| scholarly article | Q13442814 |
| P819 | ADS bibcode | 1983PNAS...80.3158F |
| P356 | DOI | 10.1073/PNAS.80.11.3158 |
| P932 | PMC publication ID | 393999 |
| P698 | PubMed publication ID | 6574477 |
| P5875 | ResearchGate publication ID | 16620791 |
| P2093 | author name string | E E Baulieu | |
| G Redeuilh | |||
| F Bayard | |||
| J C Faye | |||
| S Jozan | |||
| P2860 | cites work | Protein measurement with the Folin phenol reagent | Q20900776 |
| Antibodies to estrogen receptor: Immunochemical similarity of estrophilin from various mammalian species | Q35048365 | ||
| Estradiol receptor of calf uterus: interactions with heparin-agarose and purification | Q35060551 | ||
| Estrogen and Antiestrogen Action in Reproductive Tissues and Tumors | Q38041110 | ||
| A method for determining the sedimentation behavior of enzymes: application to protein mixtures | Q39512885 | ||
| Production and detection of antibodies against the estrogen receptor from calf uterine cytosol | Q39984511 | ||
| Tamoxifen and metabolites in MCF7 cells: correlation between binding to estrogen receptor and inhibition of cell growth. | Q41619173 | ||
| The effects of estrogens and antiestrogens on hormone-responsive human breast cancer in long-term tissue culture | Q42803245 | ||
| Nuclear estrogen receptor release from antiestrogen suppression: amplified induction of progesterone receptor in MCF-7 human breast cancer cells | Q43411264 | ||
| Monohydroxytamoxifen: An antioestrogen with high affinity for the chick oviduct oestrogen receptor | Q43634735 | ||
| A monohydroxylated metabolite of tamoxifen with potent antioestrogenic activity | Q44004732 | ||
| Cytoplasmic and nuclear estradiol and progesterone receptors in human endometrium | Q45004310 | ||
| New biospecific adsorbents for the purification of estradiol receptor | Q53815622 | ||
| [Mechanism of action of a triphenylethylene type antiestrogen on growth of the human breast cancer cell line. MCF-7 in culture] | Q54537535 | ||
| Tamoxifen is a potent "pure" anti-oestrogen in chick oviduct | Q59080823 | ||
| High-affinity anti-oestrogen binding site distinct from the oestrogen receptor | Q59082035 | ||
| Differential binding of antiestrogens by rat uterine and chick oviduct cytosol | Q66979028 | ||
| High-affinity binding of the antiestrogen [3H]tamoxifen to the 8S estradiol receptor | Q67367424 | ||
| Estrogen control of progesterone receptor in human breast cancer: role of estradiol and antiestrogen | Q67446195 | ||
| Antiestrogen specific, high affinity saturable binding sites in rat uterine cytosol | Q70650484 | ||
| Modifications in the aminoether side chain of clomiphene influence affinity for a specific antiestrogen binding site in MCF 7 cells cytosol | Q70899616 | ||
| Calf uterine estradiol receptor. Effects of molybdate on salt-induced transformation process and characterization of a nontransformed receptor state | Q70975881 | ||
| Inhibition of uterine estrogen receptor transformation by sodium molybdate | Q71241824 | ||
| High-affinity binding to the estrogen receptor of [3H]4-hydroxytamoxifen, an active antiestrogen metabolite | Q71397987 | ||
| Different effects of oestradiol, oestriol, oestetrol and of oestrone on human breast cancer cells (MCF-7) in long term tissue culture | Q71569150 | ||
| Properties of a uterine oestradiol receptor | Q72093764 | ||
| P4510 | describes a project that uses | MCF-7/RTx6 | Q54904377 |
| P433 | issue | 11 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | cell line | Q21014462 |
| P304 | page(s) | 3158-3162 | |
| P577 | publication date | 1983-06-01 | |
| P1433 | published in | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
| P1476 | title | Physicochemical and genetic evidence for specific antiestrogen binding sites | |
| P478 | volume | 80 |
| Q68674574 | A study on the correlation between estrogen receptor, progesterone receptor and tamoxifen binding sites in human breast cancer tissues |
| Q43505469 | Anti-proliferative effects of 1,2-diphenylethane oestrogens and anti-oestrogens on human breast cancer cells |
| Q43685275 | Antiestrogen action in breast cancer cells: modulation of proliferation and protein synthesis, and interaction with estrogen receptors and additional antiestrogen binding sites |
| Q34786218 | Changes in vascularization of human breast cancer xenografts responding to antiestrogen therapy |
| Q73226598 | Diphenyl quinolines and isoquinolines: synthesis and primary biological evaluation |
| Q54393577 | Estrogen inhibits the growth of MCF-7 cell variants resistant to transforming growth factor-beta. |
| Q25257588 | Farnesyl-transferase inhibitor R115,777 enhances tamoxifen inhibition of MCF-7 cell growth through estrogen receptor dependent and independent pathways. |
| Q68581882 | Fatty acid modulation of antiestrogen action and antiestrogen-binding protein in cultured lymphoid cells |
| Q42150530 | Interaction of unsaturated fatty acids with anti-oestrogen-binding sites |
| Q41463841 | Mechanisms of tamoxifen resistance in the treatment of advanced breast cancer |
| Q42853991 | Microsomal binding sites for antioestrogens in rat liver. Properties and detergent solubilization |
| Q39715988 | Microsomal epoxide hydrolase expression in the endometrial uterine corpus is regulated by progesterone during the menstrual cycle |
| Q28568639 | Microsomal epoxide hydrolase of rat liver is a subunit of theanti-oestrogen-binding site |
| Q40971042 | Modifications of benzylphenoxy ethanamine antiestrogen molecules: influence affinity for antiestrogen binding site (AEBS) and cell cytotoxicity |
| Q24631017 | Phenol red in tissue culture media is a weak estrogen: implications concerning the study of estrogen-responsive cells in culture |
| Q44100624 | Regulation of breast tumor growth by high dose estrogen is independent of the presence of estrogen receptors |
| Q30403555 | Solubilization of a tamoxifen-binding protein. Assessment of its molecular mass |
| Q40913236 | Structural similitudes between cytotoxic antiestrogen-binding site (AEBS) ligands and cytotoxic sigma receptor ligands. Evidence for a relationship between cytotoxicity and affinity for AEBS or sigma-2 receptor but not for sigma-1 receptor |
| Q72995250 | Synthesis, binding and structure-affinity studies of new ligands for the microsomal anti-estrogen binding site (AEBS) |
| Q41979321 | Unsaturated fatty acids as endogenous inhibitors of tamoxifen binding to anti-oestrogen-binding sites |
| Q54904377 | MCF-7/RTx6 | described by source | P1343 |
Search more.