-
1
-
-
0026319635
-
Endocrine therapy for prostate cancer
-
Labrie F., Endocrine therapy for prostate cancer. Endocrinol. Metab. Clin. North Am. 20 (1991) 845-872.
-
(1991)
Endocrinol. Metab. Clin. North Am.
, vol.20
, pp. 845-872
-
-
Labrie, F.1
-
2
-
-
0025346719
-
The role of endocrine therapy in primary breast cancer
-
Baum M., The role of endocrine therapy in primary breast cancer. J. Steroid. Biochem. 36 (1990) 187-189.
-
(1990)
J. Steroid. Biochem.
, vol.36
, pp. 187-189
-
-
Baum, M.1
-
3
-
-
0013283803
-
The estrogen receptor as a target for rational drug design
-
R. G. Landes Company, Austin, TX, 237 pp.
-
Von Angerer, E., The estrogen receptor as a target for rational drug design. In Molecular Biology Intelligence Unit. R. G. Landes Company, Austin, TX, 1995, 237 pp.
-
(1995)
Molecular Biology Intelligence Unit
-
-
Von Angerer, E.1
-
5
-
-
0027401411
-
The future of new pure antiestrogens in clinical breast cancer
-
Wakeling A. E., The future of new pure antiestrogens in clinical breast cancer. Breast Cancer Res. Treat. 25 (1993) 1-9.
-
(1993)
Breast Cancer Res. Treat.
, vol.25
, pp. 1-9
-
-
Wakeling, A.E.1
-
6
-
-
0028861402
-
Response to a specific antiestrogen (ICI 182780) in tamoxifen-resistant breast cancer
-
Howell A., DeFriend D., Robertson J., Blamey R. and Walton P., Response to a specific antiestrogen (ICI 182780) in tamoxifen-resistant breast cancer. Lancet 345 (1995) 29-30.
-
(1995)
Lancet
, vol.345
, pp. 29-30
-
-
Howell, A.1
DeFriend, D.2
Robertson, J.3
Blamey, R.4
Walton, P.5
-
7
-
-
0028267672
-
RU 58668, a new pure antiestrogen inducing a regression of human mammary carcinoma implanted in nude mice
-
De Velde P. V., Nique F., Bouchoux F., Brémaud J., Hameau M.-C., Lucas D., Moratile C., Viet S., Philibert D. and Teutsch G., RU 58668, a new pure antiestrogen inducing a regression of human mammary carcinoma implanted in nude mice. J. Steroid Biochem. Molec. Biol. 48 (1994) 187-196.
-
(1994)
J. Steroid Biochem. Molec. Biol.
, vol.48
, pp. 187-196
-
-
De Velde, P.V.1
Nique, F.2
Bouchoux, F.3
Brémaud, J.4
Hameau, M.-C.5
Lucas, D.6
Moratile, C.7
Viet, S.8
Philibert, D.9
Teutsch, G.10
-
9
-
-
0028223692
-
Structure, regulation and role of 3β-hydroxysteroid dehydrogenase, 17β-hydroxysteroid dehydrogenase and aromatase enzymes in the formation of sex steroids in classical and peripheral intracrine tissues
-
Labrie F., Simard J., Luu-The V., Pelletier G., Belghmi K. and Bélanger A., Structure, regulation and role of 3β-hydroxysteroid dehydrogenase, 17β-hydroxysteroid dehydrogenase and aromatase enzymes in the formation of sex steroids in classical and peripheral intracrine tissues. Baillière's Clin. Endocrinol. Metab. 8 (1994) 451-474.
-
(1994)
Baillière's Clin. Endocrinol. Metab.
, vol.8
, pp. 451-474
-
-
Labrie, F.1
Simard, J.2
Luu-The, V.3
Pelletier, G.4
Belghmi, K.5
Bélanger, A.6
-
10
-
-
0018088560
-
Synthesis and biochemical evaluation of inhibitors of estrogen biosynthesis
-
Brueggemeier R. W., Floyd E. E. and Counsell R. E., Synthesis and biochemical evaluation of inhibitors of estrogen biosynthesis. J. Med. Chem. 21 (1978) 1007-1011.
-
(1978)
J. Med. Chem.
, vol.21
, pp. 1007-1011
-
-
Brueggemeier, R.W.1
Floyd, E.E.2
Counsell, R.E.3
-
11
-
-
0026446844
-
Phase I and endocrine study of exemestrane (FCE 24304), a new aromatase inhibitor, in postmenopausal women
-
Evans T. R. J., Salle E. D., Ornati G., Lassus M., Benedetti M. S., Pianezolla E. and Coombies R. C., Phase I and endocrine study of exemestrane (FCE 24304), a new aromatase inhibitor, in postmenopausal women. Cancer Res. 52 (1992) 5933-5939.
-
(1992)
Cancer Res.
