(Q28378344)

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The aryl hydrocarbon receptor (AHR)/AHR nuclear translocator (ARNT) heterodimer interacts with naturally occurring estrogen response elements

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3 November 2019

The aryl hydrocarbon receptor (AHR)/AHR nuclear translocator (ARNT) heterodimer interacts with naturally occurring estrogen response elements (English)

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3 November 2019

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Carolyn M. Klinge

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3 November 2019

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J L Bowers

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3 November 2019

P C Kulakosky

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3 November 2019

K K Kamboj

4

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3 November 2019

H I Swanson

5

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3 November 2019

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1 November 1999

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3 November 2019

Molecular and Cellular Endocrinology

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3 November 2019

157

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3 November 2019

1-2

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3 November 2019

105-119

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3 November 2019

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Activation of pS2 gene transcription is a primary response to estrogen in the human breast cancer cell line MCF-7.

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Polynuclear aromatic hydrocarbon carcinogens as antiestrogens in MCF-7 human breast cancer cells: role of the Ah receptor

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Sequence Requirements for Estrogen Receptor Binding to Estrogen Response Elements

1 reference

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Identification of a motif within the 5' regulatory region of pS2 which is responsible for AP-1 binding and TCDD-mediated suppression

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Identification and characterization of an estrogen-responsive element binding protein repressed by estradiol

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Estrogen does not inhibit 2,3,7, 8-tetrachlorodibenzo-p-dioxin-mediated effects in MCF-7 and Hepa 1c1c7 cells

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Inhibition of 7,12-dimethylbenzanthracene-induced rat mammary tumor growth by 2,3,7,8-tetrachlorodibenzo-p-dioxin

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A CBP integrator complex mediates transcriptional activation and AP-1 inhibition by nuclear receptors

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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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Editorial: A New Actor in the Estrogen Receptor Drama--Enter ER-

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7 January 2021

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Antiestrogenic effects of 2,3,7,8-tetrachlorodibenzo-p-dioxin are mediated by direct transcriptional interference with the liganded estrogen receptor. Cross-talk between aryl hydrocarbon- and estrogen-mediated signaling

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Dissociation of 4-hydroxytamoxifen, but not estradiol or tamoxifen aziridine, from the estrogen receptor as the receptor binds estrogen response element DNA

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Chicken Ovalbumin Upstream Promoter-Transcription Factor Interacts with Estrogen Receptor, Binds to Estrogen Response Elements and Half-Sites, and Inhibits Estrogen-induced Gene Expression

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7 January 2021

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Comparison of tamoxifen ligands on estrogen receptor interaction with estrogen response elements

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7 January 2021

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Identification of multiple, widely spaced estrogen-responsive regions in the rat progesterone receptor gene

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Polychlorinated Biphenyls (PCBs), Dibenzo-p-dioxins (PCDDs), and Dibenzofurans (PCDFs) as Antiestrogens in MCF-7 Human Breast Cancer Cells: Quantitative Structure-Activity Relationships

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Molecular mechanism of inhibition of estrogen-induced cathepsin D gene expression by 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) in MCF-7 cells

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Interference between progesterone and dioxin signal transduction pathways. Different mechanisms are involved in repression by the progesterone receptor A and B isoforms

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Cloning of a novel receptor expressed in rat prostate and ovary

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Comparison of the ligand binding specificity and transcript tissue distribution of estrogen receptors alpha and beta

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1 reference

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1 reference

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7 January 2021

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1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

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1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

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1 reference

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7 January 2021

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1 reference

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7 January 2021

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1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

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1 reference

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7 January 2021

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inferred from DOI database lookup

Identifiers

10.1016/S0303-7207(99)00165-3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10619402%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10619402%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

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