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This locus encodes the transforming growth factor (TGF)-beta type III receptor.
Showing 7 out of 10 products:
Inhibition of genes for betaglycan and FIBP (show FIBP Proteins) in granulosa cells in vitro suggests that they inhibit estradiol production in regressing subordinate follicles.
describe a detailed characterization of TbetaRIII expression in lymphocyte subpopulations demonstrating that this co-receptor is significantly expressed in T but not B lymphocytes and among them, preferentially expressed on naive and central memory T cells
TGF-beta (show TGFB1 Proteins) type I, II, and III receptors were all identified in pregnant serum; all were substantially elevated in early-onset but not late-onset PE. Endoglin (show ENG Proteins) was increased in both subtypes.
TGFBR3 and/or MGEA5 (show MGEA5 Proteins) rearrangements are much more common in hybrid hemosiderotic fibrolipomatous tumor-myxoinflammatory fibroblastic sarcomas than in classical myxoinflammatory fibroblastic sarcomas.
opposing functions for the different GAG modifications on TbetaRIII suggesting that Wnt (show WNT2 Proteins) interactions with the TbetaRIII heparan sulfate chains result in inhibition of Wnt (show WNT2 Proteins) signaling, likely via Wnt (show WNT2 Proteins) sequestration, whereas the chondroitin sulfate GAG chains on TbetaRIII promote Wnt3a (show WNT3A Proteins) signaling.
Results suggest that high expression levels of alpha-inhibin and beta-glycan transcripts in secretory phase endometrium are associated with a lower chance of achieving pregnancy with in vitro fertilization.
Results show decreased TbetaRIII expression with hepatocellullar carcinoma (HCC (show FAM126A Proteins)) progression leading to the activation of Smad2 (show SMAD2 Proteins) and suggest that TbetaRIII acts as a suppressive factor in regulating the migration and invasion of HCC (show FAM126A Proteins), by inhibiting Smad2 (show SMAD2 Proteins) and Akt (show AKT1 Proteins) pathways.
Study shows that TbetaRIII expression is significantly decreased in salivary glands adenoid cystic carcinoma (ACC) patients and defines TbetaRIII as a biomarker exerting antitumor action on ACC progression.
No correlation of loss of heterozygosity at the TGFBR3 locus with clinicopathological parameters suggests that allelic imbalance may be an early genetic event during neoplastic transformation of human endometrium.
Study shows that GDF10 (show GDF10 Proteins) is down-regulated in patients with oral squamous cell carcinoma, and is an independent risk factor for overall survival. Its expression is regulated by TGFBR3 which shares the signaling inhibiting epithelial-mesenchymal transition.
rs1192415 of TGFBR3 is associated with primary open angle glaucoma.
TGFbetaR3 promotes apoptosis of cardiomyocytes via a p38 (show CRK Proteins) pathway-associated mechanism, and loss of TGFbetaR3 reduces myocardial infarction injury.
BMP2 (show BMP2 Proteins) also requires Src (show SRC Proteins) for filamentous actin polymerization in Tgfbr3(-/-) epicardial cells.
Study identified a novel major binding site for TGF-beta (show TGFB1 Proteins)-like growth factors in TGFR-3. Findings potentially provide novel experimental insight into the general function of zona pellucida domain-containing proteins.
Retinoic acid enhanced TbetaRIII expression and that this increase contributed to LF-stimulated IgA production.
Pro-fibrotic cardiac effect of miR (show MLXIP Proteins)-328 was mediated by down-regulating TGFbR3 and up-regulating TGFb1 (show TGFB1 Proteins).
These data demonstrate that TbetaRIII regulates BMP-mediated signaling and biological effects, primarily through the ligand sequestration effects of sTbetaRIII in normal and cancerous mammary epithelial cells.
Glucocorticoids recruit Tgfbr3 and Smad1 (show SMAD1 Proteins) to shift transforming growth factor-beta signaling from the Tgfbr1 (show TGFBR1 Proteins)/Smad2 (show SMAD2 Proteins)/3 axis to the Acvrl1 (show ACVRL1 Proteins)/Smad1 (show SMAD1 Proteins) axis in lung fibroblasts.
work reveals a 'seed and soil' mechanism where TGF-beta2 (show TGFB2 Proteins) and TGF-beta (show TGFB1 Proteins)-RIII signalling through p38alpha (show MAPK14 Proteins)/beta regulates DTC dormancy and defines restrictive (BM) and permissive (lung) microenvironments for HNSCC metastasis
TGFBR3 mediated suppression of cancer progression includes effects on the tumor immune microenvironment.
This study provides evidence that the expressions of inhibin alpha subunit (show INHA Proteins) and betaglycan are inferior in cystic follicles, and this may be caused by the decrease in FSH (show BRD2 Proteins) in the presence of a cystic follicle.
This locus encodes the transforming growth factor (TGF)-beta type III receptor. The encoded receptor is a membrane proteoglycan that often functions as a co-receptor with other TGF-beta receptor superfamily members. Ectodomain shedding produces soluble TGFBR3, which may inhibit TGFB signaling. Decreased expression of this receptor has been observed in various cancers. Alternatively spliced transcript variants encoding different isoforms have been identified for this gene.
transforming growth factor, beta receptor III
, transforming growth factor, beta receptor III (betaglycan, 300kDa)
, transforming growth factor beta receptor type 3-like
, TGF-beta receptor type 3
, TGF-beta receptor type III
, betaglycan proteoglycan
, transforming growth factor beta receptor type 3
, transforming growth factor, beta receptor 3
, TGF-beta type III receptor
, transforming growth factor beta receptor III
, transforming growth factor-beta type III receptor