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Ana L. Jongen-Rêlo

Researcher at ETH Zurich

Publications -  18
Citations -  1864

Ana L. Jongen-Rêlo is an academic researcher from ETH Zurich. The author has contributed to research in topics: Nucleus accumbens & Hippocampal formation. The author has an hindex of 16, co-authored 18 publications receiving 1763 citations.

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Effect of social isolation on stress-related behavioural and neuroendocrine state in the rat.

TL;DR: It is suggested that chronic SI increases emotional reactivity to stress and produces a hyperfunction of the HPA axis in adult rats, particularly in males.
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Highly specific neuron loss preserves lateral inhibitory circuits in the dentate gyrus of kainate-induced epileptic rats.

TL;DR: The findings support hypotheses of temporal lobe epileptogenesis that involve mossy cell and somatostatinergic neuron loss and suggest that lateral inhibition in the dentate gyrus does not require mossy cells but, instead, may be generated directly by GABAergic interneurons.
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Dissociation of function between the dorsal and the ventral hippocampus in spatial learning abilities of the rat: a within-subject, within-task comparison of reference and working spatial memory

TL;DR: It was shown that dorsal lesions were as effective as complete lesions in severely disrupting both reference and working spatial memory, whereas rats with ventral lesions performed at a level comparable with controls, lending further support to the existence of a functional dissociation between the dorsal and the ventral hippocampus.
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Double dissociation of the effects of selective nucleus accumbens core and shell lesions on impulsive-choice behaviour and salience learning in rats.

TL;DR: The double dissociations demonstrated here support a functional segregation between nucleus accumbens core and shell, and add weight to the hypothesis that the core, but not the shell, subregion of the nucleus Accumbens is preferentially involved in the control of choice behaviour under delayed reinforcement conditions and in the inhibitory control of goal‐directed behaviour.
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ApoE4 impairs hippocampal plasticity isoform-specifically and blocks the environmental stimulation of synaptogenesis and memory.

TL;DR: It is shown that apoE4 impairs hippocampal plasticity and isoform-specifically blocks the environmental stimulation of synaptogenesis and memory, which provides a novel mechanism by which environmental factors can modulate the function and phenotypic expression of the APoE genotype.