结论脾气虚证发生有免疫相关基因组学基础，脾虚时机体免疫功能紊乱。
ConclusionThe genesis of Pi-Qi deficiency syndrome has its immune associated genomic basis, and the immune functions are disordered in patients with that syndrome.
目的对卵巢癌患者血细胞天然免疫活性与红细胞CR1密度相关基因组多态性的相关性进行对比研究。
Objective To study the relationship between CR1 density polymorphism and innate immune activity of red cell and blood corpuscle in patients with ovarian carcinoma.
目的：探讨原发性肾病综合征（PNS）患者红细胞CR1密度相关基因组多态性及数量表达、黏附活性与临床疗效的关系。
Objective: To study the clinical effect and erythrocytes CR1 genomic density and quantitative expression, adhesive active in primary nephrosis syndrome(PNS).
然而，如果血液和组织细胞在基因上原本并不一致，那么就证明那些雄心勃勃而又昂贵的全基因组相关的研究很可能一开始就有本质上的缺陷。
However, if it turns out that blood and tissue cells do not match genetically, these ambitious and expensive genome-wide association studies may prove to have been essentially flawed from the outset.
从一个古代北极熊颚骨上测得的最古老哺乳动物基因组，为动物与气候的紧密相关提供了线索。
The sequencing of the oldest mammalian genome from an ancient polar bear jawbone provides clues about these.
他们试图发现：在一些从研究对象身上取出的DNA遗传物质标记和个性兴趣维度之间，是否可以知道全基因组显著的相关性。
They looked to see whether they could find genomewide significant associations between some of the snips of genetic material taken from subjects' DNA and the personality dimensions of interest.
从人类基因组计划数据库中获取基因的信息可以帮助科学家对肿瘤样本中的相关基因进行定位和拷贝。
Obtaining the details of these genes from the genome project's databases made it possible for the researchers to locate and make copies of each relevant gene from each cancer sample.
2000年，我在清华大学读研究生时参与了人类基因组工程的相关研究。
In 2000, I took part in the research of Human Genome Project at Tsinghua University.
他们也认为浏览人类基因组来寻找疾病相关基因是有效的做法。
They also said it showed it was useful to scan people's entire genome to look for disease-causing genes.
该学科包括医学遗传学，生物化学技术，基因组定位技术，毒理学及相关学科。
Studies include medical genetics, biochemical techniques, genome mapping, genetic toxicology, and related subjects.
用线粒体的基因组来测量相关性是基因学家用以发现很久以前生存过的共同祖先的这一艰巨任务的简化方式。
Using mitochondrial genomes to gauge relatedness is a way for geneticists to simplify the task of finding common ancestors that lived long ago.
这个突然的新发现标志着寻找疾病相关基因能力的提高，也可能是其中一个转折点，是1989年开始的人类基因组计划希望的长远结果。
And the sudden spate of new results mark an acceleration, and perhaps a turning point, in the ability to find disease genes, the long-promised payoff from the human genome project that began in 1989.
在基因组坐标位置下放置有注释的通道，允许快速可视化不同类型信息间的相关性。
It places annotation tracks beneath genome coordinate positions, allowing rapid visual correlation of different types of information.
结论PASG基因作为上游调控基因，通过改变基因组甲基化水平调控下游一系列细胞增殖分化相关基因表达。
Conclusions AS an upstream regulator, PASG can regulate expression of a series of cell proliferation, differentiation relevant downstream genes through changing methylation levels of genomic DNA.
甲基化修饰是脊椎动物DNA唯一的自然修饰方式，动物基因组甲基化与基因表达密切相关。
The methylation beautification is the vertebrate DNA only nature beautification way, the animal genome team methylation and the gene expression close related.
但主题来自于从不同角度对基因组相关性研究结果处理时产生的三种意见。
The main course, however, is provided by three opinion pieces tackling the recent results of genome-wide association studies from quite different angles.
人类基因组计划的完成及相关分子遗传学技术在青光眼研究领域的应用，使青光眼的病因学研究取得了重要进展。
Progress in human genome project (HGP) and the application of molecular genetics in the study of glaucoma has leaded to an important progress in the understanding of etiology of glaucoma.
而对于高血压来说，大型基因组范围研究还未发现与高血压发病风险相关联的普通变异。
In the case of high blood pressure, for instance, large genome-wide studies have thus far found no common variants that are associated with the risk of developing hypertension.
介绍了基因工程及其在基因检测与基因治疗、生物反应器工程、蛋白质工程与代谢工程，基因组计划与生物信息学等相关领域的进展。
Recent progress in gene engineering and related fields such as gene diagnosis, therapy, bioreactor, protein engineering, metabolism engineering, human genome project, bioinformatics is reviewed.
脂质代谢组学在营养学、功能基因组学等相关学科中的应用已有许多报道。
The applications of lipidomics in related subjects are widely reported, such as nutrition and functional genomics.
该网站还收集了基因组中最佳代表基因，并提供了常规的软件分析系统以及一些相关的数据库和实验等等。
It also provides the collections designed to optimally represent each gene in the genome as well as conventional software analysis system and some relevant databases and experiments etc.
蛋白质组学是功能基因组学的重要组成部分，已被广泛应用于人类疾病等相关研究领域。
Proteomics is an important component of functional genomics, which already widely used in disease-related researches.
随着1988年生物质谱相关软电离技术的发明和2001年人类基因组测序完成，蛋白质组学进入了高速发展期。
The development of biomass related ionization method in 1988 and the accomplishment of human genome sequencing in 2001 are major breakthrough for Proteomic study.
功能基因组学另一个研究重点是人类疾病相关基因。
Another important aspect of functional genomics is the research on human disease - related genes.
简要介绍了目前我国在食品相关的功能基因组学将要和正在进行的相关工作。
This thesis briefly introduced the correlation work of the function genome of food in China.
但是，目前对遗传相关的估计主要是基于全基因组的黑箱式整体估计。
However, up to date, the estimation of genetic correlation is chiefly based on a holistic evaluation of the total genome from a blackbox consideration.
对于所有的序列，关于相关基因、外显子、内含子、基因产物和分类学，以及挑选的基因组图谱和RNA二级结构信息是可利用的。
For all sequences, information on related genes, exons, introns, gene products and taxonomy is available, as well as selected genome maps and RNA secondary structures.
结论：所构建的基因组d NA消减文库为进一步筛选UPEC132中与致病相关基因奠定了基础。
Conclusion: The DNA subtractive library may provide a solid foundation for screening and cloning pathogenic genes of UPEC132.
随着人类基因组计划的快速进展及为人类的健康事业提供的便利，遗传性听力损害相关基因的定位克隆工作近十年来取得了令人瞩目的进展。
With the advances in Human Genome Project and the genomics offering for human health, our understanding of the genetics of hearing impairment has advanced rapidly during the last decade.
随着人类基因组计划的快速进展及为人类的健康事业提供的便利，遗传性听力损害相关基因的定位克隆工作近十年来取得了令人瞩目的进展。
With the advances in Human Genome Project and the genomics offering for human health, our understanding of the genetics of hearing impairment has advanced rapidly during the last decade.
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