Muscular dystrophies are associated with mutations in genes encoding several classes of proteins. These range from extracellular matrix and integral membrane proteins to cytoskeletal proteins, but also include a heteroge-neous group of proteins including proteases, nuclear proteins, and signalling molecules. Muscular dystrophy phenotypes have also become evident in studies on various knockout mice defective in proteins not pre-viously considered or known to be mutated in muscular dystrophies. Some unifying themes are beginning to emerge from all of these data. This review will consider recent advances in our understanding of the molecules involved and bring together data that suggest a role for the cytoskeleton and cell adhesion in muscular...
Muscular dystrophies are a heterogeneous group of inherited disorders that share similar clinical fe...
Muscular dystrophies are a heterogeneous group of inherited disorders that share similar clinical fe...
AbstractDuchenne muscular dystrophy is the most prevalent and severe form of human muscular dystroph...
INVITED REVIEW ABSTRACT: Muscular dystrophies represent a heterogeneous group of disorders, which ha...
The study of the muscle cell in the muscular dystrophies (MDs) has shown that mutant proteins result...
The dystrophin–glycoprotein complex (DGC) can be considered as a specialized adhesion complex, linki...
Context Over the past 15 years the causative genes of several inherited muscular dystrophies have be...
The extracellular matrix provides a solid scaffold and signals to cells through extracellular matrix...
Duchenne muscular dystrophy (DMD) is secondary to loss-of-function mutations in the dystrophin gene....
During the past year significant progress has been made in understanding how dystrophin deficiency l...
During the past year significant progress has been made in understanding how dystrophin deficiency l...
During the past year significant progress has been made in understanding how dystrophin deficiency l...
Muscular dystrophies are heterogeneous genetic disorders that share progressive muscle wasting. This...
Duchenne muscular dystrophy (DMD) is caused by the absence of functional dystrophin (Blake et al. 20...
Dystrophin, the protein product of the DMD gene, is a component of the muscle-membrane cytoskeleton....
Muscular dystrophies are a heterogeneous group of inherited disorders that share similar clinical fe...
Muscular dystrophies are a heterogeneous group of inherited disorders that share similar clinical fe...
AbstractDuchenne muscular dystrophy is the most prevalent and severe form of human muscular dystroph...
INVITED REVIEW ABSTRACT: Muscular dystrophies represent a heterogeneous group of disorders, which ha...
The study of the muscle cell in the muscular dystrophies (MDs) has shown that mutant proteins result...
The dystrophin–glycoprotein complex (DGC) can be considered as a specialized adhesion complex, linki...
Context Over the past 15 years the causative genes of several inherited muscular dystrophies have be...
The extracellular matrix provides a solid scaffold and signals to cells through extracellular matrix...
Duchenne muscular dystrophy (DMD) is secondary to loss-of-function mutations in the dystrophin gene....
During the past year significant progress has been made in understanding how dystrophin deficiency l...
During the past year significant progress has been made in understanding how dystrophin deficiency l...
During the past year significant progress has been made in understanding how dystrophin deficiency l...
Muscular dystrophies are heterogeneous genetic disorders that share progressive muscle wasting. This...
Duchenne muscular dystrophy (DMD) is caused by the absence of functional dystrophin (Blake et al. 20...
Dystrophin, the protein product of the DMD gene, is a component of the muscle-membrane cytoskeleton....
Muscular dystrophies are a heterogeneous group of inherited disorders that share similar clinical fe...
Muscular dystrophies are a heterogeneous group of inherited disorders that share similar clinical fe...
AbstractDuchenne muscular dystrophy is the most prevalent and severe form of human muscular dystroph...