International audienceInduced pluripotent stem cells (iPSCs) obtained by reprogramming primary somatic cells have revolutionized the fields of cell biology and disease modeling. However, the number protocols for generating mature muscle fibers with sarcolemmal organization using iPSCs remain limited, and partly mimic the complexity of mature skeletal muscle. Methods: We used a novel combination of small molecules added in a precise sequence for the simultaneous codifferentiation of human iPSCs into skeletal muscle cells and motor neurons. Results: We show that the presence of both cell types reduces the production time for millimeter-long multinucleated muscle fibers with sarcolemmal organization. Muscle fiber contractions are visible in 19...
Muscular dystrophy is a disease characterized by progressive muscle weakness and degeneration. There...
AbstractStriated skeletal muscle cells from humans represent a valuable source for in vitro studies ...
International audienceDuchenne muscular dystrophy (DMD) is a devastating genetic disease leading to ...
International audienceOnly a limited number of large-scale protocols describe the production of matu...
International audienceInduced pluripotent stem cells (iPSC) represent an innovative, easily obtained...
Summary: Generating human skeletal muscle models is instrumental for investigating muscle pathology ...
: Induced pluripotent stem cells (iPSCs) offer an unlimited resource of cells to be used for the stu...
International audienceProgress toward finding a cure for muscle diseases has been slow because of th...
International audienceKey cell types including skeletal muscle have proven difficult to differentiat...
In vitro organoids derived from human pluripotent stem cells (hPSCs) have been developed as essentia...
textabstractAlthough skeletal muscle cells can be generated from human induced pluripotent stem cell...
Induced pluripotent stem cells (iPSCs) offer an unlimited resource of cells to be used for the study...
The establishment of human induced pluripotent stem cells (hiPSCs) has enabled the production of in ...
<div><p>The establishment of human induced pluripotent stem cells (hiPSCs) has enabled the productio...
Neuromuscular diseases are caused by functional defects of skeletal muscles, directly via muscle pat...
Muscular dystrophy is a disease characterized by progressive muscle weakness and degeneration. There...
AbstractStriated skeletal muscle cells from humans represent a valuable source for in vitro studies ...
International audienceDuchenne muscular dystrophy (DMD) is a devastating genetic disease leading to ...
International audienceOnly a limited number of large-scale protocols describe the production of matu...
International audienceInduced pluripotent stem cells (iPSC) represent an innovative, easily obtained...
Summary: Generating human skeletal muscle models is instrumental for investigating muscle pathology ...
: Induced pluripotent stem cells (iPSCs) offer an unlimited resource of cells to be used for the stu...
International audienceProgress toward finding a cure for muscle diseases has been slow because of th...
International audienceKey cell types including skeletal muscle have proven difficult to differentiat...
In vitro organoids derived from human pluripotent stem cells (hPSCs) have been developed as essentia...
textabstractAlthough skeletal muscle cells can be generated from human induced pluripotent stem cell...
Induced pluripotent stem cells (iPSCs) offer an unlimited resource of cells to be used for the study...
The establishment of human induced pluripotent stem cells (hiPSCs) has enabled the production of in ...
<div><p>The establishment of human induced pluripotent stem cells (hiPSCs) has enabled the productio...
Neuromuscular diseases are caused by functional defects of skeletal muscles, directly via muscle pat...
Muscular dystrophy is a disease characterized by progressive muscle weakness and degeneration. There...
AbstractStriated skeletal muscle cells from humans represent a valuable source for in vitro studies ...
International audienceDuchenne muscular dystrophy (DMD) is a devastating genetic disease leading to ...