Early embryo-endometrial signaling modulates the regulation of matrix metalloproteinase-3
Fertility and Sterility, ISSN: 0015-0282, Vol: 82, Issue: SUPPL. 3, Page: 1029-1035
2004
- 4Citations
- 6Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations4
- Citation Indexes4
- CrossRef3
- Captures6
- Readers6
Article Description
To examine matrix metalloproteinase-3 (MMP-3) expression in human stromal cell culture after P stimulation and the effect of conditioned medium from human embryo-epithelial cells coculture on its expression and activity. Metabolic and endocrine studies on human tissue. In vitro fertilization (IVF) unit and endocrine research unit. Infertile patients undergoing endometrial tissue sampling for dating at the luteal phase before IVF. Endometrial sampling and collection of human embryos culture media. Expression and activity of secreted MMP-3 by P-induced stromal cells, and in stromal cells exposed to conditioned medium from embryo-epithelial cell coculture. Expression and activity of MMP-3 in human stromal cells decrease after P induction. Following incubation of these stromal-derived decidual cells with conditioned medium from embryo-epithelial cell coculture, MMP-3 expression and activity increased in a statistically significant manner. Progesterone inhibition of MMP-3 expression and its support of endometrial integrity were prevented by local expression of MMP-3 in response to embryonic signaling.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0015028204012658; http://dx.doi.org/10.1016/j.fertnstert.2004.06.026; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=5044219862&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/15474069; https://linkinghub.elsevier.com/retrieve/pii/S0015028204012658; https://dx.doi.org/10.1016/j.fertnstert.2004.06.026
Elsevier BV
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