-
1
-
-
0028283503
-
Molecular mechanisms of action of steroid/thyroid receptor superfamily members
-
Tsai M.-J., O'Malley B.W. Molecular mechanisms of action of steroid/thyroid receptor superfamily members. Annu. Rev. Biochem. 63:1994;451-486.
-
(1994)
Annu. Rev. Biochem.
, vol.63
, pp. 451-486
-
-
Tsai, M.-J.1
O'Malley, B.W.2
-
2
-
-
0030451142
-
Interaction of steroid hormone receptors with the transcription initiation complex
-
Beato M., Sanchez-Pacheco A. Interaction of steroid hormone receptors with the transcription initiation complex. Endocrinol. Rev. 17:1996;587-609.
-
(1996)
Endocrinol. Rev.
, vol.17
, pp. 587-609
-
-
Beato, M.1
Sanchez-Pacheco, A.2
-
4
-
-
0030667676
-
Molecular basis of agonism and antagonism in the oestrogen receptor
-
Brzozowski A.M., Pike A.C.W., Dauter Z., Hubbard R.W., Bonn T., Engström O., Öhman L., Greene G.L., Gustafsson J.-Å., Carlquist M. Molecular basis of agonism and antagonism in the oestrogen receptor. Nature. 389:1997;753-758.
-
(1997)
Nature
, vol.389
, pp. 753-758
-
-
Brzozowski, A.M.1
Pike, A.C.W.2
Dauter, Z.3
Hubbard, R.W.4
Bonn, T.5
Engström, O.6
Öhman, L.7
Greene, G.L.8
Gustafsson, J.-Å.9
Carlquist, M.10
-
5
-
-
0032511086
-
Hormone dependent coactivator binding to a hydrophobic cleft on nuclear receptors
-
Feng W., Ribeiro R.C.J., Wagner R.L., Nguyen H., Apriletti J.W., Fletterick R.J., Baxter J.D., Kushner P.J., West B.L. Hormone dependent coactivator binding to a hydrophobic cleft on nuclear receptors. Science. 280:1998;1747-1749.
-
(1998)
Science
, vol.280
, pp. 1747-1749
-
-
Feng, W.1
Ribeiro, R.C.J.2
Wagner, R.L.3
Nguyen, H.4
Apriletti, J.W.5
Fletterick, R.J.6
Baxter, J.D.7
Kushner, P.J.8
West, B.L.9
-
6
-
-
0025338591
-
Development of antiestrogens and their use in breast cancer: Eighth Cain memorial award lecture
-
Lerner L.J., Jordan V.C. Development of antiestrogens and their use in breast cancer: Eighth Cain memorial award lecture. Cancer Res. 50:1990;4177-4189.
-
(1990)
Cancer Res.
, vol.50
, pp. 4177-4189
-
-
Lerner, L.J.1
Jordan, V.C.2
-
7
-
-
0032446607
-
The structural basis of estrogen receptor/coactivator recognition and the antagonism of this interaction by tamoxifen
-
Shiau A.K., Barstad D., Loria P.M., Cheng L., Kushner P.J., Agard D.A., Greene G.L. The structural basis of estrogen receptor/coactivator recognition and the antagonism of this interaction by tamoxifen. Cell. 95:1998;927-937.
-
(1998)
Cell
, vol.95
, pp. 927-937
-
-
Shiau, A.K.1
Barstad, D.2
Loria, P.M.3
Cheng, L.4
Kushner, P.J.5
Agard, D.A.6
Greene, G.L.7
-
8
-
-
0037153283
-
Investigations on the estrogen receptor binding. The estrogenic, antiestrogenic and cytotoxic properties of C2-alkyl substituted 1,1-bis(4-hydroxyphenyl)-2-phenylethenes
-
Lubczyk V., Bachmann H., Gust R. Investigations on the estrogen receptor binding. The estrogenic, antiestrogenic and cytotoxic properties of C2-alkyl substituted 1,1-bis(4-hydroxyphenyl)-2-phenylethenes. J. Med. Chem. 45:2002;5358-5364.
-
(2002)
J. Med. Chem.
, vol.45
, pp. 5358-5364
-
-
Lubczyk, V.1
Bachmann, H.2
Gust, R.3
-
9
-
-
0037431405
-
Antiestrogenically active 1,1,2-tris(4-hydroxyphenyl)alkenes without basic side chain. Synthesis and biological activity
-
Lubczyk V., Bachmann H., Gust R. Antiestrogenically active 1,1,2-tris(4-hydroxyphenyl)alkenes without basic side chain. Synthesis and biological activity. J. Med. Chem. 46:2003;1484-1491.
