Matthew Kostek

Blood pressure response to strength training may be influenced by angiotensinogen A-20C and angiotensin II type I receptor A1166C genotypes in older men and women.

Vitamin D receptor FokI genotype influences bone mineral density response to strength training, but not aerobic training.

Muscle strength response to strength training is influenced by insulin-like growth factor 1 genotype in older adults.

Effects of moderate-velocity strength training on peak muscle power and movement velocity: do women respond differently than men?

AMPD1 gene polymorphism and the vasodilatory response to ischemia.

ACE ID genotype and the muscle strength and size response to unilateral resistance training.

Muscle-power quality: does sex or race affect movement velocity in older adults?

Alpha-actinin-3 (ACTN3) R577X polymorphism influences knee extensor peak power response to strength training in older men and women.

Gene expression responses over 24 h to lengthening and shortening contractions in human muscle: major changes in CSRP3, MUSTN1, SIX1, and FBXO32.

Subcutaneous fat alterations resulting from an upper-body resistance training program.

Influence of promoter region variants of insulin-like growth factor pathway genes on the strength-training response of muscle phenotypes in older adults.

Myostatin and follistatin polymorphisms interact with muscle phenotypes and ethnicity.

A polymorphism near IGF1 is associated with body composition and muscle function in women from the Health, Aging, and Body Composition Study.

Training and detraining in older men.

Age-related changes in adult muscle morphology.

Does insulin-like growth factor 1 genotype influence muscle power response to strength training in older men and women?

Therapeutic ultrasound affects IGF-1 splice variant expression in human skeletal muscle.

The regulation of skeletal muscle protein turnover during the progression of cancer cachexia in the Apc(Min/+) mouse.

Six1 and Six1 cofactor expression is altered during early skeletal muscle overload in mice.

IL-6 signaling blockade increases inflammation but does not affect muscle function in the mdx mouse.

IL-6 regulation on skeletal muscle mitochondrial remodeling during cancer cachexia in the ApcMin/+ mouse.

Resveratrol decreases inflammation and increases utrophin gene expression in the mdx mouse model of Duchenne muscular dystrophy.

Exercise increases utrophin protein expression in the mdx mouse model of Duchenne muscular dystrophy.

Resveratrol improves muscle function but not oxidative capacity in young mdx mice.

Glucocorticoid Receptor (NR3C1) Variants Associate with the Muscle Strength and Size Response to Resistance Training.

A Combination Of Exericse And Resveratrol Produces Additive Effects In Reducing Muscle Pathology In Mdx Mouse: 3165 Board #230 June 3, 2: 00 PM - 3: 30 PM.

Continuous Ultrasound Decreases Pain Perception and Increases Pain Threshold in Damaged Skeletal Muscle.