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anti-Human FZD4 Anticorps:
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Human Monoclonal FZD4 Primary Antibody pour IHC (fro), FACS - ABIN2689205
Ells, Guernsey, Wallace, Zheng, Vincer, Allen, Ingram, DaSilva, Siebert, Sheidow, Beis, Robitaille: Severe retinopathy of prematurity associated with FZD4 mutations. dans Ophthalmic genetics 2010
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Cow (Bovine) Polyclonal FZD4 Primary Antibody pour IHC, WB - ABIN2776715
Dufourcq, Leroux, Ezan, Descamps, Lamazière, Costet, Basoni, Moreau, Deutsch, Couffinhal, Duplàa: Regulation of endothelial cell cytoskeletal reorganization by a secreted frizzled-related protein-1 and frizzled 4- and frizzled 7-dependent pathway: role in neovessel formation. dans The American journal of pathology 2008
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Human Monoclonal FZD4 Primary Antibody pour CyTOF, FACS - ABIN4900304
Baksh, Boland, Tuan: Cross-talk between Wnt signaling pathways in human mesenchymal stem cells leads to functional antagonism during osteogenic differentiation. dans Journal of cellular biochemistry 2007
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Human Polyclonal FZD4 Primary Antibody pour ELISA, WB - ABIN408660
You, Nguyen, Albers, Lin, Holcombe: Wnt pathway-related gene expression in inflammatory bowel disease. dans Digestive diseases and sciences 2008
Human Monoclonal FZD4 Primary Antibody pour FACS, ICC - ABIN4898976
Despeaux, Chicanne, Rouer, De Toni-Costes, Bertrand, Mansat-De Mas, Vergnolle, Eaves, Payrastre, Girault, Racaud-Sultan: Focal adhesion kinase splice variants maintain primitive acute myeloid leukemia cells through altered Wnt signaling. dans Stem cells (Dayton, Ohio) 2012
Knockdown of Tc-fz1 alone interfered with the formation of the proximo-distal and the dorso-ventral axes during leg development, whereas no effect was observed with single Tc-fz2 (Montrer FZD2 Anticorps) or Tc-fz4 RNAi knockdowns.
This is the first study to report a group of patients with digenic familial exudative vitreoretinopathy (FEVR (Montrer NDP Anticorps)). In most affected eyes, the stage was more severe than stage 3. We speculate that the phenotype of FEVR (Montrer NDP Anticorps) is more severe in patients with digenic rather than monogenic variants of FEVR (Montrer NDP Anticorps)-related genes.
FzM1.8 is an allosteric agonist of FZD4. In the absence of any WNT (Montrer WNT2 Anticorps) ligand, FzM1.8 binds to FZD4, promotes recruitment of heterotrimeric G proteins, and biases WNT (Montrer WNT2 Anticorps) signaling toward a noncanonical route that involves PI3K (Montrer PIK3CA Anticorps). In colon cancer cells, the FZD4/PI3K (Montrer PIK3CA Anticorps) axis elicited by FzM1.8 preserves stemness and promotes proliferation of undifferentiated cells.
FZD4 Tyrosine 250(2.39) is crucial for DVL2 (Montrer DVL2 Anticorps) interaction and DVL2 (Montrer DVL2 Anticorps) translocation to the plasma membrane.
Accessory proteins in Frizzled (FZD) receptor complexes are thought to determine ligand selectivity and signaling amplitude.
FZD4 was confirmed to be a downstream target of miR (Montrer MLXIP Anticorps)-505, and found to be up-regulated in cervical cancer patients.
The screening of candidate genes namely NDP (Montrer NDP Anticorps), FZD4 and TSPAN12 (Montrer TSPAN12 Anticorps) led to the identification of six major coding region variants in 36 ROP (Montrer STXBP1 Anticorps) probands.
Seven novel mutations found in this study have broadened the spectrum of mutations in FZD4 known to cause familial exudative vitreoretinopathy (FEVR (Montrer NDP Anticorps)), providing a deeper understanding of this disease. The results show that mutations in FZD4 are associated with the phenotypes of retinal folds or ectopic macula in FEVR (Montrer NDP Anticorps)
Three affected individuals within a family with FEVR (Montrer NDP Anticorps) presented with variable disease severity. All three affected family members harboured mutation c.349T>C (p.Cys117Arg) in FZD4.
The findings in this family support the concept that some mutated FZD4 alleles can be associated with recessive rather than dominant disease.
novel role of let-7b/Fzd4 axis through wnt (Montrer WNT2 Anticorps) signaling
Hnf1beta (Montrer HNF1B Anticorps) and Fzd4/Fzd4s appear to be involved in pre-patterning events of the embryonic endoderm that allow pancreas formation in Xenopus.
A splice variant of the Frizzled-4 receptor modulates Wnt (Montrer WNT2 Anticorps) signalling in a dose-dependent, biphasic manner.
results provide functional and biochemical dissection of Fzd4 in Norrin (Montrer NDP Anticorps) signaling.
FZD4 was upregulated during cyclic mechanical stretch (CMS (Montrer Cd2ap Anticorps))-induced osteogenic differentiation, and the JNK (Montrer MAPK8 Anticorps) signalling pathway was activated. FZD4 knockdown inhibited the mechanical stimuli-induced osteogenesis and JNK (Montrer MAPK8 Anticorps) activity.
These data expose a stromal component that regulates the earliest stages of tumorigenesis in the cerebellum, and a novel role for the Norrin (Montrer NDP Anticorps)/Fzd4 axis as an endogenous anti-tumor signal in the preneoplastic niche.
Fzd4 and Fzd6 (Montrer FZD6 Anticorps) genes have a deep patterning effect on arterial vessel morphogenesis that may determine its functional efficiency
Study identified a novel Wnt5a (Montrer WNT5A Anticorps)/Fzd4 signaling pathway that contributes to the regulation of dendrite morphogenesis
These results question the conclusion that a dominant-negative mechanism would explain the dominance of the mutant L501fsX533 Fz4 allele in the transmission of a form of Familial exudative vitreoretinopathy.
The data reveal both cell-autonomous and cell-nonautonomous effects, and they imply a central role for Norrin (Montrer NDP Anticorps)/Fz4 signaling in central nervous system vascular development and in the maintenance of the blood brain barrier/blood retina barrier state.
Frizzled 4 regulates arterial network organization through noncanonical Wnt (Montrer WNT2 Anticorps)/planar cell polarity signaling.
Frizzled4 wnt (Montrer WNT2 Anticorps) receptors are significantly increased in pathological neovascularization in a mouse model of oxygen-induced proliferative retinopathy.
targeted inactivation of the TSK (Montrer FBN1 Anticorps) gene in mice causes expansion of the ciliary body and up-regulation of Wnt2b (Montrer WNT2B Anticorps) and Fzd4 expression in the developing peripheral eye
This gene is a member of the frizzled gene family. Members of this family encode seven-transmembrane domain proteins that are receptors for the Wingless type MMTV integration site family of signaling proteins. Most frizzled receptors are coupled to the beta-catenin canonical signaling pathway. This protein may play a role as a positive regulator of the Wingless type MMTV integration site signaling pathway. A transcript variant retaining intronic sequence and encoding a shorter isoform has been described, however, its expression is not supported by other experimental evidence.
, frizzled homolog 1
, frizzled homolog 4
, WNT receptor frizzled-4
, frizzled 4, seven transmembrane spanning receptor
, frizzled receptor 4
, frizzled 4 protein