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an inverse septal-to-temporal increase in the expression of sfrp3 that emerges during postnatal development, is reported.
The spatiotemporally dynamic expression ofsFRP3 strongly suggests that sFRP3 has potential functions in the sensory neuron genesis and sensory circuitry formation.
Our results suggest that FrzB may have a protective role on cartilage degradation and matrix metalloproteinase (show MMP20 ELISA Kits) induction in mouse chondrocytes
left ventricles from post-MI mice showed an increased sFRP3 mRNA level, particularly in cardiac fibroblasts, and (iv) mechanical stretch enhanced sFRP3 expression and release in myocardial fibroblasts
Secreted frizzled-related protein 3 (sFRP3) regulates antidepressant responses in mice.
Study identifies sFRP3 as an inhibitory niche factor from local mature dentate granule neurons that regulates multiple phases of adult hippocampal neurogenesis.
Data indicate an important role for frizzled-related protein (Frzb) in joint homeostasis and highlight the complex biology of WNT (show WNT2 ELISA Kits) signaling in the joint.
Secreted Frizzled-related proteins (sFrps) are expressed in the postnatal cerebral cortex in regional and lamina patterns in the major subdivisions of the cerebral cortex: the olfactory bulb, the hippocampal formation, and the neocortex.
sFRP3 may stimulate differentiation through a beta (show SUCLA2 ELISA Kits)-catenin (show CTNNB1 ELISA Kits)-independent pathway in addition to its previously known function as a decoy receptor for Wnt's
Loss of Frzb may contribute to cartilage damage by increasing the expression and activity of MMPs, in a WNT (show WNT2 ELISA Kits)-dependent and WNT (show WNT2 ELISA Kits)-independent manner. This may contribute to the development of osteoarthritis.
FRZB expression was up-regulated in hepatocellular carcinoma bone metastasis tissue, which suggested that FRZB might play a key role in the HCC (show FAM126A ELISA Kits) bone metastasis.
Positive expression of FRZB was statistically significantly associated with poor prognosis of patients with colon carcinoma hepatic metastasis.
Secreted Frizzled-Related Protein 3 (SFRP3) Is Required for Tumorigenesis of PAX3 (show PAX3 ELISA Kits)-FOXO1 (show FOXO1 ELISA Kits)-Positive Alveolar Rhabdomyosarcoma
Intermediate SFRP3 levels are associated with better survival and fewer cardiovascular events than low or high SFRP3 levels, independently of conventional risk factors, in older patients with chronic systolic Heart Failure of ischemic origin.
Intermediate levels of sFRP3 were a predictor of all-cause mortality and re-hospitalization in acute coronary syndromes.
Data suggest secreted FRP3 (frizzled related protein-3 (show HSPB3 ELISA Kits)) interacts with ADAM17 (show ADAM17 ELISA Kits) (A disintegrin/metalloprotease (show ADAM8 ELISA Kits) 17) substrate IL6R (interleukin-6 receptor (show IL6R ELISA Kits)) release; this interaction is down-regulated in osteoarthritis due to rare double variant in FRP3 (show FOLR2 ELISA Kits).
study indicates that increased expression of both SFRP1 (show SFRP1 ELISA Kits) and SFRP3 may contribute to the pathogenesis of IUGR placental dysfunction, whereas the loss of these proteins may be involved in the development of human trophoblastic tumors.
Our results suggest that the sFRP3 c.970C>G and sFRP4 (show SFRP4 ELISA Kits) c.958C>A polymorphisms may be genetic factors associated with the prevalence of osteoporosis at the femoral neck in postmenopausal Korean women.
Promoter hypermethylation of SFRP3 is a common event hepatocellular carcinoma.
FRZB knockdown may upregulate the Wnt/betacatenin pathway and promote aggressiveness in gastric cancer.
The protein encoded by this gene is a secreted protein that is involved in the regulation of bone development. Defects in this gene are a cause of female-specific osteoarthritis (OA) susceptibility.
frizzled-related protein 1
, secreted frizzled-related protein 3
, secreted frizzled-related sequence protein 3
, frizzled homolog-related