Objective Mutations of 13 CODIS (Combined DNA Index System) STR core loci in 532 cases of paternity testing were observed in confirming paternity, the mutation rate and the mutation type were studied.
目的观察美国CODIS系统的13个STR基因座在532例认定亲子关系的亲子鉴定案中的基因突变情况，探讨STR基因座突变率及突变类型。
That increased metabolism would, in turn, generate more oxygen-rich molecules of a type known as free radicals, which are potent inducers of mutation.
代谢速率的增加反过来会产生更多的富氧分子，即自由基。 后者这是一种诱发突变的蛋白质。
Longo's research led him first to a particular type of genetic mutation and ultimately to the mountains of southern Ecuador to study people with Laron syndrome.
朗格首先发现了一种特殊的基因变异，然后顺藤摸瓜，找到了厄瓜多尔南部山区的一群有莱伦氏综合症的人。
The mutation itself is in a gene for a nerve-cell protein of a type known as an ion channel.
变异的基因是编码一种叫做离子通道的神经细胞蛋白质。
"By using a different assay, we were able to pick up a completely distinct yet equally important type of genetic mutation that is likely to persist throughout a child's lifetime," Grant said.
Grant说，通过不同的化验分析方法，我们还发现了一种截然不同但同样重要的基因突变，而这种基因突变很可能在小孩的一生当中都会存在。
A partial tandem duplication is a type of gene mutation that occurs when a section of a gene is repeated, like a stutter in the gene's DNA.
部分串联复制是基因突变的一个类型，当一个基因片断重复时发生，就像停顿基因。
To identify the AKT1 mutation, the researchers analyzed 150 tumor samples from patients with either breast, colorectal or ovarian cancer (50 samples from each tumor type).
为了鉴定AKT1基因突变，研究人员共筛选了150份肿瘤样本，其中乳腺癌、直结肠癌和卵巢癌各50份。
Objective To study the gene mutation and clinical characteristic of hereditary spinocerebellar ataxia type 7 (SCA7).
目的研究遗传性脊髓小脑性共济失调7型（SCA7）的基因突变和临床特征。
Considering the data flow description in protocol security testing, mutation analysis is introduced based on constructed type algebra, and a new protocol security testing method is proposed.
针对协议安全测试中数据流的描述问题，在构造类别代数的基础上引入变异分析，由此提出了一种协议安全测试方法。
Complete response rates were similar for children with either mutation and children with wild-type FLT3, the authors report.
作者报道，有突变患儿和野生型FLT3患儿的完全有效率是相似的。
The researchers did not observe any differences in disease metastatic patterns, according to the presence of mutations in serum or the type of mutation.
通过分析血浆中的变异或变异类型，研究者并未观察到疾病转移方式的差异。
Conclusion Construction of the eukaryotic expression vectors of wild type and mutant PRPF31 genes is basic work for research on the mechanisms of retinitis pigmentosa caused by PRPF31 mutation.
结论野生型和突变型PRPF31基因真核表达载体的构建，为研究PRPF31基因突变引起视网膜色素变性的机制奠定了基础。
Methods We screened a family affected by long-QT syndrome type 1 and identified an autosomal dominant missense mutation (R190Q) in the KCNQ1 gene.
方法：筛选出患长qt综合征1型的家庭成员，并鉴定KCNQ1基因中一个常染色体显性遗传突变基因(R190 Q)。
Objective To generate rescued viruses with deletion mutation of capsid protein from dengue virus type 2 isolated in China (DEN2-43).
目的制备登革2型病毒中国分离株(DEN2 - 43)的衣壳蛋白缺失突变病毒。
Youzhan 8, selected from a natural mutation of variety Aojinzhan by Rice Research Institute of GXAAS, is a fine grain quality inbred variety of indica type.
油占8号是广西农科院水稻所从“澳粳占”自然变异植株中选育而成的优质常规稻新品种。
Objective: To analyse the significance and relationship between p53 gene mutation and the expression of mutant type p53 gene protein in the laryngeal carcinomas.
目的：探讨喉癌P53基因突变与突变性P 53基因蛋白表达之间的相互关系及意义。
What we are doing here is precisely matching a treatment to a specific type of cancer cell mutation and abnormal protein signaling pathways that may activate cancer cell growth.
我们在此所做的就是精确匹配治疗方案。一种治疗方案针对一种特殊类型的癌症突变细胞和可能激活癌症细胞生长的异常蛋白信号通路。
Information on locus heterogeneity, type of mutation, clinical and biochemical data, geographical location and common mutations are furnished based on published literature.
基于发表的文献，提供了有关基因座异质性、突变类型、临床和生化数据、地理位置和常见突变的信息。
Objective to detect the mutation on exons 32, 33 of Chinese the neurofibromatosis type 1 (NF1) gene.
目的检测中国人神经纤维瘤病1型(nf1)基因32、33外显子突变。
He said that the bacteria had adapted to pump out both the disinfectant and antibiotic from their cells, as well as showing a DNA mutation that made them resistant to ciprofloxacin-type antibiotics.
他说，这种细菌已经具有把消毒剂和抗生素从它们的细胞中提取出来的功能，也就是说它们的DNA突变使得它们对ciprofloxacin环丙沙星一类的抗生素有了耐药性。
Therefore mutation of insulin gene promoter might not be a major genetic factor for type 2 diabetes mellitus in Chinese patients.
结论：胰岛素基因启动子突变可能不是中国人2型糖尿病的重要遗传因素。
Therefore, the dwarf mutation in X. helleri is caused by the developmental defect in spinal column, and the vertebral malformation underlies the body type alteration anatomically.
因而推测，剑尾鱼的侏儒突变是由于脊椎的发育缺陷所致，椎体异常是其体型变化的结构基础。
The result reveals that I164T mutation is not a major predisposing genetic factor for type 2 diabetes and the mutation in adiponectin gene is different in rac…
提示I164T突变可能不是本组2型糖尿病的重要遗传因素，且该基因位点突变具有种族异质性。
Roughly one in 1,000 Europeans and Americans have inherited the mutation from both parents, and Huetter set out to find one such person among donors that matched the patient's marrow type.
每1000个欧洲和美国人中约有一人从父母遗传了这种突变，Huetter从捐献者中找出一名突变者与患者骨髓相配。
Methods The mutation had been screened from 116 unrelated patients with type 1 diabetes mellitus by ApaI digestion of product of polymerase chain reaction amplification.
方法对116例随机收集的1型糖尿病患者用聚合酶链反应-限制性内切酶消化作该点突变的筛选；
Methods The mutation had been screened from 116 unrelated patients with type 1 diabetes mellitus by ApaI digestion of product of polymerase chain reaction amplification.
方法对116例随机收集的1型糖尿病患者用聚合酶链反应-限制性内切酶消化作该点突变的筛选；
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