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{
"n": "",
"doi": "10.1113/jp287265",
"claim": "Characterizing optogenetically mediated rebound effects in anaesthetized mouse primary visual cortex.",
"title": null,
"cite_key": "Shapiro2025",
"evidence": "Characterizing optogenetically mediated rebound effects in anaesthetized mouse primary visual cortex.. Optogenetic tools have been used to investigate neural circuits in mouse primary visual cortex (V1), where channelrhodopsin-mediated activation (photostimulation) of inhibitory interneuron subtypes expressing parvalbumin (Pvalb+), somatostatin (SOM+) or vasoactive intestinal peptide (VIP+) can alter the responses of excitatory pyramidal neurons. Some studies have mentioned rebound spiking after this photostimulation, but no systematic analysis of these post-inhibitory rebound effects has yet ",
"effect_size": null,
"text_access": "fulltext",
"study_system": "cortex/HC",
"_source_cluster": "cluster_05_synaptic_connectivity",
"replication_status": "single",
"_source_cluster_index": 177,
"claim_source_sentence": null,
"replication_evidence_dois": []
}- source_refs
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"paper:paper-410b852f3cc3"
]
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{
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}
]- source_policy
{
"mode": "public_source_pointer_with_short_context",
"notes": [
"Local review repositories are read-only inputs.",
"SciDEX stores paper metadata, structured evidence, file pointers, and short citation contexts; it does not copy full review prose."
],
"source_commit_sha": "95e761177f7d2ec565983d3307c14ec238f9677c",
"source_repository_url": "https://github.com/AllenNeuralDynamics/ComputationalReviewVIP"
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Characterizing optogenetically mediated rebound effects in anaesthetized mouse primary visual cortex.. Optogenetic tools have been used to investigate neural circuits in mouse primary visual cortex (V1), where channelrhodopsin-mediated activation (photostimulation) of inhibitory interneuron subtypes expressing parvalbumin (Pvalb+), somatostatin (SOM+) or vasoactive intestinal peptide (VIP+) can alter the responses of excitatory pyramidal neurons. Some studies have mentioned rebound spiking after this photostimulation, but no systematic analysis of these post-inhibitory rebound effects has yet