1)NGX6 geneNGX6基因
1.Expression and significance of NGX6 gene in human hepatocellular carcinoma;NGX6基因在肝细胞癌中的表达及意义
2.Previous overall studies showed that NGX6 gene with all the transcripts low-regulated in colorectal carcinoma and the expression of NGX6 in colorectal carcinoma with lymph-node or distance metastasis was significantly lower than that in CRC without metastasis, which indicated that low-regulated or deletion of NGX6 gene may related to colorectal carcinoma\'s occurrence, development and metastasis.前期研究检测了NGX6所有转录本的表达,结果显示NGX6在结直肠癌中存在着表达下调,尤其是在伴有淋巴结转移及远处转移的结直肠癌样本中NGX6表达明显下调或缺失,提示NGX6基因的表达下调或缺失可能与结直肠癌的发生、发展及转移相关。
英文短句/例句
1.Studies on the Effects of NGX6 Gene in Wnt/Beta-catenin Signaling Pathway;NGX6基因在Wnt/Beta-catenin信号传导通路中的作用机制研究
2.The Study of the Expression of Two Transcripts of NGX6 Gene and Clinicopathological Features of Colorectal Carcinoma结直肠癌中NGX6基因两个转录本的表达及临床病理特征的研究
3.Nasopharyngeal carcinomaassociated gene 6 inhibits tumor angiogenesis in colon cancer抑瘤基因NGX6对结肠癌血管形成的影响
4.Cloning and Analysis of the NGX6 Gene Promoter;抑瘤基因NGX6启动子的克隆及初步功能研究
5.Effect of NGX6 Gene on the Protein Exprssion Profiles in Colon Cancer Cells抑瘤基因NGX6对结肠癌细胞蛋白质表达谱的影响
6.Expression of NGX6 Protein in NPC and Its Correlation to Expression of VEGF and LMVDNGX6蛋白在鼻咽癌中的表达及其与VEGF表达和LMVD的相关性研究
7.The Expression of NGX6 mRNA and Some Important Proteins in the WNT Signaling Pathway in Colorectal Cancer by Tissue Microarrays;组织芯片技术检测结直肠癌中NGX6和WNT通路中重要蛋白的表达及其相关性研究
8.extinguisher loci消失基因座，绝灭基因座
9.Of, relating to, produced by, or being genes or a gene.基因的基因的，与基因有关的，基因产生的
10.Genes are described as DOMINANT or RECESSIVE.基因分为显性基因和隐性基因。
11.hypomorphic allele次等位因素对偶基因
12.Studies on Polymorphism of Prolactin Receptor Gene and Follicle-Stimulating Hormone Beta Subunit Gene in Swine;猪PRLR基因和FSHβ亚基基因多态性研究
13.Research on Hte Microarray Based Gene Mining Algorithm;基于基因表达谱的基因挖掘算法研究
14.Human Genome Project,Post-genome Research and Gene Medicine --New Century of Diagnosis,Pharmaceutics and Therapy with Gene Technique;人类基因组计划、后基因组研究与基因医学——基因诊断、基因制药与基因治疗的新世纪
15.Genetic material produced by gene-splicing.重组基因材料基因分割而产生的基因材料
16.Gene distribution was out of balance. Dominant genes were more than recessive ones.基因的分布是不对称的,显性基因多于隐性基因。
17.Association of apoE Gene, A2M Gene and ACE Gene Polymorphism with Alzheimer s Disease;apoE基因、A2M基因、ACE基因与汉人Alzheimer病的相关性研究
18.Study on Inheritance of the Quality Transgenes Over-expressed in Transgenic Wheat;转基因小麦外源基因品质基因表达的遗传研究
相关短句/例句
NGX 6 geneNGX6基因
1.Recently, a NGX 6 gene was cloned, which is located in the region of minimal heterozygosity deletion at 9p21.NGX6基因是本研究室在鼻咽癌 9p最小共同缺失区内新克隆的鼻咽癌候选抑瘤基因。
3)NGX6 proteinNGX6蛋白
1.Results: In Experiment one, the immunoreactive products of NGX6 protein were stained into Buffy granules, located in cytoplasm and cell membrane of nasopharyngeal epithelial cells and tumor cells.第一部分鼻咽癌中NGX6蛋白的表达及其意义目的:研究鼻咽癌中鼻咽癌相关基因6(nasopharyngeal carcinoma associatedgene 6,NGX6)在蛋白水平的表达,及其与年龄、性别、淋巴结转移以及T、N和临床分期等因素的关系。
4)gene[英][d?i:n][美][d?in]基因
1.Study of the Preparation and the Characteristics of pRc/CMV-BChE Gene-chitosan nanoparticles ①;丁酰胆碱酯酶基因-壳聚糖纳米粒初步研究
2.Correlation between traditional Chinese medicine syndromes in primary immunoglobulin A nephropathy and A267G in 5'-untranslated region within exonal of megsin gene;Megsin基因E1-5’UTR区A267G与免疫球蛋白A型肾病阴虚证的相关性
3.Study on gene chip of leiomyoma of uterus;子宫肌瘤基因芯片的研究
5)Genes基因
1.Study on Apoptosis of Human Leukemia Cells and Its Related Genes Regulation Induced by ~(235) U;浓缩铀诱发细胞凋亡的形态及基因调控
2.Screening of lymphatic metastasis-associated genes in esophageal squamous cell carcinoma;食管癌淋巴结转移相关基因筛选的研究
3.Study on the Genotyping of Aminoglycoside Modifying Enzymes Genes from Pan-drug Resistant Acinetobacter Baumannii.;泛耐药鲍曼不动杆菌氨基糖苷类修饰酶基因研究
6)Polymorphism[英][,p?li'm?:fiz?m][美][,pɑl?'m?rf?zm?]基因
1.The Study on Apolipoprotein E Gene Polymorphism Characteristics of Cerebral Infarction and Intracerebral Hemorrhage;脑梗死与脑出血apoE-基因多态性特点研究
2.The Relations of Gene Polymorphisms of eNOS and FⅦ with Coronary Heart Disease in Henan Han Population;河南汉族人群一氧化氮合酶和凝血因子Ⅶ基因多态性与冠心病相关性分析
3.Methods:Polymorphism of the 677th site C/T of MTHFR gene and the 66th site A/G of MTRR gene were detected by polymerase chain reaction-restrction fragment length polymorphism in disease group(n=64) and normal controls(n=104).目的:研究同型半胱氨酸相关酶中亚甲基四氢叶酸还原酶(MTHFR)及蛋氨酸合成酶还原酶(MTRR)基因的多态性与先天神经管缺陷的关系。
延伸阅读
J基因分子式：CAS号：性质：为免疫球蛋白V区与C区之间的连接区(J区)编码的基因。
