gene therapy

gene therapy

美 　英

• n.基因疗法；基因治疗
• 网络基因治療；基因療法；基因医疗

英汉双解

英汉解释

un.	1. 基因治疗 2. 基因疗法

英英解释

n.	1. a medical treatment in which genes are put into cells in the body in order to cure some types of illness

例句

TMAdV's rarity in humans could make it a potentially powerful tool as a viral vehicle for delivering gene therapy, Chiu adds.

Chiu补充说，伶猴腺病毒（TMAdV）在人类身上罕见，这让它可能成为一个潜在的强大工具，在基因治疗中充当病毒载体。

Gene therapy has never before been used to treat a degenerative brain disease in humans and the success represents an important landmark.

以前基因治疗从未用于人类的神经退行性疾病，所以此研究是一个重要的里程碑。

Although thousands of patients have received gene therapy for a variety of conditions, only a few have shown any clinical benefit.

尽管成千上万不同条件的病人都接受过基因治疗，只有一小部分表现出临床上的受益。

Gene therapy has been used to enhance the healing of allografts in a murine model.

基因疗法已被用于加强鼠类模型同种异体移植骨愈合。

Presently, retroviral vector was extensively used for gene therapy, exogenous gene expression and genetically engineering vaccine.

目前广泛应用于基因治疗、外源基因表达、基因工程疫苗等方面。

Slowly and cautiously, Ali's group and others have been trying out an AAV-based gene therapy in people with an inherited form of blindness.

阿里的团队以及其它团队已经在小心翼翼的测试基于AAV的基因疗法，用于遗传性失明的人群。

Human artificial chromosome(HAC) will solve some critical problems of gene therapy if it was used as the vector for gene therapy.

人类人工染色体（HAC）作为基因治疗载体将解决基因治疗存在的一些关键问题。

The researchers have begun clinical trials to test the gene therapy as a treatment for a rare form of childhood blindness.

这些研究者已着手进行临床试验，检测这种基因疗法对一种罕见儿童失明症的疗效。

Partly thanks to work in the eye, gene therapy is seeing something of a renaissance.

从某一程度上说，幸亏在眼睛的基因疗法，才使得整个基因疗法开始复兴。

It has been a difficult decade for gene therapy, but Wilson believes that its fall from favor was inevitable.

对于基因疗法领域来说，这是个痛苦的10年，但是威尔森相信它从受到关注到失宠是无法避免的。

But he said it could inspire researchers to pursue gene therapy as a means to block or suppress HIV.

但他说这可激励研究者用基因治疗作为阻断或抑制HIV的方法。

Cancer has always been a worry with gene therapy.

在基因治疗中，癌症常常是一个受到担心的因素。

Previous work using animal models has demonstrated that this gene therapy can improve and preserve vision.

先前利用动物模型的试验表明，这一基因治疗能保护及改善视力。

The method of gene therapy have been emerging in recent years did not enter clinical stages.

而近年来出现的基因治疗方法亦大多没有进入临床阶段。

The lack of a safe, efficient delivery system for DNA has been a major barrier to clinical use of gene therapy.

缺乏安全有效的DNA运送系统是基因治疗临床应用的主要瓶颈。

If it works in people, it would provide a highly targeted mechanism for delivering cancer-fighting gene therapy.

如果这种方法在人体有作用，就将提供一种高度靶向抗癌基因治疗的新方法。

The X-SCID and ADA-deficiency trials have proved the validity of the concept of in vivo selection for gene therapy.

关于X-SCID和ADA缺乏症的试验证实了基因治疗中体内选择这个概念的真实性。

At present, the main vectors are virus vectors and non-virus vectors, but viral vectors are the most widely vectors used in gene therapy.

目前应用的载体主要有包括病毒和非病毒载体，但在基因治疗中应用最为广泛的载体是病毒载体。

Besides, bifidobacterium can produce a marked effect on cancer gene therapy because of its obligate anaerobic character.

此外，双歧杆菌专性厌氧的特性使其在肿瘤的基因治疗中起重要的作用。

Some researchers are working on the idea of gene therapy to treat or try to cure HIV, but the technology is still in experimental stages.

