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Ian Duguid
Researcher at University of Edinburgh
Publications - 33
Citations - 2266
Ian Duguid is an academic researcher from University of Edinburgh. The author has contributed to research in topics: Motor cortex & Cerebellum. The author has an hindex of 19, co-authored 29 publications receiving 2023 citations. Previous affiliations of Ian Duguid include University College London.
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High-fidelity transmission of sensory information by single cerebellar mossy fibre boutons.
TL;DR: It is shown that sensory stimulation can produce bursts of spikes in single boutons at very high instantaneous firing frequencies (more than 700 Hz), and suggested that the relay from mossy fibre to granule cell can act in a ‘detonator’ fashion, such that a single presynaptic afferent may be sufficient to transmit the sensory message.
Journal ArticleDOI
The GDP-GTP Exchange Factor Collybistin: An Essential Determinant of Neuronal Gephyrin Clustering
Kirsten Harvey,Ian Duguid,Melissa J. Alldred,Sarah Beatty,H. E. Ward,Nicholas H. Keep,Sue E. Lingenfelter,Brian Pearce,Johan Lundgren,Michael John Owen,Trevor G. Smart,Bernhard Lüscher,Mark I. Rees,Mark I. Rees,Robert J. Harvey +14 more
TL;DR: The characterization of several new variants of collybistin are reported, which are created by alternative splicing of exons encoding an N-terminal src homology 3 (SH3) domain and three alternate C termini (CB1, CB2, and CB3).
Journal ArticleDOI
Retrograde activation of presynaptic NMDA receptors enhances GABA release at cerebellar interneuron–Purkinje cell synapses
Ian Duguid,Trevor G. Smart +1 more
TL;DR: A newly identified form of inhibitory synaptic plasticity, termed depolarization-induced potentiation of inhibition, in rodents is reported, triggered by an elevation of Ca2+ in Purkinje cells and the subsequent retrograde activation of presynaptic NMDA receptors.
Journal ArticleDOI
Encoding of Oscillations by Axonal Bursts in Inferior Olive Neurons
TL;DR: The results challenge the view that the climbing fiber conveys an all-or-none signal to the cerebellar cortex and help to link learning and timing theories of olivocerebellar function.
Journal ArticleDOI
Mutations in the gene encoding GlyT2 (SLC6A5) define a presynaptic component of human startle disease.
Mark I. Rees,Mark I. Rees,Kirsten Harvey,Brian Pearce,Seo-Kyung Chung,Seo-Kyung Chung,Ian Duguid,Philip Thomas,Sarah Beatty,Gail E. Graham,Linlea Armstrong,Rita Shiang,Kim J. Abbott,Sameer M. Zuberi,John B.P. Stephenson,Michael John Owen,Marina A. J. Tijssen,Arn M. J. M. van den Maagdenberg,Trevor G. Smart,Stéphane Supplisson,Robert J. Harvey +20 more
TL;DR: It is shown that missense, nonsense and frameshift mutations in SLC6A5 (ref. 8), encoding the presynaptic glycine transporter 2 (GlyT2), also cause hyperekplexia.