K
Katrina F. Cooper
Researcher at Rowan University
Publications - 39
Citations - 1151
Katrina F. Cooper is an academic researcher from Rowan University. The author has contributed to research in topics: Cyclin & Cyclin A. The author has an hindex of 16, co-authored 36 publications receiving 904 citations. Previous affiliations of Katrina F. Cooper include University of Medicine and Dentistry of New Jersey & Drexel University.
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Reactive Oxygen Species and Mitochondrial Dynamics: The Yin and Yang of Mitochondrial Dysfunction and Cancer Progression
TL;DR: The latest findings on the intricate relationship between mitochondrial dynamics and ROS production are reviewed, focusing mainly on its role in malignant disease.
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Meiosis-specific destruction of the Ume6p repressor by the Cdc20-directed APC/C
TL;DR: Results indicate that Ume6p degradation is required for normal meiotic gene induction and meiotic progression, and demonstrate a direct connection between the transcription machinery and ubiquitin-mediated proteolysis that is developmentally regulated.
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Regulation of the Oxidative Stress Response Through Slt2p-Dependent Destruction of Cyclin C in Saccharomyces cerevisiae
TL;DR: A new role for the Slt2p MAP kinase cascade in protecting the cell from programmed cell death through cyclin C destruction is demonstrated, demonstrating the need for this destruction pathway in cells exposed to reactive oxygen species.
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Till Death Do Us Part: The Marriage of Autophagy and Apoptosis
TL;DR: This work has shown that the autophagic and cell death machines both respond to the same stresses and share key regulatory proteins, suggesting that the pathways are intricately connected.
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Oxidative-stress-induced nuclear to cytoplasmic relocalization is required for Not4-dependent cyclin C destruction
Katrina F. Cooper,Matthew S. Scarnati,Elizabeth Krasley,Michael J. Mallory,Chunyan Jin,Michael J. Law,Randy Strich +6 more
TL;DR: A stress-induced proteolytic pathway regulating cyclin C that requires nuclear to cytoplasmic relocalization and Not4p-mediated ubiquitylation is identified, which is required for H2O2-inducedcyclin C destruction in vivo and in vitro.