-
(2003)
J. Med. Chem.
, vol.46
, pp. 1484-1491
-
-
Lubczyk, V.1
Bachmann, H.2
Gust, R.3
-
10
-
-
0036234964
-
Structural characterization of a subtype-selective ligand reveals a novel mode of estrogen antagonism
-
Shiau A.K., Barstad D., Radek J.T., Meyers M.J., Nettles K.W., Katzenellenbogen B.S., Katzenellenbogen J.A., Agard D.A., Greene G.L. Structural characterization of a subtype-selective ligand reveals a novel mode of estrogen antagonism. Nat. Struct. Biol. 9:2002;359-364.
-
(2002)
Nat. Struct. Biol.
, vol.9
, pp. 359-364
-
-
Shiau, A.K.1
Barstad, D.2
Radek, J.T.3
Meyers, M.J.4
Nettles, K.W.5
Katzenellenbogen, B.S.6
Katzenellenbogen, J.A.7
Agard, D.A.8
Greene, G.L.9
-
11
-
-
0344417000
-
Estrogen receptor subtype-selective ligands: Asymmetric synthesis and biological evaluation of cis- and trans-5,11-dialkyl-5,6,11,12-tetrahydrochrysenes
-
Meyers M.J., Sun J., Carlson K.E., Katzenellenbogen B.S., Katzenellenbogen J.A. Estrogen receptor subtype-selective ligands: Asymmetric synthesis and biological evaluation of cis- and trans-5,11-dialkyl-5,6,11,12-tetrahydrochrysenes. J. Med. Chem. 42:1999;2456-2468.
-
(1999)
J. Med. Chem.
, vol.42
, pp. 2456-2468
-
-
Meyers, M.J.1
Sun, J.2
Carlson, K.E.3
Katzenellenbogen, B.S.4
Katzenellenbogen, J.A.5
-
12
-
-
0004752110
-
Novel ligands that function as selective estrogens or antiestrogens for estrogen receptor-alpha or estrogen receptor-beta
-
Sun J., J Meyers M., E Fink B., Rajendran R., Katzenellenbogen J.A., Katzenellenbogen B.S. Novel ligands that function as selective estrogens or antiestrogens for estrogen receptor-alpha or estrogen receptor-beta. Endocrinology. 140:1999;800-804.
-
(1999)
Endocrinology
, vol.140
, pp. 800-804
-
-
Sun, J.1
J Meyers, M.2
E Fink, B.3
Rajendran, R.4
Katzenellenbogen, J.A.5
Katzenellenbogen, B.S.6
-
13
-
-
0023896334
-
The seed stock concept and quality control for cell lines
-
Hay R.J. The seed stock concept and quality control for cell lines. Anal. Biochem. 171:1988;225-237.
-
(1988)
Anal. Biochem.
, vol.171
, pp. 225-237
-
-
Hay, R.J.1
-
14
-
-
0018825761
-
Antiestrogens. Synthesis and evaluation of mammary tumor inhibiting activity of 1,1,2,2-tetraalkyl-1,2-diphenylethanes
-
Hartmann R., Kranzfelder G., von Angerer E., Schönenberger H. Antiestrogens. Synthesis and evaluation of mammary tumor inhibiting activity of 1,1,2,2-tetraalkyl-1,2-diphenylethanes. J. Med. Chem. 23:1980;841-847.
-
(1980)
J. Med. Chem.
, vol.23
, pp. 841-847
-
-
Hartmann, R.1
Kranzfelder, G.2
Von Angerer, E.3
Schönenberger, H.4
-
15
-
-
0030199499
-
Effect of growth factors on estrogen receptor mediated gene expression
-
Hafner F., Holler E., von Angerer E. Effect of growth factors on estrogen receptor mediated gene expression. J. Steroid Biochem. Mol. Biol. 58:1996;385-393.
-
(1996)
J. Steroid Biochem. Mol. Biol.
, vol.58
, pp. 385-393
-
-
Hafner, F.1
Holler, E.2
Von Angerer, E.3
-
16
-
-
0017184389
-
A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding
-
Bradford M.M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal. Biochem. 72:1976;248-254.
-
(1976)
Anal. Biochem.
