它将带来更好的控制血糖，并防止脂肪细胞的不良基因变异。
It led to better blood sugar control and less undesirable genetic variation in fat cells.
重要的是要注意，不过，在不同的肌营养不良基因突变可能需要不同的寡核苷酸药物。
It is important to note, however, that different mutations in the dystrophin gene could require different oligonucleotide drugs.
因为带有特定基因的患者会对此药物产生不良反应。
Because patients with a particular genetic variant might not respond well to that drug.
然而，很大程度上因为在实验中有像在SCID实验中产生的那些不良的副作用，至今为止没有一项基因疗法被美国和欧洲的卫生当局授权进行临床实验。
Yet, largely because of undesirable side-effects like those in the SCID trials, none has hitherto been granted the ultimate go-ahead by health authorities in America and Europe.
科学家们分析了200多个家庭的基因构成，认为有9个基因与男孩子的大脑发育不良有关。
Scientists linked nine genes to poor brain development in young men after analysing the genetic makeup of more than 200 families.
面部匀称可能是男性稳定性的一个体现，说明在个人成长过程中较少有疾病、毒素、营养不良或有害的基因突变等问题的困扰。
Facial symmetry may be a reflection of stability in men, indicating fewer disturbances such as diseases, toxins, malnutrition or harmful genetic mutations during an individual's development.
此时，母亲的不良的Dio3基因会使得大脑充满甲状腺激素，进而破坏神经元。
Now mom's bad Dio3 allows the brain to be flooded with thyroid hormone, damaging the hippocampus.
一项新的研究显示，基因比不良饮食习惯更能导致儿童过度肥胖。
A new study shows genes are more likely to blame for obesity in children than poor eating habits.
最新研究发现的6个基因当中，有5个基因能够激活大脑神经，这表明比起新陈代谢不良，大量的饮食依然是导致肥胖的主要原因。
Five of the six newly discovered genes are active in the brain, suggesting appetite plays a larger part in obesity than metabolism. Photograph: Rex features.
总体来说，癌症是不好的运气、糟糕的环境和不良的遗传基因的综合作用产生的结果。
Cancer is in general a combination of bad luck, bad environment and bad inherited genes.
这种疾病的致病原因未明，但是基因和外部环境不良因素的综合影响被认为是其致病的重要原因。
Its cause is unknown, but a complex mixture of genetic and environmental risk factors is thought to be to blame in many cases.
BIGH3基因突变有关的角膜营养不良现今已是角膜营养不良最常见的遗传学致病因素。
Nowadays, BIGH3 gene mutation related corneal dystrophy is the most common etiological factor leading to corneal dystrophy in genetics.
目的对导致肌营养不良症的基因编码产物进行检测，从分子水平为临床诊断和分型提供依据。
Objective To provide a useful tool based on molecular level for clinical diagnosis and classification by detecting gene products encoded by disease genes of muscular dystrophy.
肌营养不良卵白基因位于人类X染色体，携带基因突变的母亲会遗传给婴儿。
The dystrophin gene is found on the X chromosome and passed on to children through a mother who is a carrier.
结论在外周血中存在HBV截短型囊膜蛋白编码基因，可能与患者不良预后有关。
Conclusions Truncated middle S gene is found in the circulation of patients with chronical HBV infection, suggestive of a poor prognosis.
目的为探讨假肥大型肌营养不良症（DMD）基因内含子的核苷酸序列特点与存在于内含子中的多个断裂点的关系。
Objective The purpose of the study was to investigate the relationship between the character of nucleic acids and the multiple breakpoints in the introns of DMD gene.
经浙江省医学科学院急性毒性试验和致突变试验结果表明，反义PEP转基因菜籽油食用安全，对哺乳动物健康无不良影响。
The results shew that the anti-PEP-transgene rape oil was safe and had no bad effect on the health of mammal animal after the acute poison and mutation test by Zhejiang MedicalAcademy.
目的对面肩肱型肌营养不良症（FSHD）患者进行基因诊断并总结其临床特征，以提高FSHD的诊断水平。
Objective To perform gene diagnosis and summarize clinical features of facioscapulohumeral muscular dystrophy(FSHD)in order to improve its diagnosis.
在肌营养不良蛋白基因，在人类基因大多数，这种遗传信息不连续的。
In the dystrophin gene, and in most of human genes, this genetic information is not contiguous.
目的：探讨我国多发性骨骺发育不良患者中软骨寡聚物基质蛋白（COMP）基因的突变情况。
Objective: Our aim was to study the characteristics of mutation of cartilage oligomeric matrix protein (COMP) gene in Chinese patients with multiple epiphyseal dysplasia( MED).
野生稻种蕴藏有抗病虫害和耐受不良环境等有潜在利用价值的重要基因。
The wild species are valuable resources of genes for resistance to major diseases and insects and for tolerance of abiotic stresses.
我们综述了各种相对多见的遗传性角膜营养不良的发病机制研究新进展，重点涉及基因功能、突变蛋白、异常的酶活性等方面。
This article summarizes the current achievemant about the pathogenesis of the disease, with emphasis on the genes, mutant proteins, inactive enzymes activity and so on.
目的对5例x -连锁肾上腺脑白质营养不良(X -ALD)患儿及其中2例的母亲进行ABCD 1基因突变分析。
Objective To analyze the ABCD1 gene mutations in 5 cases of X-linked adrenoleukodystrophy (X-ALD) patients and 2 cases of their mothers.
介绍了静脉注射用脂肪乳剂在提高药物溶解度和稳定性、减轻药物不良反应、缓释、靶向给药和基因治疗等方面的研究进展。
The progress of drug loaded intravenous lipid emulsions in enhancing drug solubility and stability, reducing side effects, sustained release, targeted delivery and gene therapy is introduced.
目的探讨面肩肱型肌营养不良症（FSHD）1A的基因型与临床表型之间的相关关系。
Objective To explore the genotype-phenotype correlation of facioscapulohumeral muscular dystrophy (FSHD) 1A gene.
该研究小组说，基因疗法还可能用于治疗GUCY2D的突变引起的锥杆营养不良（线）的隐性和显性的形式。
The research team says that the gene therapy might also be used in treating recessive and dominant forms of cone-rod dystrophy (CORD) caused by mutations in GUCY2D.
目的探讨X-连锁迟发性脊椎骨骺发育不良（SEDL）基因逃避X染色体失活（XCI）及与临床表型的关系。
Objective To explore the relationship between X - linked spondyloepiphyseal dysplasia tarda (SEDL) gene escaping X chromosome inactivation( XCI) and SEDL phenotype.
目的探讨X-连锁迟发性脊椎骨骺发育不良（SEDL）基因逃避X染色体失活（XCI）及与临床表型的关系。
Objective To explore the relationship between X - linked spondyloepiphyseal dysplasia tarda (SEDL) gene escaping X chromosome inactivation( XCI) and SEDL phenotype.
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