Multipotent cells that can give rise to bone, cartilage, fat, connective tissue, and skeletal and cardiac muscle are termed mesenchymal stem cells. These cells were first identified in the bone marrow, distinct from blood-forming stem cells. Based on the embryologic derivation, availability, and various pro-regenerative characteristics, research exploring their use in cell therapy shows great promise for patients with degenerative muscle diseases and a number of other conditions. In this review, the authors explore the potential for mesenchymal stem cell therapy in the emerging field of regenerative medicine with a focus on treatment for Duchenne muscular dystrophy
Muscular dystrophies are heterogeneous neuromuscular disorders of inherited origin, including Duchen...
Cell therapy is one promising approach to correct genetic diseases by contributing to tissue regener...
Indexación: Scopus.Duchene Muscular Dystrophy (DMD) is the most frequent muscular dystrophy and one ...
Mesenchymal stem cells (MSCs) are multipotent stem cells that can be isolated from both foetal and a...
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...
AbstractMuscular dystrophies comprise a heterogeneous group of neuromuscular disorders, characterize...
There is currently no cure for muscular dystrophies, although several promising strategies are in ba...
Muscular dystrophies are heritable, heterogeneous neuromuscular disorders and include Duchenne and B...
University of Minnesota Ph.D. dissertation. August 2008. Major Biomedical Engineering. Advisors: Cat...
Duchenne muscular dystrophy (DMD) is a progressive muscular degenerative disease affecting 1 in 3,50...
Cell therapy is one promising approach to correct genetic diseases by contributing to tissue regener...
This chapter focuses on stem cell-based therapies to treat muscular dystrophy. It reviews previous ...
Mutations in the dystrophin gene cause an X-linked genetic disorder: Duchenne muscular dystrophy (DM...
Muscular dystrophies are heterogeneous neuromuscular disorders of inherited origin, including Duchen...
Cell therapy is one promising approach to correct genetic diseases by contributing to tissue regener...
Indexación: Scopus.Duchene Muscular Dystrophy (DMD) is the most frequent muscular dystrophy and one ...
Mesenchymal stem cells (MSCs) are multipotent stem cells that can be isolated from both foetal and a...
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...
AbstractMuscular dystrophies comprise a heterogeneous group of neuromuscular disorders, characterize...
There is currently no cure for muscular dystrophies, although several promising strategies are in ba...
Muscular dystrophies are heritable, heterogeneous neuromuscular disorders and include Duchenne and B...
University of Minnesota Ph.D. dissertation. August 2008. Major Biomedical Engineering. Advisors: Cat...
Duchenne muscular dystrophy (DMD) is a progressive muscular degenerative disease affecting 1 in 3,50...
Cell therapy is one promising approach to correct genetic diseases by contributing to tissue regener...
This chapter focuses on stem cell-based therapies to treat muscular dystrophy. It reviews previous ...
Mutations in the dystrophin gene cause an X-linked genetic disorder: Duchenne muscular dystrophy (DM...
Muscular dystrophies are heterogeneous neuromuscular disorders of inherited origin, including Duchen...
Cell therapy is one promising approach to correct genetic diseases by contributing to tissue regener...
Indexación: Scopus.Duchene Muscular Dystrophy (DMD) is the most frequent muscular dystrophy and one ...