aav

The construction of general tetracycline-regulatable AAV vectors and the study of its application in genetic therapy of PD

通用型四环素调控腺相关病毒载体的构建及其治疗帕金森病的应用研究

First they want to find out if the AAV vector can program muscles in humans to make the levels of antibody that would be needed to protect against HIV .

首先他们希望找出腺相关病毒（AAV）是否可以在人类肌肉上按照我们的预设发挥作用，这个作用表现在产生我们所需不同程度的抗体来保护我们免受HIV感染。

RESULTS The transduction efficiency of AAV is distinct in the three lines .

结果经统计学分析显示，不同血清型AAV对三种细胞系转染率有显著差异。

These advantages make AAV an ideal vector .

这些优点使得AAV成为目前最接近理想载体的病毒。

Recombinant AAV was obtained from the cell culture supernatant after adding helper virus .

重组质粒转染BHK细胞，加入辅助病毒后，得到表达目的蛋白的重组AAV。

Expression of Extracellular Domain of VEGF Receptor KDR with Recombinant AAV

用腺相关病毒载体介导人血管内皮生长因子受体KDR胞外区基因的表达

The Construction of Recombinant AAV Vector Mediated Double Regulatory Suicide Gene and the Detection of its Activity

携带靶向性可调控自杀基因的重组相关腺病毒载体的构建及其活性检测

Production of Insulin-expressing Adeno-associated Virus ( AAV ) Using Baculovirus System

利用昆虫病毒系统生产表达胰岛素的腺相关病毒

The transduction rate was elevated with the increase of AAV quantity and prolonged cold preservation time .

转导率随病毒剂量的增加、冷保存时间的延长而提高；

Besides , AAV also has outstanding performances in nervous system diseases , metabolic diseases , as well as tumors .

除此之外，AAV在神经系统疾病、代谢疾病以及肿瘤等应用中都有着较好的表现。

The possible role of neurotoxic action of AAV in severe cases of the snake bite was discussed .

本研究发现的AAV神经毒性作用可能有一定实践意义。

The gene can be delivered to the eye using a virus called Adeno-Associated Virus ( AAV ) .

该基因可交付使用眼病毒称为腺相关病毒（腺）。

Expression of AAV vector receptor in miniature pig 's parotid glands and submandibular glands

小型猪腮腺和颌下腺中的AAV载体受体表达研究

Objective To construct a recombinant AAV reporter virus expressing GFP and observe its expression in NIH3T3 cell .

目的构建以绿色荧光蛋白为报告基因的重组腺相关病毒载体和报告病毒，并观察其在真核细胞的表达。

The company used an adeno-associated virus ( AAV ) to deliver a gene with the aim of suppressing inflammation .

公司通过应用一种腺伴随病毒（AAV）传递基因来减轻炎症。

The AAV virus with high-purity , high enrichment and high titer are got though protein electrophoresis detection and virus electric mirror picture .

通过蛋白电泳检测及病毒电镜图片显示最终得到高纯度、高浓缩、高滴度的AAV病毒。

An adeno-associated virus ( AAV ), a therapeutic virus , was used to deliver the treatment to the cones .

一个腺病毒群（AAV）病毒治疗物质，是用于运送治疗物到视锥细胞。

Collecting fresh peripheral blood samples of AAV patients and healthy volunteers , neutrophils were isolated by density gradient centrifugation method . 2 .

第二部分AAV患者NETs的产生及LL37释放1.收集AAV患者及健康志愿者新鲜外周静脉血标本，采用PolymorphprepTM密度梯度离心法分离中性粒细胞并进行体外培养。

These results suggested that the existence of AAV ITRs played an active role for long-term transgene expression even without tans elements .

这一结果提示我们，在离体条件下，即使没有反式因子的参与，AAVITR序列的存在仍然对转基因的长期表达有着积极的作用。

ANCA-associated vasculitis ( AAV ) causing bilateral cerebral infarction and subsequent intracerebral hemorrhage without renal and respiratory dysfunction

ANCA相关血管炎（AAV）导致双侧脑梗死和继发性脑内出血而无肾功能和呼吸功能障碍

Through the four rounds of screening , we got chimeric AAV ( cAAV ) preliminary .

通过四轮的筛选，初步得到了嵌合型AAV（cAAV）。

To detect the rates of infection of AAV to the different tissues of the normal population by the PCR amplification with degenerated primers .

AAV对正常人不同组织的感染率的研究AAV是目前最具希望的基因治疗的载体。

We intend to construct recombinant AAV vector , so that BDNF can be expressed in CNS for the treatment of AD.

故我们拟构建重组AAV载体，以期有效的将BDNF送入中枢神经系统，达到对AD的治疗目的。

Objective To construct plasmids that express target genes in hepatoma cell line using adeno associated virus ( AAV ) vectors containing human AFP promoter .

目的利用含有人甲胎蛋白启动子的腺相关病毒载体，构建能在人肝癌细胞株中特异表达目的基因的质粒。

Confirmed its ability to effectively prevent SIV infection , the researchers through gene transfer technology , this group of proteins into the adenovirus ( AAV ) .

在证实其能够有效防止SIV感染后，研究人员通过基因转移技术，将此蛋白置入腺群病毒（AAV）。

It is concluded that AAV vector can contribute to increase transfection efficiency in hepatoma and suitable to compare function of different gene constructs in AAV vector .

所得到的结论即是利用AAV病毒载体可提高肝肿瘤的转染效率，且能比较不同载体其基因功能的表现。

AIM : To construct an AAV based vector carrying human endothelial nitric-oxide synthase ( eNOS ) cDNA and study its expression in vitro for future gene therapy .

目的：构建一个新型的携带有人内皮一氧化氮合酶（eNOS）cDNA的质粒载体并研究其体外表达，以用于基因治疗。

However , because of the replicative characteristic of AAV , the strategy of packaging rAAV with high efficiency and low cost has been a technological bottleneck in clinical application .

然而由于AAV的复制特性，高效、低成本的重组腺相关病毒（rAAV）的制备一直是AAV基础与临床应用领域的一大技术瓶颈。

Objective An adeno associated virus ( AAV ) vector targeted to hepatoma cells was constructed in order to be used in the apoptosis inducing gene therapy of liver cancer .

目的构建一种肝癌细胞靶向性的腺相关病毒载体以用于肝癌的促凋亡基因治疗的研究。

The viruses that are commonly used for this purpose are adenovirus , adeno-associated virus ( AAV ), retrovirus , lentivirus and herpes virus .

使用的病毒可以是腺病毒、AAV、反转录病毒、疱疹病毒。