, vol.72
, pp. 248-254
-
-
Bradford, M.M.1
-
18
-
-
0021201213
-
Antiestrogens. 2. Structure-activity studies in a series of 3-aroyl-2-arylbenzo[b]thiophene derivatives leading to [6-hydroxy-2-(4-hydroxyphenyl)benzo[b]thien-3-yl] [4-[2-(1-piperidinyl)ethoxy]phenyl]methanone hydrochloride (LY156758), a remarkably effective estrogen antagonist with only minimal intrinsic estrogenicity
-
Jones C.D., Jevnikar M.G., Pike A.J., Peters M.K., Black L.J., Thompson A.R., Falcone J.F., Clemens J.A. Antiestrogens. 2. Structure-activity studies in a series of 3-aroyl-2-arylbenzo[b]thiophene derivatives leading to [6-hydroxy-2-(4-hydroxyphenyl)benzo[b]thien-3-yl] [4-[2-(1-piperidinyl)ethoxy]phenyl]methanone hydrochloride (LY156758), a remarkably effective estrogen antagonist with only minimal intrinsic estrogenicity. J. Med. Chem. 27:1984;1057-1066.
-
(1984)
J. Med. Chem.
, vol.27
, pp. 1057-1066
-
-
Jones, C.D.1
Jevnikar, M.G.2
Pike, A.J.3
Peters, M.K.4
Black, L.J.5
Thompson, A.R.6
Falcone, J.F.7
Clemens, J.A.8
-
19
-
-
0037088656
-
Structure-function relationships of the raloxifene-estrogen receptor-α complex for regulating transforming growth factor-α expression in breast cancer cells
-
Liu H., Park W.C., Bentrem D.J., McKian K.P., De Los R.A., Loweth J.A., MacGregor Schafer J., Zapf J.W., Jordan V.C. Structure-function relationships of the raloxifene-estrogen receptor-α complex for regulating transforming growth factor-α expression in breast cancer cells. J. Biol. Chem. 277:2002;9189-9198.
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 9189-9198
-
-
Liu, H.1
Park, W.C.2
Bentrem, D.J.3
McKian, K.P.4
De Los, R.A.5
Loweth, J.A.6
MacGregor Schafer, J.7
Zapf, J.W.8
Jordan, V.C.9
-
20
-
-
0023219107
-
Cytotoxic esters of 1,1-bis(4-hydroxyphenyl)-2-phenylbut-1-ene with selective antitumor activity against estrogen receptor-containing mammary tumors
-
Schuderer M.L., Schneider M.R. Cytotoxic esters of 1,1-bis(4-hydroxyphenyl)-2-phenylbut-1-ene with selective antitumor activity against estrogen receptor-containing mammary tumors. J. Cancer Res. Clin. Oncol. 113:1987;230-234.
-
(1987)
J. Cancer Res. Clin. Oncol.
, vol.113
, pp. 230-234
-
-
Schuderer, M.L.1
Schneider, M.R.2
-
21
-
-
0022450323
-
2-Alkyl-substituted 1,1-bis(4-acetoxyphenyl)-2-phenylethenes. Estrogen receptor affinity, estrogenic and antiestrogenic properties, and mammary tumor inhibiting activity
-
Schneider M.R. 2-Alkyl-substituted 1,1-bis(4-acetoxyphenyl)-2-phenylethenes. Estrogen receptor affinity, estrogenic and antiestrogenic properties, and mammary tumor inhibiting activity. J. Med. Chem. 29:1986;1494-1498.
-
(1986)
J. Med. Chem.
, vol.29
, pp. 1494-1498
-
-
Schneider, M.R.1
-
22
-
-
0023180857
-
Influence of derivatisation of the hydroxy groups in 1,1-bis(4-hydroxyphenyl)-2-phenylbut-1-ene on estradiol receptor affinity and mammary tumor inhibiting properties
-
Schuderer M.L., Schneider M.R. Influence of derivatisation of the hydroxy groups in 1,1-bis(4-hydroxyphenyl)-2-phenylbut-1-ene on estradiol receptor affinity and mammary tumor inhibiting properties. Arch. Pharm. 320:1987;635-641.
-
(1987)
Arch. Pharm.
, vol.320
, pp. 635-641
-
-
Schuderer, M.L.1
Schneider, M.R.2
-
23
-
-
0022635946
-
Studies on the mammary tumor-inhibiting effects of diethylstilbestrol and its mono- and diphosphate
-
Schneider M.R., von Angerer E., Prekajac J., Brade W.P. Studies on the mammary tumor-inhibiting effects of diethylstilbestrol and its mono- and diphosphate. J. Cancer Res. Clin. Oncol. 111:1986;110-114.
-
(1986)
J. Cancer Res. Clin. Oncol.
, vol.111
, pp. 110-114
-
-
Schneider, M.R.1
Von Angerer, E.2
Prekajac, J.3
Brade, W.P.4
-
24
-
-
0026553312
-
7 cell proliferation
-
7 cell proliferation. J. Med. Chem. 35:1992;573-583.