, vol.52
, pp. 5933-5939
-
-
Evans, T.R.J.1
Salle, E.D.2
Ornati, G.3
Lassus, M.4
Benedetti, M.S.5
Pianezolla, E.6
Coombies, R.C.7
-
12
-
-
0027228206
-
Phase I study of the oral nonsteroidal aromatase inhibitor CGS 20267 in healthy postmenopausal women
-
Iveson T. J., Smith I. E., Ahern J., Smithers D. A., Trunet P. F. and Dowsett M., Phase I study of the oral nonsteroidal aromatase inhibitor CGS 20267 in healthy postmenopausal women. J. Clin. Endocrinol. Metab. 77 (1993) 324-331.
-
(1993)
J. Clin. Endocrinol. Metab.
, vol.77
, pp. 324-331
-
-
Iveson, T.J.1
Smith, I.E.2
Ahern, J.3
Smithers, D.A.4
Trunet, P.F.5
Dowsett, M.6
-
13
-
-
0027997441
-
Aromatase inhibitors in the treatment of breast cancer
-
Brodie A. M. H., Aromatase inhibitors in the treatment of breast cancer. J. Steroid. Biochem. Molec. Biol. 48 (1994) 281-287.
-
(1994)
J. Steroid. Biochem. Molec. Biol.
, vol.48
, pp. 281-287
-
-
Brodie, A.M.H.1
-
14
-
-
0028003740
-
Aromatase inhibitors-mechanisms of steroidal inhibitors
-
Brueggemeier R. W., Aromatase inhibitors-mechanisms of steroidal inhibitors. Breast Cancer Res. Treat. 30 (1994) 31-42.
-
(1994)
Breast Cancer Res. Treat.
, vol.30
, pp. 31-42
-
-
Brueggemeier, R.W.1
-
15
-
-
0028077626
-
Clinical and endocrine effects of the oral aromatase inhibitor vorozole in postmenopausal patients with advanced breast cancer
-
Johnston S. R., Smith I. E., Doody D., Jacobs S., Robertshaw H. and Dowsett M., Clinical and endocrine effects of the oral aromatase inhibitor vorozole in postmenopausal patients with advanced breast cancer. Cancer Res. 54 (1994) 5875-5881.
-
(1994)
Cancer Res.
, vol.54
, pp. 5875-5881
-
-
Johnston, S.R.1
Smith, I.E.2
Doody, D.3
Jacobs, S.4
Robertshaw, H.5
Dowsett, M.6
-
16
-
-
0028003744
-
Second generation aromatase inhibitor-4-hydroxyandrostenedione
-
Dowsett M. and Coombes R. C., Second generation aromatase inhibitor-4-hydroxyandrostenedione. Breast Cancer Res. Treat. 30 (1994) 81-87.
-
(1994)
Breast Cancer Res. Treat.
, vol.30
, pp. 81-87
-
-
Dowsett, M.1
Coombes, R.C.2
-
17
-
-
0028125210
-
Formestane: Effective therapy in postmenopausal women with advanced breast cancer
-
Bajetta E., Zilembo N., Buzzoni R., Noberasco C., Martinetti A., Ferrari L., Bartoli C., Sacchini V., Attili A. and Lepera P., Formestane: effective therapy in postmenopausal women with advanced breast cancer. Ann. Oncol. 5 (Suppl. 7) (1994) S15-S17.
-
(1994)
Ann. Oncol.
, vol.5
, Issue.7 SUPPL.
-
-
Bajetta, E.1
Zilembo, N.2
Buzzoni, R.3
Noberasco, C.4
Martinetti, A.5
Ferrari, L.6
Bartoli, C.7
Sacchini, V.8
Attili, A.9
Lepera, P.10
-
19
-
-
0028990478
-
ARIMIDEX: A new oral, once-a-day aromatase inhibitor
-
Plourde P. V., Dyroff M., Dowsett M., Demers L., Yates R. and Webster A., ARIMIDEX: a new oral, once-a-day aromatase inhibitor. J. Steroid Biochem. Mol. Biol. 53 (1995) 175-179.
-
(1995)
J. Steroid Biochem. Mol. Biol.
, vol.53
, pp. 175-179
-
-
Plourde, P.V.1
Dyroff, M.2
Dowsett, M.3
Demers, L.4
Yates, R.5
Webster, A.6
-
20
-
-
0030041360
-
Therapeutic effects of the aromatase inhibitor fadrozole hydrochloride in advanced breast cancer
-
Bonnefoi H. R., Smith I. E., Dowsett M., Trunet P. F., Houston S. J., Da Luz R. J., Rubens R. D., Coombes R. C. and Powles T. J., Therapeutic effects of the aromatase inhibitor fadrozole hydrochloride in advanced breast cancer. Br. J. Cancer 73 (1996) 539-542.
