Mesenchymal stem cells (MSCs) are multipotent stem cells that can be isolated from both foetal and adult tissues. Several groups demonstrated that transplantation of MSCs promoted the regeneration of skeletal muscle and ameliorated muscular dystrophy in animal models. Mesenchymal stem cells in skeletal muscle, also known as fibro-adipogenic progenitors (FAPs), are essential for the maintenance of skeletal muscle. Importantly, they contribute to fibrosis and fat accumulation in dystrophic muscle. Therefore, MSCs in muscle are a pharmacological target for the treatment of muscular dystrophies. In this chapter, we briefly update the knowledge on mesenchymal stem/progenitor cells and discuss their therapeutic potential as a regenerative medicin...
PhD ThesisMuscular dystrophies are a category of diseases in which the muscle fibres degrade over ti...
Duchenne muscular dystrophy (DMD) is the most prevalent genetic neuromuscular disorder and affects 1...
Thesis (Ph.D.)--University of Washington, 2012Cell-based therapies have the potential to contribute ...
Multipotent cells that can give rise to bone, cartilage, fat, connective tissue, and skeletal and ca...
As one of the most common genetic conditions, Duchenne muscular dystrophy (DMD) is a fatal disease c...
Understanding stem cell commitment and differentiation is a critical step towards clinical translati...
Muscular dystrophies are heritable, heterogeneous neuromuscular disorders and include Duchenne and B...
Adult skeletal muscle possesses a remarkable regenerative ability, which largely depends on satellit...
Skeletal muscle tissue engineering is one of the important ways for regenerating functionally defect...
AbstractMuscular dystrophies comprise a heterogeneous group of neuromuscular disorders, characterize...
This chapter focuses on stem cell-based therapies to treat muscular dystrophy. It reviews previous ...
Muscular dystrophies are heritable, heterogeneous neuromuscular disorders and include Duchenne and B...
Genetic mutations in muscle structural genes can compromise myofiber integrity, causing repeated mus...
Includes bibliographical references (pages 79-92)Duchenne Muscular Dystrophy (DMD) is a devastating ...
© 2016 Dr. Mahsa RashidiDuchenne muscular dystrophy (DMD) is the most common form of muscular dystro...
PhD ThesisMuscular dystrophies are a category of diseases in which the muscle fibres degrade over ti...
Duchenne muscular dystrophy (DMD) is the most prevalent genetic neuromuscular disorder and affects 1...
Thesis (Ph.D.)--University of Washington, 2012Cell-based therapies have the potential to contribute ...
Multipotent cells that can give rise to bone, cartilage, fat, connective tissue, and skeletal and ca...
As one of the most common genetic conditions, Duchenne muscular dystrophy (DMD) is a fatal disease c...
Understanding stem cell commitment and differentiation is a critical step towards clinical translati...
Muscular dystrophies are heritable, heterogeneous neuromuscular disorders and include Duchenne and B...
Adult skeletal muscle possesses a remarkable regenerative ability, which largely depends on satellit...
Skeletal muscle tissue engineering is one of the important ways for regenerating functionally defect...
AbstractMuscular dystrophies comprise a heterogeneous group of neuromuscular disorders, characterize...
This chapter focuses on stem cell-based therapies to treat muscular dystrophy. It reviews previous ...
Muscular dystrophies are heritable, heterogeneous neuromuscular disorders and include Duchenne and B...
Genetic mutations in muscle structural genes can compromise myofiber integrity, causing repeated mus...
Includes bibliographical references (pages 79-92)Duchenne Muscular Dystrophy (DMD) is a devastating ...
© 2016 Dr. Mahsa RashidiDuchenne muscular dystrophy (DMD) is the most common form of muscular dystro...
PhD ThesisMuscular dystrophies are a category of diseases in which the muscle fibres degrade over ti...
Duchenne muscular dystrophy (DMD) is the most prevalent genetic neuromuscular disorder and affects 1...
Thesis (Ph.D.)--University of Washington, 2012Cell-based therapies have the potential to contribute ...