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Bruce P. Graham
Researcher at University of Stirling
Publications - 107
Citations - 2420
Bruce P. Graham is an academic researcher from University of Stirling. The author has contributed to research in topics: Postsynaptic potential & Calyx of Held. The author has an hindex of 25, co-authored 107 publications receiving 2168 citations. Previous affiliations of Bruce P. Graham include University of Queensland & University of Edinburgh.
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Principles of Computational Modelling in Neuroscience
TL;DR: In this paper, the Hodgkin Huxley model of the action potential was used to model the neuron's electrical activity in the brain. But the model was not suitable for the development of the nervous system.
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Nitric oxide is a volume transmitter regulating postsynaptic excitability at a glutamatergic synapse.
Joern R. Steinert,Cornelia Kopp-Scheinpflug,Claire A. Baker,R. A. John Challiss,Raj Mistry,Martin D. Haustein,Sarah J. Griffin,Huaxia Tong,Bruce P. Graham,Ian D. Forsythe +9 more
TL;DR: It is concluded that NO serves as a volume transmitter and slow dynamic modulator, integrating spontaneous and evoked neuronal firing, thereby providing an index of global activity and regulating information transmission across a population of active and inactive neurons.
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Encoding and retrieval in a model of the hippocampal CA1 microcircuit.
TL;DR: The model simulates the timing of firing of different hippocampal cell types relative to the theta rhythm in anesthetized animals and proposes experimentally confirmed functional roles for the different classes of inhibitory interneurons in the storage and recall cycles.
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Distinguishing between Presynaptic and Postsynaptic Mechanisms of Short-Term Depression during Action Potential Trains
TL;DR: Although presynaptic vesicle depletion makes the dominant contribution to short-term depression, the results show that AMPA receptor desensitization contributes to the depression at auditory synapses after hearing onset and in a frequency-dependent manner.
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A simulation of action potentials in synaptic boutons during presynaptic inhibition
TL;DR: The object of the simulation has been to determine the magnitude of a chloride conductance required to reduce transmitter release, for various diameters of synaptic boutons, connected to axons with diameters in the range 0.1-1.0 microns.