Entity Detail — Knowledge Graph Node
This page aggregates everything SciDEX knows about NEUROLOGICAL DISEASES: 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.
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| Name | NEUROLOGICAL DISEASES |
| Key Genes/Proteins | GPR37 |
graph TD
NEUROLOGICAL_DISEASES["NEUROLOGICAL DISEASES"]
mTOR["mTOR"] -->|"risk_factor_for"| NEUROLOGICAL_DISEASES
HDAC_Inhibitors["HDAC Inhibitors"] -->|"treats"| NEUROLOGICAL_DISEASES
STING["STING"] -->|"targets"| NEUROLOGICAL_DISEASES
Thyroid_Hormone_Transport_Defe["Thyroid Hormone Transport Defects"] -->|"risk_factor_for"| NEUROLOGICAL_DISEASES
Microglia["Microglia"] -->|"targets"| NEUROLOGICAL_DISEASES
Cns_Macrophages["Cns Macrophages"] -->|"involved_in"| NEUROLOGICAL_DISEASES
HCN4["HCN4"] -->|"implicated in"| NEUROLOGICAL_DISEASES| Target | Relation | Type | Str |
|---|---|---|---|
| No outgoing edges | |||
| Source | Relation | Type | Str |
|---|---|---|---|
| STING | associated_with | protein | 0.95 |
| mTOR | risk_factor_for | protein | 0.90 |
| microbiota-gut-brain axis | implicated_in | pathway | 0.90 |
| Hdac Inhibitors | treats | drug | 0.88 |
| SHH | therapeutic_target | protein | 0.88 |
| Swi/Snf Mutations | causes | biomarker | 0.85 |
| Optogenetic Stimulation | treats | process | 0.85 |
| HDAC Inhibitors | treats | drug | 0.85 |
| STING | targets | protein | 0.85 |
| Optogenetic Modulation | treats | mechanism | 0.82 |
| GPR37 | implicated_in | gene | 0.80 |
| Tryptophan Metabolites | associated_with | compound | 0.80 |
| Thyroid Hormone Transport Defect | contributes_to | phenotype | 0.80 |
| gut microbiota | implicated_in | cell_type | 0.80 |
| GFAP | biomarker_for | protein | 0.80 |
| neurovascular unit | associated_with | cell_type | 0.80 |
| Cns Macrophages | involved_in | cell_type | 0.80 |
| optogenetic stimulation | treats | process | 0.80 |
| Microglia | targets | cell_type | 0.80 |
| Microglia | involved_in | cell_type | 0.80 |
| Thyroid Hormone Transport Defects | risk_factor_for | mechanism | 0.80 |
| PI3K/AKT | associated_with | pathway | 0.75 |
| mitophagy | associated_with | process | 0.70 |
| OPTN | associated_with | protein | 0.70 |
| selective autophagy | associated_with | process | 0.70 |
| NBR1 | associated_with | protein | 0.70 |
| NF-κB | associated_with | pathway | 0.65 |
| HCN4 | implicated_in | gene | 0.50 |
| HCN2 | implicated_in | gene | 0.50 |
| HCN1 | implicated_in | gene | 0.50 |
| PARP1 | implicated_in | gene | 0.50 |
| NAD | implicated_in | gene | 0.50 |
Hypotheses where this entity is a therapeutic target
| Hypothesis | Score | Disease | Analysis |
|---|---|---|---|
| Tissue-specific interactome destabilization drives phenotype | 0.280 | Mendelian neurological diseases (neurodegeneration) | What molecular mechanisms drive tissue-s |
Scientific analyses that reference this entity
No analyses mention this entity
Experimental studies targeting or related to this entity
| Experiment | Type | Disease | Score | Feasibility | Model | Status | Est. Cost |
|---|---|---|---|---|---|---|---|
| No experiments found | |||||||
Scientific publications cited in analyses involving this entity
| Title & PMID | Authors | Journal | Year | Citations |
|---|---|---|---|---|
| No papers found | ||||
Multi-agent debates referencing this entity
No debates reference this entity
Hypotheses and analyses mentioning NEUROLOGICAL DISEASES in their description or question text
No additional research found