HbCP1基因,HbCP1英語短句,例句大全

HbCP1基因,HbCP1
1)HbCP1HbCP1基因
1.The expression vectors pET-30a-HbCP1 and pET-30a-EHbCP1 were constructed and expressed in E.為研究巴西橡膠樹半胱氨酸蛋白酶生物學功能,利用筆者從橡膠樹中克隆的半胱氨酸蛋白酶基因(HbCP1)(GenBank登錄號:DQ642886)序列,構建了HbCP1基因的原核表達載體,并在大腸桿菌中誘導表達。
2)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;丁酰膽堿酯酶基因-殼聚糖納米粒初步研究
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區A267G與免疫球蛋白A型腎病陰虛證的相關性
3.Study on gene chip of leiomyoma of uterus;子宮肌瘤基因芯片的研究

英文短句/例句

1.extinguisher loci消失基因座，絕滅基因座
2.Of, relating to, produced by, or being genes or a gene.基因的基因的，與基因有關的，基因產生的
3.Genes are described as DOMINANT or RECESSIVE.基因分為顯性基因和隱性基因。
4.hypomorphic allele次等位因素對偶基因
5.Studies on Polymorphism of Prolactin Receptor Gene and Follicle-Stimulating Hormone Beta Subunit Gene in Swine;豬PRLR基因和FSHβ亞基基因多態性研究
6.Research on Hte Microarray Based Gene Mining Algorithm;基于基因表達譜的基因挖掘算法研究
7.Human Genome Project,Post-genome Research and Gene Medicine --New Century of Diagnosis,Pharmaceutics and Therapy with Gene Technique;人類基因組計劃、后基因組研究與基因醫學——基因診斷、基因制藥與基因治療的新世紀
8.Genetic material produced by gene-splicing.重組基因材料基因分割而產生的基因材料
9.Gene distribution was out of balance. Dominant genes were more than recessive ones.基因的分布是不對稱的,顯性基因多于隱性基因。
10.Association of apoE Gene, A2M Gene and ACE Gene Polymorphism with Alzheimer s Disease;apoE基因、A2M基因、ACE基因與漢人Alzheimer病的相關性研究
11.Study on Inheritance of the Quality Transgenes Over-expressed in Transgenic Wheat;轉基因小麥外源基因品質基因表達的遺傳研究
12.Legal Research on Gene Science and Technology--Does Gene Belong to Invention or Discovery;基因科技的法律問題研究——“發明”基因?“發現”基因?
13.Mapping of Genetic Modifiers of Eyal~(bor/bor) Mice定位Eyal~(bor/bor)基因型小鼠Eyal基因的遺傳修飾基因
14.Analyses of Genome-wide Disease Resistance Genes and Their Expansion in Medicago truncatula蒺藜苜蓿全基因組抗病基因和基因擴張分析
15.allelic diversity等位（基因）多樣化
16.gene transplantationph.1. 基因移植
17.Functional Analysis of LLAG1 and LLGLO1 and Construction of Their RNAi Vectors;百合LLAG1和LLGLO1基因
18.State Key Laboratory of Oncogenes and Reiated Genes癌基因與相關基因國家重點實驗室

相關短句/例句

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;丁酰膽堿酯酶基因-殼聚糖納米粒初步研究
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區A267G與免疫球蛋白A型腎病陰虛證的相關性
3.Study on gene chip of leiomyoma of uterus;子宮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;濃縮鈾誘發細胞凋亡的形態及基因調控
2.Screening of lymphatic metastasis-associated genes in esophageal squamous cell carcinoma;食管癌淋巴結轉移相關基因篩選的研究
3.Study on the Genotyping of Aminoglycoside Modifying Enzymes Genes from Pan-drug Resistant Acinetobacter Baumannii.;泛耐藥鮑曼不動桿菌氨基糖苷類修飾酶基因研究
4)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;腦梗死與腦出血apoE-基因多態性特點研究
2.The Relations of Gene Polymorphisms of eNOS and FⅦ with Coronary Heart Disease in Henan Han Population;河南漢族人群一氧化氮合酶和凝血因子Ⅶ基因多態性與冠心病相關性分析
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關酶中亞甲基四氫葉酸還原酶(MTHFR)及蛋氨酸合成酶還原酶(MTRR)基因的多態性與先天神經管缺陷的關系。
5)AS geneAS基因
6)Genetic[英][d??'net?k][美][d??'n?t?k]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維生素D受體基因多態性與漢族人肺結核發病的關系
3.MTHER genetic C677T polymorphisms were determined by PCR-RFLP.N5, 10 亞甲基四氫葉酸還原酶(MTHFR)是參與甲硫氨酸-葉酸代謝的關鍵酶,其基因677位點C→T錯義突變可造成此酶活性降低,導致高同型半胱氨酸血癥,現已證明高同型半胱氨酸是誘發胎兒出生缺陷和心血管疾病的一個獨立危險因素。