-
(1996)
Br. J. Cancer
, vol.73
, pp. 539-542
-
-
Bonnefoi, H.R.1
Smith, I.E.2
Dowsett, M.3
Trunet, P.F.4
Houston, S.J.5
Da Luz, R.J.6
Rubens, R.D.7
Coombes, R.C.8
Powles, T.J.9
-
21
-
-
0029783837
-
Aromatase inhibitors in clinical practice: Current status and a look to the future
-
Harvey H. A., Aromatase inhibitors in clinical practice: current status and a look to the future. Semin. Oncol. 23 (1996) 33-38.
-
(1996)
Semin. Oncol.
, vol.23
, pp. 33-38
-
-
Harvey, H.A.1
-
22
-
-
0026587358
-
Distribution of 17β-hydroxysteroid dehydrogenase gene expression and activity in rat and human tissues
-
Martel C., Rhéaume E., Takahashi M., Trudel C., Couët J., Luu-The V., Simard J. and Labrie F., Distribution of 17β-hydroxysteroid dehydrogenase gene expression and activity in rat and human tissues. J. Steroid Biochem. Molec. Biol. 41 (1992) 597-603.
-
(1992)
J. Steroid Biochem. Molec. Biol.
, vol.41
, pp. 597-603
-
-
Martel, C.1
Rhéaume, E.2
Takahashi, M.3
Trudel, C.4
Couët, J.5
Luu-The, V.6
Simard, J.7
Labrie, F.8
-
23
-
-
0021149871
-
In situ estrogen production via the estrone sulfatase pathway in breast tumors: Relative importance versus the aromatase pathway
-
Santner S. J., Feil P. D. and Santen R. J., In situ estrogen production via the estrone sulfatase pathway in breast tumors: relative importance versus the aromatase pathway. J. Clin. Endocrinol. Metab. 59 (1984) 29-33.
-
(1984)
J. Clin. Endocrinol. Metab.
, vol.59
, pp. 29-33
-
-
Santner, S.J.1
Feil, P.D.2
Santen, R.J.3
-
24
-
-
0029621925
-
Role of 17β-hydroxysteroid dehydrogenase type I in endocrine and intracrine estradiol biosynthesis
-
Poutanen M., Isomaa V., Peltoketo H. and Vihko R., Role of 17β-hydroxysteroid dehydrogenase type I in endocrine and intracrine estradiol biosynthesis. J. Steroid. Biochem. Molec. Biol. 55 (1995) 525-532.
-
(1995)
J. Steroid. Biochem. Molec. Biol.
, vol.55
, pp. 525-532
-
-
Poutanen, M.1
Isomaa, V.2
Peltoketo, H.3
Vihko, R.4
-
25
-
-
0031023049
-
The key role of 17β-hydroxysteroid dehydrogenase in sex steroid biology
-
Labrie F., Luu-The V., Lin S.-X., Labrie C., Simard J., Breton R. and Bélanger A., The key role of 17β-hydroxysteroid dehydrogenase in sex steroid biology. Steroids 62 (1997) 148-158.
-
(1997)
Steroids
, vol.62
, pp. 148-158
-
-
Labrie, F.1
Luu-The, V.2
Lin, S.-X.3
Labrie, C.4
Simard, J.5
Breton, R.6
Bélanger, A.7
-
26
-
-
0024361957
-
Characterization of cDNAs for human estradiol 17β-hydroxysteroid dehydrogenase and assignment of the gene to chromosome 17: Evidence of two mRNA species with distinct 5′-termini in human placenta
-
Luu-The V., Labrie C., Zhao H.-R., Couët J., Lachance Y., Simard J., Leblanc G., Côté J., Bérubé D., Gagné R. and Labrie F., Characterization of cDNAs for human estradiol 17β-hydroxysteroid dehydrogenase and assignment of the gene to chromosome 17: evidence of two mRNA species with distinct 5′-termini in human placenta. Mol. Endocrinol. 3 (1989) 1301-1309.
-
(1989)
Mol. Endocrinol.
, vol.3
, pp. 1301-1309
-
-
Luu-The, V.1
Labrie, C.2
Zhao, H.-R.3
Couët, J.4
Lachance, Y.5
Simard, J.6
Leblanc, G.7
Côté, J.8
Bérubé, D.9
Gagné, R.10
Labrie, F.11
-
27
-
-
0027225486
-
Expression cloning and characterization of human 17β-hydroxysteroid dehydrogenase type 2, a microsomal enzyme possessing 20α-hydroxysteroid dehydrogenase activity
-
Wu L., Einstein M., Geissler W. M., Chan H. K., Elliston K. O. and Anderson S., Expression cloning and characterization of human 17β-hydroxysteroid dehydrogenase type 2, a microsomal enzyme possessing 20α-hydroxysteroid dehydrogenase activity. J. Biol. Chem. 268 (1993) 12964-12969.
