-
1
-
-
0001877218
-
The androgen receptor: A mediator of diverse responses
-
Keller, E. T., Ershler, W. B. and Chang, C. (1996) The androgen receptor: a mediator of diverse responses. Front. Biosci. 1, d59-d71
-
(1996)
Front. Biosci.
, vol.1
-
-
Keller, E.T.1
Ershler, W.B.2
Chang, C.3
-
2
-
-
0036755404
-
Androgen receptor as a target in androgen-independent prostate cancer
-
Balk, S. P. (2002) Androgen receptor as a target in androgen-independent prostate cancer. Urology 60, 132-138
-
(2002)
Urology
, vol.60
, pp. 132-138
-
-
Balk, S.P.1
-
3
-
-
0026591729
-
Anti-androgens and the mutated androgen receptor of LNCaP cells: Differential effects on binding affinity, heat-shock protein interaction, and transcription activation
-
Veldscholte, J., Berrevoets, C. A., Brinkmann, A. O., Grootegoed, J. A. and Mulder, E. (1992) Anti-androgens and the mutated androgen receptor of LNCaP cells: differential effects on binding affinity, heat-shock protein interaction, and transcription activation. Biochemistry 31, 2393-2399
-
(1992)
Biochemistry
, vol.31
, pp. 2393-2399
-
-
Veldscholte, J.1
Berrevoets, C.A.2
Brinkmann, A.O.3
Grootegoed, J.A.4
Mulder, E.5
-
4
-
-
0029069878
-
Androgen receptor defects: Historical, clinical, and molecular perspectives
-
Quigley, C. A., de Bellis, A., Marschke, K. B., El-Awady, M. K., Wilson, E. M. and French, F. S. (1995) Androgen receptor defects: historical, clinical, and molecular perspectives. Endocrinol. Rev. 16, 271-321
-
(1995)
Endocrinol. Rev.
, vol.16
, pp. 271-321
-
-
Quigley, C.A.1
De Bellis, A.2
Marschke, K.B.3
El-Awady, M.K.4
Wilson, E.M.5
French, F.S.6
-
5
-
-
0033013799
-
Mechanisms of androgen receptor activation and function
-
Brinkmann, A. O., Blok, L. J., de Ruiter, P. E., Doesburg, P., Steketee, K., Berrevoets, C. A. and Trapman, J. (1999) Mechanisms of androgen receptor activation and function. J. Steroid Biochem. Mol. Biol. 69, 307-313
-
(1999)
J. Steroid Biochem. Mol. Biol.
, vol.69
, pp. 307-313
-
-
Brinkmann, A.O.1
Blok, L.J.2
De Ruiter, P.E.3
Doesburg, P.4
Steketee, K.5
Berrevoets, C.A.6
Trapman, J.7
-
6
-
-
0036793098
-
The roles of androgen receptors and androgen-binding proteins in nongenomic androgen actions
-
Heinlein, C. A., and Chang, C. (2002) The roles of androgen receptors and androgen-binding proteins in nongenomic androgen actions. Mol. Endocrinol. 16, 2181-2187
-
(2002)
Mol. Endocrinol.
, vol.16
, pp. 2181-2187
-
-
Heinlein, C.A.1
Chang, C.2
-
7
-
-
0034454583
-
Nuclear hormone receptor coregulators in action: Diversity for shared tasks
-
Robyr, D., Wolffe, A. P. and Wahli, W. (2000) Nuclear hormone receptor coregulators in action: diversity for shared tasks. Mol. Endocrinol. 14, 329-347
-
(2000)
Mol. Endocrinol.
, vol.14
, pp. 329-347
-
-
Robyr, D.1
Wolffe, A.P.2
Wahli, W.3
-
8
-
-
0036515648
-
Nuclear receptor coregulators: Multiple modes of modification
-
Hermanson, O., Glass, C. K. and Rosenfeld, M. G. (2002) Nuclear receptor coregulators: multiple modes of modification. Trends Endocrinol. Metab. 13, 55-60
-
(2002)
Trends Endocrinol. Metab.
