-induced antitumorigenic/ antiestrogenic action synergized by a selective aryl hydrocarbon receptor modulator
-
McDougal A, Wormke M, Calvin J, Safe S. Tamoxifen-induced antitumorigenic/ antiestrogenic action synergized by a selective aryl hydrocarbon receptor modulator. Cancer Res 2001;61:3902-7.
-
(2001)
Cancer Res
, vol.61
, pp. 3902-3907
-
-
McDougal, A.1
Wormke, M.2
Calvin, J.3
Safe, S.4
-
18
-
-
0034665358
-
Allosteric silencing of activating function 1 in the 4-hydroxytamoxifen estrogen receptor complex is induced by substituting glycine for aspartate at amino acid 351
-
MacGregor Schafer J, Liu H, Bentrem DJ, Zapf JW, Jordan VC. Allosteric silencing of activating function 1 in the 4-hydroxytamoxifen estrogen receptor complex is induced by substituting glycine for aspartate at amino acid 351. Cancer Res 2000; 60:5097-105.
-
(2000)
Cancer Res
, vol.60
, pp. 5097-5105
-
-
MacGregor Schafer, J.1
Liu, H.2
Bentrem, D.J.3
Zapf, J.W.4
Jordan, V.C.5
-
19
-
-
0035328727
-
Silencing and reactivation of the selective estrogen receptor modulator-estrogen receptor α complex
-
Liu H, Lee ES, Deb Los Reyes A, Zapf JW, Jordan VC. Silencing and reactivation of the selective estrogen receptor modulator-estrogen receptor α complex. Cancer Res 2001;61:3632-9.
-
(2001)
Cancer Res
, vol.61
, pp. 3632-3639
-
-
Liu, H.1
Lee, E.S.2
Deb Los Reyes, A.3
Zapf, J.W.4
Jordan, V.C.5
-
21
-
-
0037470164
-
Modulation of estrogen receptor α function and stability by tamoxifen and a critical amino acid (Asp-538) in helix 12
-
Pearce ST, Liu H, Jordan VC. Modulation of estrogen receptor α function and stability by tamoxifen and a critical amino acid (Asp-538) in helix 12. J Biol Chem 2003;278:7630-8.
-
(2003)
J Biol Chem
, vol.278
, pp. 7630-7638
-
-
Pearce, S.T.1
Liu, H.2
Jordan, V.C.3
-
22
-
-
0038100188
-
Modulation of oestrogen receptor signalling by association with the activated dioxin receptor
-
Ohtake F, Takeyama K, Matsumoto T, et al. Modulation of oestrogen receptor signalling by association with the activated dioxin receptor. Nature (Lond) 2003;423: 545-50.
-
(2003)
Nature (Lond)
, vol.423
, pp. 545-550
-
-
Ohtake, F.1
Takeyama, K.2
Matsumoto, T.3
-
23
-
-
0026520381
-
Growth regulation of estrogen receptor-negative breast cancer cells transfected with complementary DNAs for estrogen receptor
-
Jiang SY, Jordan VC. Growth regulation of estrogen receptor-negative breast cancer cells transfected with complementary DNAs for estrogen receptor. J Natl Cancer Inst (Bethesda) 1992;84:580-91.
-
(1992)
J Natl Cancer Inst (Bethesda)
, vol.84
, pp. 580-591
-
-
Jiang, S.Y.1
Jordan, V.C.2
-
24
-
-
0029844145
-
Irreversible loss of the oestrogen receptor in T47D breast cancer cells following prolonged oestrogen deprivation
-
Pink JJ, Bilimoria MM, Assikis J, Jordan VC. Irreversible loss of the oestrogen receptor in T47D breast cancer cells following prolonged oestrogen deprivation. Br J Cancer 1996:74:1227-36.
