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P. Lawlor

Researcher at University of Auckland

Publications -  41
Citations -  5848

P. Lawlor is an academic researcher from University of Auckland. The author has contributed to research in topics: Long-term potentiation & Immediate early gene. The author has an hindex of 32, co-authored 41 publications receiving 5683 citations. Previous affiliations of P. Lawlor include Health Science University.

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Safety and tolerability of gene therapy with an adeno-associated virus (AAV) borne GAD gene for Parkinson's disease: an open label, phase I trial.

TL;DR: AAV-GAD gene therapy of the subthalamic nucleus is safe and well tolerated by patients with advanced Parkinson's disease, suggesting that in-vivo gene therapy in the adult brain might be safe for various neurodegenerative diseases.
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Environmental enrichment inhibits spontaneous apoptosis, prevents seizures and is neuroprotective.

TL;DR: In addition to its effects on neurogenesis, an enriched environment reduces spontaneous apoptotic cell death in the rat hippocampus by 45%.
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In situ evidence for DNA fragmentation in Huntington's disease striatum and Alzheimer's disease temporal lobes.

TL;DR: Evidence of DNA fragmentation in cells in temporal cortex and hippocampus from patients with AD and in striatum from those with HD is found, suggesting that apoptosis may be involved in these disorders.
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Correlations between immediate early gene induction and the persistence of long-term potentiation

TL;DR: Data provide support for the hypothesis that long-term potentiation 3 involves mechanisms additional to those for long- Term potentiation 2, and one possible mechanism is altered gene expression, initiated by immediate early gene transcription factors such as zif/268 and possibly homo- or heterodimers of Fos and Jun family members, that then contributes to the stabilization or maintenance of long- term potentiation3.
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An oral vaccine against NMDAR1 with efficacy in experimental stroke and epilepsy.

TL;DR: A single-dose AAV vaccine was associated with strong anti-epileptic and neuroprotective activity in rats for both a kainate-induced seizure model and also a middle cerebral artery occlusion stroke model at 1 to 5 months following vaccination.