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Tamás F. Freund

Researcher at Hungarian Academy of Sciences

Publications -  237
Citations -  33521

Tamás F. Freund is an academic researcher from Hungarian Academy of Sciences. The author has contributed to research in topics: Hippocampal formation & Parvalbumin. The author has an hindex of 96, co-authored 235 publications receiving 31361 citations. Previous affiliations of Tamás F. Freund include Pázmány Péter Catholic University & University of Szeged.

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Role of Endogenous Cannabinoids in Synaptic Signaling

TL;DR: The synthetic pathways of endocannabinoids are discussed, along with the putative mechanisms of their release, uptake, and degradation, and the fine-grain anatomical distribution of the neuronal cannabinoid receptor CB1 is described in most brain areas, emphasizing its general presynaptic localization and role in controlling neurotransmitter release.
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Presynaptically Located CB1 Cannabinoid Receptors Regulate GABA Release from Axon Terminals of Specific Hippocampal Interneurons

TL;DR: The results suggest that cannabinoid-mediated modulation of hippocampal interneuron networks operate largely via presynaptic receptors on CCK-immunoreactive basket cell terminals, the likely mechanism by which both endogenous and exogenous CB1 ligands interfere with hippocampal network oscillations and associated cognitive functions.
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Differences between somatic and dendritic inhibition in the hippocampus

TL;DR: Hippocampal synaptic inhibition is mediated by distinct groups of inhibitory cells that may differentially control dendritic electrogenesis and axonal output of hippocampal pyramidal cells.
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Total number and distribution of inhibitory and excitatory synapses on hippocampal CA1 pyramidal cells

TL;DR: The results indicate that the highly convergent excitation arriving onto the distal dendrites of pyramidal cells is primarily controlled by proximally located inhibition and the organization of excitatory and inhibitory inputs in layers receiving Schaffer collateral input (radiatum/oriens) versus perforant path input (lacunosum-moleculare) is significantly different.