, vol.13
, pp. 55-60
-
-
Hermanson, O.1
Glass, C.K.2
Rosenfeld, M.G.3
-
9
-
-
0028237201
-
Mechanism of antiandrogen action: Conformational changes of the receptor
-
Kuil, C. W. and Mulder, E. (1994) Mechanism of antiandrogen action: conformational changes of the receptor. Mol. Cell. Endocrinol. 102, R1-R5
-
(1994)
Mol. Cell. Endocrinol.
, vol.102
-
-
Kuil, C.W.1
Mulder, E.2
-
10
-
-
0033378278
-
Antiandrogens in prostate cancer
-
Reid, P., Kantoff, P. and Oh, W. (1999) Antiandrogens in prostate cancer. Invest. New Drugs 17, 271-284
-
(1999)
Invest. New Drugs
, vol.17
, pp. 271-284
-
-
Reid, P.1
Kantoff, P.2
Oh, W.3
-
11
-
-
0028891989
-
Ligand-induced conformational alterations of the androgen receptor analyzed by limited trypsinization. Studies on the mechanism of antiandrogen action
-
Kuil, C. W., Berrevoets, C. A. and Mulder, E. (1995) Ligand-induced conformational alterations of the androgen receptor analyzed by limited trypsinization. Studies on the mechanism of antiandrogen action, J. Biol. Chem. 270, 27569-27576
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 27569-27576
-
-
Kuil, C.W.1
Berrevoets, C.A.2
Mulder, E.3
-
12
-
-
0029825669
-
Codon 877 mutation in the androgen receptor gene in advanced prostate cancer: Relation to antiandrogen withdrawal syndrome
-
Suzuki, H., Akakura, K., Komiya, A., Aida, S., Akimoto, S. and Shimazaki, J. (1996) Codon 877 mutation in the androgen receptor gene in advanced prostate cancer: relation to antiandrogen withdrawal syndrome. Prostate 29, 153-158
-
(1996)
Prostate
, vol.29
, pp. 153-158
-
-
Suzuki, H.1
Akakura, K.2
Komiya, A.3
Aida, S.4
Akimoto, S.5
Shimazaki, J.6
-
13
-
-
0033152164
-
Selection for androgen receptor mutations in prostate cancers treated with androgen antagonist
-
Taplin, M. E., Bubley, G. J., Ko, Y. J., Small, E. J., Upton, M., Rajeshkumar, B. and Balk, S. P. (1999) Selection for androgen receptor mutations in prostate cancers treated with androgen antagonist. Cancer Res. 59, 2511-2515
-
(1999)
Cancer Res.
, vol.59
, pp. 2511-2515
-
-
Taplin, M.E.1
Bubley, G.J.2
Ko, Y.J.3
Small, E.J.4
Upton, M.5
Rajeshkumar, B.6
Balk, S.P.7
-
14
-
-
0025644325
-
A mutation in the ligand binding domain of the androgen receptor of human LNCaP cells affects steroid binding characteristics and response to anti-androgens
-
Veldscholte, J., Ris-Stalpers, C., Kuiper, G. G., Jenster, G., Berrevoets, C., Claassen, E., van Rooij, H. C., Trapman, J., Brinkmann, A. O. and Mulder, E. (1990) A mutation in the ligand binding domain of the androgen receptor of human LNCaP cells affects steroid binding characteristics and response to anti-androgens. Biochem. Biophys. Res. Commun. 173, 534-540
-
(1990)
Biochem. Biophys. Res. Commun.
, vol.173
, pp. 534-540
-
-
Veldscholte, J.1
Ris-Stalpers, C.2
Kuiper, G.G.3
Jenster, G.4
Berrevoets, C.5
Claassen, E.6
Van Rooij, H.C.7
Trapman, J.8
Brinkmann, A.O.9
Mulder, E.10
-
15
-
-
0036494196
-
Functional analysis of 44 mutant androgen receptors from human prostate cancer
-
Shi, X. B., Ma, A. H., Xia, L., Kung, H. J. and de Vere White, R. W. (2002) Functional analysis of 44 mutant androgen receptors from human prostate cancer. Cancer Res. 62, 1496-1502
-
(2002)
Cancer Res.