-
(1993)
J. Biol. Chem.
, vol.268
, pp. 12964-12969
-
-
Wu, L.1
Einstein, M.2
Geissler, W.M.3
Chan, H.K.4
Elliston, K.O.5
Anderson, S.6
-
28
-
-
0027930787
-
Male pseudohermaphroditism caused by mutations of testicular 17β-hydroxysteroid dehydrogenase 3
-
Geissler W. M., Davis D. L., Wu L., Bradshaw K. D., Sushma P., Mendonca B. B., Elliston K. O., Wilson J. D., Russel D. W. and Andersson S., Male pseudohermaphroditism caused by mutations of testicular 17β-hydroxysteroid dehydrogenase 3. Nature Genet. 7 (1994) 34-39.
-
(1994)
Nature Genet.
, vol.7
, pp. 34-39
-
-
Geissler, W.M.1
Davis, D.L.2
Wu, L.3
Bradshaw, K.D.4
Sushma, P.5
Mendonca, B.B.6
Elliston, K.O.7
Wilson, J.D.8
Russel, D.W.9
Andersson, S.10
-
29
-
-
0028847134
-
Molecular cloning of a novel widely expressed human 80 kDa 17β-hydroxysteroid dehydrogenase IV
-
Adamski J., Normand T., Leenders F., Monté D., Begue A., Stéhelin D., JungbIut P. W. and De Launoit Y., Molecular cloning of a novel widely expressed human 80 kDa 17β-hydroxysteroid dehydrogenase IV. Biochem. J. 311 (1995) 437-443.
-
(1995)
Biochem. J.
, vol.311
, pp. 437-443
-
-
Adamski, J.1
Normand, T.2
Leenders, F.3
Monté, D.4
Begue, A.5
Stéhelin, D.6
Jungbiut, P.W.7
De Launoit, Y.8
-
30
-
-
0013487279
-
Cloning and expression of human type V 17β-hydroxysteroid dehydrogenase
-
[abstract P3-614], Washington, DC, Bethesda, MD, The Endrocrine Society
-
Zhang, Y., Dufort, I., Soucy, P., Labrie, F. and Luu-The, V., Cloning and expression of human type V 17β-hydroxysteroid dehydrogenase [abstract P3-614]. Proceedings of the 77th Annual Meeting of the Endocrine Society, Washington, DC, Bethesda, MD, The Endrocrine Society, p. 622.
-
Proceedings of the 77th Annual Meeting of the Endocrine Society
, pp. 622
-
-
Zhang, Y.1
Dufort, I.2
Soucy, P.3
Labrie, F.4
Luu-The, V.5
-
31
-
-
0029620941
-
Kinetic analysis of enzymic activities: Prediction of multiple forms of 17β-hydroxysteroid dehydrogenase
-
Blomquist C. H., Kinetic analysis of enzymic activities: prediction of multiple forms of 17β-hydroxysteroid dehydrogenase. J. Steroid Biochem. Molec. Biol. 55 (1995) 515-524.
-
(1995)
J. Steroid Biochem. Molec. Biol.
, vol.55
, pp. 515-524
-
-
Blomquist, C.H.1
-
32
-
-
0021884506
-
17β-hydroxysteroid and 20α-hydroxysteroid dehydrogenase activities of human placental microsomes: Kinetics evidence for two enzymes differing in substrate specificity
-
Blomquist C. H., Lindemann N. J. and Hakanson E. Y., 17β-hydroxysteroid and 20α-hydroxysteroid dehydrogenase activities of human placental microsomes: kinetics evidence for two enzymes differing in substrate specificity. Arch. Biochem. Biophys. 239 (1985) 206-215.
-
(1985)
Arch. Biochem. Biophys.
, vol.239
, pp. 206-215
-
-
Blomquist, C.H.1
Lindemann, N.J.2
Hakanson, E.Y.3
-
33
-
-
0029998812
-
17β-Hydroxysteroid dehydrogenase: Inhibitors and inhibitor design
-
Penning T. M., 17β-Hydroxysteroid dehydrogenase: inhibitors and inhibitor design. Endocrine-related cancer 3 (1996) 41-56.
-
(1996)
Endocrine-related Cancer
, vol.3
, pp. 41-56
-
-
Penning, T.M.1
-
34
-
-
0016593954
-
Synthesis of 16α-bromoacetoxyestradiol 3-methyl ether and study of the binding site of human placental estradiol 17β-dehydrogenase
-
Chin C. C. and Warren J. C., Synthesis of 16α-bromoacetoxyestradiol 3-methyl ether and study of the binding site of human placental estradiol 17β-dehydrogenase. J. Biol. Chem. 250 (1975) 7682-7686.
-
(1975)
J. Biol. Chem.
, vol.250
, pp. 7682-7686
-
-
Chin, C.C.1
Warren, J.C.2
-
35
-
-
0017819395
-
Synthesis of 4-bromoacetamidoestrone methyl ether and study of steroid binding site of human placental estradiol 17β-dehydrogenase
-
Bhatnagar Y. M., Chin C. C. and Warren J. C., Synthesis of 4-bromoacetamidoestrone methyl ether and study of steroid binding site of human placental estradiol 17β-dehydrogenase. J. Biol. Chem. 253 (1978) 811-815.
