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Bryan E. Snow

Researcher at Princess Margaret Cancer Centre

Publications -  43
Citations -  9855

Bryan E. Snow is an academic researcher from Princess Margaret Cancer Centre. The author has contributed to research in topics: Telomere & RGS Proteins. The author has an hindex of 31, co-authored 41 publications receiving 9289 citations. Previous affiliations of Bryan E. Snow include University of Toronto & Ontario Institute for Cancer Research.

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Molecular characterization of mitochondrial apoptosis-inducing factor

TL;DR: The identification and cloning of an apoptosis-inducing factor, AIF, which is sufficient to induce apoptosis of isolated nuclei is reported, indicating that AIF is a mitochondrial effector of apoptotic cell death.
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Regulation of PTEN transcription by p53.

TL;DR: A unique role for p53 in regulation of cellular survival and an interesting connection in tumor suppressor signaling is revealed and a new element controlling constitutive expression of PTEN is identified.
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DJ-1, a novel regulator of the tumor suppressor PTEN.

TL;DR: DJ-1 expression was increased compared to paired nonneoplastic lung tissue, and correlated positively with relapse incidence, and is thus a key negative regulator of PTEN that may be a useful prognostic marker for cancer.
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Overexpression of AKT2/Protein Kinase Bβ Leads to Up-Regulation of β1 Integrins, Increased Invasion, and Metastasis of Human Breast and Ovarian Cancer Cells

TL;DR: Overexpression of AKT2, but not AKT1 or AKT3, was sufficient to duplicate the invasive effects of phosphoinositide 3-OH kinase (PI3-K) transfected in breast cancer cells, indicating thatAKT2 mediates PI3- K-dependent effects on adhesion, motility, invasion, and metastasis in vivo.
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Dynamic Regulation of RGS2 Suggests a Novel Mechanism in G-Protein Signaling and Neuronal Plasticity

TL;DR: It is demonstrated that mRNA encoding a member of the regulator of G-protein signaling (RGS) family, RGS2, is rapidly induced in neurons of the hippocampus, cortex, and striatum in response to stimuli that evoke plasticity.