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SOSTDC1 is a member of the sclerostin family and encodes an N-glycosylated, secreted protein with a C-terminal cystine knot-like domain. Additionally we are shipping SOSTDC1 Antibodies (47) and SOSTDC1 Kits (22) and many more products for this protein.
Showing 8 out of 9 products:
Human SOSTDC1 Protein expressed in Wheat germ - ABIN1320977
Lee, Miyazawa, Shin, Kwon, Kang, Choi, Lee, Kondo, Cho, Jung: Shh signaling is essential for rugae morphogenesis in mice. in Histochemistry and cell biology 2011
Down-regulation of SOSTDC1 promotes thyroid cancer cell proliferation via regulating cyclin A2 (show CCNA2 Proteins) and cyclin E2 (show CCNE2 Proteins).
Results conclude that the transcriptional repressor E4BP4 (show NFIL3 Proteins) plays a role in repressing epigenetically regulated SOSTDC1 expression in breast cancer cells, which can be reverted by E4BP4 (show NFIL3 Proteins) silencing.
Epigenetic silencing of SOSTDC1 through methylation is increased in prostate cancer and is associated with accelerated disease progression in patients with prostate cancer
Unliganded VDR (show CYP27B1 Proteins) upregulates the expression of hairless, the gene product of which acts as a downstream comodulator to feedback-repress DKKL1 and SOSTDC1.
DNA methylation (show HELLS Proteins) is involved in the down-regulation of SOSTDC1 expression in gastric cancer.
SOSTDC1 is expressed in normal breast tissue and this expression is reduced in breast cancer.
Results indicate for the first time that the genetic polymorphisms in SOSTDC1 have an effect on attainment and maintenance of peak bone mass in Chinese women.
genetic aberrations near SOSTDC1 are not uncommon in renal cancer, and occur in adult as well as pediatric renal tumors.
Data suggest that ectodin is a novel bone morphogenetic protein (BMP) inhibitor which integrates BMP signaling with the SHH and FGF signal pathways
USAG1 is expressed in the kidney and functions as a bone morphogenetic protein antagonist.
suggest that RUNX2 (show RUNX2 Proteins) and USAG-1 act in an antagonistic manner
the in vivo inter-relationships between Bmp7 (show BMP7 Proteins) and Usag-1, was examined.
Findings strongly suggest that Wise and Sost (show SOST Proteins) are key modulators of bone development through the ability of their encoded proteins to interact with Lrp5 (show LRP5 Proteins) and control the balance or levels of Wnt (show WNT2 Proteins) signaling.
Interactions between BMP-7 (show BMP7 Proteins) and USAG-1 (uterine sensitization-associated gene-1) regulate supernumerary organ formations
Sost (show SOST Proteins) and its paralog Sostdc1 coordinate digit number in a Gli3 (show GLI3 Proteins)-dependent manner.
Wise controls the number and distribution of the mammary epithelial cells via inhibition of Wnt (show WNT2 Proteins)/beta-catenin (show CTNNB1 Proteins) signaling.
Data suggest that Sostdc1 primarily regulates bone morphogenetic protein pathway in pancreatic islets; knockout/mutation of Sostdc1 enhances down-regulation of Ctgf (connective tissue growth factor (show CTGF Proteins)) and gremlin (show GREM1 Proteins) in islets after high-fat diet.
The data demonstrate that simvastatin contributes to prevent the progression of renal fibrosis by upregulating BMP-7 (show BMP7 Proteins)-mediated anti-fibrotic signaling and that one aspect of crucial efficacies is achieved by regulating HOXA13 (show HOXA13 Proteins) and USAG-1.
The data suggested that functions of Sostdc1 can be largely attributed to its ability to attenuate Wnt (show WNT2 Proteins)/beta-catenin (show CTNNB1 Proteins) signaling.
We propose a new reaction-diffusion model in which Wnt (show WNT2 Proteins), Shh (show SHH Proteins) and Sostdc1 act as the activator, mediator and inhibitor, respectively, and confirm that such interactions can generate the tooth pattern of a wild-type mouse.
This gene is a member of the sclerostin family and encodes an N-glycosylated, secreted protein with a C-terminal cystine knot-like domain. This protein functions as a bone morphogenetic protein (BMP) antagonist. Specifically, it directly associates with BMPs, prohibiting them from binding their receptors, thereby regulating BMP signaling during cellular proliferation, differentiation, and programmed cell death.
sclerostin domain containing 1
, sclerostin domain-containing protein 1
, Sclerostin domain-containing protein 1
, uterine sensitization-associated gene 1 protein
, wnt-signaling modulator
, cystine-knot containing secreted protein
, ectodermal BMP inhibitor
, uterine sensitization-associated protein-1
, sclerostin-like protein
, uterine sensitization-associated protein 1
, context-dependent activator and inhibitor of Wnt signalling protein Wise