, vol.62
, pp. 1496-1502
-
-
Shi, X.B.1
Ma, A.H.2
Xia, L.3
Kung, H.J.4
De Vere White, R.W.5
-
16
-
-
0037143096
-
Broadened ligand responsiveness of androgen receptor mutants obtained by random amino acid substitution of H874 and mutation hot spot T877 in prostate cancer
-
Steketee, K., Timmerman, L., Ziel-van der Made, A. C. J., Doesburg, P., Brinkmann, A. O. and Trapman, J. (2002) Broadened ligand responsiveness of androgen receptor mutants obtained by random amino acid substitution of H874 and mutation hot spot T877 in prostate cancer. Int. J. Cancer. 100, 309-317
-
(2002)
Int. J. Cancer.
, vol.100
, pp. 309-317
-
-
Steketee, K.1
Timmerman, L.2
Ziel-van Der Made, A.C.J.3
Doesburg, P.4
Brinkmann, A.O.5
Trapman, J.6
-
17
-
-
0036218706
-
Evaluation of ligand-dependent changes in AR structure using peptide probes
-
Chang, C.-Y. and McDonnel, D. P. (2002) Evaluation of ligand-dependent changes in AR structure using peptide probes. Mol. Endocrinol. 16, 647-660
-
(2002)
Mol. Endocrinol.
, vol.16
, pp. 647-660
-
-
Chang, C.-Y.1
McDonnel, D.P.2
-
18
-
-
0030998328
-
The partial agonist activity of antagonist-occupied steroid receptors is controlled by a novel hinge domain-binding coactivator L7/SPA and the corepressors N-CoR or SMRT
-
Jackson, T. A., Richer, J. K., Bain, D. L., Takimoto, G. S., Tung, L. and Horwitz, K. B. (1997) The partial agonist activity of antagonist-occupied steroid receptors is controlled by a novel hinge domain-binding coactivator L7/SPA and the corepressors N-CoR or SMRT. Mol. Endocrinol. 11, 693-705
-
(1997)
Mol. Endocrinol.
, vol.11
, pp. 693-705
-
-
Jackson, T.A.1
Richer, J.K.2
Bain, D.L.3
Takimoto, G.S.4
Tung, L.5
Horwitz, K.B.6
-
19
-
-
0030946198
-
Coactivator and corepressor regulation of the agonist/antagonist activity of the mixed antiestrogen, 4-hydroxytamoxifen
-
Smith, C. L., Nawaz, Z. and O'Malley, B. W. (1997) Coactivator and corepressor regulation of the agonist/antagonist activity of the mixed antiestrogen, 4-hydroxytamoxifen. Mol. Endocrinol. 11, 657-666
-
(1997)
Mol. Endocrinol.
, vol.11
, pp. 657-666
-
-
Smith, C.L.1
Nawaz, Z.2
O'Malley, B.W.3
-
20
-
-
0032230289
-
A nuclear receptor corepressor modulates transcriptional activity of antagonist-occupied steroid hormone receptor
-
Zhang, X., Jeyakumar, M., Petukhov, S. and Bagchi, M. K. (1998) A nuclear receptor corepressor modulates transcriptional activity of antagonist-occupied steroid hormone receptor. Mol. Endocrinol. 12, 513-524
-
(1998)
Mol. Endocrinol.
