1) CXCR2 gene
CXCR2基因
1.
Study on the relationships between polymorphisms of CXCR2 gene and milk quality and mastitis of dairy cow;
CXCR2基因多态性与奶牛乳房炎和乳品质的关联
2.
2) gene and the relationship between the polymorphisms of cattle CXCR2 gene and cattle mastitis in 160 tattles including Chinese Holstain cattle, Chinese simmental cattle and Tongjiang huangniu were detected by PCR-SSCP test with six different pairs of primers.
本文采用单链构象多态性分析法，以中国荷斯坦牛、中国西门塔尔牛和通江黄牛为研究对象，研究了CXCR2基因的多态性及其对牛奶品质性状的遗传效应，结论如下： 在扩增的6个片段中共发现3个SNP多态位点，分别位于CXCR2基因序列的684bp、777bp和861bp处。
2) CXCR1&CXCR2 gene
CXCR1&CXCR2基因
1.
The single nucleotide polymorphisms(SNPs) within the coding regions of CXCR1&CXCR2 gene in Holstein cattle were investigated by nested-PCR,DNA sequencing and CRS-PCR.
本研究采用巢氏PCR、DNA测序和CRS-PCR-RFLP方法,分析了中国荷斯坦牛、鲁西黄牛以及渤海黑牛的CXCR1&CXCR2基因编码区部分片段的遗传多态性,验证了CXCR1基因上已经发现的735(C/G),816(C/A),819(A/G)3个位点;发现了CXCR1基因上980(G/A)、995(G/A)和1008(C/T)3个新的SNPs位点和CXCR2基因上的938(C/T)、959(C/T)2个SNPs位点。
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