Autologous skeletal muscle derived cells expressing a novel functional dystrophin provide a potential therapy for Duchenne Muscular Dystrophy.
about
Lentiviral vectors can be used for full-length dystrophin gene therapyBiomaterial-Guided Gene Delivery for Musculoskeletal Tissue Repair.Creation of Dystrophin Expressing Chimeric Cells of Myoblast Origin as a Novel Stem Cell Based Therapy for Duchenne Muscular Dystrophy.Intratesticular injection followed by electroporation allows gene transfer in caprine spermatogenic cells.SU9516 Increases α7β1 Integrin and Ameliorates Disease Progression in the mdx Mouse Model of Duchenne Muscular Dystrophy.Lentiviral vectors can be used for full-length dystrophin gene therapy.Foamy Virus Vectors Transduce Visceral Organs and Hippocampal Structures following In Vivo Delivery to Neonatal Mice
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P2860
Autologous skeletal muscle derived cells expressing a novel functional dystrophin provide a potential therapy for Duchenne Muscular Dystrophy.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
2016年论文
@zh
2016年论文
@zh-cn
name
Autologous skeletal muscle der ...... r Duchenne Muscular Dystrophy.
@ast
Autologous skeletal muscle der ...... r Duchenne Muscular Dystrophy.
@en
type
label
Autologous skeletal muscle der ...... r Duchenne Muscular Dystrophy.
@ast
Autologous skeletal muscle der ...... r Duchenne Muscular Dystrophy.
@en
prefLabel
Autologous skeletal muscle der ...... r Duchenne Muscular Dystrophy.
@ast
Autologous skeletal muscle der ...... r Duchenne Muscular Dystrophy.
@en
P2093
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Autologous skeletal muscle der ...... r Duchenne Muscular Dystrophy.
@en
P2093
Adrian Thrasher
Francesco Muntoni
Jennifer E Morgan
Jinhong Meng
John R Counsell
Mojgan Reza
Olivier Danos
Steven H Laval
P2860
P2888
P356
10.1038/SREP19750
P407
P577
2016-01-27T00:00:00Z
P5875
P6179
1007156354