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Stem Cell Res ; 71: 103187, 2023 09.
Article de Anglais | MEDLINE | ID: mdl-37643496

RÉSUMÉ

Here, we present newly derived in vitro model for modeling Duchenne muscular dystrophy. Our new cell line was derived by reprogramming of peripheral blood mononuclear cells (isolated from blood from pediatric patient) with Sendai virus encoding Yamanaka factors. Derived iPS cells are capable to differentiate in vitro into three germ layers as verified by immunocytochemistry. When differentiated in special medium, our iPSc formed spontaneously beating cardiomyocytes. As cardiomyopathy is the main clinical complication in patients with Duchenne muscular dystrophy, the cell line bearing the dystrophin gene mutation might be of interest to the research community.


Sujet(s)
Cellules souches pluripotentes induites , Myopathie de Duchenne , Humains , Enfant , Agranulocytes , Différenciation cellulaire , Lignée cellulaire
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