, vol.12
, pp. 513-524
-
-
Zhang, X.1
Jeyakumar, M.2
Petukhov, S.3
Bagchi, M.K.4
-
21
-
-
0030959244
-
Role for N-CoR and histone deacetylase in Sin3-mediated transcriptional repression
-
Alland, L., Muhle, R., Hou, H., Jr, Potes, J., Chin, L., Schreiber-Agus, N. and DePinho, R. A. (1997) Role for N-CoR and histone deacetylase in Sin3-mediated transcriptional repression. Nature (London) 387, 49-55
-
(1997)
Nature (London)
, vol.387
, pp. 49-55
-
-
Alland, L.1
Muhle, R.2
Hou Jr., H.3
Potes, J.4
Chin, L.5
Schreiber-Agus, N.6
DePinho, R.A.7
-
22
-
-
17744413444
-
A complex containing N-CoR, mSin3 and histone deacetylase mediates transcriptional repression
-
Heinzel, T., Lavinsky, R. M., Mullen, T. M., Soderstrom, M., Laherty, C. D., Torchia, J., Yang, W. M., Brard, G., Ngo, S. D., Davie, J. R. et al. (1997) A complex containing N-CoR, mSin3 and histone deacetylase mediates transcriptional repression. Nature (London) 387, 43-48
-
(1997)
Nature (London)
, vol.387
, pp. 43-48
-
-
Heinzel, T.1
Lavinsky, R.M.2
Mullen, T.M.3
Soderstrom, M.4
Laherty, C.D.5
Torchia, J.6
Yang, W.M.7
Brard, G.8
Ngo, S.D.9
Davie, J.R.10
-
23
-
-
0030953186
-
Nuclear receptor repression mediated by a complex containing SMRT, mSin3A, and histone deacetylase
-
Cambridge, Mass.
-
Nagy, L., Kao, H. Y., Chakravarti, D., Lin, R. J., Hassig, C. A., Ayer, D. E., Schreiber, S. L. and Evans, R. M. (1997) Nuclear receptor repression mediated by a complex containing SMRT, mSin3A, and histone deacetylase. Cell (Cambridge, Mass.) 89, 373-380
-
(1997)
Cell
, vol.89
, pp. 373-380
-
-
Nagy, L.1
Kao, H.Y.2
Chakravarti, D.3
Lin, R.J.4
Hassig, C.A.5
Ayer, D.E.6
Schreiber, S.L.7
Evans, R.M.8
-
24
-
-
0033957792
-
Nuclear receptor co-repressors partner with class II histone deacetylases in a Sin3-independent repression pathway
-
Huang, E. Y., Zhang, J., Miska, E. A., Guenther, M. G., Kouzarides, T. and Lazar, M. A. (2000) Nuclear receptor co-repressors partner with class II histone deacetylases in a Sin3-independent repression pathway. Genes Dev. 14, 45-54
-
(2000)
Genes Dev.
, vol.14
, pp. 45-54
-
-
Huang, E.Y.1
Zhang, J.2
Miska, E.A.3
Guenther, M.G.4
Kouzarides, T.5
Lazar, M.A.6
-
25
-
-
0036208492
-
Formation of the androgen receptor transcription complex
-
Shang, Y., Myers, M. and Brown, M. (2002) Formation of the androgen receptor transcription complex. Mol. Cell 9, 601-610
-
(2002)
Mol. Cell
, vol.9
, pp. 601-610
-
-
Shang, Y.1
Myers, M.2
Brown, M.3
-
26
-
-
0036218774
-
The amino terminus of the human AR is target for corepressor action and antihormone agonism
-
Dotzlaw, H., Moehren, U., Mink, S., Cato, A. C. B., Iniguez, L. and Baniahmad, A. (2002) The amino terminus of the human AR is target for corepressor action and antihormone agonism. Mol. Endocrinol. 16, 661-673
-
(2002)
Mol. Endocrinol.
, vol.16
, pp. 661-673
-
-
Dotzlaw, H.1
Moehren, U.2
Mink, S.3
Cato, A.C.B.4
Iniguez, L.5
Baniahmad, A.6
-
27
-
-
85047683640
-
Inhibition of the dihydrotestosterone-activated androgen receptor by nuclear receptor corepressor
-
Cheng, S., Brzostek, S., Lee, S. R., Hollenberg, A. N. and Balk, S. P. (2002) Inhibition of the dihydrotestosterone-activated androgen receptor by nuclear receptor corepressor. Mol. Endocrinol. 16, 1492-1501
-
(2002)
Mol. Endocrinol.
