Research Project
Grant-in-Aid for Young Scientists (B)
We are intended to develop the gene therapy for neuromuscular disease, especially about muscular dystrophy. Lentiviral vector can stably transduced therapeutic dystrophin gene into mdx muscle fibers and satellite cells. The transduced satellite cells can contribute to muscle regeneration process and keep providing a therapeutic gene product, dystrophin. Mdx respiratory muscle may be an appropriate target for in vivo direct gene delivery approach. LvMSCV-EGFP transgenic mice showed fiber type-dependent variations in EGFP protein expression.
All 2014 2013 2012 2011 Other
All Journal Article (21 results) (of which Peer Reviewed: 8 results) Presentation (35 results) Book (1 results) Remarks (2 results)
ブレインナーシング
Volume: 30 Pages: 24-25
Volume: 30 Pages: 25-26
診断と治療
Volume: 102 (2014年増刊号) Pages: 129-137
J Clin Neurol
Volume: (in press)
Journal of Clinical Neurology
Volume: in press
Clin Neurol Neurosurg
Volume: 115(5) Issue: 5 Pages: 603-6
10.1016/j.clineuro.2012.07.019
Neurol Asia
Volume: 18 (1) Pages: 103-105
Volume: 29 Pages: 708-709
Progress in Medicine
Volume: 33 Pages: 1765-1770
分子脳血管病
Volume: 12 Pages: 362-368
medicina
Volume: 50 (2013年増刊号) Pages: 290-295
別冊日本臨床 神経症候群
Volume: (第2版) I—その他の神経疾患を含めて— Pages: 126-132
Neurology Asia
Volume: 18 Pages: 103-105
日本臨床 神経症候群 (第2版) I―その他の神経疾患を含めて―
Volume: 別冊 Pages: 126-132
European Neurology
Volume: 68 Issue: 2 Pages: 117-121
10.1159/000338474
Lab Invest
Volume: 78 Issue: 8 Pages: 1100-1114
10.1038/labinvest.2012.78
Journal of Neurplogy
Volume: 259 Issue: 6 Pages: 1039-1044
10.1007/s00415-011-6292-6
http://www2.kuh.kumamoto-u.ac.jp/neurology/