-
1
-
-
0023913120
-
The steroid and thyroid hormone receptor superfamily
-
Evans, R. M. The steroid and thyroid hormone receptor superfamily. Science 1986, 240, 889-895.
-
(1986)
Science
, vol.240
, pp. 889-895
-
-
Evans, R.M.1
-
2
-
-
0012473279
-
The nuclear receptor superfamily: The second decade
-
Mangelsdorf, D. J.; Thummel, C.; Beato, M.; Herrlich, P.; Schutz, G.; Umesono, K.; Blunberg, G.; Kastner, P.; Mark, M.; Chambon, P.; Evans, R. M. The nuclear receptor superfamily: the second decade. Cell 1995, 83, 835-839.
-
(1995)
Cell
, vol.83
, pp. 835-839
-
-
Mangelsdorf, D.J.1
Thummel, C.2
Beato, M.3
Herrlich, P.4
Schutz, G.5
Umesono, K.6
Blunberg, G.7
Kastner, P.8
Mark, M.9
Chambon, P.10
Evans, R.M.11
-
3
-
-
0025335811
-
Solution structure of the glucocorticoid receptor DNA binding domain
-
Hard, T.; Kellenbach, E.; Boelens, R.; Maler, B. A.; Dahlman, K.; Freedman, L.P.; Carstedt-Duke, J.; Yamamoto, K. R.; Gustafsson, J.-A. Solution structure of the glucocorticoid receptor DNA binding domain. Science 1990, 249, 157-160.
-
(1990)
Science
, vol.249
, pp. 157-160
-
-
Hard, T.1
Kellenbach, E.2
Boelens, R.3
Maler, B.A.4
Dahlman, K.5
Freedman, L.P.6
Carstedt-Duke, J.7
Yamamoto, K.R.8
Gustafsson, J.-A.9
-
4
-
-
0025223160
-
Solution structure of the DNA-binding domain of the oestrogen receptor
-
Schwabe, J. W. R.; Neuhaus, D.; Rhodes, D. Solution structure of the DNA-binding domain of the oestrogen receptor. Nature 1990, 348, 458-461.
-
(1990)
Nature
, vol.348
, pp. 458-461
-
-
Schwabe, J.W.R.1
Neuhaus, D.2
Rhodes, D.3
-
5
-
-
0025780755
-
Crystallographic analysis of the interaction of the glucocorticoid receptor with DNA
-
Luisi, B. F.; Xu, W. X.; Otwinowski, Z.; Freedman, L. P.; Yamamoto, K. R.; Sigler, B. P. Crystallographic analysis of the interaction of the glucocorticoid receptor with DNA. Nature 1991, 352, 497-505.
-
(1991)
Nature
, vol.352
, pp. 497-505
-
-
Luisi, B.F.1
Xu, W.X.2
Otwinowski, Z.3
Freedman, L.P.4
Yamamoto, K.R.5
Sigler, B.P.6
-
6
-
-
0029012163
-
Crystal structure of the ligand-binding domain of the human nuclear receptor RXRα
-
Bourguet, W.; Ruff, M.; Chambon, P.; Gronemeyer, H.; Moras, D. Crystal structure of the ligand-binding domain of the human nuclear receptor RXRα. Nature 1995, 375, 377-382.
-
(1995)
Nature
, vol.375
, pp. 377-382
-
-
Bourguet, W.1
Ruff, M.2
Chambon, P.3
Gronemeyer, H.4
Moras, D.5
-
7
-
-
0029643780
-
Crystal structure of the RAR-γ ligand binding domain bound to all-trans retinoic acid
-
Renaud, J.-P.; Rochel, N.; Ruff, M.; Vivat, V.; Chambon, P.; Gronemeyer, H.; Moras, D. Crystal structure of the RAR-γ ligand binding domain bound to all-trans retinoic acid. Nature 1995, 378, 681-689.
-
(1995)
Nature
, vol.378
, pp. 681-689
-
-
Renaud, J.-P.1
Rochel, N.2
Ruff, M.3
Vivat, V.4
Chambon, P.5
Gronemeyer, H.6
Moras, D.7
-
8
-
-
0029643769
-
A structural role for hormone in the thyroid hormone receptor
-
Wagner, R. L.; Apriletti, J. W.; Mc Grath, M. E.; West, B. L.; Baxter, J. D.; Fletterick, R. J. A structural role for hormone in the thyroid hormone receptor. Nature 1995, 378, 690-697.