, vol.16
, pp. 1492-1501
-
-
Cheng, S.1
Brzostek, S.2
Lee, S.R.3
Hollenberg, A.N.4
Balk, S.P.5
-
28
-
-
0038475953
-
Regulation of androgen receptor activity by the nuclear receptor corepressor SMRT
-
Liao, G., Chen, L. Y., Zhang, A., Godavarthy, A., Xia, F., Ghosh, J. C., Li, H. and Chen, J. D. (2003) Regulation of androgen receptor activity by the nuclear receptor corepressor SMRT. J. Biol. Chem. 278, 5052-5061
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 5052-5061
-
-
Liao, G.1
Chen, L.Y.2
Zhang, A.3
Godavarthy, A.4
Xia, F.5
Ghosh, J.C.6
Li, H.7
Chen, J.D.8
-
29
-
-
0029132202
-
Ligand-independent repression by the thyroid hormone receptor mediated by a nuclear receptor co-repressor
-
Horlein, A. J., Naar, A. M., Heinzel, T., Torchia, J., Gloss, B., Kurokawa, R., Ryan, A., Kamei, Y., Soderstrom, M. and Glass, C. K. (1995) Ligand-independent repression by the thyroid hormone receptor mediated by a nuclear receptor co-repressor. Nature (London) 377, 397-404
-
(1995)
Nature (London)
, vol.377
, pp. 397-404
-
-
Horlein, A.J.1
Naar, A.M.2
Heinzel, T.3
Torchia, J.4
Gloss, B.5
Kurokawa, R.6
Ryan, A.7
Kamei, Y.8
Soderstrom, M.9
Glass, C.K.10
-
30
-
-
0024848136
-
The human androgen receptor: Domain structure, genomic organization and regulation of expression
-
Brinkmann, A. O., Faber, P. W., van Rooij, H. C., Kuiper, G. G., Ris, C., Klaassen, P., van der Korput, J. A., Voorhorst, M. M., van Laar, J. H. and Mulder, E. (1989) The human androgen receptor: domain structure, genomic organization and regulation of expression. J. Steroid Biochem. 34, 307-310
-
(1989)
J. Steroid Biochem.
, vol.34
, pp. 307-310
-
-
Brinkmann, A.O.1
Faber, P.W.2
Van Rooij, H.C.3
Kuiper, G.G.4
Ris, C.5
Klaassen, P.6
Van Der Korput, J.A.7
Voorhorst, M.M.8
Van Laar, J.H.9
Mulder, E.10
-
31
-
-
0032230283
-
Functional interactions of the AF-2 activation domain core region of the human androgen receptor with the amino-terminal domain and with the transcriptional coactivator TIF2 (transcriptional intermediary factor 2)
-
Berrevoets, C. A., Doesburg, P., Steketee, K., Trapman, J. and Brinkmann, A. O. (1998) Functional interactions of the AF-2 activation domain core region of the human androgen receptor with the amino-terminal domain and with the transcriptional coactivator TIF2 (transcriptional intermediary factor 2). Mol. Endocrinol. 12, 1172-1183
-
(1998)
Mol. Endocrinol.
, vol.12
, pp. 1172-1183
-
-
Berrevoets, C.A.1
Doesburg, P.2
Steketee, K.3
Trapman, J.4
Brinkmann, A.O.5
-
32
-
-
0027474938
-
Localization and hormonal stimulation of phosphorylation sites in the LNCaP-cell androgen receptor
-
Kuiper, G. G., de Ruiter, P. E., Trapman, J., Boersma, W. J., Grootegoed, J. A. and Brinkmann, A. O. (1993) Localization and hormonal stimulation of phosphorylation sites in the LNCaP-cell androgen receptor. Biochem. J. 291, 95-101
-
(1993)
Biochem. J.