-
(1996)
Br J Cancer
, vol.74
, pp. 1227-1236
-
-
Pink, J.J.1
Bilimoria, M.M.2
Assikis, J.3
Jordan, V.C.4
-
25
-
-
0024307356
-
6-Substituted-1,3,8-trichlorodibenzofurans as 2,3,7,8-tetrachlorodibenzo-p-dioxin antagonists in the rat: Structure activity relationships
-
Astroff B, Safe S. 6-Substituted-1,3,8-trichlorodibenzofurans as 2,3,7,8-tetrachlorodibenzo-p-dioxin antagonists in the rat: structure activity relationships. Toxicology 1989;59:285-96.
-
(1989)
Toxicology
, vol.59
, pp. 285-296
-
-
Astroff, B.1
Safe, S.2
-
26
-
-
0018850985
-
A simple, rapid, and sensitive DNA assay procedure
-
La Barca C, Paigen K. A simple, rapid, and sensitive DNA assay procedure. Anal Biochem 1980;102:344-52.
-
(1980)
Anal Biochem
, vol.102
, pp. 344-352
-
-
La Barca, C.1
Paigen, K.2
-
27
-
-
0029028741
-
Increasing the number of tandem estrogen response elements increases the estrogenic activity of a tamoxifen analogue
-
Catherino WH, Jordan VC. Increasing the number of tandem estrogen response elements increases the estrogenic activity of a tamoxifen analogue. Cancer Lett 1995;92:39-47.
-
(1995)
Cancer Lett
, vol.92
, pp. 39-47
-
-
Catherino, W.H.1
Jordan, V.C.2
-
28
-
-
0029858911
-
p300 is a component of an estrogen receptor coactivator complex
-
Hanstein B, Eckner R, DiRenzo J, et al. p300 is a component of an estrogen receptor coactivator complex. Proc Natl Acad Sci USA 1996;93:11540-5.
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, pp. 11540-11545
-
-
Hanstein, B.1
Eckner, R.2
DiRenzo, J.3
-
29
-
-
0032568527
-
Crystallographic comparison of the estrogen and progesterone receptor's ligand binding domains
-
Tanenbaum DM, Wang Y, Williams SP, Sigler PB. Crystallographic comparison of the estrogen and progesterone receptor's ligand binding domains. Proc Natl Acad Sci USA 1998;95:5998-6003.
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, pp. 5998-6003
-
-
Tanenbaum, D.M.1
Wang, Y.2
Williams, S.P.3
Sigler, P.B.4
-
30
-
-
0028233383
-
Estrogen receptor-associated proteins: Possible mediators of hormone-induced transcription
-
Halachmi S, Marden E, Martin G, et al. Estrogen receptor-associated proteins: possible mediators of hormone-induced transcription. Science (Wash DC) 1994;264: 1455-8.
-
(1994)
Science (Wash DC)
, vol.264
, pp. 1455-1458
-
-
Halachmi, S.1
Marden, E.2
Martin, G.3
-
31
-
-
0030797902
-
AIB1, a steroid receptor coactivator amplified in breast and ovarian cancer
-
Anzick SL, Kononen J, Walker RL, et al. AIB1, a steroid receptor coactivator amplified in breast and ovarian cancer. Science (Wash DC) 1997;277:965-8.
-
(1997)
Science (Wash DC)
, vol.277
, pp. 965-968
-
-
Anzick, S.L.1
Kononen, J.2
Walker, R.L.3
-
32
-
-
0037764668
-
Aryl hydrocarbon receptor gene silencing with small inhibitory RNA differentially modulates Ah-responsiveness in MCF-7 and HepG2 cancer cells
-
Abdelrahim M, Smith R III, Safe S. Aryl hydrocarbon receptor gene silencing with small inhibitory RNA differentially modulates Ah-responsiveness in MCF-7 and HepG2 cancer cells. Mol Pharmacol 2003;63:1373-81.
-
(2003)
Mol Pharmacol
, vol.63
, pp. 1373-1381
-
-
Abdelrahim, M.1
Smith III, R.2
Safe, S.3
-
33
-
-
0033514930
-
Proteasome-dependent degradation of the human estrogen receptor
-
Nawaz Z, Lonard DM, Dennis AP, Smith CL, O'Malley BW. Proteasome-dependent degradation of the human estrogen receptor. Proc Natl Acad Sci USA 1999;96:1858-62.
