1.
Cloning brings hope to families with inherited genetic diseases by opening the way to gene therapy.
克隆技术开放了基因治疗法，为有遗传基因疾病的家庭带来了希望。
2.
Cloning also brings hope to families with inherited genetic diseases by opening the way to gene therapy.
克隆技术还开放了基因治疗法，为有遗传性基因疾病的家庭带来了希望。
3.
Can the gene be fixed with gene therapy?
这种基因能用基因疗法治疗吗？
4.
Streamlined Delivery
基因疗法治肌营养不良
5.
Therefore, massage complements with acupuncture and becomes an essential method in acupuncture treatment.
因此，推拿与针灸治疗可以互补，并成为一种基本的治疗方法。
6.
Although there are risks with gene therapy, Thrasher believes it is safer than conventional bone marrow transplants which often involve chemotherapy.
虽然基因治疗有风险，思拉舍还是认为基因治疗比常需配合化学疗法的常规骨髓移植更加安全。
7.
A Fundamental Research of Tumor Immune Gene Therapy s Curative Effect to Metastasis Malignant Tumor;
免疫基因疗法对转移性恶性肿瘤治疗作用的基础研究
8.
Scientists have attempted to treat the disease with gene therapy, whereby the defective gene is swapped for a healthy one.
科学家一直希望用基因疗法治疗此病，即用健康基因把失去功能的基因替换掉。
9.
The verdict on the pioneering children of great therapy: So far,so good.
关于用开闯性的的基因疗法治疗儿童的疾病的结论:鼓舞人心.
10.
Effects of Wide-type p53 Gene Transfection Combined with Photodynamic Therapy in Lung Cancer;
野生型p53基因转染联合光动力疗法对肺癌治疗作用的实验研究
11.
Antitumor Effects of Human Interferon-Alpha Gene Therapy in Melonoma;
α-干扰素基因疗法治疗人黑色素瘤的实验与临床研究
12.
The Experimental Study of the Combined Treatment for Lewis Lung Carcinoma with Adenoviral Vectors Mediated Murine Interleukin 12 Gene Therapy and Photodynamic Therapy;
腺病毒介导的鼠白细胞介素12基因治疗联合光动力疗法治疗Lewis肺癌的实验研究
13.
Effect of vector factors on hGH gene therapy in vivo
载体因素对非病毒基因治疗体内实验方法的影响
14.
The second way to exploit genes to treat disease is known as small-molecule therapy.
第二种应用基因治疗疾病的方法，那就是人们所了解的小分子治疗方法。
15.
Contradiction and Consideration of Vascular Endothelial Growth Factor Gene Therapy;
关于血管内皮细胞生长因子基因治疗
16.
Gene or bone marrow-derived cells transfer cons titu tes an alternative strategy for accomplishing therapeutic angiogenesis and for h ealing of myocardial infarction in patients with coronary heart diseases.
基因和骨髓干细胞移植是治疗缺血性冠心病的一种新方法。
17.
Exploration the New Approach for AIDS Therapy by ApplyingRNA Interference to Nef Gene Expression;
应用RNAi技术干扰SIV的Nef基因以探寻艾滋病治疗新方法
18.
Study on Therapy for Asthma by Aerosolizing Delivery of CpGODN Mediated by a New Type Cationic Liposome;
新型阳离子脂质体雾化介导CpGODN哮喘基因治疗方法的探讨