-
(1978)
J. Biol. Chem.
, vol.253
, pp. 811-815
-
-
Bhatnagar, Y.M.1
Chin, C.C.2
Warren, J.C.3
-
36
-
-
0019195581
-
Photoaffinity labeling of human placental estradiol dehydrogenase with 3-(arylazido-β-alanine)
-
Inano H. and Engel L. L., Photoaffinity labeling of human placental estradiol dehydrogenase with 3-(arylazido-β-alanine). J. Biol Chem. 255 (1980) 7694-7699.
-
(1980)
J. Biol Chem.
, vol.255
, pp. 7694-7699
-
-
Inano, H.1
Engel, L.L.2
-
37
-
-
0019313854
-
Synthesis of 2-bromoacetamidoestrone methyl ether and study of steroid-binding site of human placental estradiol 17β-dehydrogenase
-
Chin C. C., Asmar P. and Warren J. C., Synthesis of 2-bromoacetamidoestrone methyl ether and study of steroid-binding site of human placental estradiol 17β-dehydrogenase. J. Biol. Chem. 255 (1980) 3660-3664.
-
(1980)
J. Biol. Chem.
, vol.255
, pp. 3660-3664
-
-
Chin, C.C.1
Asmar, P.2
Warren, J.C.3
-
38
-
-
0019876493
-
Human placental 17β-estradiol dehydrogenase and 20α-hydroxysteroid dehydrogenase
-
Strickler R. C., Tobas B. and Covey D. R., Human placental 17β-estradiol dehydrogenase and 20α-hydroxysteroid dehydrogenase. J. Biol. Chem. 256 (1981) 316-321.
-
(1981)
J. Biol. Chem.
, vol.256
, pp. 316-321
-
-
Strickler, R.C.1
Tobas, B.2
Covey, D.R.3
-
39
-
-
0022901572
-
The affinity alkylators 11α-bromoacetoxyprogesterone and estrone 3-bromoacetate, modify a common histidyl residue in the active site of human placental 17β,20α-hydroxysteroid dehydrogenase
-
Thomas J. L., Asibey-Berko E. and Strickler R. C., The affinity alkylators 11α-bromoacetoxyprogesterone and estrone 3-bromoacetate, modify a common histidyl residue in the active site of human placental 17β,20α-hydroxysteroid dehydrogenase. J. Steroid Biochem. 25 (1986) 203-208.
-
(1986)
J. Steroid Biochem.
, vol.25
, pp. 203-208
-
-
Thomas, J.L.1
Asibey-Berko, E.2
Strickler, R.C.3
-
40
-
-
0023914945
-
Human placental estradiol 17β-dehydrogenase: Evidence for inverted substrate orientation (wrong-way binding) at the active site
-
Murdock G. L., Warren J. C. and Sweet F., Human placental estradiol 17β-dehydrogenase: Evidence for inverted substrate orientation (wrong-way binding) at the active site. Biochemistry 27 (1988) 4452-4458.
-
(1988)
Biochemistry
, vol.27
, pp. 4452-4458
-
-
Murdock, G.L.1
Warren, J.C.2
Sweet, F.3
-
41
-
-
0020514222
-
Inactivation of human placental 17β,20α-hydroxysteroid dehydrogenase by 16-methylene estrone, as affinity alkylator enzymatically generated from 16-methylene estradiol
-
Thomas J. L., LaRochelle M. C., Covey D. F. and Strickler R. C., Inactivation of human placental 17β,20α-hydroxysteroid dehydrogenase by 16-methylene estrone, as affinity alkylator enzymatically generated from 16-methylene estradiol. J. Biol. Chem. 258 (1983) 11500-11504.
-
(1983)
J. Biol. Chem.
, vol.258
, pp. 11500-11504
-
-
Thomas, J.L.1
LaRochelle, M.C.2
Covey, D.F.3
Strickler, R.C.4
-
42
-
-
0022845066
-
Mechanism-based inactivation of 17β,20α-hydroxysteroid dehydrogenase by an acetylenic secoestradiol
-
Auchus R. J. and Covey D. F., Mechanism-based inactivation of 17β,20α-hydroxysteroid dehydrogenase by an acetylenic secoestradiol. Biochemistry 25 (1986) 7295-7300.
-
(1986)
Biochemistry
, vol.25
, pp. 7295-7300
-
-
Auchus, R.J.1
Covey, D.F.2
-
43
-
-
0020675055
-
Affinity labelling of arginyl residues at the catalytic region of estradiol 17β-hydroxysteroid dehydrogenase from human placenta by 16-oxo-estrone
-
Inano H. and Tamaoki B., Affinity labelling of arginyl residues at the catalytic region of estradiol 17β-hydroxysteroid dehydrogenase from human placenta by 16-oxo-estrone. Eur. J. Biochem. 129 (1983) 691-695.
