ANDREW P. GARNHAM

This study shows that free testosterone is linked to skeletal muscle transcriptome changes but not to muscle mass or strength in males aged 18-80.

This study examines how muscle mass and denervation affect maximal power and rapid force in adult females across their lifespan.

This study examines how normobaric hypoxia affects gene expression in skeletal muscle after high-intensity interval exercise, finding more differentially expressed genes in hypoxia at 24 h post-exercise.

The study compares the transcriptomic profiles of human muscle biopsies and their derived primary myocytes, finding minimal retention of age and sex-related gene expression patterns in culture.

Nine vastus lateralis biopsies from before exercise to 48 h after one high-intensity interval session reveal 16,625 exercise-responsive genes; only four respond differently between males and females.

This study compares mitochondrial remodelling in humans after moderate-intensity continuous exercise and sprint-interval exercise, showing divergent adaptations in mitochondrial structure, function, and protein expression.

This study finds that total testosterone is not linked to muscle mass or strength in pre-menopausal females, but bioavailable testosterone and nuclear-localized androgen receptor are associated with muscle hypertrophy.

This study integrates multi-OMIC data from 12 cohorts to identify exercise-specific molecular signatures and gene regulatory patterns in human skeletal muscle.

This study examines how sleep restriction and resistance exercise interact to affect skeletal muscle transcriptomics in young females, finding that sleep loss moderates the gene expression response to exercise.

This study compares exercise-induced changes in autophagy markers in human and rodent skeletal muscle, finding differences in LC3B-II protein levels and autophagy flux responses.