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Jeffrey G. Edwards

Researcher at Brigham Young University

Publications -  62
Citations -  3137

Jeffrey G. Edwards is an academic researcher from Brigham Young University. The author has contributed to research in topics: Medicine & Synaptic plasticity. The author has an hindex of 25, co-authored 48 publications receiving 2931 citations. Previous affiliations of Jeffrey G. Edwards include Queen's University & Brown University.

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Recycling Endosomes Supply AMPA Receptors for LTP

TL;DR: It is reported that AMPA receptors are transported from recycling endosomes to the plasma membrane for LTP and provide a mechanistic link between synaptic potentiation and membrane remodeling during synapse modification.
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Myosin Vb Mobilizes Recycling Endosomes and AMPA Receptors for Postsynaptic Plasticity

TL;DR: It is demonstrated that myosin Vb (MyoVb), a Ca2+-sensitive motor, conducts spine trafficking during long-term potentiation (LTP) of synaptic strength, providing a mechanistic link between the induction and expression of postsynaptic plasticity.
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TRPV1 Channels Mediate Long-Term Depression at Synapses on Hippocampal Interneurons

TL;DR: The results suggest that, in the hippocampus, TRPV1 receptor activation selectively modifies synapses onto interneurons, which may have a role in long-term changes in physiological and pathological circuit behavior during learning and epileptic activity.
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Seroprevalence of human herpesvirus-8 (HHV-8) in countries of Southeast Asia compared to the USA, the Caribbean and Africa

TL;DR: Nasopharyngeal and oral carcinoma patients from Malaysia, Hong Kong and Sri Lanka who have very high EBV titres show that there is little, if any, cross-reactivity between antibodies to these two gamma viruses, suggesting that human herpes virus-8 (HHV-8) may be either a recently introduced virus or one that has extremely low infectivity.
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The international epidemiology of disseminated Mycobacterium avium complex infection in AIDS

TL;DR: Rates of disseminated MAC in AIDS are higher in developed than developing countries and are due to both differences in exposure and differences in immunity, providing a rationale for prevention of MAC through both active immunization and reduction in exposure to the organism.