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。
He will continue to run his Salk Institute lab where he studies gene therapy, cancer genetics, and inflammation.
为了了解那些基因云发生的情况，遗传学研究者们必须找到开启和关闭基因的生物学开关。
Hoping to understand what's happening in those clouds, epigenetics researchers have focused on biochemical switches that turn genes on and off.
科学家们发现多基因和基因突变似乎和自闭症有关，但它比遗传学更加复杂。
Scientists have identified multiple genes and mutations that seem to be related to ASDs, but it's more complex than just genetics.
另一篇是发表于2010年1月的论文，表明ART胚胎里的基因和非art基因比，承受着不同的表观遗传学标志物。
Another paper, from January 2010, shows that the genes in ART embryos bear different epigenetic marks than non-ART embryos.
一个叫做表观修饰(表观遗传学)的过程——它关闭了那些对环境刺激起反应的基因——可能使得他们起作用的基因组和实际的基因组不一致。
A process called epigenesis, which shuts down genes in response to environmental prompts, may make their effective genomes different from their actual ones.
近期压力研究方面的进展（基因学、表观遗传学和分子的结果）反向印证了有关环境/基因相关性与先天/后天分界线的假设。
Recent advances in stress research (focused on genetic, epigenetic, and molecular events) are inverting implicit assumptions about gene/environment relationships and the nature/nurture divide.
AFLP已广泛应用于分类学、病理学、种群遗传学、DNA指纹分析的研究和建立数量性状基因图谱，成为最主要的遗传标记。
AFLP has been emerged as a major new type of genetic marker with broad application in systematic, pathology, population genetics, DNA fingerprinting and quantitative trait loci (QTL) mapping.
遗传学和基因研究的重要性不断增强。基因能影响许多事情，比如会影响着我们的长相。吃什么食物可能会引起疾病，需要被治疗。
Genetics, the study of genes, is gaining increasing importance. Genes can influence many things, from whom we look like to what we eat to possible treatments for diseases.
以下是关于乳腺癌遗传学方面的一些问题和回答，以及关于新近发现的基因和基因标志物的新闻报道。
Below are some questions and answers regarding breast cancer genetics and the latest news regarding the newly discovered genes and genetic markers.
通过染色体核型和显带分析，为研究松辽黑猪起源进化、品种形成和基因定位提供细胞遗传学方面的基础数据；
It was to provide basic data of cytogenetics for origin, evolution and gene location of Songliao black pig by caryotype and banding.
食物与健康之间的关系与表现遗传学有关，那是一门研究生活方式和环境如何影响人们基因的学科。
The link between food and health has to do with epigenetics, the study of how lifestyle and environment influence the expression of your genes.
据《自然遗传学》报道，研究人员宣称2号染色体和16号染色体发生基因变异会增加雌激素受体阳性的乳腺癌发病率。
Reporting in Nature Genetics, researchers said genetic variants on chromosome 2 and on chromosome 16 May increase the risk of estrogen-receptor-positive breast cancer.
毕业生可在制药工程和基因研究类企业，学术机构和其他研究遗传学的组织中找到工作。
Graduates find job opportunities with pharmaceutical and genetic research firms, academic institutions, and other organizations investigating genetics.
我们报道了11例成年起病的亚历山大病详细的临床和基因数据，进行了为期4年多的观察，并回顾了先前报道的25例通过遗传学证实的成年起病的亚历山大病。
We report detailed clinical and genetic data of 11 cases of AOAD, observed over a 4-year period, and a review of the previously reported 25 cases of genetically confirmed AOAD.
作者承认遗传学研究真正进步，并列举了BRCA1和BRCA2基因发现的例子，以及它们在乳癌中的作用。
The authors admit that genetic research is progressing, and they cite the example of the discovery of the BRCA1 and BRCA2 genes and their role in breast cancer.
这些研究人员在《自然》杂志上发表了他们的研究结果。桑格研究所是英国一家非营利性的基因学和遗传学研究所。
These researchers published their findings in the scientific journal Nature. Sanger is a non-profit British genomics and genetics research institute.
书的剩馀部分献身于遗传学的绘图和异形基因的克隆。
The remainder of the book is devoted to genetic mapping and cloning of mutant genes.
动物遗传学的学生研究多细胞动物的遗传学。他们通过实验，医学和兽医角度研究不同动物的遗传基因码。
Students in this major study the genetics of multicellular animals. They compare the genetic codes of different animals and approach the topic from experimental, medical, and veterinary perspectives.
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。
Gene Mapping of human diseases, especially the complex genetic diseases, has been the difficulty and hotspot in medical genetics and gene study.
鉴定的微卫星分子标记为进行银鲫群体遗传学和进化遗传学研究，以及银鲫的分子标记育种和进行基因组作图提供了理想的工具。
The microsatellite markers produced by this study will be of benefit to further studies on the evolutionary genetics and provide useful tools for marker assisted selection breeding or genetic map.
对OSA的分子遗传学研究可帮助理解OSA的病因和发病机理，并能促进对OSA的基因诊断和预防。
The molecular genetic research on OSA can assist us in understanding the pathogenesis of OSA and promote genetic diagnosis and prevention of OSA.
迄今为止，用连锁分析和细胞遗传学方法对小眼球相关基因进行了基因定位并进一步对候选基因进行突变分析。
Up to date, on the bases of linkage analysis and cytogenetic analysis, the loci associated with microphthalmia have been identified and mutation analysis of the candidate loci are performed.
化学遗传学和化学基因组学是近几年兴起的新研究领域。
Chemical genetics and chemical genomics are new approaches developed recently in genetics researches.
本文综述了全基因组技术及其种类和原理和其在法医遗传学方面的应用前景。
This article gives a review on whole genome amplification, including the species, principle and application prospect in forensic genetics.
其内容包括利用原生质体融合、基因工程等技术进行菌株遗传改良和利用酶谱分析、分子遗传学等技术研究其遗传变异。
This included genetic improvement of strains by protoplast fusion and molecular biology and studies on genetic variability by zymogram technology and molecular genetics.
行为遗传学的发展前景将是定量遗传学和分子遗传学以行为基因组学为中心的整合。
The future for behavior genetics is integration of quantitative genetics and molecular genetics centering on behavior genomics.
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。
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。
Conclusion: D12S1686 is such a valuable genetic marker that it can be used to gene linkage analysis and population genetics research.
应用推荐