查询词典 modifier gene

Among all, deleted in liver cell (DLC-1) gene was found to play an important role in hepatoma in 1998, and after that hypermethylation on the promoter of the DLC-1 gene was found in many other cancers, suggesting that epigenetic modification is another way to control the carcinogenesis. Another gene, Endothelin type B receptor, was found to cause megacolon syndrome by accident while searching the cause of white spot in mouse, and was also found hypermethylation on its promoter in some cancer cells.

在此中，DLC-1基因自从1998年后被发现在肝癌的演化上扮演重要的角色后，在许多其他的癌症上也发现此基因上位於promoter的CpG islands有过度甲基化的现象，推论DLC-1基因的过度甲基化是一种经由epigenetic modification调节细胞癌化的方式。

The result indicates that there are one dominant and one recessive complementary gene that are effective against the Indian race 2E16. However, the monosomic analysis results indicated there was one resistant gene to the Indian race 2E16 and the gene was located on chromosome 3B. The current study shows that it is different from the known genes.

采用常规杂交分析方法，对铭贤169与阿夫杂交的F_1、F_2、BC_1代及其亲本进行抗性鉴定和统计分析，结果表明，阿夫对2E16菌系的抗性至少由1对显性抗条锈基因控制；通过单体分析将阿夫抗2E16菌系的1对显性基因定位在3B染色体上，等位性分析表明该基因不同于目前的已知基因。

The Sry gene sequence of Muntiacus crinifrons was acquired and the conclution was that there are 83% homology between the human and Muntiacus crinifrons. It was testified that in all mammal Sry gene is consertive. On the other side the Sry gene was located to the Y2 chromosome of the Muntiacus crinifrons.

最后提取雄性黑麂的基因组DNA，并用同一对引物对其进行扩增，亦得到Sry基因的片段，对此扩增片段进行克隆，测序，结果表明其与Y2染色体得到的Sry基因片段完全一样，与人SRY基因的同源性均为83%。

They all contain 13 protein coding gene,2 rRNA gene,22 tRNA gene and 1 D-Loop.The base composition for the four nucleotides is A-32.0%,C-27.6%,G-14.7%,T-25.8%,And it is A-32.5%,C-26.9%,G-14.1%,T-26.5%for Yellow-throated Marten.But there are some definite differences in base composition,the using of Initiation codon and Stop codon,and the mode of repeat sequences in control region.The codon usages of Manes have bias,and the ttiird locations of codon of protein-coding genes have the higher frequency in using A and C.There may be some relativity with the content of A and C in D-loop,namely,it has relation with the mode of repeat sequences.The complete mitochondrial genome of the Sable and Yellow-throated Marten were submitted to GenBank,and the accession number are FJ429093 and FJ719367 respectively.3、The complete mitochondrial genome of 6 other species of Mustelidae from GenBank and some sequences of D-loop from the 6 species were aligned.

分析紫貂大兴安岭亚种、长白山亚种、阿尔泰亚种和北欧亚种间的基因流及进化历史得知：大兴安岭种群与新疆种群和长白山种群间的基因流水平最高(Nm=0.1260和0.1427)，新疆与长白山种群间最低Nm=0.0053紫貂种群在进化过程中可能发生过种群膨胀，经历过种群增长过程。2、对紫貂和黄喉貂的线粒体全基因组结构进行分析发现：全长分别为16 523bp和16549bp，均包含13个蛋白质编码基因、2个rRNA基因、22个tRNA基因和1个非编码序列区(D-Loop区，紫貂全序列中碱基组成为A-32.0%，C-27.6%，G-14.7%，T-25.8%，黄喉貂为A-32.5%，C-26.9%，G-14.1%，T-26.5%；基因排列顺序与日本貂和貂熊的一致，但碱基组成、起始密码子和终止密码子的使用及控制区中串联重复序列模式等均存在一定差异。

Opportunistically expressed (usually at the basal levels of transcription), but still permit the continued expression of genes that are regulated by strong promoters/enhancers (such as housing-keeping gene), the expresison of these genes might play a key role in the embryonic development; 5 The sum of these two opposing processes-activation and repression-would dictate the final pattern of gene expression that manifests itself as a dramatic reprogramming of gene expression during the maternal-to-zygotic transition and support further embryonic development.

