错配
- mismatch;mispairing
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DNA错配修复系统基因多态性与大肠癌易感
Polymorphisms of the DNA Mismatch Repair Genes and Susceptibility to Colorectal Cancer
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DNA错配修复基因甲基化在肝细胞癌发生发展中的作用
Methylation of mismatch repair gene ( MMR ) in primary hepatocellular carcinoma
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幽门螺杆菌与DNA错配修复系统
Relationship between Helicobacter pylori and DNA mismatch repair system
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DNA错配修复与癌症的发生及治疗
DNA mismatch repair and occurrence and therapy of cancer
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缺损DNA错配修复决定一个近侧结肠癌特异的转录模式
Defective DNA mismatch repair determines a characteristic transcriptional profile in proximal colon cancers
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DNA错配修复系统研究进展
Advances of Researches on DNA Mismatch Repair System
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DNA错配修复、染色体不稳定和肿瘤的关系
DNA Mismatch Repair , Chromosome Instability and Cancer
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此外,此体系对目标DNA的识别能力非常强,能够区分单碱基错配的目标DNA。
Furthermore , the recognition capability of this system for target DNA was strong .
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DNA错配修复基因产物表达与肿瘤恶性程度相关性的初步探讨
The preliminary research of significance of DNA mismatch repair gene product expressions in tumor cells
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DNA错配修复基因hMSH2蛋白表达与胃癌发生关系的探讨
Study of relationship between expression of DNA mismatch repair gene hMSH_2 and generation of gastric cancer
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微卫星不稳定性可间接反映DNA错配修复系统功能的缺陷。
Microsatellite instability can thus reflect the deficiency in DNA mismatch repair system to some extend .
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对结肠癌DNA错配修复基因突变携带者的识别及存活率的评估
Identification and survival of carriers of mutations in DNA mismatch - repair genes in colon cancer
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DNA错配修复系统可以识别并修复这种错误,对维持微卫星长度稳定相当重要。
DNA mismatch repair system is one of the systems in maintaining the length of Microsatellites loci .
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错配PCR和DNA改组技术提高抗肝癌单链抗体亲和力
Affinity maturation of a single-chain antibody for hepatocellular carcinoma by error-prone PCR and DNA shuffling
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错配PCR致突变的实验条件研究
The condition for error - prone PCR induced mutation
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青年人结直肠癌DNA错配修复基因表达和DNA倍性检测
The expression of DNA mismatch repair genes and detection of DNA ploidy in young patients with colorectal carcinoma
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5-氮-2′-脱氧胞苷对人卵巢癌细胞凋亡及DNA错配修复基因表达的影响
Effects of 5-aza-2 ' - deoxycytidine on apoptosis of ovarian cancer cells and on expression of mismatch repair genes
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对rrrA基因83位C-T的点突变,设计错配引物,以错配PCR的方法检测福氏志贺菌的耐药突变。
To fixed point mutant , mismatch primer was designed and Shield flexneri were detected by mismatch PCR .
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错配的双链RNA及其稳定性研究
Studies on mismatched double stranded RNA and their stabilities
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子宫颈癌错配修复基因产物与p53表达
Mismatch Repair Gene Protein Product and the p53 Expression in Cervical Squamous Cancer
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它利用引物在低严谨条件下会与模板发生错配结合的特性,使一端引物与已知序列退火,而另一端引物则与未知侧翼区的部分相似序列退火来实现完整的PCR扩增。
It utilized the character that mismatch occurred between the primer and the template under low stringency .
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科学家给出的解释认为有一些聚合酶在延伸DNA时特别容易发生错配。
A likely explanation is that some polymerase enzyme is particularly prone to errors when it 's weaving a strand of DNA .
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方法使用不同指示剂,分别检测单链DNA电极在完全互补与三碱基错配DNA中的电化学信号。
Means To detect the electronic signal with different indictors respectively on ssDNA , completely complementary dsDNA and incompletely complementary hybridization dsDNA .
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其中腺嘌呤甲基化在原核生物限制-修饰系统、DNA复制、DNA错配修复和基因表达调控中发挥着重要的作用。
Adenine methylation plays important roles in restriction-modificaton system , DNA replication , DNA mismatch repair and gene expression regulation in prokaryotes .
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强度错配双界面约束条件下纯铝层TEM原位拉伸观察
In-Situ TEM Tension Observation of Pure Al Sheet Constrained by Bi-Interface with Strength Match
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在实验选定的最佳条件下,体系的化学发光强度随单碱基错配目标DNA的浓度的增大而增强,验证了该实验方案的可行性。
Under the optimum conditions , the CL intensity increased with the concentration of target DNA , which proved the feasibility of the DNA biosensor .
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异源双链DNA体外错配修复功能检测模型的构建及弥漫性大B细胞性淋巴瘤中错配修复系统的分析
Construction of Heteroduplex DNA and in Vitro Model of Functional Analysis of Mismatch Repair as Well as Its Application in the Diffuse Large B Cell Lymphoma
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目的建立一种以多重PCR-高效液相色谱(Highperformanceliquidchromatography,HPLC)分析为基础的错配修复基因DNA大片段缺失检测技术。
Objective Establishing a new method on the basis of multiplex PCR-high performance liquid chromatography ( HPLC ) for screening a large deletion in mismatch repair genes .
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幽门螺杆菌对AGS细胞DNA错配修复基因表达的影响
Effects of Helicobacter pylori on expression of DNA mismatch repair genes in AGS cell line
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其中修复DNA复制中发生的碱基错配的系统称为错配修复系统,可避免复制错误的产生与积累。
The system is called mismatch repair system whose function is to repair the mismatch of nucleotide in replication and avoid the accumulation of replication errors .