-
(1995)
Nature
, vol.378
, pp. 690-697
-
-
Wagner, R.L.1
Apriletti, J.W.2
Mc Grath, M.E.3
West, B.L.4
Baxter, J.D.5
Fletterick, R.J.6
-
9
-
-
0030056997
-
A canonical structure for the ligand-binding domain of nuclear receptors
-
Wurtz, J.-M.; Bourguet, W.; Renaud, J.-P.; Vivat, V.; Chambon, P.; Moras, D.; Gronemeyer, H. A canonical structure for the ligand-binding domain of nuclear receptors. Nature Struct. Biol. 1996, 3, 87-94.
-
(1996)
Nature Struct. Biol.
, vol.3
, pp. 87-94
-
-
Wurtz, J.-M.1
Bourguet, W.2
Renaud, J.-P.3
Vivat, V.4
Chambon, P.5
Moras, D.6
Gronemeyer, H.7
-
10
-
-
0020619686
-
3H] tamoxifen aziridine
-
3H] tamoxifen aziridine. J. Biol. Chem. 1983, 258, 3487-3495.
-
(1983)
J. Biol. Chem.
, vol.258
, pp. 3487-3495
-
-
Katzenellenbogen, J.A.1
Carlson, K.E.2
Heiman, D.F.3
Robertson, D.W.4
Wei, L.L.5
Katzenellenbogen, B.S.6
-
11
-
-
0023177450
-
Estrogenic affinity labels: Synthesis, irreversible receptor binding, and bioactivity of aziridine substituted hexestrols derivatives
-
Zablocki, J. A.; Katzenellenbogen, J. A.; Carlson, K. E.; Norman, M. J.; Katzenellenbogen, B. S. Estrogenic affinity labels: synthesis, irreversible receptor binding, and bioactivity of aziridine substituted hexestrols derivatives. J. Med. Chem. 1987, 30, 829-838.
-
(1987)
J. Med. Chem.
, vol.30
, pp. 829-838
-
-
Zablocki, J.A.1
Katzenellenbogen, J.A.2
Carlson, K.E.3
Norman, M.J.4
Katzenellenbogen, B.S.5
-
12
-
-
0025793207
-
Efficient and selective photoaffinity labeling of the estrogen receptor using two nonsteroidal ligands that embody aryl azide and tetrafluoroaryl azide photoreactive functions
-
Pinney, K. G.; Carlson, K. E.; Katzenellenbogen, B. S.; Katzenellenbogen, J. A. Efficient and selective photoaffinity labeling of the estrogen receptor using two nonsteroidal ligands that embody aryl azide and tetrafluoroaryl azide photoreactive functions. Biochemistry 1991, 30, 2421-2431.
-
(1991)
Biochemistry
, vol.30
, pp. 2421-2431
-
-
Pinney, K.G.1
Carlson, K.E.2
Katzenellenbogen, B.S.3
Katzenellenbogen, J.A.4
-
13
-
-
0026507149
-
Nonsteroidal estrogens bearing acyl azide functions: Potential electrophilic and photoaffinity labeling agents for the estrogen receptor
-
Pinney, K. G.; Carlson, K. E.; Katzenellenbogen, J. A. Nonsteroidal estrogens bearing acyl azide functions: potential electrophilic and photoaffinity labeling agents for the estrogen receptor. Steroids 1992, 57, 222-232.
-
(1992)
Steroids
, vol.57
, pp. 222-232
-
-
Pinney, K.G.1
Carlson, K.E.2
Katzenellenbogen, J.A.3
-
14
-
-
0028399010
-
Hexestrol diaziridine photoaffinity labeling reagent for the estrogen receptor
-
Bergmann, K. E.; Carlson, K. E.; Katzenellenbogen, J. A. Hexestrol diaziridine photoaffinity labeling reagent for the estrogen receptor. Bioconjugate Chem. 1994, 5, 141-150.
-
(1994)
Bioconjugate Chem.
, vol.5
, pp. 141-150
-
-
Bergmann, K.E.1
Carlson, K.E.2
Katzenellenbogen, J.A.3
-
15
-
-
0027363644
-
Steroidal affinity labels of the estrogen receptor. 1. 17α-(bromoacetoxy)alkyl/ alkynylestradiols
-
El Garrouj, D.; Aumelas, A.; Borgna, J.-L. Steroidal affinity labels of the estrogen receptor. 1. 17α-(bromoacetoxy)alkyl/ alkynylestradiols. J. Med. Chem. 1993, 36, 2973-2983.
