Progesterone receptor contains a proline-rich motif that directly interacts with SH3 domains and activates c-Src family tyrosine kinases.
By Viroj Boonyaratanakornkit, M. Scott, V. Ribon, Lori Sherman, S. Anderson, J. Maller, W. Miller, D. Edwards. Molecules and Cells, 2001
602 citations recorded by the source corpus.
Subfields: Genetics, Molecular Biology, Oncology
View Paper: https://www.semanticscholar.org/paper/630929c121a1dced846ef3f6cd1e899413ffcff3
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Citations in the corpus
- Overview of Nomenclature of Nuclear Receptors (2006, background): “However, it now seems that at least some of the reported effects can be attributed to the same steroid receptors that are known as NRs (Migliaccio et al., 1996; Simoncini et al., 2000; Boonyaratanakornkit et al., 2001; Castoria et al., 2001; Kousteni et al., 2001).”
- Src family kinases in tumor progression and metastasis (2003, background): “[95] demonstrated that the progesterone receptor was capable of directly activating SFKs, through displacement of the SH3 domain/linker intramolecular interaction, in response to progestin.”
- Nongenomic actions of steroid hormones (2003, neutral): “uk/interpro/IEntry?ac=IPR001452">SH3 ) domains of various proteins in response to progesteron”
- Ovarian follicle growth, maturation, and ovulation in teleost fish (2004, background): “It is tempting to speculate that both novel (Thomas et al. 2002) and classical (Bagovski et al. 2001; Boonyaratanakornkit et al. 2001) forms of progestin receptors are involved in the regulation of MIH-dependent meiotic resumption.”