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ULK1 and Parkinson disease are reported together in 1 article.
Gene
ULK1
- HGNC
- HGNC:12558
9articles
9mentions
0variants with confirmed gene link
Most co-reported phenotypes (articles)
Phenotype
Parkinson disease
280articles
280mentions
12co-reported genes shown
Most co-reported genes (articles)
Counts are literature co-mentions in SaudiVarKB, not clinical or causal assertions. Gene details: HGNC; variant status: ClinVar via dbSNP.
Publications
1 records shown · first 60Resveratrol alleviates neurological disorders and motor dysfunction in 3-NP induced- Huntington's Disease in rats: Role of activating AMPK/SIRT1/ULK1 autophagy pathway.
PMID 42331250 | DOI 10.1016/j.neuropharm.2026.111084 · Neuropharmacology · 2026 · 4 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | ULK1 | “Resveratrol alleviates neurological disorders and motor dysfunction in 3-NP induced- Huntington's Disease in rats: Role of activating AMPK/SIRT1/ULK1 autophagy pathway.” | 0.98 | hgnc_dict_v1 |
| phenotype | Parkinson disease | “RESV showed promising neuroprotective effects against Alzheimer's and Parkinson's disease.” | 0.93 | phenotype_alias_lexicon_v2 |
| gene | SIRT1 | “Resveratrol alleviates neurological disorders and motor dysfunction in 3-NP induced- Huntington's Disease in rats: Role of activating AMPK/SIRT1/ULK1 autophagy pathway.” | 0.98 | hgnc_dict_v1 |
| phenotype | intellectual disability | “Huntington's disease (HD) is a genetic neurodegenerative disease characterized by striatum damage, which results in a number of uncontrollable muscle movements alongside intellectual and cognitive impairment.” | 0.93 | phenotype_alias_lexicon_v2 |