-
(1999)
Proc Natl Acad Sci USA
, vol.96
, pp. 1858-1862
-
-
Nawaz, Z.1
Lonard, D.M.2
Dennis, A.P.3
Smith, C.L.4
O'Malley, B.W.5
-
34
-
-
0033060824
-
Implication of proteasome in estrogen receptor degradation
-
El Khissiin A, Leclercq G. Implication of proteasome in estrogen receptor degradation. FEBS Lett 1999;448:160-6.
-
(1999)
FEBS Lett
, vol.448
, pp. 160-166
-
-
El Khissiin, A.1
Leclercq, G.2
-
35
-
-
0033304776
-
Proteasome-mediated proteolysis of estrogen receptor: A novel component in autologous down-regulation
-
Alarid ET, Bakopoulos N, Solodin N. Proteasome-mediated proteolysis of estrogen receptor: a novel component in autologous down-regulation. Mol Endocrinol 1999; 13:1522-34.
-
(1999)
Mol Endocrinol
, vol.13
, pp. 1522-1534
-
-
Alarid, E.T.1
Bakopoulos, N.2
Solodin, N.3
-
36
-
-
0035929585
-
The human estrogen receptor-α is a ubiquitinated protein whose stability is affected differentially by agonists, antagonists, and selective estrogen receptor modulators
-
Wijayaratne AL, McDonnell DP. The human estrogen receptor-α is a ubiquitinated protein whose stability is affected differentially by agonists, antagonists, and selective estrogen receptor modulators. J Biol Chem 2001;276:35684-92.
-
(2001)
J Biol Chem
, vol.276
, pp. 35684-35692
-
-
Wijayaratne, A.L.1
McDonnell, D.P.2
-
37
-
-
0037373474
-
The aryl hydrocarbon receptor mediates degradation of estrogen receptor α through activation of proteasomes
-
Wormke M, Stoner M, Saville B, et al. The aryl hydrocarbon receptor mediates degradation of estrogen receptor α through activation of proteasomes. Mol Cell Biol 2003;23:1843-55.
-
(2003)
Mol Cell Biol
, vol.23
, pp. 1843-1855
-
-
Wormke, M.1
Stoner, M.2
Saville, B.3
-
38
-
-
0028179816
-
Restoration of aryl hydrocarbon (Ah) responsiveness in MDA-MB-231 human breast cancer cells by transient expression of the estrogen receptor
-
Thomsen JS, Wang X, Hines RN, Safe S. Restoration of aryl hydrocarbon (Ah) responsiveness in MDA-MB-231 human breast cancer cells by transient expression of the estrogen receptor. Carcinogenesis (Lond) 1994;15:933-7.
-
(1994)
Carcinogenesis (Lond)
, vol.15
, pp. 933-937
-
-
Thomsen, J.S.1
Wang, X.2
Hines, R.N.3
Safe, S.4
-
39
-
-
0026496895
-
2,3,7,8-Tetrachlorodibenzo-p-dioxin-dependent regulation of transforming growth factors-α and -β2 expression in a human keratinocyte cell line involves both transcriptional and post-transcriptional control
-
Gaido KW, Maness SC, Leonard LS, Greenlee WF. 2,3,7,8-Tetrachlorodibenzo-p-dioxin-dependent regulation of transforming growth factors-α and -β2 expression in a human keratinocyte cell line involves both transcriptional and post-transcriptional control. J Biol Chem 1992;267:24591-5.
-
(1992)
J Biol Chem
, vol.267
, pp. 24591-24595
-
-
Gaido, K.W.1
Maness, S.C.2
Leonard, L.S.3
Greenlee, W.F.4
-
40
-
-
0028109671
-
Indolo[3,2-b]carbazole: A dietary-derived factor that exhibits both antiestrogenic and estrogenic activity
-
Liu H, Wormke M, Safe SH, Bjeldanes LF. Indolo[3,2-b]carbazole: a dietary-derived factor that exhibits both antiestrogenic and estrogenic activity. J Natl Cancer Inst (Bethesda) 1994;86:1758-65.
