The scientist’s investigation covers issues in Internal medicine, Endocrinology, Neuroscience, Regulation of gene expression and Poison control. His studies deal with areas such as In situ hybridization, Depression and Sensitization as well as Internal medicine. His Endocrinology study incorporates themes from Cytokine, Immunology and Cell biology.
As part of the same scientific family, Michael O. Poulter usually focuses on Neuroscience, concentrating on Receptor and intersecting with Hormone and PDZ domain. Michael O. Poulter performs multidisciplinary studies into Poison control and Genetics in his work. The various areas that Michael O. Poulter examines in his GABAA receptor study include Olfactory bulb, Cortex and Interleukin 10 receptor, alpha subunit, G alpha subunit.
His main research concerns Neuroscience, Internal medicine, Endocrinology, GABAA receptor and Inhibitory postsynaptic potential. His work on Corticotropin-releasing hormone, NMDA receptor and Cytokine as part of general Internal medicine study is frequently connected to Regulation of gene expression, therefore bridging the gap between diverse disciplines of science and establishing a new relationship between them. His work deals with themes such as Receptor and Stressor, which intersect with Endocrinology.
He has included themes like Alpha, Neuron, G alpha subunit, Kindling and Synapse in his GABAA receptor study. His Inhibitory postsynaptic potential research integrates issues from Neuroactive steroid, Kindling model, Epileptogenesis, Neurotransmission and Disinhibition. His biological study deals with issues like Locus coeruleus, which deal with fields such as Receptor expression.
Michael O. Poulter mainly focuses on Neuroscience, Epilepsy, Excitatory postsynaptic potential, GABAergic and Macaque. His study in the field of Hippocampus, Premovement neuronal activity and Stimulus also crosses realms of Population and Automatic gain control. His Hippocampus research is multidisciplinary, incorporating elements of Brain-derived neurotrophic factor, Neuroplasticity, Depression and Brain region.
His study in Epilepsy is interdisciplinary in nature, drawing from both Clinical trial, Electrophysiology and Interneuron. His GABAergic study integrates concerns from other disciplines, such as Cerebral cortex, Gene knockdown, Cortex and Piriform cortex. His Inhibitory postsynaptic potential research incorporates elements of Kindling model, Antagonist and Amygdala.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Dysregulation in the Suicide Brain: mRNA Expression of Corticotropin-Releasing Hormone Receptors and GABAA Receptor Subunits in Frontal Cortical Brain Region
Zul Merali;Lisheng Du;Pavel Hrdina;Miklos Palkovits.
The Journal of Neuroscience (2004)
The pathogenesis of clinical depression: stressor- and cytokine-induced alterations of neuroplasticity.
Shawn Hayley;M.O. Poulter;Z. Merali;Hymie Anisman;Hymie Anisman.
Neuroscience (2005)
GABAA receptor promoter hypermethylation in suicide brain: implications for the involvement of epigenetic processes
Michael O. Poulter;Michael O. Poulter;Lisheng Du;Ian C.G. Weaver;Miklós Palkovits.
Biological Psychiatry (2008)
Cytokines as a precipitant of depressive illness: animal and human studies.
Hymie Anisman;Zul Merali;Michael O. Poulter;Shawn Hayley.
Current Pharmaceutical Design (2005)
Differential and transient expression of GABAA receptor alpha-subunit mRNAs in the developing rat CNS.
MO Poulter;JL Barker;AM O'Carroll;SJ Lolait.
The Journal of Neuroscience (1992)
CRF receptor 1 regulates anxiety behavior via sensitization of 5-HT2 receptor signaling
Ana C. Magalhaes;Kevin D. Holmes;Lianne B. Dale;Laetitia Comps-Agrar.
Nature Neuroscience (2010)
Ontogeny of GABAA receptor subunit mRNAs in rat spinal cord and dorsal root ganglia.
Wu Ma;Paul A. Saunders;Roland Somogyi;Michael O. Poulter.
The Journal of Comparative Neurology (1993)
Kindling: some old and some new.
Dan C McIntyre;Michael O Poulter;Krista Gilby.
Epilepsy Research (2002)
Corticotropin-releasing hormone, arginine vasopressin, gastrin-releasing peptide, and neuromedin B alterations in stress-relevant brain regions of suicides and control subjects.
Zul Merali;Pamela Kent;Lisheng Du;Pavel Hrdina.
Biological Psychiatry (2006)
Serotonin receptor subtype and p11 mRNA expression in stress-relevant brain regions of suicide and control subjects.
Hymie Anisman;Lisheng Du;Miklos Palkovits;Gabor Faludi.
Journal of Psychiatry & Neuroscience (2008)
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