17β-Estradiol (E2) is the main estrogenic hormone in the body and exerts many
cardiovascular protective effects. Via three receptors known to date, including estrogen …

Phytoestrogens are natural endocrine disruptors that interfere with estrogenic pathways.
They insert directly within the hormone-binding domain of ERα and β, with a preference for …

The estrogen receptor α (ERα) corresponds to a large platform in charge of the recruitment
of a panel of molecules, including steroids and related heterocyclic derivatives …

Twenty-five years ago, a class A (rhodopsin-like) G protein-coupled receptor (GPCR) was
reported to participate in the rapid physiological responses to the mammalian steroid …

Estrogen receptor α (ER-α) is a nuclear hormone receptor that controls selected genes,
thereby regulating proliferation and differentiation of target tissues, such as breast. Gene …

We have synthesized a 17‐mer peptide (ERα17p) that is issued from the hinge region of the
estrogen receptor α and which activates the proliferation of breast carcinoma cells in steroid …

The ERα (oestrogen receptor α)-derived peptide ERα17p activates rapid signalling events in
breast carcinoma cells under steroid-deprived conditions. In the present study, we …

The immunophilin FKBP52 interacts with nuclear steroid hormone receptors. Studying the
crystal structure of human estrogen receptor α (hERα) and using nuclear magnetic …

The estrogen receptor α (ERα) corresponds to a large platform in charge of the recruitment
of a panel of molecules, including steroids and related heterocyclic derivatives …

Calcineurin (CN) is a Ca 2+/calmodulin (CaM) activated serine/threonine phosphatase, and
its regulatory region (CNRR) plays a critical role in the coupling of Ca 2+ signals to cellular …