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Trevor G. Shepherd

Researcher at University of Western Ontario

Publications -  53
Citations -  7083

Trevor G. Shepherd is an academic researcher from University of Western Ontario. The author has contributed to research in topics: Ovarian cancer & Metastasis. The author has an hindex of 25, co-authored 47 publications receiving 6342 citations. Previous affiliations of Trevor G. Shepherd include McMaster University & London Health Sciences Centre.

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Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)

Daniel J. Klionsky, +2522 more
- 21 Jan 2016 - 
TL;DR: In this paper, the authors present a set of guidelines for the selection and interpretation of methods for use by investigators who aim to examine macro-autophagy and related processes, as well as for reviewers who need to provide realistic and reasonable critiques of papers that are focused on these processes.
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BMP4 induces EMT and Rho GTPase activation in human ovarian cancer cells.

TL;DR: Treatment of OvCa cells with BMP4 produced morphological alterations and increased cellular adhesion, motility and invasion, suggesting a link between autocrine BMP signalling mediated through the Rho GTPase family and Snail- and Slug-induced EMT that may collectively contribute to aggressive OvCa behaviour.
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Primary culture of ovarian surface epithelial cells and ascites-derived ovarian cancer cells from patients

TL;DR: The laboratory has refined the technique for isolating primary cultures of normal human ovarian surface epithelial cells by combining two different protocols involving the enzymatic and mechanical removal of OSE cells from ovarian biopsies by including optional steps for the immediate preparation of ascites-derived EOC cells to be used for subsequent cytological analyses.
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The pea3 subfamily ets genes are required for HER2/Neu-mediated mammary oncogenesis

TL;DR: These findings imply that one or more of the PEA3 subfamily Ets proteins or other ETS proteins with related DNA binding specificity play an essential role in Neu-mediated mammary oncogenesis and agents that inhibit the expression or activity of the pea3 sub family proteins may prove efficacious in the treatment of breast cancer.
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Contribution of reactive oxygen species to ovarian cancer cell growth arrest and killing by the anti-malarial drug artesunate.

TL;DR: Artesunate has potent anti‐proliferative and cytotoxic effects on ovarian cancer cells, and may therefore be useful in the treatment of ovarian cancer.