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Larry S. Zweifel

Researcher at University of Washington

Publications -  97
Citations -  6589

Larry S. Zweifel is an academic researcher from University of Washington. The author has contributed to research in topics: Dopamine & Ventral tegmental area. The author has an hindex of 35, co-authored 80 publications receiving 5213 citations. Previous affiliations of Larry S. Zweifel include Johns Hopkins University & Johns Hopkins University School of Medicine.

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Genetic identification of a neural circuit that suppresses appetite

TL;DR: Genetically encoded anatomical, optogenetic and pharmacogenetic tools are demonstrated that activation of neurons projecting to the central nucleus of the amygdala suppresses appetite and inhibition of these neurons increases food intake in circumstances when mice do not normally eat and prevents starvation in adult mice whose agouti-related peptide neurons are ablated.
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Functions and mechanisms of retrograde neurotrophin signalling

TL;DR: This work has established many of the cellular and molecular events that underlie retrograde signalling and the importance of these events for both development and maintenance of proper neural connectivity.
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Disruption of NMDAR-dependent burst firing by dopamine neurons provides selective assessment of phasic dopamine-dependent behavior.

TL;DR: The role of phasic DA was addressed by attenuating DA neuron burst firing and subsequent DA release, without altering tonic neural activity, and dramatically attenuated learning about cues that predicted rewarding and aversive events while leaving many other DA-dependent behaviors unaffected.
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Anxiety Cells in a Hippocampal-Hypothalamic Circuit.

TL;DR: The hippocampus encodes not only neutral but also valence-related contextual information, and the vCA1-LHA pathway is a direct route by which the hippocampus can rapidly influence innate anxiety behavior.
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A Neurotrophin Signaling Cascade Coordinates Sympathetic Neuron Development through Differential Control of TrkA Trafficking and Retrograde Signaling

TL;DR: It is proposed that a hierarchical neurotrophin signaling cascade coordinates sequential stages of sympathetic axon growth, innervation of targets, and survival in a manner dependent on the differential control of TrkA internalization, trafficking, and retrograde axonal signaling.