Details
- scope
- vip-interneurons
- claim_text
- Developmental loss of MeCP2 from VIP interneurons impairs cortical function and Rett-like behaviors
- section_id
- section_13
- source_url
- https://github.com/AllenNeuralDynamics/ComputationalReviewVIP/blob/95e761177f7d2ec565983d3307c14ec238f9677c/evidence/section_13_evidence_package.json
- review_repo
- ComputationalReviewVIP
- section_ref
- wiki_page:computationalreviewvip-13-conclusion
- source_kind
- review_finding
- source_path
- evidence/section_13_evidence_package.json
- source_span
- Rett Syndrome is a devastating neurodevelopmental disorder resulting from mutations in the gene <i>MECP2</i>.
- section_title
- Synthesis and Conclusion: Reassessing the Canonical VIP Disinhibitor
- review_bundle_ref
- analysis_bundle:ab-2ce40c33e827
- replication_status
- unevaluated
- review_package_ref
- analysis_bundle:ab-2ce40c33e827
- source_artifact_ref
- wiki_page:computationalreviewvip-13-conclusion
- origin_url
- https://github.com/AllenNeuralDynamics/ComputationalReviewVIP/blob/95e761177f7d2ec565983d3307c14ec238f9677c/evidence/section_13_evidence_package.json
- commit_sha
- 95e761177f7d2ec565983d3307c14ec238f9677c
- created_by
- persona-jerome-lecoq-gbo-neuroscience
- repository_url
- https://github.com/AllenNeuralDynamics/ComputationalReviewVIP
Raw fields (4)
- raw_fields
{ "n": null, "doi": "10.7554/elife.55639", "pmid": "32343226", "tags": [ "snowball_fwd" ], "year": "2020", "claim": "Developmental loss of MeCP2 from VIP interneurons impairs cortical function and Rett-like behaviors", "pmcid": "PMC7213975", "round": 2, "title": "Developmental loss of MeCP2 from VIP interneurons impairs cortical function and behavior", "journal": "eLife", "citation": "James M. Mossner; Renata Batista‐Brito; Rima Pant; Jessica A. Cardin", "cite_key": "Mossner2020", "effect_size": null, "text_access": "fulltext", "citedByCount": 59, "isOpenAccess": "Y", "evidence_type": "mechanism", "linked_topics": [ "snowball_fwd" ], "_source_cluster": "cluster_07_in_vivo_function", "relevance_score": 0.8, "replication_status": null, "_source_cluster_index": 55, "claim_source_sentence": "Rett Syndrome is a devastating neurodevelopmental disorder resulting from mutations in the gene <i>MECP2</i>." }- source_refs
[ "paper:paper-4effa559f79e" ]
- evidence_refs
[ { "ref": "paper:paper-4effa559f79e" } ]- 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" }