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Transcriptional factor FOXL2 interacts with DP103 and induces apoptosis
Biochemical and Biophysical Research Communications, 2005Blepharophimosis-ptosis-epicanthus inversus syndrome type I is an autosomal disorder caused by mutations in FOXL2 gene and associated with premature ovarian failure in women by a dominant inheritance. FOXL2 is a recently identified protein that belongs to forkhead family transcription factor, of which signaling pathways are still unknown. Here, we show
Kangseok, Lee +7 more
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Bioinformatics Analysis of FOXL2 Gene of Gallus gallus
2011 5th International Conference on Bioinformatics and Biomedical Engineering, 2011The Fox gene family is an ancient class of DNA binding transcription factors that has anastonishing array of functions in development, physiology, cancer and cognition. We analyzed the salient features of the FOXL2 gene and encoded protein of Gallus gallus by bioinformatics tools and highlighted its important biological characterization, which provided
San-Hu Wang, Ren-Feng Li, Xue-Bin Li
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FOXL2 Knockdown Inhibits the Progression of Endometriosis
American Journal of Reproductive ImmunologyABSTRACTProblemEndometriosis (EM) is known as a common estrogen‐dependent chronic inflammatory disease. Elevated levels of Forkhead box L2 (FOXL2) have been observed in uterine diseases, including EM. However, the molecular mechanism of FOXL2 in EM needs to be further illustrated.
Bing Zhang +5 more
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SUMOylation of Foxl2 Increases Synergistic Activation of the Mc2R Promoter by Foxl2 and SF1.
2010Wei-Hsiung Yang +4 more
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M070 ENDOMETRIAL FOXL2 EXPRESSION CHANGES THROUGHOUT MENSTRUAL CYCLE
International Journal of Gynecology & Obstetrics, 2012P. Carrarelli +7 more
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FOXL2, the gatekeeper of ovarian identity
2010Pannetier, Maëlle, Pailhoux, Eric
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