-
(1994)
J Natl Cancer Inst (Bethesda)
, vol.86
, pp. 1758-1765
-
-
Liu, H.1
Wormke, M.2
Safe, S.H.3
Bjeldanes, L.F.4
-
42
-
-
0029598803
-
Alkyl polychlorinated dibenzofurans and related compounds as antiestrogens in the female rat uterus: Structure-activity studies
-
Dickerson R, Keller LH, Safe S. Alkyl polychlorinated dibenzofurans and related compounds as antiestrogens in the female rat uterus: structure-activity studies. Toxicol Appl Pharmacol 1995;135:287-98.
-
(1995)
Toxicol Appl Pharmacol
, vol.135
, pp. 287-298
-
-
Dickerson, R.1
Keller, L.H.2
Safe, S.3
-
43
-
-
0033529692
-
Differential recruitment of coactivator RIP140 by Ah and estrogen receptors. Absence of a role for LXXLL motifs
-
Kumar MB, Tarpey RW, Perdew GH. Differential recruitment of coactivator RIP140 by Ah and estrogen receptors. Absence of a role for LXXLL motifs. J Biol Chem 1999;274:22155-64.
-
(1999)
J Biol Chem
, vol.274
, pp. 22155-22164
-
-
Kumar, M.B.1
Tarpey, R.W.2
Perdew, G.H.3
-
44
-
-
0032745979
-
The aryl hydrocarbon receptor (AHR)/AHR nuclear translocator (ARNT) heterodimer interacts with naturally occurring estrogen response elements
-
Klinge CM, Bowers JL, Kulakosky PC, Kamboj KK, Swanson HI. The aryl hydrocarbon receptor (AHR)/AHR nuclear translocator (ARNT) heterodimer interacts with naturally occurring estrogen response elements. Mol Cell Endocrinol 1999;157:105-19.
-
(1999)
Mol Cell Endocrinol
, vol.157
, pp. 105-119
-
-
Klinge, C.M.1
Bowers, J.L.2
Kulakosky, P.C.3
Kamboj, K.K.4
Swanson, H.I.5
-
46
-
-
0037204013
-
Identification of a second binding site in the estrogen receptor
-
van Hoorn WP. Identification of a second binding site in the estrogen receptor. J Med Chem 2002;45:584-9.
-
(2002)
J Med Chem
, vol.45
, pp. 584-589
-
-
Van Hoorn, W.P.1
-
47
-
-
16544387339
-
A second binding site for hydroxytamoxifen within the ligand-binding domain of estrogen receptor beta
-
Abstract No. OR34-2. Chevy Chase, MD: The Endocrine Society Press
-
Wang Y, Chirgadze NY, Briggs SL, et al. A second binding site for hydroxytamoxifen within the ligand-binding domain of estrogen receptor beta. In: Proceedings of the 85th Annual Endocrine Society Meeting, Abstract No. OR34-2. Chevy Chase, MD: The Endocrine Society Press; 2003. p. 106.
-
(2003)
Proceedings of the 85th Annual Endocrine Society Meeting
, pp. 106
-
-
Wang, Y.1
Chirgadze, N.Y.2
Briggs, S.L.3
-
48
-
-
0033305430
-
Coactivator peptides have a differential stabilizing effect on the binding of estrogens and antiestrogens with the estrogen receptor
-
Gee AC, Carlson KE, Martini PG, Katzenellenbogen BS, Katzenellenbogen JA. Coactivator peptides have a differential stabilizing effect on the binding of estrogens and antiestrogens with the estrogen receptor. Mol Endocrinol 1999;13: 1912-23.
