gene splicing的例句大全

Secondary structural characteristic of eukaryotic gene splicing sites

真核基因剪接位点二级结构特征

The major focuses of research include: clinical biochemistry, gene splicing and regulation, and neurological biochemistry.

现有临床生化、基因拼接与调控、神经生化三个研究方向。

Construction of middle fragment deletion mutant with improved gene splicing by overlap extension

用改进的重叠区扩增基因拼接法构建中间缺失突变体

Alterations in gene splicing can be much more subtle in nature but still have a major impact on the cancer cell and can be targets of therapy.

基因剪切的改变在自然界是微乎其微的，但是对癌细胞仍然是一个主要的影响并能够作为治疗的靶点。

Recombination and Mutation of some Genes with Gene Splicing by Overlap Extension

利用套叠PCR技术进行基因突变和拼接

Research of Human Gene Splicing Donor Site Recognition

人类基因剪接供体位点识别的研究

Construction of a chimeric SEA-hPLAP-1 cDNA with gene splicing by overlap extension

重叠区扩增基因拼接法在构建膜锚定金黄色葡萄球菌肠毒素A融合基因上的应用

Studies on the Splicing Ability of Wx Gene Intron 1 in Glutinous Rice

糯性水稻中蜡质基因第1内含子的剪接活性

Further analysis of the alternative splicing distribution in human duplicate pairs showed the asymmetric evolution of alternative splicing after gene duplications, i.e., the AS forms between duplicates may differ dramatically.

对人复制基因对间AS分布的进一步分析表明，基因复制后AS进化是非对称性的，如，复制基因间的AS形式数可能有很大的变化。

the study of gene mutation and alternative splicing in primary hepatocellular carcinoma using dna sequencing and oligonucleotide chip

应用DNA测序和寡聚核苷酸芯片对原发性肝癌中基因突变及变位剪接的研究

Objective: To clone and analyze the different splicing variant of Lims gene in rat.

目的：克隆与分析大鼠不同剪切的Lims基因。

Alternative Splicing of de novo Methyltransferase Gene 3b in Adult and Newborn Mice

DNA重新甲基化酶3b在成年及新生小鼠部分组织中的选择性剪接表达

Alternative splicing of gene transcription and its progress in clinical pharmacology

基因转录另路剪接及其在临床药理学的研究进展

Intronic mutations may affect gene regulation through aberrant splicing or disruption of critical DNA protein interactions.

内含子突变可以通过引起剪接异常或关键性DNA-蛋白反应中断而影响基因调控。

Conclusion The splicing mutation can affect the result of transcription and translation, and it is a specific novel mutation of ATP2C1 gene.

结论该剪接位点突变可影响基因转录和翻译产物，是ATP2C1基因新的特异性突变。

There are multiple molecular mechanisms that can cause genetic disorders such as point mutations, splicing site mutation, insertion/ deletion mutations, gene duplication, complex rearrangements and gene copy number abnormalities.

引起遗传性疾病的分子机制有多种，常见的有点突变、小片段插入/缺失突变、拼接位点突变、外显子缺失/重复突变、基因重复和复杂重排及基因拷贝数异常等。