1、

The NIH 3 T 3 infected rGFP-AAV expressed significantly GFP fluorescence, which showed that rGFP-AAV was infectious virions.

感染了重组 GFP -AAV的大鼠NIH3T3细胞表达了明显的GFP荧光.

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2、

The bioactive AAV-hVEGF _ ( 165 ) was packaged by Benyuan Zhengyang Corporation, and the AAV-hVEGF _ ( 165 ) was successfully constructed.

本元正阳公司包装出具有生物学功能的AAV-hVEGF_ ( 165 ),AAV-hVEGF_ ( 165 ) 构建成功.

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3、

This may be assessed by means of the aggregate abrasion value ( AAV ) test.

这种能力可以通过聚合物磨损值 ( AAV ) 测试来评估.

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4、

Low level of anti-HSV and anti-AAV antibodies was detected in mouse serum.

小鼠血清中可以检测到少量 抗 HSV抗体和 抗 AAV抗体.

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5、

The safety of intramuscular injection of recombinant adeno-associated virus ( AAV )-mF to rescue hemophilia B was assessed.

研究了肌注腺伴随病毒 ( adeno-associatedvirus,AAV ) 介导凝血因子基因治疗血友病B的安全性.

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6、

After 3 weeks, AAV-hTGF-� � _ 1 was injected into groups D injury intervertebral discs.

3周后, D组椎间盘显微注射AAV-hTGF-1β.

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7、

Objective Plasmid of AAV vector with HIV 1 gag and gp 120 were constructed respectively.

目的构建带有HIV1gag或gp120基因的重组腺病毒伴随病毒AAVHIVgag或AAVHIVgp120.

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8、

Results 1. The recombinant AAV expressing human VEGF 121 gene wassuccessfully constructed and confirmed by DNA sequencing.

结果:1、成功构建了rAAV-VEGF,经序列测定目的基因为VEGF_(121).

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9、

Conclusion AAV-mediated striatal transgene expression of TH, AADC and GCH is more effective for gene therapy on Parkinsonian rat.

结论AAV载体介导的TH、AADC和GCH三重基因纹状体内共表达对于帕金森病大鼠的基因治疗更为有效。

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10、

Conclusion The triple transduction of TH, AADC and GCH genes with separate AAV vectors is effective, which might be important to gene therapy for Parkinson's disease.

结论使用AAV载体进行TH、AADC、GCH三重基因共转导是有效的,这对帕金森病基因治疗的研究具有重要意义。

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11、

Protection mechanism of mice transferred by AAV 2-BPI_ ( 700)-Fc γ 1_ ( 700) recombinant virus to minimal lethal dose E.coli infection

AAV2-BPI(700)-Fcγ1(700)重组病毒导入小鼠对致死量大肠埃希菌感染的保护作用机制

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