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Nuclear receptor coactivators and corepressors

Molecular endocrinology (Baltimore, Md.), 1996-10, Vol.10 (10), p.1167-1177

1996

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Antagonist-occupied human progesterone receptors bound to DNA are functionally switched to transcriptional agonists by cAMP

The Journal of biological chemistry, 1993-05, Vol.268 (13), p.9262-9266

1993

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Antagonist-occupied human progesterone B-receptors activate transcription without binding to progesterone response elements and are dominantly inhibited by A-receptors

Molecular endocrinology (Baltimore, Md.), 1993-10, Vol.7 (10), p.1256-1265

1993

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Association of the Ku autoantigen/DNA-dependent protein kinase holoenzyme and poly(ADP-ribose) polymerase with the DNA binding domain of progesterone receptors

Journal of molecular endocrinology, 2000-04, Vol.24 (2), p.165-182

2000

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Tamoxifen resistant breast cancer: coregulators determine the direction of transcription by antagonist-occupied steroid receptors

Journal of steroid biochemistry and molecular biology, 1999-04, Vol.69 (1), p.45-50

1999

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Progesterone receptor variants found in breast cells repress transcription by wild-type receptors

Breast cancer research and treatment, 1998-04, Vol.48 (3), p.231-241

1998

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The Inhibitory Function in Human Progesterone Receptor N Termini Binds SUMO-1 Protein to Regulate Autoinhibition and Transrepression

The Journal of biological chemistry, 2002-09, Vol.277 (37), p.33950-33956

2002

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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

Molecular endocrinology (Baltimore, Md.), 1997-06, Vol.11 (6), p.693-705

1997

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Hormone-Induced Progesterone Receptor Phosphorylation Consists of Sequential DNA-Independent and DNA-Dependent Stages: Analysis with Zinc Finger Mutants and the Progesterone Antagonist ZK98299

Proceedings of the National Academy of Sciences - PNAS, 1992-04, Vol.89 (7), p.3050-3054

1992

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New T47D breast cancer cell lines for the independent study of progesterone B- and A-receptors : only antiprogestin-occupied B-receptors are switched to transcriptional agonists by cAMP

Cancer research (Chicago, Ill.), 1994-07, Vol.54 (14), p.3868-3877

1994

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An N-terminal Inhibitory Function, IF, Suppresses Transcription by the A-isoform but Not the B-isoform of Human Progesterone Receptors

The Journal of biological chemistry, 1998-03, Vol.273 (10), p.5455-5460

1998

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Functional properties of the N-terminal region of progesterone receptors and their mechanistic relationship to structure

Journal of steroid biochemistry and molecular biology, 2003-06, Vol.85 (2), p.209-219

2003

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The N-terminal region of the human progesterone A-receptor. Structural analysis and the influence of the DNA binding domain

The Journal of biological chemistry, 2000-03, Vol.275 (10), p.7313-7320

2000

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Novel mechanisms of antiprogestin action

Journal of steroid biochemistry and molecular biology, 1995-06, Vol.53 (1), p.9-17

1995

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The leucine zippers of c-fos and c-jun for progesterone receptor dimerization: A-dominance in the A/B heterodimer

The Journal of steroid biochemistry and molecular biology, 1994-12, Vol.51 (5-6), p.241-250

1994

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The N-terminal region of human progesterone B-receptors: biophysical and biochemical comparison to A-receptors

The Journal of biological chemistry, 2001-06, Vol.276 (26), p.23825-23831

2001

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Mapping the unique activation function 3 in the progesterone B-receptor upstream segment. Two LXXLL motifs and a tryptophan residue are required for activity

The Journal of biological chemistry, 2001-10, Vol.276 (43), p.39843-39851

2001

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Progesterone receptor phosphorylation complexities in defining a functional role

Trends in Endocrinology & Metabolism, 1993, Vol.4 (1), p.1-7

1993

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Novel Mechanisms of Antiprogestin Action

Acta oncologica, 1996, Vol.35 (2), p.129-140

Horwitz, Kathryn B.