-
(1993)
J. Med. Chem.
, vol.36
, pp. 2973-2983
-
-
El Garrouj, D.1
Aumelas, A.2
Borgna, J.-L.3
-
16
-
-
0029058769
-
Steroidal affinity labels of the estrogen receptor. 2. 17α-[(haloacetamido)-alkyl]estradiols
-
El Garrouj, D.; Aliau, S.; Aumelas, A.; Borgna, J.-L. Steroidal affinity labels of the estrogen receptor. 2. 17α-[(haloacetamido)-alkyl]estradiols. J. Med. Chem. 1995, 38, 2339-2348.
-
(1995)
J. Med. Chem.
, vol.38
, pp. 2339-2348
-
-
El Garrouj, D.1
Aliau, S.2
Aumelas, A.3
Borgna, J.-L.4
-
17
-
-
0024330337
-
Identification of cysteine 530 as the covalent attachment site of an affinity-labeling estrogen (ketononestrol aziridine) and antiestrogen (tamoxifen aziridine) in the human estrogen receptor
-
Harlow, K. W.; Smith, D. N.; Katzenellenbogen, J. A.; Greene, G. L.; Katzenellenbogen, B. S. Identification of cysteine 530 as the covalent attachment site of an affinity-labeling estrogen (ketononestrol aziridine) and antiestrogen (tamoxifen aziridine) in the human estrogen receptor. J. Biol. Chem. 1989, 264, 17476-17485.
-
(1989)
J. Biol. Chem.
, vol.264
, pp. 17476-17485
-
-
Harlow, K.W.1
Smith, D.N.2
Katzenellenbogen, J.A.3
Greene, G.L.4
Katzenellenbogen, B.S.5
-
18
-
-
0025797584
-
Mutagenesis of cysteines in the hormone binding domain of the human estrogen receptor
-
Reese, J. C.; Katzenellenbogen, B. S. Mutagenesis of cysteines in the hormone binding domain of the human estrogen receptor. J. Biol. Chem. 1991, 266, 10880-10887
-
(1991)
J. Biol. Chem.
, vol.266
, pp. 10880-10887
-
-
Reese, J.C.1
Katzenellenbogen, B.S.2
-
19
-
-
0342813075
-
17α-[(haloacetamido)alkyl]estradiols alkylate the human estrogen receptor at cysteine residues 417 and 530
-
in press
-
Aliau, S.; El Garrouj, D.; Yasri, A.; Katzenellenbogen, B. S.; Borgna, J.-L. 17α-[(haloacetamido)alkyl]estradiols alkylate the human estrogen receptor at cysteine residues 417 and 530. Biochemistry, 1997, in press.
-
(1997)
Biochemistry
-
-
Aliau, S.1
El Garrouj, D.2
Yasri, A.3
Katzenellenbogen, B.S.4
Borgna, J.-L.5
-
20
-
-
0019443088
-
Regio and stereospecific synthesis of 11β-substituted 19-norsteroids
-
Belanger, A.; Philibert, D.; Teutsch, G. Regio and stereospecific synthesis of 11β-substituted 19-norsteroids. Steroids 1981, 37, 361-382.
-
(1981)
Steroids
, vol.37
, pp. 361-382
-
-
Belanger, A.1
Philibert, D.2
Teutsch, G.3
-
21
-
-
15644384179
-
Steroid derivatives
-
U.S. Patent 4 447 424, 1984
-
Teutsch, G.; Costerousse, G.; Philibert, D.; Deraedt, R. Steroid derivatives. U.S. Patent 4 447 424, 1984; Chem. Abstr. 1984,101, 130975m.
-
(1984)
Chem. Abstr.
, vol.101
-
-
Teutsch, G.1
Costerousse, G.2
Philibert, D.3
Deraedt, R.4
-
22
-
-
37049089769
-
Synthesis of new steroidal 11β-substituted spirolactones
-
Faraj, H.; Claire, M.; Rondot, A.; Aumelas, A.; Auzou, G. Synthesis of new steroidal 11β-substituted spirolactones. J. Chem. Soc., Perkin Trans. 1 1990, 3045-3048.
