真核基因剪接位点是真核细胞生物基因序列中外显子和内含子的相邻区域。
The splice sites of the eukaryotic DNA are the region of the vicinity in the exons and introns of the DNA sequences of the eukaryotic cell biology.
我们使用一个已知导致剪切缺陷的83个内含子和35个外显子的突变来评估hsf的效率。
We evaluated HSF efficiency using a set of 83 intronic and 35 exonic mutations known to result in splicing defects.
目的调查广东地区汉族人群MICA基因第5外显子和MICB基因第1内含子微卫星多态性分布。
Objective To investigate the genetic polymorphism of microsatellite in the exon 5 of MICA gene and the intron 1 of MICB gene in Guangdong Han population.
青蒿鲨烯合酶基因组dna结构很复杂，包括14个外显子和13个内含子。
The AaSQS genomic DNA has a complex organization containing 14 exons and 13 introns.
为了解人类LDL受体基因内含子15的遗传背景，利用长链PCR和锚定PCR分离了LDL受体基因外显子15-内含子15-外显子16和内含于15的3’末端片段。
To understand intron 15 of human LDL receptor gene, the DNA fragments from exon 15 to exon 16 and the 3' end of intron 15 were amplified with long chain PCR and anchored PCR.
分别设计MSX1、PAX9基因特异性引物，聚合酶链反应扩增全部外显子编码区和内含子-外显子剪接序列，产物纯化后直接测序。
Specific primers were designed for MSX1 and PAX9 respectively. Mutation analysis was performed by direct sequencing of all the coding exons and intron-exon boundaries.
采用聚合酶链反应(PCR)方法扩增rho基因第1 ~ 5外显子和第1内含子基因片段，用直接dna测序法筛查rho基因突变。
Extron 1-5 of RHO gene was amplified by polymerase chain reaction (PCR), and the mutation of RHO gene was screened by direct DNA sequence measurement.
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.
这7个基因在基因簇中串联排列 ，每个基因都由6个外显子和5个内含子组成。
The 7 DFR-like genes were found to be arranged in a tandem array, and all of them comprised 6 exons and 5 introns.
因此选择对基因的表达具有重要功能的外显子1和其上游的调控区及下游外显子内含子交界区序列通过直接测序法进行SNP筛查，并进一步分析多态位点与病窦的关联性。
Therefore the other aim of our study is to discover SNPs of HCN4 exon 1, including the regulatory sequence and exon-intron boundary of it, which plays an importable role of channel function.
因此选择对基因的表达具有重要功能的外显子1和其上游的调控区及下游外显子内含子交界区序列通过直接测序法进行SNP筛查，并进一步分析多态位点与病窦的关联性。
Therefore the other aim of our study is to discover SNPs of HCN4 exon 1, including the regulatory sequence and exon-intron boundary of it, which plays an importable role of channel function.
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