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Aav Vector Mediated Gene Transfer Into Mini Dystrophin Transgenic Mdx Cvba Musclesfig

This post categorized under Vector and posted on July 27th, 2019.
AAV Vector: Aav Vector Mediated Gene Transfer Into Mini Dystrophin Transgenic Mdx Cvba Musclesfig

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An AAV type 2 vector expressing micro-dystrophin (DeltaCS1) under the control of a muscle-specific MCK promoter was injected into the tibialis anterior (TA) muscles of dystrophin-deficient mdx mice and resulted in extensive and long-term expression of micro-dystrophin that Author Takashi OkadaDOI 10.577253023Publish Year 2013Although AAV vectors are too small to package the full-graphicgth dystrophin cDNA AAV vector-mediated gene therapy with using a rod-truncated dystrophin gene provides ais promising approach (graphic et Author ShinIchi Takeda Takashi OkadaDOI 10.577218624Publish Year 2011Sustained improvement of muscle function one year after full-graphicgth dystrophin gene transfer into mdx mice by a gutted helper-dependent adenoviral vector. Hum. Gene Ther. 15 145156.Cited by 30Publish Year 2011Author Zejing graphic Stephen J. Tapscott Stephen J. Tapscott Jeffrey S. Chamberlain Jeffrey S. Chamberlai


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