Hillary F. Huber

The paper develops a web-based tool to estimate sample sizes for non-human primate longitudinal studies using natural healthspan data.

This study examines how aging affects physiological reactivity to social stress in marmosets, finding differences in HPA activity, metabolic markers, and social behavior between peri-geri and very-geri females and males.

This study computes sex-specific survival curves for 12 nonhuman primate species to characterize aging patterns and provides insights into lifespan and healthspan differences.

This study finds that aging baboons show sex-specific declines in prefrontal cortex mitochondrial bioenergetics, with males experiencing greater ETC activity loss and a link between walking speed and respiration in males.

This study identifies age-related metabolic shifts in baboon hearts that promote glycosaminoglycan accumulation via the hexosamine biosynthetic pathway, preceding cardiac hypertrophy.

This study examines the effects of maternal undernutrition on hepatic mitochondrial function in baboon offspring during aging, finding male-specific increases in mitochondrial bioenergetics without changes in plasma metabolites.

The paper compares mitochondrial bioenergetics and cellular resilience across astrocytes, hepatocytes, and fibroblasts from aged baboons under different stressors.

The paper integrates multi-omics data from female baboons to identify age-related molecular changes in the prefrontal cortex, revealing altered signaling pathways and potential biomarkers for age-related cognitive decline.

This study integrates multi-omics data from female nonhuman primates to identify aging-related molecular changes in the liver, revealing age-associated pathways in endoplasmic stress and degradation.