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16 alpha-substituted analogs of the antiprogestin RU486 induce a unique conformation in the human progesterone receptor resulting in mixed agonist activity.

Data up to Jan 2025

Published1996
Citations59
References29

Total Citations Per Year

Abstract

References (29)

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Two distinct estrogen-regulated promoters generate transcripts encoding the two functionally different human progesterone receptor forms A and B.

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1996 • 505 citations

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1995 • 502 citations

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1989 • 458 citations

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1991 • 433 citations

The mechanism of RU486 antagonism is dependent on the conformation of the carboxy-terminal tail of the human progesterone receptor

1992 • 381 citations

Hormone and antihormone induce distinct conformational changes which are central to steroid receptor activation.

1992 • 363 citations

Members of the steroid hormone receptor superfamily interact with TFIIB (S300-II).

1992 • 354 citations

The A and B isoforms of the human progesterone receptor operate through distinct signaling pathways within target cells.

1994 • 343 citations

Agonistic and antagonistic activities of RU486 on the functions of the human progesterone receptor.

1990 • 333 citations

Transcriptional activation by the estrogen receptor requires a conformational change in the ligand binding domain.

1993 • 249 citations

Identification of a New Subclass of Alu DNA Repeats Which Can Function as Estrogen Receptor-dependent Transcriptional Enhancers

1995 • 226 citations

Yeast RSP5 and Its Human Homolog hRPF1 Potentiate Hormone-Dependent Activation of Transcription by Human Progesterone and Glucocorticoid Receptors

1996 • 160 citations

A Single Amino Acid That Determines the Sensitivity of Progesterone Receptors to RU486

1992 • 141 citations

Human Progesterone Receptor Complexed with the Antagonist RU 486 Binds to Hormone Response Elements in a Structurally Altered Form

1989 • 138 citations

Ligand-induced Conformational Alterations of the Androgen Receptor Analyzed by Limited Trypsinization

1995 • 132 citations

Ligand-dependent conformational changes in the progesterone receptor are necessary for events that follow DNA binding.

1992 • 108 citations

Identification of a negative regulatory function for steroid receptors.

1992 • 98 citations

Novel estrogen response elements identified by genetic selection in yeast are differentially responsive to estrogens and antiestrogens in mammalian cells.

1994 • 92 citations

Ligands induce conformational changes in the carboxyl-terminus of progesterone receptors which are detected by a site-directed antipeptide monoclonal antibody.

1992 • 81 citations

The A and B Isoforms of the Human Progesterone Receptor Operate through Distinct Signaling Pathways within Target Cells

1994 • 77 citations

Progestin regulation of alkaline phosphatase in the human breast cancer cell line T47D.

1991 • 66 citations

Identification of a Transactivation Function in the Progesterone Receptor That Interacts with the TAFII110 Subunit of the TFIID Complex

1995 • 57 citations

Reversal of activity profile in analogs of the antiprogestin RU 486: effect of a 16 alpha-substituent on progestational (agonist) activity.

1993 • 20 citations

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16 alpha-substituted analogs of the antiprogestin RU486 induce a unique conformation in… (1996) – Proceedings of the National Academy of Sciences | Metascience Observatory Explorer