, vol.291
, pp. 95-101
-
-
Kuiper, G.G.1
De Ruiter, P.E.2
Trapman, J.3
Boersma, W.J.4
Grootegoed, J.A.5
Brinkmann, A.O.6
-
33
-
-
0025965086
-
Epitope prediction and confirmation for the human androgen receptor: Generation of monoclonal antibodies for multi-assay performance following the synthetic peptide strategy
-
Zegers, N. D., Claassen, E., Neelen, C., Mulder, E., van Laar, J. H., Voorhorst, M. M., Berrevoets, C. A., Brinkmann, A. O., van der Kwast, T. H. and Ruizeveld de Winter, J. A. (1991) Epitope prediction and confirmation for the human androgen receptor: generation of monoclonal antibodies for multi-assay performance following the synthetic peptide strategy. Biochim. Biophys. Acta 1073, 23-32
-
(1991)
Biochim. Biophys. Acta
, vol.1073
, pp. 23-32
-
-
Zegers, N.D.1
Claassen, E.2
Neelen, C.3
Mulder, E.4
Van Laar, J.H.5
Voorhorst, M.M.6
Berrevoets, C.A.7
Brinkmann, A.O.8
Van Der Kwast, T.H.9
Ruizeveld De Winter, J.A.10
-
34
-
-
0033572656
-
Molecular determinants of nuclear receptor-corepressor interaction
-
Perissi, V., Staszewski, L. M., McInerney, E. M., Kurokawa, R., Krones, A., Rose, D. W., Lambert, M. H., Milburn, M. V., Glass, C. K. and Rosenfeld, M. G. (1999) Molecular determinants of nuclear receptor-corepressor interaction. Genes Dev. 13, 3198-3208
-
(1999)
Genes Dev.
, vol.13
, pp. 3198-3208
-
-
Perissi, V.1
Staszewski, L.M.2
McInerney, E.M.3
Kurokawa, R.4
Krones, A.5
Rose, D.W.6
Lambert, M.H.7
Milburn, M.V.8
Glass, C.K.9
Rosenfeld, M.G.10
-
35
-
-
17544398986
-
Mechanism of corepressor binding and release from nuclear hormone receptors
-
Nagy, L., Kao, H. Y., Love, J. D., Li, C., Banayo, E., Gooch, J. T., Krishna, V., Chatterjee, K., Evans, R. M. and Schwabe, J. W. (1999) Mechanism of corepressor binding and release from nuclear hormone receptors. Genes Dev. 13, 3209-3216
-
(1999)
Genes Dev.
, vol.13
, pp. 3209-3216
-
-
Nagy, L.1
Kao, H.Y.2
Love, J.D.3
Li, C.4
Banayo, E.5
Gooch, J.T.6
Krishna, V.7
Chatterjee, K.8
Evans, R.M.9
Schwabe, J.W.10
-
36
-
-
0037197970
-
Interactions that determine the assembly of a retinoid X receptor/corepressor complex
-
Ghosh, J. C., Yang, X., Zhang, A., Lambert, M. H., Li, H., Xu, H. E. and Chen, J. D. (2002) Interactions that determine the assembly of a retinoid X receptor/corepressor complex. Proc. Natl. Acad. Sci. U.S.A. 99, 5842-5847
-
(2002)
Proc. Natl. Acad. Sci. U.S.A.
, vol.99
, pp. 5842-5847
-
-
Ghosh, J.C.1
Yang, X.2
Zhang, A.3
Lambert, M.H.4
Li, H.5
Xu, H.E.6
Chen, J.D.7
-
37
-
-
0026636999
-
The molecular biology of RU486. Is there a role for antiprogestins in the treatment of breast cancer?
-
Horwitz, K. B. (1992) The molecular biology of RU486. Is there a role for antiprogestins in the treatment of breast cancer? Endocrinol. Rev. 13, 146-163
-
(1992)
Endocrinol. Rev.
, vol.13
, pp. 146-163
-
-
Horwitz, K.B.1
-
38
-
-
0031051692
-
RU486 (milepristone): Mechanisms of action and clinical uses
-
Cadepond, F., Ulmann, A. and Baulieu, E. E. (1997) RU486 (milepristone): mechanisms of action and clinical uses. Annu. Rev. Med. 48, 129-156
-
(1997)
Annu. Rev. Med.
