Advanced search
Combine gene, variant, phenotype, region and year filters
Every result shows the extracted entities next to the sentences that support them; rows for the searched entities come first.
Transparent by designEvery result links extracted entities to its source sentence and publication identifier.
Knowledge-base search
About your search
SIRT3 and cardiomyopathy are reported together in 2 articles.
Gene
SIRT3
- HGNC
- HGNC:14931
13articles
13mentions
0variants with confirmed gene link
Most co-reported phenotypes (articles)
Phenotype
Cardiomyopathy
- HPO
- HP:0001638
618articles
618mentions
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
2 records shown · first 60Targeting the underlying immune mechanism of diabetes-induced myocardial dysfunction via modulation of SIRT-3/p53/TIGAR/PFKFB-3 and SIRT-3/NF-κB signaling pathways as a potential controlling strategy.
PMID 41496325 | DOI 10.1016/j.biopha.2025.118901 · Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie · 2026 · 5 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | SIRT3 | “Notably, MTX upregulated cardiac SIRT3 and PFKFB3 expression while downregulating p53/TIGAR signaling pathways, indicating an improvement in T2D-induced glycolytic disruption and reduced apoptosis.” | 0.98 | hgnc_dict_v1 |
| phenotype | cardiomyopathy | “Conclusively, MTX mitigates T2D-induced myocardial dysfunction by modulating SIRT3-related metabolic and inflammatory signaling pathways, highlighting its potential as a low-cost therapeutic option for diabetes-associated cardiomyopathy.” | 0.98 | phenotype_alias_lexicon_v2 |
| gene | TIGAR | “Targeting the underlying immune mechanism of diabetes-induced myocardial dysfunction via modulation of SIRT-3/p53/TIGAR/PFKFB-3 and SIRT-3/NF-κB signaling pathways as a potential controlling strategy.” | 0.98 | hgnc_dict_v1 |
| gene | PFKFB3 | “Notably, MTX upregulated cardiac SIRT3 and PFKFB3 expression while downregulating p53/TIGAR signaling pathways, indicating an improvement in T2D-induced glycolytic disruption and reduced apoptosis.” | 0.98 | hgnc_dict_v1 |
The enigmatic role of SIRT2 in the cardiovascular system: Deciphering its protective and detrimental actions to unlock new avenues for therapeutic intervention.
PMID 39566866 | DOI 10.1016/j.cpcardiol.2024.102929 · Current problems in cardiology · 2025 · 4 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | SIRT3 | “The Sirtuin (SIRT) family of NAD+-dependent enzymes has recently been shown to play a critical role in cardiovascular health and disease, and several SIRT isoforms, especially SIRT1 and SIRT3, have been amply investigated.” | 0.98 | hgnc_dict_v1 |
| phenotype | cardiomyopathy | “Here, we review the current understanding of the involvement of SIRT2 in various cardiovascular pathologies, such as cardiac hypertrophy, ischemia-reperfusion injury, diabetic cardiomyopathy, and vascular dysfunction, with emphasis placed on the context-dependent protective or deleterious actions of SIRT2, including its wide array of catalytic activities which span beyond deacetylation.” | 0.98 | phenotype_alias_lexicon_v2 |
| gene | SIRT2 | “The enigmatic role of SIRT2 in the cardiovascular system: Deciphering its protective and detrimental actions to unlock new avenues for therapeutic intervention.” | 0.98 | hgnc_dict_v1 |
| gene | SIRT1 | “The Sirtuin (SIRT) family of NAD+-dependent enzymes has recently been shown to play a critical role in cardiovascular health and disease, and several SIRT isoforms, especially SIRT1 and SIRT3, have been amply investigated.” | 0.98 | hgnc_dict_v1 |