-
(1999)
Mol Endocrinol
, vol.13
, pp. 1912-1923
-
-
Gee, A.C.1
Carlson, K.E.2
Martini, P.G.3
Katzenellenbogen, B.S.4
Katzenellenbogen, J.A.5
-
49
-
-
0031039888
-
Comparison of the ligand binding specificity and transcript tissue distribution of estrogen receptors α and β
-
Kuiper GG, Carlsson B, Grandien K, et al. Comparison of the ligand binding specificity and transcript tissue distribution of estrogen receptors α and β. Endocrinology 1997; 138:863-70.
-
(1997)
Endocrinology
, vol.138
, pp. 863-870
-
-
Kuiper, G.G.1
Carlsson, B.2
Grandien, K.3
-
50
-
-
0031733298
-
Interaction of estrogenic chemicals and phytoestrogens with estrogen receptor β
-
Kuiper GG, Lemmen JG, Carlsson B, et al. Interaction of estrogenic chemicals and phytoestrogens with estrogen receptor β. Endocrinology 1998;139:4252-63.
-
(1998)
Endocrinology
, vol.139
, pp. 4252-4263
-
-
Kuiper, G.G.1
Lemmen, J.G.2
Carlsson, B.3
-
51
-
-
0242526030
-
Distinct molecular conformations of the estrogen receptor α complex exploited by environmental estrogens
-
Bentrem D, Fox JE, Pearce ST, et al. Distinct molecular conformations of the estrogen receptor α complex exploited by environmental estrogens. Cancer Res 2003;63:7490-6.
-
(2003)
Cancer Res
, vol.63
, pp. 7490-7496
-
-
Bentrem, D.1
Fox, J.E.2
Pearce, S.T.3
-
52
-
-
0028280245
-
Stimulation of pS2 expression by diet-derived compounds
-
Sathyamoorthy N, Wang T, Phang J. Stimulation of pS2 expression by diet-derived compounds. Cancer Res 1994;54:957-61.
-
(1994)
Cancer Res
, vol.54
, pp. 957-961
-
-
Sathyamoorthy, N.1
Wang, T.2
Phang, J.3
-
53
-
-
0028959192
-
Estrogenic flavonoids: Structural requirements for biological activity
-
Miksicek R. Estrogenic flavonoids: structural requirements for biological activity. Proc Soc Exp Biol Med 1995;208:44-50.
-
(1995)
Proc Soc Exp Biol Med
, vol.208
, pp. 44-50
-
-
Miksicek, R.1
-
54
-
-
0031831117
-
Detection of weak estrogenic flavonoids using a recombinant yeast strain and a modified MCF7 cell proliferation assay
-
Breinholt V, Larsen JC. Detection of weak estrogenic flavonoids using a recombinant yeast strain and a modified MCF7 cell proliferation assay. Chem Res Toxicol 1998;11:622-9.
-
(1998)
Chem Res Toxicol
, vol.11
, pp. 622-629
-
-
Breinholt, V.1
Larsen, J.C.2
-
55
-
-
0033564553
-
Dietary flavonols quercetin and kaempferol are ligands of the aryl hydrocarbon receptor that affect CYP1A1 transcription differentially
-
Ciolino HP, Daschner PJ, Yeh GC. Dietary flavonols quercetin and kaempferol are ligands of the aryl hydrocarbon receptor that affect CYP1A1 transcription differentially. Biochem J 1999;340:715-22.
-
(1999)
Biochem J
, vol.340
, pp. 715-722
-
-
Ciolino, H.P.1
Daschner, P.J.2
Yeh, G.C.3
-
56
-
-
0346121452
-
Flavonoids as aryl hydrocarbon receptor agonists/antagonists effects of structure and cell context
-
Zhang S, Qin C, Safe S. Flavonoids as aryl hydrocarbon receptor agonists/antagonists effects of structure and cell context. Environ Health Perspect 2003; 111:1877-82.
-
(2003)
Environ Health Perspect
, vol.111
, pp. 1877-1882
-
-
Zhang, S.1
Qin, C.2
Safe, S.3
|