Results 81 to 90 of about 5,621 (166)
FOXL2, GATA4, and SMAD3 interaction in the transcription complex.
Both COS-7 and COV434 cells were transfected for 48 h. All cell lysates were immunoprecipitated using V5 epitope. A) COS-7 cells transfected with V5 tagged GATA4, V5 or GFP tagged wild type (WT) FOXL2 or SMAD3 overexpression vectors as indicated.
David L'Hôte (197958) +9 more
core +1 more source
FOXL2 drives the differentiation of supporting gonadal cells in early ovarian development
Background Forkhead box L2 (FOXL2) is a transcription factor from the forkhead box family primarily expressed in the pituitary, ovaries, and eyelids. Human mutations in FOXL2 cause blepharophimosis, ptosis, epicanthus and inversus syndrome (BPES), which ...
Laura Danti +4 more
doaj +1 more source
Asia arowana (Scleropages formosus) is an ornamental fish with high economic value, while its sex determination mechanism is still poorly understood. By far, no morphological evidence or molecular marker has been developed for effective distinguishment ...
Chenxi Zhao +9 more
doaj +1 more source
FOXL2 functions in endometrial physiology in cattle
L'implantation est une étape cruciale de la gestation et du développement post-natal chez les mammifères. L'implantation est définie comme l'établissement d'interactions cellulaires et permanentes entre un endomètre réceptif et un embryon compétent et ...
Lesage, Audrey
core
The study focuses on the critically endangered Dabry’s sturgeon (Acipenser dabryanus), a species on the brink of extinction in the wild. This research investigates the role of the Forkhead box protein L2 (foxl2) in the gonadal development and ...
Yacheng Hu +31 more
doaj +1 more source
BackgroundThe somatic mutation in the FOXL2 gene c.402C>G (p.Cys134Trp) has recently been identified in the vast majority of adult ovarian granulosa cell tumors (OGCTs) studied. In addition, this mutation seems to be specific to adult OGCTs and is likely
Bérénice A Benayoun +11 more
doaj +1 more source
Hypopituitarism in Patients with Blepharophimosis and FOXL2 Mutations
International audienceBackground: FOXL2 is the gene involved in blepharophimosis, ptosis, and epicanthus inversus syndrome (BPES). There have been few single case reports of growth hormone deficiency (GHD) with this syndrome, and Foxl2 is known to be ...
Roucher-Boulez, Florence +12 more
core +1 more source
Novel action of FOXL2 as mediator of Col1a2 gene autoregulation
FOXL2 belongs to the evolutionarily conserved forkhead box (FOX) superfamily and is a master transcription factor in a spectrum of developmental pathways, including ovarian and eyelid development and bone, cartilage and uterine maturation. To analyse its
Marcia, Loredana +13 more
core +1 more source
Wt FOXL2 reduces viable cell number, and GATA4 protects GCT cells from wt FOXL2 induced apoptosis.
KGN cells were transfected with wild type FOXL2, C134W mutated FOXL2, GATA4, and SMAD3 expression plasmids. A) The cell viability was measured 48 h after transfection. B) The activated caspase 3/7 was measured 24 h after transfection.
David L'Hôte (197958) +9 more
core +1 more source
The proportion of FOXL2-positive cells in cancer stroma.
The proportion of FOXL2-positive cells on each tissue section was scored using 5-tired scale and the results were plotted. High percentages of cancer stromal cells were FOXL2-positive in the ovary, whereas there were almost no FOXL2-positive cells ...
Aye Moh-Moh-Aung (5844032) +5 more
core +1 more source

