[HTML][HTML] Human ES-and iPS-derived myogenic progenitors restore DYSTROPHIN and improve contractility upon transplantation in dystrophic mice
R Darabi, RW Arpke, S Irion, JT Dimos, M Grskovic… - Cell stem cell, 2012 - cell.com
A major obstacle in the application of cell-based therapies for the treatment of
neuromuscular disorders is obtaining the appropriate number of stem/progenitor cells to …
neuromuscular disorders is obtaining the appropriate number of stem/progenitor cells to …
Functional myogenic engraftment from mouse iPS cells
R Darabi, W Pan, D Bosnakovski, J Baik… - Stem Cell Reviews and …, 2011 - Springer
Direct reprogramming of adult fibroblasts to a pluripotent state has opened new possibilities
for the generation of patient-and disease-specific stem cells. However the ability of induced …
for the generation of patient-and disease-specific stem cells. However the ability of induced …
[HTML][HTML] Direct reprogramming of mouse fibroblasts into functional skeletal muscle progenitors
Skeletal muscle harbors quiescent stem cells termed satellite cells and proliferative
progenitors termed myoblasts, which play pivotal roles during muscle regeneration …
progenitors termed myoblasts, which play pivotal roles during muscle regeneration …
[HTML][HTML] Expansion and purification are critical for the therapeutic application of pluripotent stem cell-derived myogenic progenitors
Recent reports have documented the differentiation of human pluripotent stem cells toward
the skeletal myogenic lineage using transgene-and cell purification-free approaches …
the skeletal myogenic lineage using transgene-and cell purification-free approaches …
Assessment of the Myogenic Stem Cell Compartment Following Transplantation of Pax3/Pax7-Induced Embryonic Stem Cell-Derived Progenitors
R Darabi, FNC Santos, A Filareto, W Pan, R Koene… - Stem …, 2011 - academic.oup.com
An effective long-term cell therapy for skeletal muscle regeneration requires donor
contribution to both muscle fibers and the muscle stem cell pool. Although satellite cells …
contribution to both muscle fibers and the muscle stem cell pool. Although satellite cells …
ERBB3 and NGFR mark a distinct skeletal muscle progenitor cell in human development and hPSCs
Human pluripotent stem cells (hPSCs) can be directed to differentiate into skeletal muscle
progenitor cells (SMPCs). However, the myogenicity of hPSC-SMPCs relative to human fetal …
progenitor cells (SMPCs). However, the myogenicity of hPSC-SMPCs relative to human fetal …
Efficient derivation and inducible differentiation of expandable skeletal myogenic cells from human ES and patient-specific iPS cells
SM Maffioletti, MFM Gerli, M Ragazzi, S Dastidar… - Nature protocols, 2015 - nature.com
Skeletal muscle is the most abundant human tissue; therefore, an unlimited availability of
myogenic cells has applications in regenerative medicine and drug development. Here we …
myogenic cells has applications in regenerative medicine and drug development. Here we …
Prospective isolation of skeletal muscle stem cells with a Pax7 reporter
D Bosnakovski, Z Xu, W Li, S Thet, O Cleaver… - Stem …, 2008 - academic.oup.com
Muscle regeneration occurs through activation of quiescent satellite cells whose progeny
proliferate, differentiate, and fuse to make new myofibers. We used a transgenic Pax7 …
proliferate, differentiate, and fuse to make new myofibers. We used a transgenic Pax7 …
[HTML][HTML] Selective development of myogenic mesenchymal cells from human embryonic and induced pluripotent stem cells
T Awaya, T Kato, Y Mizuno, H Chang, A Niwa… - PloS one, 2012 - journals.plos.org
Human embryonic stem (ES) cells and induced pluripotent stem (iPS) cells are promising
sources for the cell therapy of muscle diseases and can serve as powerful experimental …
sources for the cell therapy of muscle diseases and can serve as powerful experimental …
[HTML][HTML] An ex vivo gene therapy approach to treat muscular dystrophy using inducible pluripotent stem cells
Duchenne muscular dystrophy is a progressive and incurable neuromuscular disease
caused by genetic and biochemical defects of the dystrophin–glycoprotein complex. Here …
caused by genetic and biochemical defects of the dystrophin–glycoprotein complex. Here …