A new conditionally immortal satellite cell-derived cell-line, H2K 2B4, was generated from the H2K(b)-tsA58 immortomouse. Under permissive conditions H2K 2B4 cells terminally differentiate in vitro to form uniform myotubes with a myogenic protein profile comparable with freshly isolated satellite cells. Following engraftment into immunodeficient dystrophin-deficient mice, H2K 2B4 cells regenerated host muscle with donor derived myofibres that persisted for at least 24 weeks, without forming tumours. These cells were readily transfectable using both retrovirus and the non-viral transfection methods and importantly upon transplantation, were able to reconstitute the satellite cell niche with functional donor derived satellite cells. Finally u...
Duchenne muscular dystrophy (DMD) is a lethal muscle-wasting disease currently without cure. We inve...
There is currently no cure for muscular dystrophies, although several promising strategies are in ba...
Understanding stem cell commitment and differentiation is a critical step towards clinical translati...
A new conditionally immortal satellite cell-derived cell-line, H2K 2B4, was generated from the H2K(b...
Background: Investigations into both the pathophysiology and therapeutic targets in muscle dystrophi...
International audienceABSTRACT: BACKGROUND: Investigations into both the pathophysiology and therape...
PhD ThesisMuscular dystrophies are a category of diseases in which the muscle fibres degrade over ti...
The Sleeping beauty (SB) system is a non-viral DNA based vector that has been used to stably integra...
We developed different approaches to utilize genetically modified cells and animal models to underst...
BACKGROUND: A hallmark of muscular dystrophies is the replacement of muscle by connective tissue. Mu...
AbstractMuscular dystrophies comprise a heterogeneous group of neuromuscular disorders, characterize...
Summary: Myogenic differentiation of human pluripotent stem cells (hPSCs) has been done by gene over...
Item does not contain fulltextThe intrinsic regenerative capacity of skeletal muscle makes it an exc...
Duchenne muscular dystrophy (DMD) is a lethal muscle-wasting disease currently without cure. We inve...
Primary human skeletal muscle cells (hSkMCs) are invaluable tools for deciphering the basic molecula...
Duchenne muscular dystrophy (DMD) is a lethal muscle-wasting disease currently without cure. We inve...
There is currently no cure for muscular dystrophies, although several promising strategies are in ba...
Understanding stem cell commitment and differentiation is a critical step towards clinical translati...
A new conditionally immortal satellite cell-derived cell-line, H2K 2B4, was generated from the H2K(b...
Background: Investigations into both the pathophysiology and therapeutic targets in muscle dystrophi...
International audienceABSTRACT: BACKGROUND: Investigations into both the pathophysiology and therape...
PhD ThesisMuscular dystrophies are a category of diseases in which the muscle fibres degrade over ti...
The Sleeping beauty (SB) system is a non-viral DNA based vector that has been used to stably integra...
We developed different approaches to utilize genetically modified cells and animal models to underst...
BACKGROUND: A hallmark of muscular dystrophies is the replacement of muscle by connective tissue. Mu...
AbstractMuscular dystrophies comprise a heterogeneous group of neuromuscular disorders, characterize...
Summary: Myogenic differentiation of human pluripotent stem cells (hPSCs) has been done by gene over...
Item does not contain fulltextThe intrinsic regenerative capacity of skeletal muscle makes it an exc...
Duchenne muscular dystrophy (DMD) is a lethal muscle-wasting disease currently without cure. We inve...
Primary human skeletal muscle cells (hSkMCs) are invaluable tools for deciphering the basic molecula...
Duchenne muscular dystrophy (DMD) is a lethal muscle-wasting disease currently without cure. We inve...
There is currently no cure for muscular dystrophies, although several promising strategies are in ba...
Understanding stem cell commitment and differentiation is a critical step towards clinical translati...