1) IL1RAPL1 gene
IL1RAPL1基因
1.
Association between IL1RAPL1 gene polymorphism and non-specific mental retardation in the Chinese Han population of Qinba region
IL1RAPL1基因多态性与秦巴山区汉族儿童非特异精神发育迟滞的相关性研究
2.
In order to investigate the possibility of the association of IL1RAPL1 gene with children s mental retardation and intelligence in QinBa mountain area, we use three SNPs rs12847959, rs6526806 and rs6630762 as genetic marker to do the case-control association study for children in QinBa mountain.
为了进一步探讨IL1RAPL1基因与秦巴山区儿童的智力以及精神发育迟滞之间的关系，我们选择了IL1RAPL1基因上的SNP位点rs12847959、rs6526806和rs6630762作为遗传标记，对秦巴山区精神发育迟滞儿童进行了病例-对照人群研究。
3.
Our research work have investigate the possibility of the association of IL1RAPL1 gene with children s intelligence.
用IL1RAPL1基因上的微卫星DXS1218和DXS9896作为遗传标记,进行了该人群的基因频率分布研究,以及智力和遗传标记多态性之间的关联分析。
2) 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
3) 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
4) 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。
5) AS gene
AS基因
6) Genetic
[英][dʒə'netɪk] [美][dʒə'nɛtɪk]
基因
1.
Antigenic and genetic characterization of A/Shenzhen/1/99(H3N2) virus;
A/深圳/1/99(H3N2)病毒抗原性及基因特性研究
2.
Relationship between the genetic polymorphisms of VDR and susceptibility to pulmonary tuberculosis among the Chinese Han population
维生素D受体基因多态性与汉族人肺结核发病的关系
3.
MTHER genetic C677T polymorphisms were determined by PCR-RFLP.
N5, 10 亚甲基四氢叶酸还原酶(MTHFR)是参与甲硫氨酸-叶酸代谢的关键酶,其基因677位点C→T错义突变可造成此酶活性降低,导致高同型半胱氨酸血症,现已证明高同型半胱氨酸是诱发胎儿出生缺陷和心血管疾病的一个独立危险因素。
补充资料：IL-3
分子式：
CAS号：
性质：又称白细胞介素-3。主要由活化T细胞或T细胞克隆产生。含133个氨基酸残基。免疫调节剂，可刺激多能干细胞和多种祖细胞的增殖和分化。刺激皮肤上皮细胞、CD4-CD8-TCRαβ细胞、巨噬细胞、嗜碱性粒细胞的增殖，阻止巨噬细胞发生程序性细胞死亡。
CAS号：
性质：又称白细胞介素-3。主要由活化T细胞或T细胞克隆产生。含133个氨基酸残基。免疫调节剂，可刺激多能干细胞和多种祖细胞的增殖和分化。刺激皮肤上皮细胞、CD4-CD8-TCRαβ细胞、巨噬细胞、嗜碱性粒细胞的增殖，阻止巨噬细胞发生程序性细胞死亡。
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