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John Perrino

Researcher at Stanford University

Publications -  13
Citations -  2111

John Perrino is an academic researcher from Stanford University. The author has contributed to research in topics: Viral replication & Microtubule. The author has an hindex of 10, co-authored 12 publications receiving 1483 citations.

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Atomic structure of sensitive battery materials and interfaces revealed by cryo–electron microscopy

TL;DR: Cryo–electron microscopy can preserve reactive metals and thus reveal the atomic structure of a lithium metal dendrite and atomically resolve individual lithium metal atoms and their interface with the solid electrolyte interphase (SEI).
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Stepwise Recruitment of Transcellular and Paracellular Pathways Underlies Blood-Brain Barrier Breakdown in Stroke

TL;DR: Although barrier function is impaired as early as 6 hr after stroke, TJs display profound structural defects only after 2 days, therefore, stepwise impairment of transcellular followed by paracellular barrier mechanisms accounts for the BBB deficits in stroke.
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Glia engulf degenerating axons during developmental axon pruning.

TL;DR: This study reveals a key role for glia in the removal of axon fragments during developmental axon pruning, using a genetically encoded electron microscopic (EM) marker to selectively label gamma neurons in the Drosophila mushroom bodies.
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Entrapment of Viral Capsids in Nuclear PML Cages Is an Intrinsic Antiviral Host Defense against Varicella-Zoster Virus

TL;DR: This work identifies large PML-NBs that sequester newly assembled nucleocapsids (NC) in neurons and satellite cells of human dorsal root ganglia (DRG) and skin cells infected with VZV in vivo and finds that PML IV cages co-sequester HttQ72 and ORF23 protein in VzV infected cells.
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Viral Generated Inter-Organelle Contacts Redirect Lipid Flux for Genome Replication

TL;DR: It is shown that the replication compartments of enteroviruses are created through novel membrane contact sites that recruit host lipid droplets to the RCs, and that pharmacological targeting of contact sites linking viral and host compartments is a potential strategy for antiviral development.