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Stephen B. Dunnett

Researcher at Cardiff University

Publications -  564
Citations -  39986

Stephen B. Dunnett is an academic researcher from Cardiff University. The author has contributed to research in topics: Transplantation & Dopamine. The author has an hindex of 101, co-authored 561 publications receiving 38430 citations. Previous affiliations of Stephen B. Dunnett include University of Cambridge & University of Wales.

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Dopamine neuron systems in the brain: an update.

TL;DR: The purpose of the present review is to summarize the current knowledge of the diversity and neurochemical features of the nine dopamine-containing neuronal cell groups in the mammalian brain, their distinctive cellular properties, and their ability to regulate their dopaminergic transmitter machinery in response to altered functional demands and aging.
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Characterization of progressive motor deficits in mice transgenic for the human Huntington's disease mutation.

TL;DR: R6/2 mice show measurable deficits in motor behavior that begin subtly and increase progressively until death and indicate that they may be useful for evaluating therapeutic strategies for HD, particularly those aimed at reducing the severity of motor symptoms or slowing the course of the disease.
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Differential expression of immediate early genes in the hippocampus and spinal cord

TL;DR: The results suggest that no simple relationship exists between LTP, spatial learning, and immediate early gene induction, and that immediate early genes can be differentially activated within the central nervous system.
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The "staircase test": a measure of independent forelimb reaching and grasping abilities in rats.

TL;DR: A novel reaching test for the rat has been developed to assess the independent use of forelimbs in skilled reaching and grasping tasks and the simplicity of the apparatus permits many animals to be tested concurrently.
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Prospects for new restorative and neuroprotective treatments in Parkinson's disease

TL;DR: This new understanding of the pathogenesis of Parkinson's disease now offers novel prospects for therapy based on targeted neuroprotection of vulnerable neurons and effective strategies for their replacement.