一些研究者们正在设法通过基因治疗来治疗或试图治愈HIV，但这种技术仍处于实验阶段。

First, gene therapy is potentially a method of choice, but it is still far from achieving clinical success.

一种是基因治疗，这是一种很有潜力的治疗方法，但它距离实际的临床应用还很远。

Investigators evaluated the gene therapy in two mouse models of retinal degenerative disease, as well as cultures of human retinal tissue.

调查评估了在两个视网膜退行性疾病小鼠模型的基因治疗，以及人体视网膜组织的人文研究。

The first gene therapy trial took place in the United States in September 1990.

第一例基因治疗试验1990年9月在美国进行。

In addition, there was no a targeted, high-efficiency and safe gene-transfer system for gene therapy.

此前的基因治疗缺乏靶向、高效和安全的导入系统，同时缺乏用于体内实验的普通动物胰腺癌模型。

Conclusion: The lentiviral expression vector is ideal vector of gene therapy and made genes transduced stable expression in target cell.

结论：慢病毒载体系统能够使转导的基因在靶细胞中得到稳定表达，是基因治疗中的理想载体。

Gene therapy is a permanent replacement of a defective gene, usually treating an inherited disorder and usually using a viral vector.

基因治疗通常是利用病毒载体永久性地替换缺陷基因来治疗遗传性疾病。

Because adenovirus as a gene transfer has many advantages, now it has been widely used in gene therapy.

由于腺病毒作为基因转移的载体有许多优点，现已被广泛的应用于基因治疗。

Two squirrel monkeys that were colour-blind from birth have had their vision restored after receiving gene therapy.

通过接受基因疗法，两只天生色盲的松鼠猴现在已经能辨别颜色了。

Innovative means of adding beneficial genes to patients' bodies are starting to overcome the hurdles for gene therapy.

基因治疗的障碍多多，但把有益基因送入病人体内的一些创新做法，已逐步克服难关。

The first-ever choroideremia gene therapy clinical trial is now underway at the John Radcliffe Hospital in Oxford, United Kingdom.

在英国牛津的约翰拉德克利夫医院的第一次无脉络膜基因治疗临床试验目前正在进行。

The authors suggest that because of this mechanism, future drug and gene therapy targets in glaucoma might be influenced.

作者认为青光眼未来的药物治疗和基因治疗目标可能被这个机制所影响。

No method for genetically boosting IQ currently exists, of course, but strides in gene therapy might someday make it possible.

当然，目前还不存在从遗传上提高智商的办法，但是，基因疗法方面的大的进展有朝一日会使它变得可能。

Many study had investigated that the double suicide gene therapy was much better than the suicide gene therapy.

已有的研究证实双自杀基因治疗具有单自杀基因疗法无可比拟的优越性。

Gene therapy works by inserting extra copies of particular genes into the body.

基因疗法的工作原理在于把特定基因的额外拷贝植入到体内。

As a result of the rapid advance in gene therapy, cures for cancer may be not far away.

由于基因疗法的飞速进步，治愈癌症也许不远了。

Now the gene therapy against myocardial injury involving cardiopulmonary bypass is still under the stage of animal study.

心肌保护基因治疗的研究目前仍停留在动物实验阶段。

I think it opens up the general idea of gene therapy or genetic therapy.

我想这透露出基因治疗或遗传治疗的一般思想。

People is commenting in succession, biology project food, " blackart " molecular nucleic acid -- nutrition of gene therapy, gene. . .

人们纷纷议论着，生物工程食品、“魔法”分子核酸——基因治疗、基因营养……；

This review briefly introduced the phenotypes, pathologic physiology and general therapy to the disease, strongly stress the gene therapy.

本文简要地介绍戈谢氏病的不同表现型，病理生理学特性和常用的治疗措施，着重叙述基因治疗部分。

In gene therapy approaches, the genetic material may be introduced into the patient in several different ways.

在基因治疗方法中，基因材料可以以多种方式引入病人体内。