source · text/csv
source_d3c77e3939f8406e
sha256 864e219f584a6a543fe290dde02e5753fcd52c68fab5c254d5dd5e8671bb0240
by researka:v2 · 2026-06-28 02:18:54.042502+04:00
study,population,intervention_or_exposure,comparator,endpoint,effect,risk_of_bias,directness Evidence gaps in the effects of exercise on SASP-Related biomarkers in older adults: a systematic review and meta-analysis of randomized controlled trials,not extracted,not extracted,not extracted,not extracted,not extracted,not appraised in public sidecar,review-level The microRNA-34a-Induced Senescence-Associated Secretory Phenotype (SASP) Favors Vascular Smooth Muscle Cells Calcification,not extracted,not extracted,not extracted,not extracted,not extracted,not appraised in public sidecar,primary Abstract 2954: Androgen deprivation therapy (ADT) and senescence-associated secretory phenotype (SASP) in vitro: Correlation with SASP in tumor specimens as well as in the serum of patients after ADT,not extracted,not extracted,not extracted,not extracted,not extracted,not appraised in public sidecar,primary Synergistic senolytic–regenerative therapy significantly extends healthspan and lifespan,not extracted,not extracted,not extracted,not extracted,not extracted,not appraised in public sidecar,primary The cardio‐renal‐metabolic role of the nod‐like receptor protein‐3 and senescence‐associated secretory phenotype in early sodium/glucose cotransporter‐2 inhibitor therapy in people with diabetes who have had a myocardial infarction,not extracted,not extracted,not extracted,not extracted,not extracted,not appraised in public sidecar,primary Senescence-associated secretory phenotype and its impact on oral immune homeostasis,not extracted,not extracted,not extracted,not extracted,not extracted,not appraised in public sidecar,primary Senescence in head and neck squamous cell carcinoma: relationship between senescence-associated secretory phenotype (SASP) mRNA expression level and clinicopathological features,not extracted,not extracted,not extracted,not extracted,not extracted,not appraised in public sidecar,primary ROCK inhibition modulates the senescence‐associated secretory phenotype (SASP) in oral keratinocytes,not extracted,not extracted,not extracted,not extracted,not extracted,not appraised in public sidecar,primary "Proteomic Analysis of the Senescence-Associated Secretory Phenotype: GDF-15, IGFBP-2, and Cystatin-C Are Associated With Multiple Aging Traits",not extracted,not extracted,not extracted,not extracted,not extracted,not appraised in public sidecar,primary A Senescence Associated Secretory Phenotype (SASP) in Indolent Systemic Mastocytosis Compared to Healthy Controls,not extracted,not extracted,not extracted,not extracted,not extracted,not appraised in public sidecar,primary Senescence‐associated secretory phenotype (SASP) index in individuals across the Alzheimer’s disease continuum,not extracted,not extracted,not extracted,not extracted,not extracted,not appraised in public sidecar,primary Inflammaging and Senescence-Associated Secretory Phenotype (SASP) in Psoriasis – A Narrative Review of Potential Mechanisms and Anti-Inflammaging Strategies,not extracted,not extracted,not extracted,not extracted,not extracted,not appraised in public sidecar,review-level The Impact of Senescence-Associated Secretory Phenotype (SASP) on Head and Neck Cancers: From Biology to Therapy,not extracted,not extracted,not extracted,not extracted,not extracted,not appraised in public sidecar,primary Senescent Endothelial Cells Sustain Their Senescence-Associated Secretory Phenotype (SASP) through Enhanced Fatty Acid Oxidation,not extracted,not extracted,not extracted,not extracted,not extracted,not appraised in public sidecar,primary Folic Acid Supplementation Suppresses Sleep Deprivation-Induced Telomere Dysfunction and Senescence-Associated Secretory Phenotype (SASP),not extracted,not extracted,not extracted,not extracted,not extracted,not appraised in public sidecar,primary Small extracellular vesicles and their miRNA cargo are anti-apoptotic members of the senescence-associated secretory phenotype,not extracted,not extracted,not extracted,not extracted,not extracted,not appraised in public sidecar,primary Senescence-Associated Secretory Phenotypes Reveal Cell-Nonautonomous Functions of Oncogenic RAS and the p53 Tumor Suppressor,not extracted,not extracted,not extracted,not extracted,not extracted,not appraised in public sidecar,primary "**Outcome class** is assigned from the source's bound endpoint, population, and claim text; adjacent/background sources are separated from clinical outcome slices.",not extracted,not extracted,not extracted,not extracted,not extracted,not appraised in public sidecar,citation "**Directness** is coded as direct only when a source tests the topic against a clinically proximate outcome in the relevant population; a qualifying direct source would be a human interventional or hard-endpoint study of the topic itself. Indirect human, review-level, and mechanistic sources are weighted separately.",not extracted,not extracted,not extracted,not extracted,not extracted,not appraised in public sidecar,citation "**Directional signal** is counted within the assigned outcome class only. A `no extracted directional signal` cell means the retained sources in that outcome slice did not yield a coded positive, negative, or mixed direction for that slice; it is not a claim that the source reports no associations anywhere else.",not extracted,not extracted,not extracted,not extracted,not extracted,not appraised in public sidecar,citation **Evidence tier** follows the deterministic tier/directness taxonomy used in the source builder; the prose writer cannot move a source between classes after sources are frozen.,not extracted,not extracted,not extracted,not extracted,not extracted,not appraised in public sidecar,citation
metadata
{
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"sidecar_name": "evidence_table.csv",
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}