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anti-Human FOXF1 Antibodies:
anti-Mouse (Murine) FOXF1 Antibodies:
anti-Rat (Rattus) FOXF1 Antibodies:
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Cow (Bovine) Polyclonal FOXF1 Primary Antibody for IHC, WB - ABIN2779550
Mahlapuu, Pelto-Huikko, Aitola, Enerbäck, Carlsson: FREAC-1 contains a cell-type-specific transcriptional activation domain and is expressed in epithelial-mesenchymal interfaces. in Developmental biology 1998
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FOXF1 promotes prostate tumor growth and progression by activating ERK5 (show MAPK7 Antibodies) signaling
the R139Q substitution in FOXF1 causes infantile hypertrophic pyloric stenosis in a family and implies a novel pathological pathway for the condition
Single-nucleotide polymorphisms FOXF1 rs9936833 and MHC rs9257809 remained significantly associated with presence of gastroesophageal acid reflux. The association for risk allele C in FOXF1 rs9936833 and risk allele A in MHC rs9257809 with the presence of acid reflux suggests a potential pathophysiologic mechanism for the role of genetic influences in Barret Esophagus development.
FOXF1 mutations may have an extremely variable phenotype, possibly as a result of somatic mosaicism and complex gene regulation.
There were decreased levels of Gsa (show GNAS Antibodies), FOXF1, CREB1 (show CREB1 Antibodies), and phosphorylated CREB1 (show CREB1 Antibodies) proteins in intestinal muscle layers of patients with chronic intestinal pseudo-obstruction, compared with tissues from controls.
Data show that MeCP2 promotes gastric cancer (GC) cell proliferation via FOXF1-mediated Wnt5a (show WNT5A Antibodies)/beta-Catenin (show CTNNB1 Antibodies) signaling pathway, and suppresses GC cell apoptosis through MYOD1 (show MYOD1 Antibodies)-mediated Caspase-3 (show CASP3 Antibodies) signaling pathway.
Results show that FoxF1 increases invasiveness of breast cancer cells by upregulating LOX (show LOX Antibodies).
we provide supportive evidence that genetic variants at FOXP1 (show FOXP1 Antibodies), BARX1 (show BARX1 Antibodies), and FOXF1 confer risk for the development of EAC (show CYLD Antibodies).
Point mutations of FOXF1 gene is associated with alveolar capillary dysplasia.
Targeted Resequencing of 29 Candidate Genes and Mouse Expression Studies Implicate ZIC3 (show ZIC3 Antibodies) and FOXF1 in Human VATER/VACTERL Association
Results provide support for the function of FoxF1 in the development of visceral mesoderm and the organogenesis of the gut (show GUSB Antibodies).
Expression of Bmp4 (show BMP4 Antibodies) in the ureteric mesenchyme depends on HH signaling and Foxf1, and that exogenous BMP4 (show BMP4 Antibodies) rescued cell proliferation and epithelial differentiation in ureters with abrogated HH signaling or FOXF1 function.
The Gli (show GLI1 Antibodies) increased the activity of one of these long-range enhancers, which was specific to distal blood vessel, suggesting that Shh (show SHH Antibodies) regulates Foxf1 transcription in pulmonary distal blood vessel formation.
Data indicate that forkhead box F1 (Foxf1) deletion from endothelial cells decreases the abundance of sphingosine 1-phosphate receptor 1 (S1PR1 (show S1PR1 Antibodies)).
novel Shh (show SHH Antibodies)-Foxf-Fgf18 (show FGF18 Antibodies)-Shh (show SHH Antibodies) circuit in the palate development molecular network, in which Foxf1 and Foxf2 (show FOXF2 Antibodies) regulate palatal shelf growth downstream of Shh (show SHH Antibodies) signaling, at least in part, by repressing Fgf18 (show FGF18 Antibodies) expression
findings suggest that Foxf1 may serve as a target gene to disrupt progression of liver fibrosis and DBTC might provide a potentially feasible and effective tool for HSC (show FUT1 Antibodies)-specific delivery of therapeutic RNA
Our findings implicate Foxf genes(Foxf1a and Foxf2 (show FOXF2 Antibodies) ) in atrioventricular septation, describe the molecular underpinnings of the genetic interaction between Hedgehog (show SHH Antibodies) signaling and Tbx5 (show TBX5 Antibodies)
Data indicate FOXF1 transcription factor is required for the formation of embryonic vasculature by regulating endothelial genes critical for vascular development and vascular endothelial growth factor signaling.
Endodermal Shh (show SHH Antibodies) and mesenchymal Foxf1 genes expression were preserved around the hindgut cystic malformation.
This gene belongs to the forkhead family of transcription factors which is characterized by a distinct forkhead domain. The specific function of this gene has not yet been determined\; however, it may play a role in the regulation of pulmonary genes as well as embryonic development.
forkhead box F1
, forkhead box protein F1
, forkhead box F protein
, Forkhead, drosophila, homolog-like 5
, forkhead-related activator 1
, forkhead-related protein FKHL5
, forkhead-related transcription factor 1
, fork head domain-related protein 13
, forkhead box protein F1-A
, forkhead transcription factor
, HNF-3/forkhead homolog 8
, forkhead box F1a
, hepatocyte nuclear factor 3 forkhead homolog 8
, HNF-3/fork-head homolog-5 (HFH-5)
, forkhead box protein I2
, hepatocyte nuclear factor 3 forkhead homolog 5