Multimodal aging clocks accurately quantify human biological age and reveal coagulation factors as key drivers of multi-organ senescence.
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Multimodal aging clocks accurately quantify human biological age and reveal coagulation factors as key drivers of multi-organ senescence.
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Loss of Lsp2 reduces TOP mRNA translation via 4E-BP, extending Drosophila lifespan independently of rapamycin, highlighting a new longevity pathway.
Restricting larval protein intake reduces Lsp2 levels, decreases ribosomal proteins, and extends adult lifespan in Drosophila by up to a significant margin.
A miR-10a-5p-γCaMKII axis mediates peripheral signals that increase brain vulnerability during female midlife, with miR-10a-5p levels rising significantly in this period.
Transient changes in H3K27me3 in C. elegans persist for multiple generations, affecting fertility and involving specific histone modifications.
Fine-tuned Longevity-LLMs with 0.6B-9B parameters outperform larger models on aging biology tasks in the LongevityBench benchmark.
Caloric restriction enhances circadian metabolic regulation and improves glucose and fatty acid metabolism compared to fasting-refeeding cycles, with a significant impact on metabolic health.
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