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In this paper we report 3 further families with mutations in FZD6 causing Isolated recessive nail (zeige CD244 Proteine) dysplasia.
monomeric rather than dimeric form is active signal initiating unit of the receptor complex; constitutive signaling to ERK1/2 can be affected by modulating the dimeric status
the FZD6-fibronectin actin axis identified in our study could be exploited for drug development in highly metastatic forms of breast cancer
we found that FZD6 expression was negatively regulated by miR199a5p
The rs3808553 of FZD6 is obviously associated with neural tube defects in Han population of northern China
This study confirms our speculation that down-regulation of FZD6 by beta-Carotene is causally related to the observed up-regulation of cancer related genes
DVL is a master regulator of FZD6/G-protein signaling
FZD6 should be screened for pachyonychia congenita as it is a candidate gene for hereditary nail (zeige CD244 Proteine) dysplasias.
sequence analysis revealed a novel homozygous missense mutation (c.1266G>A; p.Gly422Asp) located in the transmembrane domain of the protein FZD6 in individuals of a consanguineous family exhibiting features of nail (zeige CD244 Proteine) dysplasia
The present results emphasize the role of FZD6 mutation in Wnt (zeige WNT2 Proteine) pathways in nail (zeige CD244 Proteine) development.
Fzd4 (zeige FZD4 Proteine) and Fzd6 genes have a deep patterning effect on arterial vessel morphogenesis that may determine its functional efficiency
Eliminating Fz6 in most hair follicle cells or in the inter-follicular epidermis at E15.5 suggests that planar cell polarity signaling in developing follicles is not required to maintain their orientation.
Data show that Wnt receptor, Frizzled-6 (Fzd6) -/- hematopoietic stem/progenitor cell (HSPC (zeige PSMA7 Proteine)) exhibit poor emergency hematopoiesis.
Fz3 (zeige FZD3 Proteine) and Fz6 have partly interchangeable roles in tissue polarity signaling for epithelial orientation and axon growth and guidance
Fzd6-mediated Wnt (zeige WNT2 Proteine) signaling likely regulates the overall differentiation process of nail (zeige CD244 Proteine)/claw formation.
Our results support a role of miR (zeige MLXIP Proteine)-194 in liver tumorigenesis through its endogenous target Fzd6.
FZD6 mutations can result in severe defects in nail (zeige CD244 Proteine) and claw formation through reduced or abolished membranous FZD(6) levels and several nonfunctional WNT (zeige WNT2 Proteine)-FZD pathways.
The time course of local hair follicle refinement and the resulting evolution of a montage of competing patterns in Fz6(-/-) skin, is defined.
Downregulated by dietary beta-carotene in lungs of knockout Bcmo1 (zeige BCMO1 Proteine)-deficient mice.
This gene represents a member of the 'frizzled' gene family, which encode 7-transmembrane domain proteins that are receptors for Wnt signaling proteins. The protein encoded by this family member contains a signal peptide, a cysteine-rich domain in the N-terminal extracellular region, and seven transmembrane domains, but unlike other family members, this protein does not contain a C-terminal PDZ domain-binding motif. This protein functions as a negative regulator of the canonical Wnt/beta-catenin signaling cascade, thereby inhibiting the processes that trigger oncogenic transformation, cell proliferation, and inhibition of apoptosis. Alternative splicing results in multiple transcript variants, some of which do not encode a protein with a predicted signal peptide.
, frizzled homolog 6
, frizzled 6
, frizzled 6, seven transmembrane spanning receptor
, seven transmembrane helix receptor
, involved in Wnt signaling, encoding a Wnt receptor