Epigenetics is the study of gene regulation.
表观遗传学是研究基因调控。
RNA interference (RNAi) is a powerful tool in the study of gene function.
RNA干扰已经成为基因功能研究的强大工具。
The study of gene engineering of macrolide antibiotics have made the rapid and exciting progress.
大环内酯类抗生素的基因工程研究进展十分迅速。
After the sequencing of genomes, genomics has shifted to the study of gene expression and function.
测序完成后，基因组学转向了基因表达及功能的研究。
In functional genomics ear, the study of gene function will also transfer from single genes to studying all genes.
功能基因组学时代对于基因功能的研究也由单一基因转向大规模、批量分析。
RNA interference as a very effective and powerful tool has been employed extensively in the study of gene function.
RNA干扰作为一种快捷方便的工具广泛用于基因研究。
Upon the coming of post-genomics era, the life science will from the study of gene switch to explore the function of gene.
后基因组时代的到来，预示着生命科学将从研究基因转向对基因功能的探索。
With the discovery of antisense RNA and further research, antisense RNA technique has been applied in the study of gene regulation.
随着反义rna的发现及对其研究的深入，反义rna技术已被广泛应用于基因调控的研究中。
The article expounds the progress of the study of human genome and post-genome and the current situation of the study of gene therapy and gene drugs.
本文概述了人类基因组及后基因组的研究进展及依此开展基因治疗及基因(组)药物研制等应用开发研究的现状。
Despite the advantages of using mouse es cells in the study of gene regulatory networks, further research must focus more directly on human stem cells.
除了在本研究中利用基因调控网络中的小鼠胚胎干细胞的优势外，深入研究必须更加直接地集中于人类干细胞。
The study of gene mechanism of coronary heart disease is being emphasized, which will give a new way for the treatment of coronary heart disease in molecular level.
冠心病基因机制的研究愈来愈受到重视，这将为冠心病从分子水平上彻底治疗开辟新的途径。
Because of being able to highly specifically and efficiently silence gene expression, RNAi has the potent application in the study of gene function and gene drug development.
由于其在基因沉默中的高度特异性和有效性，在基因功能和基因药物的研究中有很大潜力。
All these show that fibroblast cells harvested and cultured in this method could be safe and stable targeted cells used for the study of gene therapy of autologous skin fibroblast.
从而证明该方法所获取的大量皮肤成纤维细胞可作为一种安全、可靠的靶细胞用于自体皮肤成纤维细胞基因治疗研究。
RNA interference methods and gene inducible expression techniques to use on study of gene regulations in cells are transferred to making transgenic animals, and the ideal research results are gained.
用于细胞基因调控研究的RNA干涉技术和基因诱导表达方法，现在移植到了转基因动物中，并获得了理想结果。
Metatranscriptomics studies have been performed to study the gene expression of microbial communities.
进行了超转录组学研究以研究微生物群落的基因表达。
We would never have been able to get to this gene if not for the study of this family.
如果没有对这个家族的研究，我们永远不可能找到这个基因。
He added that the challenge was to next move beyond this correlative study to figure out how these gene variations may lead to functional changes that contribute to the molecular process of aging.
他补充说，挑战在于这一相关性研究的下一步，即弄清楚这些变异基因如何可能导致分子老化过程的功能性变化。
Highlighting the potential of further study, they found that one particular gene is involved in a previously unknown metabolic process that can lower bad cholesterol.
研究者们强调了深入研究的巨大潜力：他们发现其中一个基因参与一种未知的可降低有害胆固醇的代谢过程。
The key difference in this study was the presence of a single gene from the H3N2 human virus: the PB2 protein, which gave the hybrid viruses the ability to spread easily among the lab mice.
这项研究中一个关键的不同点就是H3N2人类流感病毒中存在一个蛋白基因：PB2蛋白，它的存在使得杂交病毒具有了在实验小鼠之间轻易传染的能力。
Scientists developed it from gene information on 226 patients, analyzed it in 640 patients, and on Monday reported a validation study of it in 526 others.
科学家从226位患者的基因信息中进行测试，在640位患者中分析了这项测试，并在周一报告了在其他526名患者中有效性的研究。
In 40 research patients in the UK that are participating in an ongoing study that has documented many aspects of their lives, researchers looked at differences in gene methylation.
英国的40名患者参加了一项持续研究，在这项研究中，他们人生中的很多方面都被记录下来，研究者们观察了他们基因甲基化的差异。
The researchers went on to study what is responsible for the difference in expression of the glucocorticoid-receptor gene.
研究者们进一步探究是什么造成了糖皮质激素受体基因表达的差异。
The study will be the first to measure which variant a teenager has of the serotonin transporter gene, which is responsible for our uptake of "feel-good" serotonin and mood control.
研究组还将首次测试青年人拥有那种转胺基因（对吸收让心情转好的胺和控制情绪起首要作用）。
In a new study, people with alterations in a gene called9p21 had an increased risk of having a heart attack.
在一项新的研究中，带有一种被称为9 p 21的基因变异体的人有增加的心脏病突发风险。
In a study of nearly 3, 000 people, around 38% inherited one copy of the gene variant and were biologically three to four years older than those who did not carry the sequence.
对近三千人的研究显示，约有38%的人带有遗传性基因变体，与没有这一基因序列的人相比，他们的生物年龄要老三到四岁。
"This is the first major study that shows how small changes in one master regulator gene can cause a cascade of other metabolic effects in other genes," said lead author Tim Spector in a statement.
“这是第一个重要的研究，它解释了主宰调解员基因中微小的变化可以引发串联的其它基因的新陈代谢变化，”主作者TimSpector在声明中说。
"We would never have been able to get to this gene if not for the study of this family."
如果没有对这个家族的研究，我们永远不可能找到这个基因。
The Blue Gene/L technology offers a powerful way to study these types of diseases, because it provides a more cost-effective (and faster) way to model the effects of protein folding and misfolding.
BlueGene/L技术提供了一种强大的方法来研究这些类型的疾病，因为它能够更加经济高效地（和更快地）建模蛋白质折叠和错误折叠的效果。
Based on a study of 13, 945 Icelandic smokers, deCODE's researchers showed that having a t in the appropriate part of the gene correlates very strongly indeed with being a heavy smoker.
基于一项样本数量为13945位冰岛吸烟者的研究，deCODE公司的研究人员证实如果胸腺嘧啶处在基因中恰当位置，就呈现出与嗜烟程度极强的相关性。
Based on a study of 13, 945 Icelandic smokers, deCODE's researchers showed that having a t in the appropriate part of the gene correlates very strongly indeed with being a heavy smoker.
基于一项样本数量为13945位冰岛吸烟者的研究，deCODE公司的研究人员证实如果胸腺嘧啶处在基因中恰当位置，就呈现出与嗜烟程度极强的相关性。
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