-
(1983)
Eur. J. Biochem.
, vol.129
, pp. 691-695
-
-
Inano, H.1
Tamaoki, B.2
-
44
-
-
0025833808
-
Hydrogen bonding in steroidogenesis: Studies on new heterocyclic analogs of estrone that inhibit human estradiol 17β-dehydrogenase
-
Sweet F., Boyd J., Medina O., Konderski L. and Murdock G. L., Hydrogen bonding in steroidogenesis: studies on new heterocyclic analogs of estrone that inhibit human estradiol 17β-dehydrogenase. Biochim. Biophys. Commun. 180 (1991) 1057-1063.
-
(1991)
Biochim. Biophys. Commun.
, vol.180
, pp. 1057-1063
-
-
Sweet, F.1
Boyd, J.2
Medina, O.3
Konderski, L.4
Murdock, G.L.5
-
45
-
-
0026571802
-
Novel compounds inhibit estrogen formation and action
-
Labrie C., Martel C., Dufour J.-M., Lévesque G., Mérand Y. and Labrie F., Novel compounds inhibit estrogen formation and action. Cancer Res. 52 (1992) 610-615.
-
(1992)
Cancer Res.
, vol.52
, pp. 610-615
-
-
Labrie, C.1
Martel, C.2
Dufour, J.-M.3
Lévesque, G.4
Mérand, Y.5
Labrie, F.6
-
46
-
-
0029593494
-
Characteristics of human types 1, 2 and 3 17β-hydroxysteroid dehydrogenase activities: Oxidation/reduction and inhibition
-
Luu-The V., Zhang Y., Poirier D. and Labrie F., Characteristics of human types 1, 2 and 3 17β-hydroxysteroid dehydrogenase activities: oxidation/reduction and inhibition. J. Steroid Biochem. Molec. Biol. 55 (1995) 581-587.
-
(1995)
J. Steroid Biochem. Molec. Biol.
, vol.55
, pp. 581-587
-
-
Luu-The, V.1
Zhang, Y.2
Poirier, D.3
Labrie, F.4
-
47
-
-
0344367421
-
C16 and C17 derivatives of estradiol as inhibitors of 17β-hydroxysteroid dehydrogenase type I: Chemical synthesis and structure-activity relationships
-
in press
-
Sam, K.-M., Boivin, R. P., Tremblay, M. R., Auger, S. and Poirier, D., C16 and C17 derivatives of estradiol as inhibitors of 17β-hydroxysteroid dehydrogenase type I: chemical synthesis and structure-activity relationships. Drug Design Discov., 1997 (in press).
-
(1997)
Drug Design Discov.
-
-
Sam, K.-M.1
Boivin, R.P.2
Tremblay, M.R.3
Auger, S.4
Poirier, D.5
-
48
-
-
0023156403
-
A short, stereoselective route to 16α-(substituted-alkyl)-estradiol derivatives
-
Fevig T. L. and Katzenellenbogen J. A., A short, stereoselective route to 16α-(substituted-alkyl)-estradiol derivatives. J. Org. Chem. 52 (1987) 247-251.
-
(1987)
J. Org. Chem.
, vol.52
, pp. 247-251
-
-
Fevig, T.L.1
Katzenellenbogen, J.A.2
-
49
-
-
0028027142
-
16α-propyl derivatives of estradiol as inhibitors of 17β-hydroxysteroid dehydrogenase type I
-
Sam K.-M., Boivin R. P., Auger S. and Poirier D., 16α-propyl derivatives of estradiol as inhibitors of 17β-hydroxysteroid dehydrogenase type I. Bioorg. Med. Chem. Lett. 4 (1994) 2129-2132.
-
(1994)
Bioorg. Med. Chem. Lett.
, vol.4
, pp. 2129-2132
-
-
Sam, K.-M.1
Boivin, R.P.2
Auger, S.3
Poirier, D.4
-
50
-
-
0029038902
-
A convenient synthetic method for alpha-alkylation of steroidal 17-ketone: Preparation of 16β-(THPO-heptyl)-estradiol
-
Tremblay M. R., Auger S. and Poirier D., A convenient synthetic method for alpha-alkylation of steroidal 17-ketone: preparation of 16β-(THPO-heptyl)-estradiol. Synth. Commun. 25 (1995) 2483-2495.
-
(1995)
Synth. Commun.
, vol.25
, pp. 2483-2495
-
-
Tremblay, M.R.1
Auger, S.2
Poirier, D.3
-
51
-
-
0029011261
-
Synthesis of 16-(bromoalkyl)-estradiols having inhibitory effect on human placental estradiol 17β-hydroxysteroid dehydrogenase (17β-HSD type I)
-
Tremblay M. R., Auger S. and Poirier D., Synthesis of 16-(bromoalkyl)-estradiols having inhibitory effect on human placental estradiol 17β-hydroxysteroid dehydrogenase (17β-HSD type I). Bioorg. Med. Chem. 3 (1995) 505-523.
