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instructive input of Frizzled-Planar cell polarity (Fz/PCP (show PRCP ELISA Kits)) signalling into polarized centriole positioning in Drosophila wings, is reported.
Studies indicate that Frizzled (Fz) is constitutively ubiquitinated and internalized to the early endosome.
We found no evidence for an essential requirement of the Fz C-terminal tail downstream of the KTxxxW motif in planar polarity and canonical Wnt (show WNT4 ELISA Kits) signaling.
Frizzled-dependent planar polarity pathway locally promotes E-cadherin (show CDH1 ELISA Kits) turnover via recruitment of RhoGEF2.
Dissecting the molecular bridges that mediate the function of Frizzled in planar cell polarity.
Frizzled and Dishevelled (show DVL2 ELISA Kits) are enriched at distal sides of each cell and hence localize at the interface with ligand-expressing cells in the non-responding cells.
Knockdown of Tc-fz1 (show FZD4 ELISA Kits) 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 (show FZD2 ELISA Kits) or Tc-fz4 (show FZD4 ELISA Kits) RNAi knockdowns.
Results describe a Frizzled-Dishevelled (show DVL2 ELISA Kits)-NuMA (show NUMA1 ELISA Kits)/Mud (show AP5M1 ELISA Kits) pathway that orients division from Drosophila to vertebrates.
dAbl positively regulates the Fz/Dishevelled (Dsh (show DVL2 ELISA Kits)) PCP (show PRCP ELISA Kits) pathway without affecting canonical Wnt/Wg-Fz signaling
A balance of ubiquitylation and deubiquitylation of the Wg/Wnt receptor Frizzled determines the cellular responsiveness to Wg/Wnt both in mammalian cells and in Drosophila.
aken together, our results suggest that Sp1 (show PSG1 ELISA Kits) plays a role in human osteoblast differentiation and mineralization, which is at least partially mediated by Sp1 (show PSG1 ELISA Kits)-dependent transactivation of FZD1.
The amplification of miR (show MLXIP ELISA Kits)-135b suppressed non-small cell lung cancer chemoresistance by directly mediating FZD1 down-regulation.
Our study suggests that Sox9 (show SOX9 ELISA Kits) siRNA inhibits the proliferation capability of human osteosarcoma cells by down-regulating the expression of Wnt1 (show WNT1 ELISA Kits) and its receptor Fzd1
FZD1 expression was down-regulated by AP2 (show GTF3A ELISA Kits) expression and mediated osteoblast differentiation and mineralization.
our data demonstrate that FZD1 regulates PKCdelta (show PKCd ELISA Kits), and the PKCdelta (show PKCd ELISA Kits)/AP-1 (show FOSB ELISA Kits) signalling transduction pathway plays an important role in drug resistance in MES (show ME1 ELISA Kits)-SA/Dx5 (show ITGA2 ELISA Kits) cells.
Polymorphisms in several genes involved in the Wnt (show WNT2 ELISA Kits) signaling pathway were associated with hepatic fibrosis or inflammation risk in HCV-infected males.
ACE2 (show ACE2 ELISA Kits) and FZD1 are prognosis markers in squamous cell/adenosquamous carcinoma and adenocarcinoma of gallbladder.
Experiments demonstrate a role of E2F1 (show E2F1 ELISA Kits) in osteoblast differentiation and mineralization and suggest that FZD1 is required, in part, for E2F1 (show E2F1 ELISA Kits) regulation of osteoblast mineralization.
Fz1 (show FZD4 ELISA Kits) is a Wnt (show WNT2 ELISA Kits) responsive gene in colon-derived tissues. Fz1 (show FZD4 ELISA Kits) expression exhibited increased expression in normal mucosa only in close proximity to colon cancer
FZD1 appears to mediate multidrug resistance by regulating the Wnt (show WNT2 ELISA Kits)/beta-catenin (show CTNNB1 ELISA Kits) pathway
FZD1 regulates specific stages of adult hippocampal neurogenesis.
Suppressed expression of Fzd1 in myogenic cells from aged mice results in a significant increase in myogenic differentiation, and its forced expression in those from young mice results in its drastic inhibition.
The results indicate the involvement of Wnt1 (show WNT1 ELISA Kits) and Fzd1 in the pathogenesis and development of amyotrophic lateral sclerosis.
Wnt (show WNT2 ELISA Kits)/Fzd signaling is involved in balancing the inflammatory response to microbial stimulation of innate immune cells of vertebrate origin
Frizzled signaling is involved in diverse tissue closure processes, defects in which account for some of the most common congenital anomalies.
Indicate that myofibroblast migration and differentiation are modulated via Wnt (show WNT2 ELISA Kits)/Fzd signalling.
Fz-1 is expressed at distinct stages of follicular development.
Direct interaction of Frizzled-1, -2, -4, and -7 with PDZ domains of PSD-95. "FZ-2, Fz-4, Fz-7"
Frizzled-1 is an antagonist of the canonical Wnt (show WNT2 ELISA Kits)/beta-catenin (show CTNNB1 ELISA Kits) signaling pathway
Data demonstrate that Wnt7b (show WNT7B ELISA Kits) signals through Fzd1 and -10 and LRP5 (show LRP5 ELISA Kits) and implicate these Wnt (show WNT2 ELISA Kits) coreceptors in the regulation of lung airway and vascular development.
Receptor for Wnt proteins. Most of frizzled receptors are coupled to the beta-catenin canonical signaling pathway, which leads to the activation of disheveled proteins, inhibition of GSK- 3 kinase, nuclear accumulation of beta-catenin and activation of Wnt target genes. A second signaling pathway involving PKC and calcium fluxes has been seen for some family members, but it is not yet clear if it represents a distinct pathway or if it can be integrated in the canonical pathway, as PKC seems to be required for Wnt-mediated inactivation of GSK-3 kinase. Both pathways seem to involve interactions with G-proteins. May be involved in transduction and intercellular transmission of polarity information during tissue morphogenesis and/or in differentiated tissues. Activated by Wnt3A, Wnt3, Wnt1 and to a lesser extent Wnt2, but not by Wnt4, Wnt5A, Wnt5B, Wnt6, Wnt7A or Wnt7B.
, frizzled 1
, frizzled 1, seven transmembrane spanning receptor
, frizzled homolog 1
, Wnt receptor
, frizzled, Drosophila, homolog of, 1
, 7-transmembrane protein frizzled-1
, Drosophila polarity gene (frizzled) homologue
, Drosophila polarity gene homolog 1
, 7-transmembrane receptor frizzled-1