Steroid hormone receptors: an update.
By M. Beato, J. Klug. Human Reproduction Update, 2000
643 citations recorded by the source corpus.
Subfields: Endocrinology, Diabetes and Metabolism, Genetics
View Paper: https://www.semanticscholar.org/paper/5e09fb51c240a4a4df544c07eb0a7d82cc1a0cbb
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In Endocrinology, Diabetes and Metabolism
In Genetics
Citations in the corpus
- Hypothalamic–pituitary–adrenal and hypothalamic–pituitary–gonadal axes: sex differences in regulation of stress responsivity (2017, background): “Transcription of target genes is initiated through activation of the pre-initiation complex (Beato, 1989; Beato & Klug, 2000; Tyagi et al., 2000).”
- Multiple actions of steroid hormones--a focus on rapid, nongenomic effects. (2000, neutral): “…structurally nor biosynthetically related, receptors for steroids, retinoic acid, vitamin D 3 , and thyroid hormones have been characterized as nuclear receptors or a superfamily of steroid and thyroid hormone receptors due to their close structural homologies (Evans, 1988; Beato and Klug, 2000).”
- Sex hormones and the immune response in humans. (2005, background): “The steroid/steroid receptor complex in the nucleus functions as a transcription factor, directly regulating expression of genes containing a binding site for this complex in the promoter region (Beato and Klung, 2000).”
- The international workshop on meibomian gland dysfunction: report of the subcommittee on anatomy, physiology, and pathophysiology of the meibomian gland. (2011, background): “It is possible that the action also involves binding to glandular membrane receptors, stimulation of signal transduction cascades, and consequent alteration of gene transcription.(249,250) In addition, androgens may act indirectly, by regulating the secretion of the hypothalamic and anterior pituita”
- Dopamine as a prolactin (PRL) inhibitor. (2001, background): “shock protein 90 and enabling receptor dimerization (185).”
- Reframing sexual differentiation of the brain (2011, background): “Steroid receptors such as androgen receptor, estrogen receptor and progesterone receptor are nuclear transcription factor receptors that are capable of directly interacting with DNA at specific response elements and modulating gene transcriptio”