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Ping Yin

Researcher at Northwestern University

Publications -  68
Citations -  3268

Ping Yin is an academic researcher from Northwestern University. The author has contributed to research in topics: Uterine leiomyoma & Leiomyoma. The author has an hindex of 30, co-authored 58 publications receiving 2808 citations. Previous affiliations of Ping Yin include Tohoku University & University of Yamanashi.

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Progesterone resistance in endometriosis: Link to failure to metabolize estradiol

TL;DR: The cellular and molecular mechanisms underlying progesterone resistance and failure to metabolize E2 in endometriosis are reviewed.
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Promoter Methylation Regulates Estrogen Receptor 2 in Human Endometrium and Endometriosis

TL;DR: Methylation of a CpG island at the ESR2 promoter region is a primary mechanism responsible for differential expression of ESR1 in endometriosis and endometrium and may be applied to a number of areas ranging from diagnosis to the treatment of endometRIosis.
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Estrogen Receptor-β, Estrogen Receptor-α, and Progesterone Resistance in Endometriosis

TL;DR: It is speculated that alterations in the relative levels of ERbeta and ERalpha in endometrial tissue dictate E2-regulated PR expression, such that a decreased ERalpha-tauomicron-ERbeta ratio may result in suppression of PR.
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Transcriptional Activation of Steroidogenic Factor-1 by Hypomethylation of the 5′ CpG Island in Endometriosis

TL;DR: This is the first demonstration of methylation-dependent regulation of SF-1 in any mammalian tissue and points to a new mechanism for targeting local estrogen biosynthesis in endometriosis.
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Paracrine activation of WNT/β-catenin pathway in uterine leiomyoma stem cells promotes tumor growth

TL;DR: It is demonstrated that wingless-type (WNT) acts as a paracrine signal from estrogen/progesterone receptor-rich mature cells to activate the canonical β-catenin pathway in leiomyoma stem cells, which enables mature myometrial or leoomyoma cells to send mitogenic signals to neighboring tissue stem cells in response to estrogen and progesterone.