-
(1995)
Bioorg. Med. Chem.
, vol.3
, pp. 505-523
-
-
Tremblay, M.R.1
Auger, S.2
Poirier, D.3
-
52
-
-
0030925164
-
Intracellular regulation of 17β-hydroxysteroid dehydrogenase type 2 catalytic activity in A431 cells
-
Blomquist C. H., Leung B. S., Beaudoin C., Poirier D. and Tremblay Y., Intracellular regulation of 17β-hydroxysteroid dehydrogenase type 2 catalytic activity in A431 cells. J. Endocrinology 153 (1997) 453-464.
-
(1997)
J. Endocrinology
, vol.153
, pp. 453-464
-
-
Blomquist, C.H.1
Leung, B.S.2
Beaudoin, C.3
Poirier, D.4
Tremblay, Y.5
-
53
-
-
0024238549
-
Estrogen receptor binding tolerance of 16α-substituted estradiol derivatives
-
Fevig T. L., Mao M. K. and Katzenellenbogen J. A., Estrogen receptor binding tolerance of 16α-substituted estradiol derivatives. Steroids 51 (1988) 471-497.
-
(1988)
Steroids
, vol.51
, pp. 471-497
-
-
Fevig, T.L.1
Mao, M.K.2
Katzenellenbogen, J.A.3
-
55
-
-
0025785380
-
Synthesis and biological activity of new halo-steroidal antiestrogens
-
Lévesque C., Mérand Y., Dufour J.-M., Labrie C. and Labrie F., Synthesis and biological activity of new halo-steroidal antiestrogens. J. Med. Chem. 34 (1991) 1624-1630.
-
(1991)
J. Med. Chem.
, vol.34
, pp. 1624-1630
-
-
Lévesque, C.1
Mérand, Y.2
Dufour, J.-M.3
Labrie, C.4
Labrie, F.5
-
56
-
-
0027161787
-
Inhibition of estrone sulfatase and 17β-hydroxysteroid dehydrogenase by antiestrogens
-
Santner S. J. and Santen R. J., Inhibition of estrone sulfatase and 17β-hydroxysteroid dehydrogenase by antiestrogens. J. Steroid Biochem. Molec. Biol. 45 (1993) 383-390.
-
(1993)
J. Steroid Biochem. Molec. Biol.
, vol.45
, pp. 383-390
-
-
Santner, S.J.1
Santen, R.J.2
-
57
-
-
0028059981
-
N-butyl, N-methyl 11-[3′,17′β (dihydroxy)-1′,3′,5′(10′)-estratrien-16′α- yl]-9 (R/S)-bromoundecanamide: Synthesis and 17β-HSD inhibiting, estrogenic and antiestrogenic activities
-
Pelletier J. D., Labrie F. and Poirier D., N-butyl, N-methyl 11-[3′,17′β (dihydroxy)-1′,3′,5′(10′)-estratrien-16′α- yl]-9 (R/S)-bromoundecanamide: synthesis and 17β-HSD inhibiting, estrogenic and antiestrogenic activities. Steroids 59 (1994) 536-547.
-
(1994)
Steroids
, vol.59
, pp. 536-547
-
-
Pelletier, J.D.1
Labrie, F.2
Poirier, D.3
-
58
-
-
0030272290
-
Synthesis and evaluation of estradiol derivatives with 16α-(bromoalkylamide), 16α-(bromoalkyl) or 16α-(bromoalkynyl) side chain as inhibitors of 17β-hydroxysteroid dehydrogenase type I without estrogenic activity
-
Pelletier J. D. and Poirier D., Synthesis and evaluation of estradiol derivatives with 16α-(bromoalkylamide), 16α-(bromoalkyl) or 16α-(bromoalkynyl) side chain as inhibitors of 17β-hydroxysteroid dehydrogenase type I without estrogenic activity. Bioorg. Med. Chem. 4 (1996) 1617-1628.
-
(1996)
Bioorg. Med. Chem.
, vol.4
, pp. 1617-1628
-
-
Pelletier, J.D.1
Poirier, D.2
-
59
-
-
0002085765
-
Synthesis of 16-[carbamoyl-(bromomethyl) alkyl]estradiol: A potential dual-action inhibitor designed to blockade estrogen action and biosynthesis
-
Tremblay M. R. and Poirier D., Synthesis of 16-[carbamoyl-(bromomethyl) alkyl]estradiol: a potential dual-action inhibitor designed to blockade estrogen action and biosynthesis. J. Chem. Soc. Perkin Trans. 1 22 (1996) 2765-2771.