-
(1990)
J. Chem. Soc., Perkin Trans. 1
, pp. 3045-3048
-
-
Faraj, H.1
Claire, M.2
Rondot, A.3
Aumelas, A.4
Auzou, G.5
-
23
-
-
84915649677
-
Relation between estrogen receptor inhibitory activity and binding to cytosol of rabbit and human uterus
-
Korenman, S. G. Relation between estrogen receptor inhibitory activity and binding to cytosol of rabbit and human uterus. Endocrinology 1970, 87, 1119-1123.
-
(1970)
Endocrinology
, vol.87
, pp. 1119-1123
-
-
Korenman, S.G.1
-
24
-
-
0023433335
-
3H]estradiol-17β: A very high affinity, reversible ligand for the estrogen receptor
-
3H]estradiol-17β: a very high affinity, reversible ligand for the estrogen receptor. J. Steroid Biochem. 1987, 28, 361-370.
-
(1987)
J. Steroid Biochem.
, vol.28
, pp. 361-370
-
-
Bindal, R.D.1
Carlson, K.E.2
Reiner, G.A.C.3
Katzenellenbogen, J.A.4
-
25
-
-
0025223142
-
Synthesis and estrogen receptor binding of novel 11β-substituted estra-1,3,5(10)-triene-3,17β-diols
-
Hanson, R. N.; Napolitano, E.; Fiaschi, R. Synthesis and estrogen receptor binding of novel 11β-substituted estra-1,3,5(10)-triene-3,17β-diols. J. Med. Chem. 1990, 33, 3155-3160.
-
(1990)
J. Med. Chem.
, vol.33
, pp. 3155-3160
-
-
Hanson, R.N.1
Napolitano, E.2
Fiaschi, R.3
-
26
-
-
0025251173
-
11β-methoxy-, 11β-ethyl- and 17α-ethynyl-substituted 16α-fluoroestradiols: Receptor-based imaging agents with enhanced uptake efficiency and selectivity
-
Pomper, M. G.; VanBrocklin, H.; Thieme, A. M.; Thomas, R. D; Kiesewetter, D. O.; Carlson, K. E.; Mathias, C. J.; Welch, M. J.; Katzenellenbogen, J. A. 11β-methoxy-, 11β-ethyl-and 17α-ethynyl-substituted 16α-fluoroestradiols: receptor-based imaging agents with enhanced uptake efficiency and selectivity. J. Med. Chem. 1990, 33, 3143-3155
-
(1990)
J. Med. Chem.
, vol.33
, pp. 3143-3155
-
-
Pomper, M.G.1
VanBrocklin, H.2
Thieme, A.M.3
Thomas, R.D.4
Kiesewetter, D.O.5
Carlson, K.E.6
Mathias, C.J.7
Welch, M.J.8
Katzenellenbogen, J.A.9
-
27
-
-
0026578544
-
11β-amidoalkylestradiols, a new series of pure antiestrogens
-
Claussner, A.; Nedelec, L.; Nique, F.; Philibert, D.; Teutsch, G.; Van de Velde, P. 11β-amidoalkylestradiols, a new series of pure antiestrogens. J. Steroid Biochem. Mol. Biol. 1992, 41, 609-614.
-
(1992)
J. Steroid Biochem. Mol. Biol.
, vol.41
, pp. 609-614
-
-
Claussner, A.1
Nedelec, L.2
Nique, F.3
Philibert, D.4
Teutsch, G.5
Van De Velde, P.6
-
28
-
-
0025187484
-
A new cellular model of response to estrogen: A bioluminescent test to characterize (anti)estrogen molecules
-
Pons, M.; Gagne, D.; Nicolas, J.-C.; Mehtali, M. A new cellular model of response to estrogen: a bioluminescent test to characterize (anti)estrogen molecules. Biotechniques 1990, 9, 450-459.
-
(1990)
Biotechniques
, vol.9
, pp. 450-459
-
-
Pons, M.1
Gagne, D.2
Nicolas, J.-C.3
Mehtali, M.4
-
29
-
-
0027365574
-
MVLN cells: A bioluminescent MCF-7-derived cell line to study the modulation of estrogenic activity
-
Demirpence, E.; Duchesne, M.-J.; Badia, E.; Gagne, D.; Pons, M. MVLN cells: a bioluminescent MCF-7-derived cell line to study the modulation of estrogenic activity. J. Steroid Biochem. Mol. Biol. 1993, 46, 355-364.