这些基因的表达对于胚胎的后继发育可能是至关重要的；5）通过胚胎基因表达的激活与抑制：这两个作用相反的机制依不同时间顺序协同作用于胚胎基因，从而在指导胚胎发育的控制权由母源性表达产物移交到胚胎特异的基因表达产物的过程中&再程序化&胚胎基因的表达，形成特定的表达模式，以支持胚胎的后继发育。

P16 gene is composed of two intervening sequences and three exons , and encodes p16 protein , which is the inhibiter of CDK4 and CDK6 . They can together prevent phosphorylation deactivation of pRB , and make the cell cycle blocked in G1 stage. P16 gene promoter region has a great of CpG islands , which can be methylated when some adverse factor appears , and so the genetic transcription of p16 can be inhibited , which leads to gene silencing, cell paraplasm, and tumor generate.

抑癌基因p16编码蛋白P16 ，是细胞周期蛋白CDK4和CDK6抑制剂，它阻止pRB磷酸化失活，使细胞周期阻滞于G1期。P16基因启动子区域富含CpG岛，当受到各种有害因素影响时，容易发生甲基化，从而抑制P16基因转录，导致基因沉默，细胞异常增生，导致肿瘤的发生[5]。

Comparing the nucleotide sequences of 16S rRNA gene and ribosomal protein gene, we could find that these two strains have the highest homology of 99.4% and 99.8%, respectively. The nucleotide sequences of 16S rRNA gene for the CWB-YN strain shared higher homology (98.5%,98.9% and 98.0%) with phytoplasma strains in Tomato big bug 16SrI-A group, Western aster yellow (16SrI-B group and Clover phyllody (16SrI-C group). But it is obviously under 97.0% with other phytoplasma groups. The CWB-GZh strain shared higher homology (98.7%,99.1% and 98.3%) with phytoplasma strains in Tomato big bug(16SrI-A group ),Western aster yellow (16SrI-B group) and Clover phyllody (16SrI-C group).

苦楝丛枝病植原体云南株系与其它组16S rRNA基因序列的同源率进行比较，结果与16SrI-A组中的番茄巨芽病植原体(Tomato big bug，BB)、16SrI-B组中的西方翠菊黄化病植原体(Western aster yellow，SAY)和16SrI-C组中的三叶草变病植原体(Clover phyllody，CPh)同源率达最高，分别为98.5%、98.9%和98.0%，而与其它组的植原体16S rRNA基因序列的同源率均低于95%；苦楝丛枝病植原体贵州株系与16Sr I-A组的番茄巨芽病植原体(Tomato big bug，BB)、16Sr I-B组的西方翠菊黄化病植原体(Western aster yellow， SAY)和16SrI-C组中的三叶草变叶病植原体(Clover phyllody，CPh)的同源率达最高，分别为98.7%、99.1%和98.3%。

Nodosus pilin and the killed D. nodosus vaccines. It also means that the IL-2 in the fused Pilin-IL2 construct may also have a potential role in stimulating vaccine antigen .Key words: D. nodosus Recombinant Pilin gene Recombinant Ovine IL-2 gene Fused Pilin-IL2 gene

用Pilin-IL-2融合基因工程疫苗免疫健康家兔的初步免疫试验结果表明，2l天后产生较高的凝集效价，达到〓，甚至稍高于加佐剂的前三种疫苗，证明绵羊IL-2基因与Pilin基因融合后，可起到一定的免疫佐剂作用。

GAP gene was found to be a good internal control for the first time for studying gene expression in H. polymorpha. It was shown by Northern hybridization that H-OLE1 gene was expressed in H.

为研究H-OLE1基因的转录及其调节规律，通过一系列实验，首次找到了可在研究多形汉逊氏酵母基因表达时用作内标的GAP基因。

Because Cx43 gene is the first a connexin gene to be associated with non-syndromic deafness, we have sequenced the coding region of Cx43 gene from 190 Taiwanese patients with prelingual deafness and 130 unrelated normal individuals.

Cx43基因是connexin α家族中第一个被发现与非症候群听障有关的基因，我们收集台湾地区190位语言学习前期听障患者，及130位听力正常人血液DNA做Cx43基因的分析。

His female bullfighter Lydia gradually Health love, but she was in a vegetative state after the Bulls Zhuangcheng away from her, just because Lydia's ex-boyfriend showed more affectionate than he is like love.

他对女斗牛士莉迪亚渐生爱意，却在她被公牛撞成植物人后离她而去，仅仅因为莉迪亚的前男友表现出好似比他更深情的爱。

I know of none which are not easy to answer, but what I am trying to do now is only by a series of hints to throw some light on the narrow path of legal doctrine, and upon two pitfalls which, as it seems to me, lie perilously near to it.

我不认为有什么难以回答的问题，但我现在要做的仅仅是通过一系列线索，来给法律理论的狭窄路径以及在我看来离它近得危险的两个陷阱提供一些启示。