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These results suggest that the availability of estrogens in the boar epididymis may be locally controlled also by steroid sulphatase (show STS Proteins) and estrogen sulphotransferase.
These results resolve the conflicting results on the localization of SULT1E1 from earlier studies and suggest that posttranscriptional mechanisms play an important role in the control of SULT1E1 expression during TGC (show TGM2 Proteins) differentiation.
the activities of free estrogens produced in bovine TGC are curtailed by SULT1E1 expressed in UTC and in fetal liver
Our study shows that estrogen sulfotransferase is present in both the intracellular and intraluminal compartments of the epididymis, suggesting that this enzyme plays different roles along the excurrent duct.
Gene profiling identifies sulfotransferase family 1E (Sult1e1), which encodes a sulfotransferase E1 responsible for inactivation of estrogen, as a gene upregulated in non-alcoholic steatohepatitis in both genders and most conspicuously in male IkbkbDeltahep mice having worst non-alcoholic steatohepatitis and lowest plasma estradiol levels.
The role of estrogen sulfotransferase, a conjugating enzyme that sulfonates and deactivates estrogens, in sepsis response is reported.
Liver ischemia and reperfusion (I/R) induced the expression of EST (show MAP3K8 Proteins) and comprised estrogen activity in an Nrf2 (show NFE2L2 Proteins)-dependent manner. EST (show MAP3K8 Proteins) ablation gender-specifically affected I/R sensitivity.
EST (show MAP3K8 Proteins) functions as a negative regulator of adipogenesis.
Murine SULT1E1 inhibition in vitro and in silico was investigated and compared this to data for the human enzyme.
results suggest that estrogen sulfotransferase plays a physiologic role in protecting Leydig cells from estrogen-induced biochemical lesions
Data show that ablation of the mouse estrogen sulfotransferase gene Sult1e1 causes placental thrombosis and spontaneous fetal loss.
estrogen sulfotransferase, the enzyme that inactivates estrogen, has been found selectively expressed in male tissues, thus suggesting a role for this enzyme to protect male-specific tissues against estrogenic activity
Elevated SULT1E1 levels and associated alterations in estrogen-regulated hepatic protein expression may play an important role in cystic fibrosis (show S100A8 Proteins) liver disease
The role of SULT1E1 in ovulation is suggested by the substantially low ovulatory response in hCG-treated SULT1E1 KO mice
Resveratrol and all its derivatives reduced also SULT1E1 mRNA transcript level. The reduced expression of AhR (show AHR Proteins), CYP1A1 (show CYP1A1 Proteins), and 1B1 was also found as a result of treatment with these compounds.
Data show that both estrogen sulfatase (STS) and estrogen sulfotransferase (EST) were highly expressed in the human umbilical vein
Effects of steroid hormone on estrogen sulfotransferase and on steroid sulfatase (show STS Proteins) expression in endometriosis tissue and stromal cells
a model that enables prediction of substrates and inhibitors of SULT1E1, is reported.
Data suggest that the substrate specificities of SULT1E1 and SULT1A1 (show SULT1A1 Proteins)*1 include metabolites of tamoxifen (endoxifen, 4-hydroxytamoxifen, and N-desmethyltamoxifen); these metabolites are weak inhibitors of sulfation of estradiol by SULT1E1/SULT1A1 (show SULT1A1 Proteins)*1.
Authors propose that the formation of this DNA loop and protein-bound complex prevents additional binding of ETS1 (show ETS1 Proteins) and p53 (show TP53 Proteins) R273H proteins to other proximal binding sites.
Data indicate that protein-ligand interaction energy by using docking Quantitative Structure-Activity Relationships(QSAR) models showed accuracy of 67.28%, 78.00% and 75.46%, for the isoforms SULT1A1, SULT1A3 and SULT1E1, respectively.
Overexpression of EST (show MAP3K8 Proteins) promoted adipogenesis.
Report diterpenoid extracts from Leonurus sibiricus L. with estrogen sulfotransferase inhibitory activity.
Knock-down of SULT1E1 in HUVECs resulted in regulation of genes involved in inflammation and lipid metabolism.
Sulfotransferase enzymes catalyze the sulfate conjugation of many hormones, neurotransmitters, drugs, and xenobiotic compounds. These cytosolic enzymes are different in their tissue distributions and substrate specificities. The gene structure (number and length of exons) is similar among family members. This gene encodes a protein that transfers a sulfo moiety to and from estrone, which may control levels of estrogen receptors.
, estrone sulfotransferase
, ste2 gene for estrogen sulfotransferase
, sulfotransferase, estrogen-preferring
, estrogen sulfotransferase
, sulfotransferase 1E1
, estrogen sulfotransferase, testis isoform
, sulfotransferase, estrogen preferring
, adrenocortical estrogen sulfotransferase
, sulfotransferase family 1E, estrogen-preferring, member 1
, sulfotransferase family 1E member 1 L homeolog
, sulfotransferase family 1E member 1 S homeolog