Forkhead box protein L2 is a protein that in humans is encoded by the FOXL2 gene. FOXL2 (OMIM 605597) is a transcription factor belonging to the forkhead...

patients as young as 15 years old. This is due to the shortening of the FOXL2 gene. Vignes (1889) probably first described this entity, a dysplasia of...

an active process, regulated by the expression of a "pro-female" gene, FOXL2. In an interview for the TimesOnline edition, study co-author Robin Lovell-Badge...

patients as young as 15 years old. BPES is caused by a mutation in the gene FOXL2, located at 3q23 (band 23 on the long arm of chromosome 3). There are two...

autoimmune diseases, enzyme defects, and resistant ovaries. Mutations in FOXL2 cause blepharophimosis, ptosis, epicanthus inversus syndrome (BPES). Premature...

COX7B CRIM1 CRYAA CRYBA4 CRYBB2 DHX38 DPYD ERCC1 ERCC5 FADD FAM111A FNBP4 FOXL2 FRAS1 FREM1 FREM2 FZD5 GDF3 GDF6 GJA1 GRIP1 HCCS HMGB3 HMX1 IGBP1 KAT6B...

FOXJ2 (erythroid), FOXJ3 FOXK1, FOXK2 (HIV, IL-2, adrenal) FOXL1 (ovary), FOXL2 FOXM1 (cell cycle, erythroid, cancer) FOXN1 (hair, thymus), FOXN2, FOXN3...

mucinous and low-grade serous 30% FMS coexpression with CSF-1 50% FOXL2 point mutation (402 C to G) adult granulosa cell ~100% JAG1 amplification...

development. An assortment of genes and proteins - such as WNT4, RSPO1, FOXL2, and various estrogen receptors - have been shown to prevent the development...

amenorrhoea and infertility FOXL2 Forkhead box L2 Isolated premature ovarian failure (POF3) associated with BPES type I; FOXL2 402C → G mutations associated...

10.1-kb DNA element which regulates the transcription of both PISRT1 and FOXL2, with the latter having been shown to be responsible for sex-determination...

the FOXL2 gene [1]. This is a somatic mutation, meaning it is not usually transmitted to descendants. Mutation c.402C>G in the sequence of FOXL2 leads...

transdifferentiate to Sertoli and Leydig cells via induced knockout of the FOXL2 gene. Similarly, Sertoli cells in the testes of adult male mice can transdifferentiate...

develop. Gradual sex reversal in developed mice can also occur when the gene FOXL2 is removed from females. Even though the gene DMRT1 is used by birds as...

Schmidt K, Justice NJ, Vale WW, Fischer WH, Bilezikjian LM (March 2009). "FoxL2 and Smad3 coordinately regulate follistatin gene transcription". The Journal...

activation of oocyte follicles is Forkhead boxL2 (Foxl2). In knock out studies, it has been shown that Foxl2 may be responsible for the cuboidal transition...

genes being expressed, where multiple pro-ovarian genes (including Wnt4, FoxL2, and Rsp01) and the lack of Sry gene expression are responsible. The lack...

hearing involvement, some implicated genes are: FOXL2, NOBOX, and FIGLA, related to ovarian development. FOXL2 mutation can cause Blepharophimosis, ptosis...

ENSG00000176678 Forkhead Known motif – High-throughput in vitro [269] RTAAACA FOXL2 ENSG00000183770 Forkhead Known motif – High-throughput in vitro [270] VBGHMAACAH...

is the amh gene, in tilapia it is tDmrt1, and in southern catfish it is foxl2. In fish, due to the fact that modes of reproduction range from gonochorism...

HGNC:23480 P85037 5809 FOXK2 HGNC:6036 Q01167 5810 FOXL1 HGNC:3817 Q12952 5811 FOXL2 HGNC:1092 P58012 5812 FOXL2NB HGNC:34428 Q6ZUU3 5813 FOXL3 HGNC:54201 A0A1W2PRP0...

mesenchymal dysgenesis FOXF1 ACD/MPV FOXI1 Enlarged vestibular aqueduct FOXL2 Premature ovarian failure 3 FOXP3 IPEX 3.5 IRF6 Van der Woude syndrome Popliteal...

person. DMRT1 is a gene that helps the testes develop. On the other hand, FOXL2 feminizes the body. Pogonomyrmex are "bearded ants." Interviewed experts:...

mesenchymal dysgenesis FOXF1 ACD/MPV FOXI1 Enlarged vestibular aqueduct FOXL2 Premature ovarian failure 3 FOXP3 IPEX 3.5 IRF6 Van der Woude syndrome Popliteal...

development. An assortment of genes and proteins - such as WNT4, RSPO1, FOXL2, and various estrogen receptors - have been shown to prevent the development...

"Differential apoptotic activities of wild-type FOXL2 and the adult-type granulosa cell tumor-associated mutant FOXL2 (C134W)". Oncogene. 30 (14): 1653–1663....

(BRWS1) ACTG1 AD Baraitser–Winter syndrome 2 (BRWS2) unknown Biemond syndrome FOXL2 AD Blepharophimosis, ptosis, epicanthus inversus syndrome (BPES) SMCHD1...

determination, females have upregulated female-specific genes, figla and foxl2, and downregulation of the male-specific genes, dmrt1 and amh, under both...

Cao A, Pilia G (Feb 2001). "The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome". Nat...

spans 2,307 base pairs. Other genes in the neighborhood include: FOXL2NB, FOXL2, PRR23B, and PRR23C. The FOXL2NB gene has tissue enriched expression in...