Mesoangioblast delivery of miniagrin ameliorates murine model of merosin-deficient congenital muscular dystrophy type 1A.
about
Intra-arterial transplantation of HLA-matched donor mesoangioblasts in Duchenne muscular dystrophy.piggyBac transposons expressing full-length human dystrophin enable genetic correction of dystrophic mesoangioblasts.Preclinical and clinical advances in transposon-based gene therapy.At the Crossroads of Clinical and Preclinical Research for Muscular Dystrophy-Are We Closer to Effective Treatment for Patients?
P2860
Mesoangioblast delivery of miniagrin ameliorates murine model of merosin-deficient congenital muscular dystrophy type 1A.
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
2015年论文
@zh
2015年论文
@zh-cn
name
Mesoangioblast delivery of min ...... al muscular dystrophy type 1A.
@ast
Mesoangioblast delivery of min ...... al muscular dystrophy type 1A.
@en
type
label
Mesoangioblast delivery of min ...... al muscular dystrophy type 1A.
@ast
Mesoangioblast delivery of min ...... al muscular dystrophy type 1A.
@en
prefLabel
Mesoangioblast delivery of min ...... al muscular dystrophy type 1A.
@ast
Mesoangioblast delivery of min ...... al muscular dystrophy type 1A.
@en
P2093
P2860
P50
P1433
P1476
Mesoangioblast delivery of min ...... tal muscular dystrophy type 1A
@en
P2093
Alessandra Biffi
Daniele Velardo
Markus A Ruegg
Rossana Tonlorenzi
Shin'ichi Takeda
Stefano Amadio
Yuko Miyagoe-Suzuki
P2860
P2888
P356
10.1186/S13395-015-0055-5
P577
2015-09-03T00:00:00Z
P5875
P6179
1011846619