, vol.48
, pp. 129-156
-
-
Cadepond, F.1
Ulmann, A.2
Baulieu, E.E.3
-
39
-
-
0037062484
-
Coactivator/corepressor ratios modulate PR-mediated transcription by the selective receptor modulator RU486
-
Liu, Z., Auboeuf, D., Wong, J., Chen, J. D., Tsai, S. Y., Tsai, M. J. and O'Malley, B. W. (2002) Coactivator/corepressor ratios modulate PR-mediated transcription by the selective receptor modulator RU486. Proc. Natl. Acad. Sci. U.S.A. 99, 7940-7944
-
(2002)
Proc. Natl. Acad. Sci. U.S.A.
, vol.99
, pp. 7940-7944
-
-
Liu, Z.1
Auboeuf, D.2
Wong, J.3
Chen, J.D.4
Tsai, S.Y.5
Tsai, M.J.6
O'Malley, B.W.7
-
40
-
-
0034664769
-
Combinatorial roles of the nuclear receptor corepressor in transcription and development
-
Cambridge, Mass.
-
Jepsen, K., Hermanson, O., Onami, T M., Gleiberman, A. S., Lunyak, V., McEvilly, R. J., Kurokawa, R., Kumar, V., Liu, F., Seto, E. et al. (2000) Combinatorial roles of the nuclear receptor corepressor in transcription and development. Cell (Cambridge, Mass.) 102, 753-763
-
(2000)
Cell
, vol.102
, pp. 753-763
-
-
Jepsen, K.1
Hermanson, O.2
Onami, T.M.3
Gleiberman, A.S.4
Lunyak, V.5
McEvilly, R.J.6
Kurokawa, R.7
Kumar, V.8
Liu, F.9
Seto, E.10
-
41
-
-
0035361340
-
A mechanism for androgen receptor-mediated prostate cancer recurrence after androgen deprivation therapy
-
Gregory, C. W., He, B., Johnson, R. T., Ford, O. H., Mohler, J. L., French, F. S. and Wilson, E. M. (2001) A mechanism for androgen receptor-mediated prostate cancer recurrence after androgen deprivation therapy. Cancer Res. 61, 4315-4319
-
(2001)
Cancer Res.
, vol.61
, pp. 4315-4319
-
-
Gregory, C.W.1
He, B.2
Johnson, R.T.3
Ford, O.H.4
Mohler, J.L.5
French, F.S.6
Wilson, E.M.7
-
42
-
-
0035942197
-
Crystallographic structures of the ligand-binding domains of the androgen receptor and its T877A mutant complexed with the natural agonist dihydrotestosterone
-
Sack, J. S., Kish, K. F., Wang, C., Attar, R. M., Kiefer, S. E., An, Y., Wu, G. Y., Scheffler, J. E., Salvati, M. E., Krystek, S. R., Jr et al. (2001) Crystallographic structures of the ligand-binding domains of the androgen receptor and its T877A mutant complexed with the natural agonist dihydrotestosterone. Proc. Natl. Acad. Sci. U.S.A. 98, 4904-4909
-
(2001)
Proc. Natl. Acad. Sci. U.S.A.
, vol.98
, pp. 4904-4909
-
-
Sack, J.S.1
Kish, K.F.2
Wang, C.3
Attar, R.M.4
Kiefer, S.E.5
An, Y.6
Wu, G.Y.7
Scheffler, J.E.8
Salvati, M.E.9
Krystek Jr., S.R.10
-
43
-
-
0037135630
-
Bicalutamide functions as an androgen receptor antagonist by assembly of a transcriptionally inactive receptor
-
Massiello, D., Cheng, S., Bubley, G. J., Lu, M. L. and Balk, S. P. (2002) Bicalutamide functions as an androgen receptor antagonist by assembly of a transcriptionally inactive receptor. J. Biol. Chem. 277, 26321-26326
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 26321-26326
-
-
Massiello, D.1
Cheng, S.2
Bubley, G.J.3
Lu, M.L.4
Balk, S.P.5
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