Chady H. Hakim

Microdystrophin Ameliorates Muscular Dystrophy in the Canine Model of Duchenne Muscular Dystrophy.

Connexin isoform expression in smooth muscle cells and endothelial cells of hamster cheek pouch arterioles and retractor feed arteries.

Nitrosative stress elicited by nNOSµ delocalization inhibits muscle force in dystrophin-null mice.

Monitoring murine skeletal muscle function for muscle gene therapy.

Genotyping mdx, mdx3cv, and mdx4cv mice by primer competition polymerase chain reaction.

The passive mechanical properties of the extensor digitorum longus muscle are compromised in 2- to 20-mo-old mdx mice.

Temperature effects on morphological integrity and Ca²⁺ signaling in freshly isolated murine feed artery endothelial cell tubes.

Gender differences in contractile and passive properties of mdx extensor digitorum longus muscle.

Dystrophin deficiency compromises force production of the extensor carpi ulnaris muscle in the canine model of Duchenne muscular dystrophy.

Truncated dystrophins reduce muscle stiffness in the extensor digitorum longus muscle of mdx mice.

A marginal level of dystrophin partially ameliorates hindlimb muscle passive mechanical properties in dystrophin-null mice.