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MicroRNA expression and regulation in mouse uterus during embryo implantation.
Differential expression and regulation of prostaglandin transporter and metabolic enzymes in mouse uterus during blastocyst implantation.
To investigate the differential expression and regulation of Gstm2 in mouse uterus during early pregnancy.
The aim of this study was to identify a novel implantation-related molecule and to examine EMO2 expression in the mouse uterus during the peri-implantation period.
To examine the spatiotemporal expression and regulation of prostaglandin transporter (PGT), 15-hydroxy-PG dehydrogenase (15-PGDH), and carbonyl reductase 1 (CBR1) messenger RNA (mRNA) and protein in the mouse uterus during embryo implantation and in related models.
The large-scale proteomic analysis in mouse uterus during embryo implantation is still lacking.
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Progesterone treatments have also been shown to alter the expression of miR-200b/429 and ZEBs in mice uterus during gestation and in isolated myometrial smooth muscle cells (MSMCs) where miR-200b/429 overexpression repressed ZEBs, oxytocin receptor, and connexin-43 (Renthal et al. 2010).
Previous studies have implicated that estrogen induces expression of numerous genes via ERα during this time in the mouse uterus (5).
The immature mouse uterus is sensitive to elevations in endogenous levels of 17β -estradiol (E2) that occur during puberty.
The kinase activity of p38 in mouse uterus was gestation stage-dependent, and was markedly increased on day 19 of gestation and during labor.
Serial analysis of gene expression in mouse uterus at the implantation site.
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