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Jean-Luc Dreyer

Researcher at University of Fribourg

Publications -  56
Citations -  2870

Jean-Luc Dreyer is an academic researcher from University of Fribourg. The author has contributed to research in topics: Nucleus accumbens & Conditioned place preference. The author has an hindex of 29, co-authored 53 publications receiving 2622 citations.

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microRNAs miR-124, let-7d and miR-181a regulate cocaine-induced plasticity.

TL;DR: The data suggest that miR-124, let-7d and mi-181a may be involved in a complex feedback loop with cocaine-responsive plasticity genes, highlighting the possibility that some miRNAs are key regulators of the reward circuit and may be implicated in addiction.
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Potential role of nuclear translocation of glyceraldehyde-3-phosphate dehydrogenase in apoptosis and oxidative stress.

TL;DR: Observations indicate that nuclear translocation of GAPDH may play a role in apoptosis and oxidative stress, probably related to the activity ofGAPDH as a DNA repair enzyme or as a nuclear carrier for pro-apoptotic molecules.
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Regulation of MiR-124, Let-7d, and MiR-181a in the accumbens affects the expression, extinction, and reinstatement of cocaine-induced conditioned place preference.

TL;DR: In vivo miRNA gain and loss of function on cocaine-induced conditioned place preference (CPP) by localized LV-miRNA regulation in the nucleus accumbens (NAc) is tested, describing a complex regulatory pathway mediated by miRNAs in cocaine-mediated neuronal adaptations.
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Associative Learning and CA3–CA1 Synaptic Plasticity Are Impaired in D1R Null, Drd1a−/− Mice and in Hippocampal siRNA Silenced Drd1a Mice

TL;DR: A functional relationship between acquisition of associative learning, increase in synaptic strength at the CA3–CA1 synapse, and Egr1 induction in the hippocampus is revealed by demonstrating that all three are dramatically impaired when D1R is eliminated or reduced.
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Specification of Distinct Dopaminergic Neural Pathways: Roles of the Eph Family Receptor EphB1 and Ligand Ephrin-B2

TL;DR: It is suggested that the ligand–receptor pair may contribute to the establishment of distinct neural pathways by selectively inhibiting the neurite outgrowth and cell survival of mistargeted neurons.