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anti-Human FOXF1 Anticorps:
anti-Mouse (Murine) FOXF1 Anticorps:
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Cow (Bovine) Polyclonal FOXF1 Primary Antibody pour 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. dans 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 (Montrer GNAS Anticorps), FOXF1, CREB1 (Montrer CREB1 Anticorps), and phosphorylated CREB1 (Montrer CREB1 Anticorps) 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 (Montrer WNT5A Anticorps)/beta-Catenin (Montrer CTNNB1 Anticorps) signaling pathway, and suppresses GC cell apoptosis through MYOD1 (Montrer MYOD1 Anticorps)-mediated Caspase-3 (Montrer CASP3 Anticorps) signaling pathway.
Results show that FoxF1 increases invasiveness of breast cancer cells by upregulating LOX (Montrer LOX Anticorps).
we provide supportive evidence that genetic variants at FOXP1 (Montrer FOXP1 Anticorps), BARX1 (Montrer BARX1 Anticorps), and FOXF1 confer risk for the development of EAC (Montrer CYLD Anticorps).
Point mutations of FOXF1 gene is associated with alveolar capillary dysplasia.
Targeted Resequencing of 29 Candidate Genes and Mouse Expression Studies Implicate ZIC3 (Montrer ZIC3 Anticorps) 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 (Montrer CDKN1A Anticorps)-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 (Montrer GUSB Anticorps).
Expression of Bmp4 (Montrer BMP4 Anticorps) in the ureteric mesenchyme depends on HH signaling and Foxf1, and that exogenous BMP4 (Montrer BMP4 Anticorps) rescued cell proliferation and epithelial differentiation in ureters with abrogated HH signaling or FOXF1 function.
The Gli (Montrer GLI1 Anticorps) increased the activity of one of these long-range enhancers, which was specific to distal blood vessel, suggesting that Shh (Montrer SHH Anticorps) 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 (Montrer S1PR1 Anticorps)).
novel Shh (Montrer SHH Anticorps)-Foxf-Fgf18 (Montrer FGF18 Anticorps)-Shh (Montrer SHH Anticorps) circuit in the palate development molecular network, in which Foxf1 and Foxf2 (Montrer FOXF2 Anticorps) regulate palatal shelf growth downstream of Shh (Montrer SHH Anticorps) signaling, at least in part, by repressing Fgf18 (Montrer FGF18 Anticorps) 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 (Montrer FUT1 Anticorps)-specific delivery of therapeutic RNA
Our findings implicate Foxf genes(Foxf1a and Foxf2 (Montrer FOXF2 Anticorps) ) in atrioventricular septation, describe the molecular underpinnings of the genetic interaction between Hedgehog (Montrer SHH Anticorps) signaling and Tbx5 (Montrer TBX5 Anticorps)
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 (Montrer SHH Anticorps) 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