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抗Human FOXF1 抗体:
抗Mouse (Murine) FOXF1 抗体:
抗Rat (Rattus) FOXF1 抗体:
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
Show all 3 Pubmed References
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 (显示 GNAS 抗体), FOXF1, CREB1 (显示 CREB1 抗体), and phosphorylated CREB1 (显示 CREB1 抗体) 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 (显示 WNT5A 抗体)/beta-Catenin (显示 CTNNB1 抗体) signaling pathway, and suppresses GC cell apoptosis through MYOD1 (显示 MYOD1 抗体)-mediated Caspase-3 (显示 CASP3 抗体) signaling pathway.
Results show that FoxF1 increases invasiveness of breast cancer cells by upregulating LOX (显示 LOX 抗体).
we provide supportive evidence that genetic variants at FOXP1 (显示 FOXP1 抗体), BARX1 (显示 BARX1 抗体), and FOXF1 confer risk for the development of EAC (显示 CYLD 抗体).
Point mutations of FOXF1 gene is associated with alveolar capillary dysplasia.
Targeted Resequencing of 29 Candidate Genes and Mouse Expression Studies Implicate ZIC3 (显示 ZIC3 抗体) and FOXF1 in Human VATER/VACTERL Association
FOXF1 inhibits hematopoietic lineage commitment during early mesoderm specification.
FOXF1 behaved not only as a reprogramming regulator that mediates stemness but also as a putative tumor suppressor that contributes to p21 (显示 CDKN1A 抗体)-regulated growth suppression during fusion process
Results provide support for the function of FoxF1 in the development of visceral mesoderm and the organogenesis of the gut (显示 GUSB 抗体).
Expression of Bmp4 (显示 BMP4 抗体) in the ureteric mesenchyme depends on HH signaling and Foxf1, and that exogenous BMP4 (显示 BMP4 抗体) rescued cell proliferation and epithelial differentiation in ureters with abrogated HH signaling or FOXF1 function.
The Gli (显示 GLI1 抗体) increased the activity of one of these long-range enhancers, which was specific to distal blood vessel, suggesting that Shh (显示 SHH 抗体) 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 (显示 S1PR1 抗体)).
novel Shh (显示 SHH 抗体)-Foxf-Fgf18 (显示 FGF18 抗体)-Shh (显示 SHH 抗体) circuit in the palate development molecular network, in which Foxf1 and Foxf2 (显示 FOXF2 抗体) regulate palatal shelf growth downstream of Shh (显示 SHH 抗体) signaling, at least in part, by repressing Fgf18 (显示 FGF18 抗体) 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 (显示 FUT1 抗体)-specific delivery of therapeutic RNA
Our findings implicate Foxf genes(Foxf1a and Foxf2 (显示 FOXF2 抗体) ) in atrioventricular septation, describe the molecular underpinnings of the genetic interaction between Hedgehog (显示 SHH 抗体) signaling and Tbx5 (显示 TBX5 抗体)
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 (显示 SHH 抗体) and mesenchymal Foxf1 genes expression were preserved around the hindgut cystic malformation.
Foxf1 also directly binds to serum response factor (SRF) and myocardin-related transcription factors (MRTFs).
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