Area of research
Physiology · Molecular Biology
Research interest
Research interests include Muscle Physiology and Disorders, Adipose Tissue and Metabolism, Nutrition and Health in Aging, and Muscle metabolism and nutrition.
Covariation MS uncovers a protein that controls cysteine catabolism
The human zinc-binding cysteine proteome
Stem cell secretome treatment improves whole‐body metabolism, reduces adiposity, and promotes skeletal muscle function in aged mice
Disuse‐induced muscle fibrosis, cellular senescence, and senescence‐associated secretory phenotype in older adults are alleviated during re‐ambulation with metformin pre‐treatment
Lipid hydroperoxides promote sarcopenia through carbonyl stress
Extracellular vesicle distribution and localization in skeletal muscle at rest and following disuse atrophy
Skeletal muscle-specific inducible AMPKα1/α2 knockout mice develop muscle weakness, glycogen depletion, and fibrosis that persists during disuse atrophy
Macrophage immunomodulation accelerates skeletal muscle functional recovery in aged mice following disuse atrophy
Short-term exposure to a clinical dose of metformin increases skeletal muscle mitochondrial H2O2 emission and production in healthy, older adults: A randomized controlled trial
Metformin and leucine increase satellite cells and collagen remodeling during disuse and recovery in aged muscle
Low lysophosphatidylcholine induces skeletal muscle myopathy that is aggravated by high‐fat diet feeding
Disrupted macrophage metabolic reprogramming in aged soleus muscle during early recovery following disuse atrophy
Influence of Exercise Training on Skeletal Muscle Insulin Resistance in Aging: Spotlight on Muscle Ceramides
PGC-1α-Targeted Therapeutic Approaches to Enhance Muscle Recovery in Aging
Ceramide Biomarkers Predictive of Cardiovascular Disease Risk Increase in Healthy Older Adults After Bed Rest
Neuromuscular electrical stimulation and protein during bed rest increases CD11b<sup>+</sup> skeletal muscle macrophages but does not correspond to muscle size or insulin sensitivity
Aging impairs mouse skeletal muscle macrophage polarization and muscle-specific abundance during recovery from disuse