-
(1993)
J. Steroid Biochem. Mol. Biol.
, vol.46
, pp. 355-364
-
-
Demirpence, E.1
Duchesne, M.-J.2
Badia, E.3
Gagne, D.4
Pons, M.5
-
30
-
-
0028077625
-
Hydroxytamoxifen induces a rapid and irreversible inactivation of an estrogenic response in an MCF-7-derived cell line
-
Badia, E.; Duchesne, M.-J.; Fournier-Bidoz, S.; Simar-Blancnet, A. E.; Terouanne, B.; Nicolas, J.-C.; Pons, M. Hydroxytamoxifen induces a rapid and irreversible inactivation of an estrogenic response in an MCF-7-derived cell line. Cancer Res. 1994, 54, 5860-5866.
-
(1994)
Cancer Res.
, vol.54
, pp. 5860-5866
-
-
Badia, E.1
Duchesne, M.-J.2
Fournier-Bidoz, S.3
Simar-Blancnet, A.E.4
Terouanne, B.5
Nicolas, J.-C.6
Pons, M.7
-
31
-
-
0020610131
-
Org-4333, a potent irreversibly binding estrogen agonist
-
Van den Broek, A.; Leemhuis, J.; de Winter, M. S.; Zeelen, F. J. Org-4333, a potent irreversibly binding estrogen agonist. Weeklab. Sci. Edit. 1983, 5, 182-183.
-
(1983)
Weeklab. Sci. Edit.
, vol.5
, pp. 182-183
-
-
Van Den Broek, A.1
Leemhuis, J.2
De Winter, M.S.3
Zeelen, F.J.4
-
32
-
-
0011201769
-
In vitro screening of cytotoxic estrogens of potential therapeutic activity
-
Raus, J., Martens, H., Leclercq, G., Eds.; Academic Press: London
-
Leclercq, G.; Devleeschouwer, N.; Legros, N.; Heuson, J. In vitro screening of cytotoxic estrogens of potential therapeutic activity. In Cytotoxic Estrogens in Hormone Receptive Tumors; Raus, J., Martens, H., Leclercq, G., Eds.; Academic Press: London, 1980; pp 165-181.
-
(1980)
Cytotoxic Estrogens in Hormone Receptive Tumors
, pp. 165-181
-
-
Leclercq, G.1
Devleeschouwer, N.2
Legros, N.3
Heuson, J.4
-
33
-
-
0019638247
-
The synthesis and study of some potential affinity labelling reagents for estrogens receptors
-
Ratajczak, T.; Sheppard, P. N.; Capon, R. J.; Hahnel, R. The synthesis and study of some potential affinity labelling reagents for estrogens receptors. Steroids 1981, 38, 537-555.
-
(1981)
Steroids
, vol.38
, pp. 537-555
-
-
Ratajczak, T.1
Sheppard, P.N.2
Capon, R.J.3
Hahnel, R.4
-
34
-
-
77957012032
-
Spectrophotometric and turbidimetric methods for measuring proteins
-
Layne, E. Spectrophotometric and turbidimetric methods for measuring proteins. Methods Enzymol. 1957, 3, 444-454.
-
(1957)
Methods Enzymol.
, vol.3
, pp. 444-454
-
-
Layne, E.1
-
36
-
-
71849104860
-
Protein measurement with the Folin phenol reagent
-
Lowry, O. H.; Rosenbrough, N. I.; Farz, A. L.; Randall, R. G. Protein measurement with the Folin phenol reagent. J. Biol. Chem. 1951, 193, 265-275.
-
(1951)
J. Biol. Chem.
, vol.193
, pp. 265-275
-
-
Lowry, O.H.1
Rosenbrough, N.I.2
Farz, A.L.3
Randall, R.G.4
-
37
-
-
0018344156
-
Assay for nanogram quantities of DNA in cellular homogenates
-
Brunk, C. F.; Jones, K. C.; James, T. W. Assay for nanogram quantities of DNA in cellular homogenates. Anal. Biochem. 1979, 92, 497-500.
-
(1979)
Anal. Biochem.
, vol.92
, pp. 497-500
-
-
Brunk, C.F.1
Jones, K.C.2
James, T.W.3
|