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Anne Hamacher-Brady

Researcher at Johns Hopkins University

Publications -  43
Citations -  10918

Anne Hamacher-Brady is an academic researcher from Johns Hopkins University. The author has contributed to research in topics: Autophagy & Mitochondrion. The author has an hindex of 28, co-authored 42 publications receiving 8860 citations. Previous affiliations of Anne Hamacher-Brady include San Diego State University & German Cancer Research Center.

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Agent-based modeling of autophagy reveals emergent regulatory behavior of spatio-temporal autophagy dynamics

TL;DR: An agent-based model (ABM) is developed to represent individual components of the autophagy pathway, subcellular vesicle dynamics and metabolic feedback with the cellular environment, thereby providing a framework to investigate spatio-temporal aspects of autophagic regulation and dynamic behavior.
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Time course decomposition of cell heterogeneity in TFEB signaling states reveals homeostatic mechanisms restricting the magnitude and duration of TFEB responses to mTOR activity modulation.

TL;DR: TFEB protein levels and subcellular localization are under control of a short-term rheostat, which is highly responsive to negative regulation by mTOR, but under conditions of mTOR inhibition, restricts TFEB activation in a manner dependent on the proteasome.

Advances in Autophagy

TL;DR: Three forms of autophagy are commonly described: macroautophagy, microautophagic, and chaperone-mediated autophagosome (CMA), along with mitophagy.
Posted ContentDOI

Listeria monocytogenes virulence factors are secreted in biologically active Extracellular Vesicles

TL;DR: It is demonstrated that L. monocytogenes utilize EVs for toxin release and implicate these structures in mammalian cytotoxicity and the deletion of plcA increased EV toxicity, suggesting PI-PLC can restrain LLO activity.
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CMLS forum reviews: mitochondrial damage control.

TL;DR: The CMLS Forum Reviews as mentioned in this paper present a collection of articles covering select topics on basic mechanisms and pathophysiological contexts of mitochondrial damage control, which can be used to support a functional mitochondrial organelle compartment.