Bryce Vissel

Professor of Neuroscience and Head

Australia

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Professor Bryce Vissel is the Head of Neuroscience at St Vincent's Hospital Sydney, Australia. His research focuses on the role of microglia in neurological diseases, the impact of learning on memory precision, and the effects of lifestyle factors on brain health. Recent publications include studies on dyskinesias related to L-Dopa treatment and the neural mechanisms underlying goal-directed actions in models of Alzheimer's disease.

Articles (12)

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2023

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2023

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2023

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2021

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2021

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2021

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2021

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2020

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2020

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2020

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2020

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2020

Collaborators (4)

Sandy Stayte

University of Sydney

AUSTRALIA

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Amanda Wright

Macquarie University

AUSTRALIA

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Kong M. Li

University of Sydney

AUSTRALIA

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Christopher Vaughan

Clinical Professor

University of Sydney

AUSTRALIA

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Bryce Vissel

Research Interests

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Articles (12)

Goal-Directed Action Is Initially Impaired in a hAPP-J20 Mouse Model of Alzheimer’s Disease

The ratio of M1 to M2 microglia in the striatum determines the severity of L‐Dopa‐induced dyskinesias

Autocrine positive feedback of tumor necrosis factor from activated microglia proposed to be of widespread relevance in chronic neurological disease

Extinction and discrimination in a Bayesian model of context fear conditioning ( <scp>BaconX</scp> )

Engram Size Varies with Learning and Reflects Memory Content and Precision

Parafascicular Thalamic and Orbitofrontal Cortical Inputs to Striatum Represent States for Goal-Directed Action Selection

Brain health is independently impaired by E-vaping and high-fat diet

A new mouse line with reduced GluA2 Q/R site RNA editing exhibits loss of dendritic spines, hippocampal CA1-neuron loss, learning and memory impairments and NMDA receptor-independent seizure vulnerability

Medial Orbitofrontal Cortex Regulates Instrumental Conditioned Punishment, but not Pavlovian Conditioned Fear

Maladaptive Properties of Context-Impoverished Memories

Targeting the cannabinoid receptor CB2 in a mouse model of l-dopa induced dyskinesia

The kainate receptor antagonist UBP310 but not single deletion of GluK1, GluK2, or GluK3 subunits, inhibits MPTP-induced degeneration in the mouse midbrain

Collaborators (4)

Sandy Stayte

Amanda Wright

Kong M. Li

Christopher Vaughan

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