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Thiruma V. Arumugam

Researcher at La Trobe University

Publications -  205
Citations -  15784

Thiruma V. Arumugam is an academic researcher from La Trobe University. The author has contributed to research in topics: Stroke & Inflammation. The author has an hindex of 61, co-authored 187 publications receiving 12921 citations. Previous affiliations of Thiruma V. Arumugam include Agency for Science, Technology and Research & LSU Health Sciences Center Shreveport.

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Temporal and Spatial Dynamics of Cerebral Immune Cell Accumulation in Stroke

TL;DR: The peculiar activation pattern and massive increase of antigen-presenting cells in temporal conjunction with regulatory cells might provide additional insight into poststroke immune regulation.
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Pivotal role for neuronal Toll-like receptors in ischemic brain injury and functional deficits

TL;DR: It is reported that neurons express several TLRs, and that the levels of TLR2 and -4 are increased in neurons in response to IFN-γ stimulation and energy deprivation, establishing a proapoptotic signaling pathway for TLR1 and -3 in neurons that may render them vulnerable to ischemic death.
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Role of T lymphocytes and interferon-gamma in ischemic stroke.

TL;DR: Findings indicate that CD4+ and CD8+ T lymphocytes, but not B lymphocyte, contribute to the inflammatory and thrombogenic responses, brain injury, and neurological deficit associated with experimental stroke.
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Hallmarks of Brain Aging: Adaptive and Pathological Modification by Metabolic States.

TL;DR: An overview of the cellular and molecular biology of brain aging, how those processes interface with disease-specific neurodegenerative pathways, and how metabolic states influence brain health is provided.
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Diabetes impairs hippocampal function through glucocorticoid-mediated effects on new and mature neurons

TL;DR: It is demonstrated that, in both insulin-deficient rats and insulin-resistant mice, diabetes impairs hippocampus-dependent memory, perforant path synaptic plasticity and adult neurogenesis, and the adrenal steroid corticosterone contributes to these adverse effects.