Some of the babies were related as they showed a congenital bone defect on their knee bones, which is a very rare gene.
一些孩子还是血脉相连的，因为他们的膝盖骨上都有一种先天性的骨质缺损，这种遗传基因是非常罕见的。
If you look in the normal population and ask what fraction of people have [a defect in methylation in the gene encoding insulin-like growth factor 2] it's about 5 percent.
如果你观察普通人群，调查多少比例的人有[胰岛素类生长因子2基因编码甲基化的缺陷]，大概是百分之5。
15 years after a gene defect was found to increase the risk of schizophrenia 30-fold, scientists have figured out how it might cause the brain disorder's debilitating symptoms
15年前，基因缺陷被发现可增加30倍的精神分裂风险，现在科学家终于查明基因缺陷是如何引起大脑功能失调症状。
Only five children born in the U.S. annually have the same type of LCA as Morehouse, but focusing on a rare single-gene defect is a good way to develop a model for treating more common ailments.
在美国出生的孩子中，每年只有5个孩子的雷伯氏先天性黑内障与豪斯为同一类型，但是从一个少见的单基因缺陷入手，是开发更普遍的治疗模型的一个很好的途径。
The gene therapy for bone defect, which overcomes the restriction of traditional therapies, has fatal research significance.
骨缺损的基因治疗克服了传统治疗方法的局限，具有重要研究意义。
Only a fraction of breast cancers result from an inherited gene mutation. Those with a defect in BRCA1 have a 65 percent risk of getting it, on average.
只有一小部分的乳腺癌是由遗传性基因突变造成的。基因brca1有缺陷的人平均患上乳腺癌的几率是65%。
Bone morphogenetic protein-2 released from carrier or gene could repair bone defect effectively.
载体或基因释放的骨形态发生蛋白2可有效修复骨缺损。
Under light and electron microscope, it was seen that HCY 2 gene resulted in structure disturbance, endocardial cushion defect and hypoplasia of heart.
HCY2基因可引起心脏结构紊乱、心内膜垫缺损和抑制心室心房发育，并可损害心肌细胞的超微结构。
Gene therapy is considered to maintain bone defect an effective therapeutic concentrations of local growth factor in the most promising methods.
基因治疗被认为是维持骨缺损局部生长因子有效治疗浓度最有希望的一种方法。
The approach combining the principles of tissue engineering with technique of gene transfection, could be of potential benefit to accelerate bone defect repair.
利用基因转染技术结合组织工程有助于深入加强骨缺损的修复研究。
But a defect in the gene may disable its proteins from performing their normal functions in mitochondria - most notably the mitochondria within the nervous system's cellular pathways.
但缺陷基因却不同产生蛋白质以维持线粒体的正常功能—尤其是神经系统细胞通路的线粒体。
PeanutsA gene defect that can triple the risk of a child developing an allergy to peanuts has been identified, scientists have said.
科学家称，他们明确了一个可导致儿童对花生过敏的风险增加三倍的基因缺陷。
Interviewer: Conditions based on a single gene defect.
主持：只要一个基因有问题，就可能出现这些病症。
In current, different kinds of methods were widely used in the animal model, such as the wild type, congenital defect and gene modification.
目前野生型、先天缺陷型、基因修饰等动物模型被广泛应用在这一研究领域。
Conclusion Targeting mutation of Fox C2 gene can result in ventricular septal defect.
结论：敲除叉头框c 2基因可使小鼠室间隔发育缺损。
The higher gene expression of IGFBP-6 may be induced the developmental skeleton defect in CCF rat.
CCF大鼠软骨组织内IGFBP-6的高表达可能与骨骼发育畸形的发生密切相关。
The higher gene expression of IGFBP-6 may be induced the developmental skeleton defect in CCF rat.
CCF大鼠软骨组织内IGFBP-6的高表达可能与骨骼发育畸形的发生密切相关。
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