Reduced Dehydroepiandrosterone-Sulfate Levels in the Mid-Luteal Subphase of the Menstrual Cycle: Implications to Women’s Health Research [PDF]
The regulation of DHEA-sulfate by steroid sulfotransferase (SULT) and steryl-sulfatase (STS) enzymes is a vital process for the downstream formation of many steroid hormones. DHEA-sulfate is the most abundant steroid hormone in the human body; thus, DHEA-
Ajna Hamidovic +5 more
doaj +2 more sources
Placental proteomic signatures of preterm birth, gestational age, and birthweight [PDF]
Background Preterm birth and low birthweight are leading contributors to infant morbidity and mortality, yet underlying mechanisms remain poorly understood.
Brennan H. Baker +11 more
doaj +2 more sources
Steroid sulfatase inhibitors and sulfated C19 steroids for proteotoxicity-related diseases: a patent spotlight. [PDF]
Al-Horani RA.
europepmc +1 more source
STS pathogenic variants in a Dutch patient cohort clinically suspected for X-linked ichthyosis show genetic heterogeneity. [PDF]
Nagtzaam IF +7 more
europepmc +1 more source
Genetic Heterogeneity of X-Linked Ichthyosis in the Republic of North Ossetia-Alania, Case Series Report. [PDF]
Vasilyeva TA +9 more
europepmc +1 more source
Characterization of Xenobiotic and Steroid Disposition Potential of Human Placental Tissue and Cell Lines (BeWo, JEG-3, JAR, and HTR-8/SVneo) by Quantitative Proteomics. [PDF]
Kruger L +11 more
europepmc +1 more source
STS and PUDP Deletion Identified by Targeted Panel Sequencing with CNV Analysis in X-Linked Ichthyosis: A Case Report and Literature Review. [PDF]
Park J, Cho YG, Kim JK, Kim HH.
europepmc +1 more source
Simultaneous expression of steroid sulfatase and androgen receptor reduced overall survival of patients with epithelial ovarian tumors. [PDF]
Calvillo-Robledo A +10 more
europepmc +1 more source
A Structural and Bioinformatics Investigation of a Fungal Squalene Synthase and Comparisons with Other Membrane Proteins. [PDF]
Malwal SR +7 more
europepmc +1 more source
Hypertrophic pyloric stenosis masked by kidney failure in a male infant with a contiguous gene deletion syndrome at Xp22.31 involving the steroid sulfatase gene: case report. [PDF]
Schierz IAM +8 more
europepmc +1 more source

