entity

miR-132

Entity Detail — Knowledge Graph Node

Understanding Entity Pages

This page aggregates everything SciDEX knows about miR-132: its mechanistic relationships (Knowledge Graph edges), hypotheses targeting it, analyses mentioning it, and supporting scientific papers. The interactive graph below shows its immediate neighbors. All content is AI-synthesized from peer-reviewed literature.

9Connections
1Hypotheses
2Analyses
8Outgoing
1Incoming
0Experiments
2Debates

No AI portrait yet

Outgoing (8)

TargetRelationTypeStr
benchmark_ot_ad_answer_key:MIR-132data_indataset_row0.00
Tau Phosphorylationinhibitsprocess0.80
Tau hyperphosphorylationinhibitsprocess0.80
memory consolidationregulatesphenotype0.70
MeCP2 mRNAregulatesgene0.70

Incoming (1)

SourceRelationTypeStr
benchmark_ot_ad_answer_key:MIR-132data_indataset_row0.00

Targeting Hypotheses (1)

Hypotheses where this entity is a therapeutic target

HypothesisScoreDiseaseAnalysis
H6: miR-132/212 Cluster Silencing Disables Neuronal Chromati 0.660 neurodegeneration Investigate mechanisms of epigenetic rep

Mentioning Analyses (2)

Scientific analyses that reference this entity

What are the specific molecular mechanisms linking ADCY8 to spatial memory conso

neuroscience | 2026-04-11 | 0 hypotheses

Can circadian interventions selectively target microglia without affecting other

neuropharmacology | 2026-04-10 | 0 hypotheses

Experiments (0)

Experimental studies targeting or related to this entity

ExperimentTypeDiseaseScoreFeasibilityModelStatusEst. Cost
No experiments found

Related Papers (0)

Scientific publications cited in analyses involving this entity

Title & PMIDAuthorsJournalYearCitations
No papers found

Debates (2)

Multi-agent debates referencing this entity

The debate highlighted a critical cell-type specificity gap where no evidence ex

closed · Rounds: 4 · Score: 0.30 · 2026-04-21

While the debate proposes ADCY8-cAMP-PKA-CREB pathways, the exact molecular step

closed · Rounds: 4 · Score: 0.30 · 2026-04-21

Related Research

Hypotheses and analyses mentioning miR-132 in their description or question text

No additional research found