1) UBAP1 gene
UBAP1基因
1.
Objective To analyze the expression and location of coding protein of UBAP1 gene and to understand the relationship between the expression pattern of the protein and cell carcinogenesis.
方法:利用生物信息学分析编码蛋白的一般性质并预测其定位,构建增强型绿色荧光蛋白(enhance green fluorescent prote in,EGFP)与UBAP1融合基因的真核表达载体pEGFP-C2-UBAP1,通过脂质体介导转染人鼻咽癌细胞系HNE1,荧光显微镜观察UBAP1基因编码蛋白在HNE1活细胞内定位。
2.
Results Two novel SNPs were found, one resides on the sixth exon of UBAP1 gene and the other on the fourth exon of CDKN2A gene.
结果 在 UBAP1基因第 6外显子及 CDKN2 A基因第 4外显子中各发现一个新的 SNP位点 ,db SNP登录号为 rs3135 92 9和 rs30 884 4 0 ,其多态信息含量分别为 0 。
3.
Recently, UBAP1 gene, which is located in the region of minimal heterozygosity deletion at 9p21 3～22 1 and down expressed in NPC, has been cloned.
UBAP1基因是在鼻咽癌 9p最小共同缺失区内新克隆的鼻咽癌候选抑瘤基因 ,通过采用病例 对照研究方法 ,对 10 5例鼻咽癌患者和 183例正常人UBAP1基因的 5个单核苷酸多态 (SNPs)用测序法进行了分型 ,在实验过程中 ,偶然发现了一个新的SNP位点 ,并已登录至dbSNP (登录号 :rs3135 92 9) 。
2) UBAP1
UBAP1基因
1.
Identification and Digitalized Expression Analysis of Murine UBAP1 Gene by Means of EST Database Searching;
表达序列标签数据库搜索鉴定小鼠UBAP1基因及其数字化表达分析
2.
Background &Objectives:This study was designed to identify d ifferential expression patterns in tumor and normal tissues of the human novel gene,UBAP1,a putative nasopharyngeal carcinoma (NPC)relate gene,which is located at human chromosome 9p21-22where loss of heterozygosity frequently occurs in NPC.
进一步地,我们应用EST策略鉴定UBAP1基因在多种肿瘤组织中的差异表达谱。
3) gene
[英][dʒi:n] [美][dʒin]
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
4) 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
5) Polymorphism
[英][,pɔli'mɔ:fizəm] [美][,pɑlɪ'mɔrfɪzṃ]
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。
6) AS gene
AS基因
补充资料：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。
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。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条