Related Experiment Video
Updated: Oct 14, 2025

07:44
CRISPR/Cas9 Technology in Restoring Dystrophin Expression in iPSC-Derived Muscle Progenitors
Published on: September 14, 2019
8.6K
Editorial: Gene, Cell and Protein Replacement Therapy for Genetic Muscle, Bone and Skin Disorders
Holm Schneider1, Michele De Luca2
1Department of Pediatrics, University Hospital Erlangen, Friedrich-Alexander University Erlangen-Nürnberg, Erlangen, Germany.
Frontiers in Genetics
|November 4, 2021
Abstract
No abstract available in PubMed .
Keywords:
duchenne muscular dystrophy (DMD)ectodermal dysplasiaepidermolysis bullosagene therapymyogenic cell transplantationprotein replacementMore Related Videos
10:28Direct Reprogramming of Human Fibroblasts into Myoblasts to Investigate Therapies for Neuromuscular Disorders
Published on: April 3, 2021
6.6K
10:03Transplantation of Induced Pluripotent Stem Cell-derived Mesoangioblast-like Myogenic Progenitors in Mouse Models of Muscle Regeneration
Published on: January 20, 2014
9.8K