-
(1996)
J. Chem. Soc. Perkin Trans. 1
, vol.22
, pp. 2765-2771
-
-
Tremblay, M.R.1
Poirier, D.2
-
60
-
-
0026784736
-
Effects of antiestrogens on the DNA binding activity of estrogen receptors in vitro
-
Arbuckle N. D., Dauvois S. and Parker M. G., Effects of antiestrogens on the DNA binding activity of estrogen receptors in vitro. Nucleic Acids Res. 20 (1992) 3839-3844.
-
(1992)
Nucleic Acids Res.
, vol.20
, pp. 3839-3844
-
-
Arbuckle, N.D.1
Dauvois, S.2
Parker, M.G.3
-
61
-
-
0031596753
-
A 6β-(thiaheptanamide) derivative of estradiol as inhibitor of 17β-hydroxysteroid dehydrogenase type I
-
Poirier D., Dionne P. and Auger S., A 6β-(thiaheptanamide) derivative of estradiol as inhibitor of 17β-hydroxysteroid dehydrogenase type I. J. Steroid Biochem. Molec. Biol. 64 (1998) 83-90.
-
(1998)
J. Steroid Biochem. Molec. Biol.
, vol.64
, pp. 83-90
-
-
Poirier, D.1
Dionne, P.2
Auger, S.3
-
63
-
-
0030571293
-
D-ring alkylamide derivatives of estradiol: Effect on ER-binding affinity and antiestrogenic activity
-
Poirier D., Mérand Y., Labrie C. and Labrie F., D-ring alkylamide derivatives of estradiol: effect on ER-binding affinity and antiestrogenic activity. Bioorg. Med. Chem. Lett. 6 (1996) 2537-2542.
-
(1996)
Bioorg. Med. Chem. Lett.
, vol.6
, pp. 2537-2542
-
-
Poirier, D.1
Mérand, Y.2
Labrie, C.3
Labrie, F.4
-
64
-
-
0029644733
-
Structure of human estrogenic 17β-hydroxysteroid dehydrogenase at 2.20 a resolution
-
Ghosh D., Pletnev V. Z., Zhu D.-W., Wawrzak Z., Duax W. L., Pangborn W., Labrie F. and Lin S.-X., Structure of human estrogenic 17β-hydroxysteroid dehydrogenase at 2.20 A resolution. Structure 3 (1995) 503-513.
-
(1995)
Structure
, vol.3
, pp. 503-513
-
-
Ghosh, D.1
Pletnev, V.Z.2
Zhu, D.-W.3
Wawrzak, Z.4
Duax, W.L.5
Pangborn, W.6
Labrie, F.7
Lin, S.-X.8
-
65
-
-
0029761692
-
Crystal structure of human estrogenic 17β-hydroxysteroid dehydrogenase complexed with 17β-estradiol
-
Azzi A., Rehse P., Zhu D.-W., Campbell R. L., Labrie F. and Lin S.-X., Crystal structure of human estrogenic 17β-hydroxysteroid dehydrogenase complexed with 17β-estradiol. Nature Struct. Biol. 3 (1996) 665-668.
-
(1996)
Nature Struct. Biol.
, vol.3
, pp. 665-668
-
-
Azzi, A.1
Rehse, P.2
Zhu, D.-W.3
Campbell, R.L.4
Labrie, F.5
Lin, S.-X.6
-
66
-
-
0030586820
-
The structure of a complex of human 17β-hydroxysteroid dehydrogenase with estradiol and NADP identifies two principal targets for the design of inhibitors
-
Breton R., Housset D., Mazza C. and Frontecilla-Camps J. C., The structure of a complex of human 17β-hydroxysteroid dehydrogenase with estradiol and NADP identifies two principal targets for the design of inhibitors. Structure 4 (1996) 905-915.
-
(1996)
Structure
, vol.4
, pp. 905-915
-
-
Breton, R.1
Housset, D.2
Mazza, C.3
Frontecilla-Camps, J.C.4
-
67
-
-
0031059270
-
The estradiol pharmacophore: Ligand structure-estrogen receptor binding affinity relationships and a model for the receptor binding site
-
Anstead G. M., Carlson K. E. and Katzenellenbogen J. A., The estradiol pharmacophore: ligand structure-estrogen receptor binding affinity relationships and a model for the receptor binding site. Steroids 62 (1997) 268-303.
-
(1997)
Steroids
, vol.62
, pp. 268-303
-
-
Anstead, G.M.1
Carlson, K.E.2
Katzenellenbogen, J.A.3
-
68
-
-
0027141842
-
DNA recognition by the oestrogen receptor: From solution to the crystal
-
Schwabe J. W. R., Chapman L., Finch J. T., Rhodes D. and Nenhaus D., DNA recognition by the oestrogen receptor: from solution to the crystal. Structure 1 (1993) 187-204.
-
(1993)
Structure
, vol.1
, pp. 187-204
-
-
Schwabe, J.W.R.1
Chapman, L.2
Finch, J.T.3
Rhodes, D.4
Nenhaus, R.5
|