- raw_fields
{
"n": 540,
"doi": "10.1113/jp287265",
"claim": "We found converging evidence that rebounds were largest when interneuron photostimulation was coupled with visual stimuli that strongly activate V1.",
"evidence": "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",
"effect_size": null,
"text_access": "fulltext",
"study_system": "mouse cortex",
"replication_status": "replication_unknown",
"claim_source_sentence": "We found converging evidence that rebounds were largest when interneuron photostimulation was coupled with visual stimuli that strongly activate V1.",
"replication_evidence_dois": [],
"effect_size_source_sentence": null
}- source_refs
[
"paper:paper-410b852f3cc3"
]
- evidence_refs
[
{
"ref": "paper:paper-410b852f3cc3"
}
]- 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": "df9fc7e8d455b084152c9d713558dae0013cef21",
"source_repository_url": "https://github.com/AllenNeuralDynamics/ComputationalReviewPV"
}- evidence_summary
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