Select Publications
Journal articles
2024, 'Faster and lower dose imaging: evaluating adaptive, constant gantry velocity and angular separation in fast low-dose 4D cone beam CT imaging', Medical Physics, 51, pp. 1364 - 1382, http://dx.doi.org/10.1002/mp.16585
,2022, 'Cannabinoids and Opioids Differentially Target Extrinsic and Intrinsic GABAergic Inputs onto the Periaqueductal Grey Descending Pathway', Journal of Neuroscience, 42, pp. 7744 - 7756, http://dx.doi.org/10.1523/JNEUROSCI.0997-22.2022
,2022, 'Reducing 4DCBCT imaging dose and time: Exploring the limits of adaptive acquisition and motion compensated reconstruction', Physics in Medicine and Biology, 67, http://dx.doi.org/10.1088/1361-6560/ac55a4
,2021, 'The first-in-human implementation of adaptive 4D cone beam CT for lung cancer radiotherapy: 4DCBCT in less time with less dose', Radiotherapy and Oncology, 161, pp. 29 - 34, http://dx.doi.org/10.1016/j.radonc.2021.05.021
,2021, 'Reducing 4DCBCT scan time and dose through motion compensated acquisition and reconstruction', Physics in Medicine and Biology, 66, http://dx.doi.org/10.1088/1361-6560/abebfb
,2020, 'Mu-opioids suppress gabaergic synaptic transmission onto orbitofrontal cortex pyramidal neurons with subregional selectivity', Journal of Neuroscience, 40, pp. 5894 - 5907, http://dx.doi.org/10.1523/JNEUROSCI.2049-19.2020
,2020, 'Opioid presynaptic disinhibition of the midbrain periaqueductal grey descending analgesic pathway', British Journal of Pharmacology, 177, pp. 2320 - 2332, http://dx.doi.org/10.1111/bph.14982
,2020, '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', Molecular Brain, 13, http://dx.doi.org/10.1186/s13041-020-0545-1
,2017, 'Endocannabinoid modulation of homeostatic and non-homeostatic feeding circuits', Neuropharmacology, 124, pp. 38 - 51, http://dx.doi.org/10.1016/j.neuropharm.2017.05.033
,2017, 'Projection-Target-Defined Effects of Orexin and Dynorphin on VTA Dopamine Neurons', Cell Reports, 18, pp. 1346 - 1355, http://dx.doi.org/10.1016/j.celrep.2017.01.030
,2017, 'Endocannabinoids control vesicle release mode at midbrain periaqueductal grey inhibitory synapses', Journal of Physiology, 595, pp. 165 - 178, http://dx.doi.org/10.1113/JP272292
,2016, 'Age-dependent D1-D2 receptor coactivation in the lateral orbitofrontal cortex potentiates NMDA receptors and facilitates cognitive flexibility', Cerebral Cortex, 26, pp. 4524 - 4539, http://dx.doi.org/10.1093/cercor/bhv222
,2015, 'Repeated morphine treatment alters cannabinoid modulation of GABAergic synaptic transmission within the rat periaqueductal grey', British Journal of Pharmacology, 172, pp. 681 - 690, http://dx.doi.org/10.1111/bph.12809
,2014, 'Endocannabinoid modulation by FAAH and monoacylglycerol lipase within the analgesic circuitry of the periaqueductal grey', British Journal of Pharmacology, 171, pp. 5225 - 5236, http://dx.doi.org/10.1111/bph.12839
,2014, 'Descending modulation of pain: The GABA disinhibition hypothesis of analgesia', Current Opinion in Neurobiology, 29, pp. 159 - 164, http://dx.doi.org/10.1016/j.conb.2014.07.010
,2014, 'Menthol enhances phasic and tonic GABA
2014, 'Targeting the endogenous cannabinoid system to treat neuropathic pain', Frontiers in Pharmacology, 5 MAR, http://dx.doi.org/10.3389/fphar.2014.00028
,2009, 'Substance P drives endocannabinoid-mediated disinhibition in a midbrain descending analgesic pathway', Journal of Neuroscience, 29, pp. 7220 - 7229, http://dx.doi.org/10.1523/JNEUROSCI.4362-08.2009
,2008, 'Muscarinic modulation of synaptic transmission via endocannabinoid signalling in the rat midbrain periaqueductal gray', Molecular Pharmacology, 74, pp. 1392 - 1398, http://dx.doi.org/10.1124/mol.108.045872
,Preprints
2020, Mu-opioids suppress GABAergic synaptic transmission onto orbitofrontal cortex pyramidal neurons with subregional selectivity, http://dx.doi.org/10.1101/2020.05.12.091678
,2020, Obesity-induced astrocyte dysfunction impairs heterosynaptic plasticity in the orbitofrontal cortex, http://dx.doi.org/10.1101/2020.05.01.073205
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