1996

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BCL3 rearrangements and t(14;19) in chronic lymphocytic leukemia and other B-cell malignancies: A molecular and cytogenetic study

Genes chromosomes & cancer, 1997-09, Vol.20 (1), p.64-72

1997

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Role of Phosphorylation on DNA Binding and Transcriptional Functions of Human Progesterone Receptors

The Journal of biological chemistry, 1996-06, Vol.271 (23), p.13308-13316

1996

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Epitope mapping of the anti-human progesterone receptor monoclonal antibody, AB-52

The Journal of steroid biochemistry and molecular biology, 1991-11, Vol.39 (5), p.687-692

1991

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Differential sensitivity of hypothalamic norepinephrine and striatal dopamine to catecholamine-depleting agents

The Journal of pharmacology and experimental therapeutics, 1983-08, Vol.226 (2), p.432

1983

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Effects of nitroprusside-induced hypotension on sympathetic nerve activity, tyrosine hydroxylase activity and [3H]norepinephrine uptake in rabbit vascular tissues

The Journal of pharmacology and experimental therapeutics, 1981-11, Vol.219 (2), p.420

1981

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Evidence for the transsynaptic activation of tyrosine hydroxylase in rabbit portal vein mediated through a cyclic AMP-independent mechanism

The Journal of pharmacology and experimental therapeutics, 1981-10, Vol.219 (1), p.97

1981

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Nuclear receptor coactivators and corepressors

Antagonist-occupied human progesterone receptors bound to DNA are functionally switched to transcriptional agonists by cAMP

Antagonist-occupied human progesterone B-receptors activate transcription without binding to progesterone response elements and are dominantly inhibited by A-receptors

Association of the Ku autoantigen/DNA-dependent protein kinase holoenzyme and poly(ADP-ribose) polymerase with the DNA binding domain of progesterone receptors

Tamoxifen resistant breast cancer: coregulators determine the direction of transcription by antagonist-occupied steroid receptors

Progesterone receptor variants found in breast cells repress transcription by wild-type receptors

The Inhibitory Function in Human Progesterone Receptor N Termini Binds SUMO-1 Protein to Regulate Autoinhibition and Transrepression

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

Hormone-Induced Progesterone Receptor Phosphorylation Consists of Sequential DNA-Independent and DNA-Dependent Stages: Analysis with Zinc Finger Mutants and the Progesterone Antagonist ZK98299

New T47D breast cancer cell lines for the independent study of progesterone B- and A-receptors : only antiprogestin-occupied B-receptors are switched to transcriptional agonists by cAMP

An N-terminal Inhibitory Function, IF, Suppresses Transcription by the A-isoform but Not the B-isoform of Human Progesterone Receptors

Functional properties of the N-terminal region of progesterone receptors and their mechanistic relationship to structure

The N-terminal region of the human progesterone A-receptor. Structural analysis and the influence of the DNA binding domain

Novel mechanisms of antiprogestin action

The leucine zippers of c-fos and c-jun for progesterone receptor dimerization: A-dominance in the A/B heterodimer

The N-terminal region of human progesterone B-receptors: biophysical and biochemical comparison to A-receptors

Mapping the unique activation function 3 in the progesterone B-receptor upstream segment. Two LXXLL motifs and a tryptophan residue are required for activity

Progesterone receptor phosphorylation complexities in defining a functional role

Novel Mechanisms of Antiprogestin Action

BCL3 rearrangements and t(14;19) in chronic lymphocytic leukemia and other B-cell malignancies: A molecular and cytogenetic study

Role of Phosphorylation on DNA Binding and Transcriptional Functions of Human Progesterone Receptors

Epitope mapping of the anti-human progesterone receptor monoclonal antibody, AB-52

Differential sensitivity of hypothalamic norepinephrine and striatal dopamine to catecholamine-depleting agents

Effects of nitroprusside-induced hypotension on sympathetic nerve activity, tyrosine hydroxylase activity and [3H]norepinephrine uptake in rabbit vascular tissues

Evidence for the transsynaptic activation of tyrosine hydroxylase in rabbit portal vein mediated through a cyclic AMP-independent mechanism

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