Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

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

1 May 1992

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Estrogen and related hormone effects
Share to Hormonal Regulation and Hypertension
Share to Neurobiology and Insect Physiology Research

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 1586949
DOI: 10.1016/0092-8674(92)90234-4

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The mechanism of RU486 antagonism is dependent on the conformation of the carboxy-terminal tail of the human progesterone receptorPMID 1586949Read ↗

Mechanism of Action of Progesterone AntagonistsSemantic proximity Read ↗

The evolution of progesterone receptor ligandsSemantic proximity Read ↗

Unfolding the action of progesterone receptors.Semantic proximity Read ↗

Molecular determinants of context-dependent progesterone receptor action in breast cancerSemantic proximity Read ↗

Clinical pharmacology of RU 486—an antiprogestin and antiglucocorticoidSemantic proximity Read ↗

History and perspectives of antiprogestins from the chemist's point of viewSemantic proximity Read ↗

Regulation by Progestins, Corticosteroids and RU486 of Activation of Elephant Shark and Human Progesterone Receptors: An Evolutionary PerspectiveSemantic proximity Read ↗

Met909 plays a key role in the activation of the progesterone receptor and also in the high potency of 13-ethyl progestins.Semantic proximity Read ↗

Regulation by Progestins, Corticosteroids and RU486 of Activation of Elephant Shark and Human Progesterone Receptors: An Evolutionary PerspectiveSemantic proximity Read ↗

The Novel Progesterone Receptor Antagonists RTI 3021–012 and RTI3021–022 Exhibit Complex Glucocorticoid Receptor Antagonist Activities: Implications for the Development of Dissociated Antiprogestins*Semantic proximity Read ↗

Structure of human follicle-stimulating hormone in complex with its receptorSemantic proximity Read ↗

Reversal of multidrug resistance by RU 486.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.