## Abstract ## Background Adeno‐associated viral (AAV) vectors are potent delivery vehicles for gene transfer strategies directed at the central nervous system (CNS), muscle and liver. However, comparatively few studies have described AAV‐mediated gene transfer to tumor tissues. We have previously
✦ LIBER ✦
Adeno-associated virus serotype 2 mediated transduction and coexpression of the human apoAI and SR-BI gene in HepG2 cells
✍ Scribed by Bingnan Li; Juan Zhang; Zhiyan Li; Mengqun Tan
- Publisher
- Springer
- Year
- 2011
- Tongue
- English
- Weight
- 424 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0301-4851
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## Abstract This study quantified and compared the transduction efficiencies of adenoviral (Ad), Arg‐Gly‐Asp (RGD)‐modified Ad, adeno‐associated viral serotype 2 (AAV2), and self‐complementary AAV2 (scAAV2) vectors within full‐thickness osteoarthritic (OA) and unaffected canine cartilage explants i