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Evan R. Simpson

Researcher at Hudson Institute of Medical Research

Publications -  159
Citations -  15354

Evan R. Simpson is an academic researcher from Hudson Institute of Medical Research. The author has contributed to research in topics: Aromatase & Estrogen. The author has an hindex of 61, co-authored 159 publications receiving 14473 citations. Previous affiliations of Evan R. Simpson include Hudson Institute & University of Texas Southwestern Medical Center.

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Aromatase Cytochrome P450, The Enzyme Responsible for Estrogen Biosynthesis*

TL;DR: The biosynthesis of estrogens appears to occur throughout the entire vertebrate phylum including mammals, birds, reptiles, amphibians, teleost and elasmobranch fish, and Agnatha, and in the protochordate Amphioxus.
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Sources of estrogen and their importance.

TL;DR: The importance of this unique aspect of the tissue-specific regulation of aromatase expression lies in the fact that the low circulating levels of estrogens which are observed in postmenopausal women have little bearing on the concentrations of estrogen in, for example, a breast tumor, which can reach levels at least one order of magnitude greater than those present in the circulation, due to local synthesis within the breast.
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Estrogen and spermatogenesis.

TL;DR: In this paper, a review summarizes the current knowledge on the localization of estrogen receptors and aromatase in the testis in an effort to understand the likely sites of estrogen action.
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Aromatase—A Brief Overview

TL;DR: In principle, it should be possible to develop selective aromatase modulators (SAMs) that block aromat enzyme expression in breast, but allow unimpaired estrogen synthesis in other tissues such as bone.
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Control of mammary stem cell function by steroid hormone signalling

TL;DR: It is demonstrated that mouse mammary stem cells (MaSCs) are highly responsive to steroid hormone signalling, despite lacking the oestrogen and progesterone receptors, and indicates that breast cancer chemoprevention may be achieved, in part, through suppression of MaSC function.