By comparing the DNA of Japanese with each type, the researchers were able to identify the gene that controls which type a person has, they report in the Monday issue of Nature Genetics.
通过比较两种类型耳垢的日本人的DNA，研究人员鉴定出了控制耳垢类型的基因，研究结果刊登在周一发布的《自然遗传学》期刊上。
He will continue to run his Salk Institute lab where he studies gene therapy, cancer genetics, and inflammation.
他将在索尔克研究所的实验室内继续基因治疗，癌症遗传学和炎症的研究工作。
The Molecular Genetics of schizophrenia (MGS) consortium pinpointed an association between schizophrenia and genes in the chromosome-6 region that mediate gene expression, such as histones.
精神分裂症的分子遗传学院会(MGS)精确确定了精神分裂症和6号染色体区域上的基因间的联系，它介导基因表达，比如组蛋白。
Most dog genetics researchers limit their work to gene scans of DNA collected from hundreds of pet owners.
多数狗遗传学研究人员只是对从上百只宠物狗身上收集的DNA进行基因扫描，因而使得他们的研究受到局限。
Reporting in the Jan. 9 issue of the American Journal of Human Genetics, the team describes how a variation in the neuregulin 3 gene influences delusions associated with schizophrenia.
研究报告发表在1月9日出版的《美国人类学遗传》杂志上，研究小组描述了neuregulin3基因的变异影响着和精神分裂症及相关的妄想症。
The genetics of the two groups reflect the disparity: They have different versions of a gene called pantophysin I, whose function isn't known.
两种鳕鱼的遗传特征也反映了这种差异：它们拥有不同版本的pantophysin I基因，但这个基因的功能尚不清楚。
For example we used data from gene-disease associations in the psychiatric genetics literature to see whether studies that overestimate or underestimate an effect have anything in common.
比如，我们分析了从精神病学遗传学文献中获取的基因与疾病相关性数据，以了解在那些高估或低估基因影响力的研究之间是否存在什么共性。
Some researchers thought the survival difference was due to genetics, but they could never find the gene responsible.
一些研究人员认为这两类小鼠之间的差异是源于基因的不同，但是他们未能发现基因方面存在的问题。
The public debate on plant genetics focuses almost entirely on the pros and cons (mostly cons) of genetic modification—putting a gene from one species into another.
公众对于植物基因学的争论几乎全部聚焦于转基因的正负两个方面的影响，绝大多数是负面影响。 转基因通常就是把一个种属的基因注入到里一个种属里。
However, the current Nature Genetics report associates SLE with a polymorphism at gene TNFSF4.
然而，当期《自然-遗传学》杂志报告sle与TNFSF4基因多态性有关。
Nowadays, BIGH3 gene mutation related corneal dystrophy is the most common etiological factor leading to corneal dystrophy in genetics.
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。
Although a recent study found that a single gene mutation heightened the risk of obesity by up to 67 percent, genetics cannot explain the skyrocketing obesity trend.
尽管最近的研究发现单基因突变使肥胖的风险增加高达67%，但是遗传不能解释飞涨的肥胖趋势。
The much touted anti-leukemia drug Gleevec here appears as the hero of modern, genetics-based cancer therapy, a “rationally designed” drug specifically directed against a known cancer gene.
格列卫（Gleevec）这种广为宣传的抗白血病药物在这里成了现代基因癌症治疗的英雄，是一种“理性设计”出来专门针对特定肿瘤基因的药物。
By combining advanced gene-sequencing technologies with privileged access to the genetic data of Icelanders, DeCode Genetics pioneered the field of personal genomics.
由于拥有先进的基因序列分析技术和获得冰岛人基因资料的特权。DeCodeGenetics公司在个人染色体领域处于领先地位。
Their study, published in the magazine Nature Genetics, shows that halting the activity of this gene in mice predisposed to cancer slowed the growth of — and in some cases, prevented — tumors.
他们的刊登在《自然遗传杂志上》研究，显示了在小鼠中这个基因活性的不完善可以使癌症增长减缓并且在某些情况下阻止肿瘤的发生。
Gene transfer techniques make a new way for the fish genetics and breeding.
基因转移为鱼类遗传育种开辟了一条新的途径。
The results will improve the application of plant cell engineering and gene engineering on cotton genetics and breeding.
该结果的获得必将大大促进植物细胞工程和基因工程在棉花遗传改良上的应用。
As the new study approach, molecular genetics now is trying to find specific genes, and will focus in understanding how gene works.
分子遗传学作为新兴的研究途径，目前以寻找基因为主，将来则以认识基因如何工作为重。
Gene Mapping of human diseases, especially the complex genetic diseases, has been the difficulty and hotspot in medical genetics and gene study.
人类疾病，特别是多基因遗传病相关基因的定位，是目前医学遗传学和基因研究中的难点和热点。
Law of changes of gene frequency was core of research on population genetics, was also a key of understanding biological evolution.
基因频率变化规律是群体遗传学研究的核心，也是理解生物进化的关键。
STR and its typing characteristics and applications in genetic map, forensic identification, anthropology, population genetics, gene diagnosis and organ transplantation are reviewed in this paper.
本文介绍了STR及其分型特点，以及STR应用于遗传制图、法医学鉴定、人类学、群体遗传学、基因诊断、器官移植等方面内容。
Since the split gene was found in 1977, the processing mechanism transcribed and the function of intron have been a popular subject about the study of molecular genetics ineucaryote.
自1977年发现不连续基因（断裂基因）以来，有关内元（内含子）的功用以及转录后的加工机制是真核生物分子遗传研究的一个热门。
For example, transfer of virulence gene and transmission of drug-resistant gene mediated by a phage results in gene polymorphism of bacteria, which is an important problem in medicine and genetics.
如由噬菌体介导的细菌毒力基因的转移、细菌耐药基因的传递等导致了病原菌基因表型的多态性，这在医学与遗传学中是一个日益严峻的重要问题。
Conclusion: D12S1686 is such a valuable genetic marker that it can be used to gene linkage analysis and population genetics research.
结论D 12s1686位点具有较高的杂合度和多态信息含量，在基因连锁分析和群体遗传学研究中具有重要的应用价值。
Genetics: Associated with mutation of the GNAQ gene, almost always sporadic (familial inheritance pattern is exceedingly rare).
遗传学：和GNAQ基因突变有关，散发，家族性遗传极其罕见。
Main interests in Human Molecular Genetics, relationship between genes and diseases, technology and application of gene chip.
人类分子遗传学、基因与疾病、基因芯片技术和应用、基因工程及相关生物信息学研究。
The genetics and gene location were studied through F_1 and F_2 generations.
通过F_1和F_2代的性状表现研究雄性不育性的遗传和基因定位。
The gene therapy, also called "the gene transfer", means to have intention to carries on genetics to manipulate towards living the cell heredity materials.
基因治疗，又称“基因转移”，是指有意对活细胞遗传物质进行遗传学操纵。
It is regarded as a replicator of culture that is a basic unit in cultural evolutionism, similar to the gene of genetics.
它被看作是一个文化复制因子，是文化进化的基本单位，其性质类似于遗传学中的基因。
It is regarded as a replicator of culture that is a basic unit in cultural evolutionism, similar to the gene of genetics.
它被看作是一个文化复制因子，是文化进化的基本单位，其性质类似于遗传学中的基因。
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