-
(1992)
J. Med. Chem.
, vol.35
, pp. 573-583
-
-
Doré, J.C.1
Gilbert, J.2
Bignon, E.3
Crastes de Paulet, A.4
Ojasoo, T.5
Pons, M.6
Raynaud, J.-P.7
Miquel, J.-F.8
-
25
-
-
0024470812
-
Effect of triphenylacrylonitrile derivatives on estradiol-receptor binding and on human breast cancer cell growth
-
Bignon E., Pons M., Crastes de Paulet A., Doré J.-C., Gilbert J., Abecassis J., Miquel J.-F., Ojasoo T., Raynaud J.-P. Effect of triphenylacrylonitrile derivatives on estradiol-receptor binding and on human breast cancer cell growth. J. Med. Chem. 32:1989;2092-2103.
-
(1989)
J. Med. Chem.
, vol.32
, pp. 2092-2103
-
-
Bignon, E.1
Pons, M.2
Crastes de Paulet, A.3
Doré, J.-C.4
Gilbert, J.5
Abecassis, J.6
Miquel, J.-F.7
Ojasoo, T.8
Raynaud, J.-P.9
-
26
-
-
0017838558
-
Synthèse de polyphényléthylènes et interferences avec le récepteur œstrogène d'utérus de souris
-
Miquel J.-F., Sekera A.S., Chaudron T. Synthèse de polyphényléthylènes et interferences avec le récepteur œstrogène d'utérus de souris. C. R. Acad. Sci. Paris. Ser. C. 286:1978;151-154.
-
(1978)
C. R. Acad. Sci. Paris. Ser. C
, vol.286
, pp. 151-154
-
-
Miquel, J.-F.1
Sekera, A.S.2
Chaudron, T.3
-
27
-
-
0035099225
-
Structural insights into the mode of action of a pure antiestrogen
-
Pike A.C., Brzozowski A.M., Walton J., Hubbard R.E., Thorsell A.G., Li Y.L., Gustafsson J.A., Carlquist M. Structural insights into the mode of action of a pure antiestrogen. Structure. 9:2001;145-153.
-
(2001)
Structure
, vol.9
, pp. 145-153
-
-
Pike, A.C.1
Brzozowski, A.M.2
Walton, J.3
Hubbard, R.E.4
Thorsell, A.G.5
Li, Y.L.6
Gustafsson, J.A.7
Carlquist, M.8
-
28
-
-
0025329841
-
Characterization and colocalization of steroid binding and dimerization activities in the mouse estrogen receptor
-
Fawell S.E., Lees J.A., White R., Parker M.G. Characterization and colocalization of steroid binding and dimerization activities in the mouse estrogen receptor. Cell. 60:1990;953-962.
-
(1990)
Cell
, vol.60
, pp. 953-962
-
-
Fawell, S.E.1
Lees, J.A.2
White, R.3
Parker, M.G.4
-
29
-
-
0026560435
-
Antiestrogen ICI 164,384 reduces cellular estrogen receptor content by increasing its turnover
-
Dauvois S., Danielian P.S., White R., Parker M.G. Antiestrogen ICI 164,384 reduces cellular estrogen receptor content by increasing its turnover. Proc. Natl. Acad. Sci. U.S.A. 89:1992;4037-4041.
-
(1992)
Proc. Natl. Acad. Sci. U.S.A.
, vol.89
, pp. 4037-4041
-
-
Dauvois, S.1
Danielian, P.S.2
White, R.3
Parker, M.G.4
-
30
-
-
0027768899
-
The antiestrogen ICI 182 780 disrupts estrogen receptor nucleocytoplasmic shuttling
-
Dauvois S., White R., Parker M.G. The antiestrogen ICI 182 780 disrupts estrogen receptor nucleocytoplasmic shuttling. J. Cell Sci. 106:1993;1377-1388.
-
(1993)
J. Cell Sci.
, vol.106
, pp. 1377-1388
-
-
Dauvois, S.1
White, R.2
Parker, M.G.3
-
31
-
-
0036681599
-
(4R,5S)/(4S,5R)-4,5-bis(4-Hydroxyphenyl)-2-imidazolines: Ligands for the estrogen receptor with a novel binding mode
-
Gust R., Keilitz R., Schmidt K., von Rauch M. (4R,5S)/(4S,5R)-4,5-bis(4-Hydroxyphenyl)-2-imidazolines: ligands for the estrogen receptor with a novel binding mode. J. Med. Chem. 45:2002;3356-3365.
-
(2002)
J. Med. Chem.
, vol.45
, pp. 3356-3365
-
-
Gust, R.1
Keilitz, R.2
Schmidt, K.3
Von Rauch, M.4
|