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- Live5/17/2026, 4:35:28 PM
09e83627f10cContent snapshot
{ "scope": "mouse neocortex, Scn1a knock-in model", "claim_text": "Nav1.1 is clustered predominantly at the axon initial segments of parvalbumin-positive inhibitory interneurons in developing neocortex, and heterozygous Scn1a loss-of-function causes pronounced spike amplitude decrement during sustained firing in these fast-spiking cells.", "raw_fields": { "n": 0, "doi": "10.1523/jneurosci.5270-06.2007", "claim": "Nav1.1 is clustered predominantly at the axon initial segments of parvalbumin-positive inhibitory interneurons in developing neocortex, and heterozygous Scn1a loss-of-function causes pronounced spike amplitude decrement during sustained firing in these fast-spiking cells.", "evidence": "Knock-in mouse line with loss-of-function nonsense mutation in Scn1a developed epileptic seizures within first postnatal month. Trains of evoked APs in PV-FS cells showed pronounced spike amplitude decrement late in burst.", "effect_size": "pronounced spike amplitude decrement in heterozygous knock-in FS cells during sustained burst firing", "text_access": "abstract_only", "study_system": "mouse neocortex, Scn1a knock-in model", "replication_status": "independently_replicated", "claim_source_sentence": "Immunohistochemical analyses revealed that, in the developing neocortex, Nav1.1 was clustered predominantly at the axon initial segments of parvalbumin-positive (PV) interneurons.", "replication_evidence_dois": [ "10.1073/pnas.1411131111", "10.1523/jneurosci.0721-14.2014" ], "effect_size_source_sentence": "In heterozygous knock-in mice, trains of evoked action potentials in these fast-spiking, inhibitory cells exhibited pronounced spike amplitude decrement late in the burst." }, "section_id": "section_05_evidence_package", "source_url": "https://github.com/AllenNeuralDynamics/ComputationalReviewPV/blob/df9fc7e8d455b084152c9d713558dae0013cef21/evidence/section_05_evidence_package.json", "effect_size": "pronounced spike amplitude decrement in heterozygous knock-in FS cells during sustained burst firing", "review_repo": "ComputationalReviewPV", "section_ref": "wiki_page:computationalreviewpv-05", "source_kind": "review_finding", "source_path": "evidence/section_05_evidence_package.json", "source_refs": [ "paper:paper-fd8f15e7c2e1" ], "source_span": "Immunohistochemical analyses revealed that, in the developing neocortex, Nav1.1 was clustered predominantly at the axon initial segments of parvalbumin-positive (PV) interneurons.", "study_system": "mouse neocortex, Scn1a knock-in model", "evidence_refs": [ { "ref": "paper:paper-fd8f15e7c2e1" } ], "section_title": "Intrinsic Electrophysiology: The Fast-Spiking Phenotype and Its Variants", "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": "Knock-in mouse line with loss-of-function nonsense mutation in Scn1a developed epileptic seizures within first postnatal month. Trains of evoked APs in PV-FS cells showed pronounced spike amplitude decrement late in burst.", "review_bundle_ref": "analysis_bundle:ab-e6261c8263e7", "replication_status": "independently_replicated", "review_package_ref": "analysis_bundle:ab-e6261c8263e7", "source_artifact_ref": "wiki_page:computationalreviewpv-05", "origin_url": "https://github.com/AllenNeuralDynamics/ComputationalReviewPV/blob/df9fc7e8d455b084152c9d713558dae0013cef21/evidence/section_05_evidence_package.json", "commit_sha": "df9fc7e8d455b084152c9d713558dae0013cef21", "created_by": "persona-jerome-lecoq-gbo-neuroscience", "repository_url": "https://github.com/AllenNeuralDynamics/ComputationalReviewPV" }