AbstractMetabolic profiles from 1H nuclear magnetic resonance spectroscopy have been used to describe both one and two protein systems in four mouse models related to Duchenne muscular dystrophy using the pattern recognition technique partial least squares. Robust statistical models were built for extracts and intact cardiac tissue, distinguishing mice according to expression of dystrophin. Using metabolic profiles of diaphragm, models were built describing dystrophin and utrophin, a dystrophin related protein, expression. Increased utrophin expression counteracted some of the deficits associated with dystrophic tissue. This suggests the method may be ideal for following treatment regimes such as gene therapy
Facioscapulohumeral muscular dystrophy (FSHD) is a hereditary neuromuscular disorder characterized b...
Duchenne muscular dystrophy (DMD) is an X-linked recessive disease caused, in most cases, by the com...
Duchenne muscular dystrophy (DMD) is an inherited, severe muscle wasting disease caused by the loss ...
Metabolic profiles from (1)H nuclear magnetic resonance spectroscopy have been used to describe both...
AbstractMetabolic profiles from 1H nuclear magnetic resonance spectroscopy have been used to describ...
A principal problem in understanding the functional genomics of a pathology is the wide-reaching bio...
Duchenne muscular dystrophy (DMD) is a recessive X-linked form of muscular dystrophy characterized b...
31P NMR spectroscopy was used to study the energy metabolism of dystrophin-deficient skeletal muscle...
AbstractThe absence of dystrophin at the muscle membrane leads to Duchenne muscular dystrophy (DMD),...
Dystrophin, its functions and the consequences of its absence are briefly reviewed. The animal model...
Duchenne Muscular Dystrophy is a lethal childhood disorder which results in progressive muscle weakn...
AbstractDystrophin is a cytoskeletal protein of muscle fibers; its loss in humans leads to Duchenne ...
Duchenne muscular dystrophy (DMD) is the most common fatal form of muscular dystrophy characterized ...
Duchenne muscular dystrophy is a fatal childhood disease caused by mutations that abolish the expres...
Extraocular muscles (EOMs) represent a specialized type of contractile tissue with unique cellular, ...
Facioscapulohumeral muscular dystrophy (FSHD) is a hereditary neuromuscular disorder characterized b...
Duchenne muscular dystrophy (DMD) is an X-linked recessive disease caused, in most cases, by the com...
Duchenne muscular dystrophy (DMD) is an inherited, severe muscle wasting disease caused by the loss ...
Metabolic profiles from (1)H nuclear magnetic resonance spectroscopy have been used to describe both...
AbstractMetabolic profiles from 1H nuclear magnetic resonance spectroscopy have been used to describ...
A principal problem in understanding the functional genomics of a pathology is the wide-reaching bio...
Duchenne muscular dystrophy (DMD) is a recessive X-linked form of muscular dystrophy characterized b...
31P NMR spectroscopy was used to study the energy metabolism of dystrophin-deficient skeletal muscle...
AbstractThe absence of dystrophin at the muscle membrane leads to Duchenne muscular dystrophy (DMD),...
Dystrophin, its functions and the consequences of its absence are briefly reviewed. The animal model...
Duchenne Muscular Dystrophy is a lethal childhood disorder which results in progressive muscle weakn...
AbstractDystrophin is a cytoskeletal protein of muscle fibers; its loss in humans leads to Duchenne ...
Duchenne muscular dystrophy (DMD) is the most common fatal form of muscular dystrophy characterized ...
Duchenne muscular dystrophy is a fatal childhood disease caused by mutations that abolish the expres...
Extraocular muscles (EOMs) represent a specialized type of contractile tissue with unique cellular, ...
Facioscapulohumeral muscular dystrophy (FSHD) is a hereditary neuromuscular disorder characterized b...
Duchenne muscular dystrophy (DMD) is an X-linked recessive disease caused, in most cases, by the com...
Duchenne muscular dystrophy (DMD) is an inherited, severe muscle wasting disease caused by the loss ...