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Data show that cytochrome P450 (show CYP ELISA Kits) enzymes Cyp17 (show CYP17A1 ELISA Kits)-I, Cyp11c1 (show CYP11B2 ELISA Kits), Cyp19a1a and Cyp19a1b and one of their regulators forkhead protein (show FOXO4 ELISA Kits) Foxl2a were detected both in the testis and ovary.
Data indicate taht monocrotophos (MCP) exposure modulated gene expression of forkhead transcription factor gene L2 (foxl2), doublesex/mab-3 related transcription factor 1 (dmrt1), gonadal aromatase (cyp19a1a) and brain aromatase (cyp19a1b).
Effects of sexual steroids on the expression of foxl2 in Gobiocypris rarus
Xenopus W-linked DM-W induces foxl2 expression during ovary formation.
direct overexpression of Foxl2 decreased the expression of Sertoli cell-specific genes in primary Sertoli cells. Taken together, these results demonstrate that repression of beta-catenin (CTNNB1 (show CTNNB1 ELISA Kits)) signaling is required for lineage maintenance of Sertoli cells.
evidence that FOXL2 modulates Col1a2 (show COL1A2 ELISA Kits) transcription through interaction with a response element 65 Kb upstream of the transcription start site
Data indicate that a balance between supporting cell (show PTPRJ ELISA Kits) self-renewal and differentiation is maintained in the developing ovary by relative Wnt4 (show WNT4 ELISA Kits) protein/beta-catenin (show CTNNB1 ELISA Kits) and p27Kip1 (show CDKN1B ELISA Kits) protein (p27 (show CDKN1B ELISA Kits))/Forkhead box L2 (FOXL2) activities.
Data indicate that the hypothalamic-pituitary-gonadal axis controls expression of Foxl2 in pituitary gonadotropes primarily through positive feedback from ovarian hormones.
FOXL2 mobilizes estrogen signaling to establish a coherent feed-forward loop repressing Sox9.
Foxl2 has a crucial role in postnatal uterine maturation and could help to understand sub-fertility predisposition in women.
Results support FOXL2 as a master transcription factor in a spectrum of developmental processes, including growth, cartilage and bone formation. Its action overlaps that of SOX9 (show SOX9 ELISA Kits), though they are antagonistic in female vs male gonadal sex determination but conjoint in cartilage and skeletal development.
Microarray expression profiling of whole adrenal mRNA from ovariectomized vs. intact mice demonstrated selective upregulation of gonadal-like genes including Spinlw1 and Insl3 (show INSL3 ELISA Kits) in GDX (show UBL4A ELISA Kits)-induced adrenocortical tumors of the mouse.
our results demonstrate the necessity of FOXL2 for proper FSH (show BRD2 ELISA Kits) production in mice and implicate FOXL2 in integration of transcription factors at the level of the FSHbeta promoter.
Results show that a piggyBac insertion ~160 kb upstream of the transcription start site of Foxl2 partially disrupted its expression resulting in BPES (Blepharophimosis, ptosis, epicanthus inversus syndrome)-like conditions.
Despite exhibiting an immunophenotype characteristic of a sex cord-stromal tumor, mutations in FOXL2 and DICER1 (show DICER1 ELISA Kits), the 2 most common mutations hitherto reported in ovarian sex cord-stromal tumors, are not a feature of Uterine tumor resembling ovarian sex cord tumor (UTROSCT).
This report describes the preservation of heterozygous c.402C>G FOXL2 mutation in recurrent aGCTs. This finding adds further credence to the concept that the c.402C>G FOXL2 mutation is oncogenic and integral to this disease.
The novel mutations of the FOXL2 are associated with blepharophimosis, ptosis and epicanthus inversus syndrome.
this study identified a novel regulatory circuit for ovarian AMH (show AMH ELISA Kits) production; specifically, through the coordinated interplay between FOXL2 and SF-1 (show NR5A1 ELISA Kits) that could control ovarian follicle development.
we report the identification of two novel and two recurrent heterozygous NOBOX (show NOBOX ELISA Kits) variants in 7 out of 107 patients, with a prevalence of 6.5% (upper 95% confidence limit of 11.17%). Several variants conserve the ability to interact with FOXL2 in intracellular aggregates
This is the first study reporting lacrimal gland(LG) volumes in BPES, describing a significant number of patients with LG agenesis. Molecular analysis of the FOXL2 gene revealed the presence of 8 distinct mutations.
In the case of aGCT, a well characterized mutation in the FOXL2 transcription factor (FOXL2 C134W) is found in almost all cases, which arguably defines the disease, although the molecular events that determine the stage, behavior and prognosis of aGCT remain to be determined.
We highlight the cooperation of WNT4 (show WNT4 ELISA Kits), RSPO1 (show RSPO1 ELISA Kits) and FOXL2 within a regulatory network and the need for further research to better understand their role in defining and maintaining ovarian identity.
The de novo mutation rate in FOXL2 is exceptionally high compared with other dominant disorders manifesting with an ocular phenotype.
SUMOylation of FOXL2 and PML (show PML ELISA Kits) Bodies
This gene encodes a forkhead transcription factor. The protein contains a fork-head DNA-binding domain and may play a role in ovarian development and function. Mutations in this gene are a cause of blepharophimosis syndrome and premature ovarian failure 3.
forkhead box L2
, forkhead box protein L2
, transcription factor FOXL2
, forkhead transcription factor L2
, foxl2 protein
, fork-head box L2 transcription factor
, pituitary forkhead factor
, putative transcription factor foxl2
, forkhead transcription factor FOXL2
, Forkhead box protein L2