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David J. Simon

Researcher at Stanford University

Publications -  23
Citations -  2508

David J. Simon is an academic researcher from Stanford University. The author has contributed to research in topics: Axon & Spectrin. The author has an hindex of 15, co-authored 22 publications receiving 1917 citations. Previous affiliations of David J. Simon include Rockefeller University & Cornell University.

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iDISCO: A Simple, Rapid Method to Immunolabel Large Tissue Samples for Volume Imaging

TL;DR: iDISCO enables facile volume imaging of immunolabeled structures in complex tissues and reveals unexpected variability in number of apoptotic neurons within individual sensory ganglia despite tight control of total number in all ganglia.
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Pathological Axonal Death through a MAPK Cascade that Triggers a Local Energy Deficit

TL;DR: Using traumatic injury as a model, this work systematically investigates mitogen-activated protein kinase (MAPK) families and delineates a MAPK cascade that represents the early degenerative response to axonal injury, revealing a regulatory mechanism that integrates distinct signals to instruct pathological axon degeneration.
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The MicroRNA miR-1 Regulates a MEF-2-Dependent Retrograde Signal at Neuromuscular Junctions

TL;DR: It is proposed that miR-1 refines synaptic function by coupling changes in muscle activity to changes in presynaptic function, suggesting that MEF-2 activity in muscles controls a retrograde signal.
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A Caspase Cascade Regulating Developmental Axon Degeneration

TL;DR: In vitro, it is shown that genetic deletion of Caspase-3 is fully protective against sensory axon degeneration initiated by trophic factor withdrawal, but not injury-induced Wallerian degeneration, and a biochemical cascade from prosurvival Bcl2 family regulators to Caspasase-9, then Caspases-3, and then Cazase-6 is defined.
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Prevalent presence of periodic actin–spectrin-based membrane skeleton in a broad range of neuronal cell types and animal species

TL;DR: It is demonstrated that this membrane-associated periodic skeleton (MPS) is present in a broad range of neuronal cell types cultured from the central and peripheral nervous systems of rodents, and that spectrin is capable of adopting a similar periodic organization in neurons of a variety of animal species.