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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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Journal ArticleDOI
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.
Journal ArticleDOI
Pathological Axonal Death through a MAPK Cascade that Triggers a Local Energy Deficit
Jing Yang,Zhuhao Wu,Nicolas Renier,David J. Simon,Kunihiro Uryu,David S. Park,Peter A. Greer,Cathy Tournier,Roger J. Davis,Marc Tessier-Lavigne +9 more
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.
Journal ArticleDOI
The MicroRNA miR-1 Regulates a MEF-2-Dependent Retrograde Signal at Neuromuscular Junctions
David J. Simon,Jon M. Madison,Annie L. Conery,Katherine L. Thompson-Peer,Michael J. Soskis,Gary Ruvkun,Joshua M. Kaplan,John Kim +7 more
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.
Journal ArticleDOI
A Caspase Cascade Regulating Developmental Axon Degeneration
David J. Simon,Robby M. Weimer,Todd McLaughlin,Dara Y. Kallop,Karen Stanger,Jing Yang,Dennis D.M. O'Leary,Rami N. Hannoush,Marc Tessier-Lavigne +8 more
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.
Journal ArticleDOI
Prevalent presence of periodic actin–spectrin-based membrane skeleton in a broad range of neuronal cell types and animal species
Jiang He,Ruobo Zhou,Zhuhao Wu,Monica A. Carrasco,Peri T. Kurshan,Jonathan E. Farley,David J. Simon,Guiping Wang,Boran Han,Junjie Hao,Evan Heller,Marc R. Freeman,Kang Shen,Tom Maniatis,Marc Tessier-Lavigne,Xiaowei Zhuang +15 more
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.