Genomic and Nongenomic Effects of Mifepristone at the Cardiovascular Level: A Review.

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Genomic and Nongenomic Effects of Mifepristone at the Cardiovascular Level: A Review.

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2016 nî lūn-bûn

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2016年の論文

@ja

2016年論文

@yue

2016年論文

@zh-hant

2016年論文

@zh-hk

2016年論文

@zh-mo

2016年論文

@zh-tw

2016年论文

@wuu

2016年论文

@zh

2016年论文

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name

Genomic and Nongenomic Effects of Mifepristone at the Cardiovascular Level: A Review.

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label

Genomic and Nongenomic Effects of Mifepristone at the Cardiovascular Level: A Review.

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prefLabel

Genomic and Nongenomic Effects of Mifepristone at the Cardiovascular Level: A Review.

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P1476

Genomic and Nongenomic Effects of Mifepristone at the Cardiovascular Level: A Review.

@en

P2093

Elisa Cairrão

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Ignacio Verde

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Joana Feiteiro

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Melissa Mariana

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P2860

A transmembrane intracellular estrogen receptor mediates rapid cell signaling

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The steroid and thyroid hormone receptor superfamily

Coactivator/corepressor ratios modulate PR-mediated transcription by the selective receptor modulator RU486

Selective progesterone receptor modulators and progesterone antagonists: mechanisms of action and clinical applications

Selective progesterone receptor modulators in reproductive medicine: pharmacology, clinical efficacy and safety

In vitro antiprogestational/antiglucocorticoid activity and progestin and glucocorticoid receptor binding of the putative metabolites and synthetic derivatives of CDB-2914, CDB-4124, and mifepristone

The nuclear corepressors NCoR and SMRT are key regulators of both ligand- and 8-bromo-cyclic AMP-dependent transcriptional activity of the human progesterone receptor.

14 beta-Hydroxyprogesterone binds to the digitalis receptor, inhibits the sodium pump and enhances cardiac contractility

P304

976-988

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P31

scholarly article

P356

10.1177/1933719116671002

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P433

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P478

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P50

P577

2016-09-27T00:00:00Z

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P698

27678094

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