Conclusion 2cvn fusion gene was successfully constructed and highly expressed.
结论已成功构建了2cvn融合基因，并获得高效表达。
The authors subsequently found that this fusion gene was present in the tumors of other patients.
作者逐渐发现混合基因存在于其他病人的肿瘤种。
Results:The expression signals of BCR/ABL fusion gene were dark violet-blue or brown precipitates.
结果 ：BCR/ABL融合基因表达信号为深紫 蓝色或棕色沉淀。
In BCR-ABL fusion gene negative myeloproliferative diseases, the discovery of JAK2V617F point mutation is an important landmark.
在BCR- ABL阴性的骨髓增殖性疾病的发病机制中，JAK2V 617 F点突变的发现是一个重大的突破。
In the lab, they tested an inhibitor of ALK against cancer cells with this fusion gene and found that it dramatically inhibited their growth.
实验中，他们实验了一种ALK的抑制剂发现大幅抑制了肿瘤的生长。
The secretion expression vector of fusion gene in E. coli has constructed by fussing the proinsulin gene to the gene of staphylococcal protein a.
将胰岛素原基因融合到金色葡萄球菌蛋白a的基因上，构建成大肠杆菌中基因融合的外分泌表达载体。
Southern blotting indicates that the pf40-gfp fusion gene integrate into the genome of tobacco transgenic plants from different transformed cases.
不同植株中基因整合位置不同，各植株是由不同的转化事件产生的。
Objective: To study the influence of tetracycline-controlled system on expression of the DT390-VEGF165 fusion gene in human gastric carcinoma cell.
目的：研究四环素调控系统对DT390-VEGF165融合基因在人胃癌细胞中表达的影响。
Conclusion KDR promoter may regulate the CDglyTK fusion gene system to selectively kill the KDR-expressing SCG7901 cells and to induce the cell apoptosis.
结论KD R启动子可以调控融合基因体系选择性地杀伤人胃癌scg7901细胞，并且该体系可以诱导胃癌细胞凋亡。
The construction and application of fusion gene of Farnesyl Pyrophosphate synthase carrying plastid transit peptide belongs to plant genetic engineering field.
携带质体转运肽的法呢基焦磷酸合成酶融合基因的构建及应用，属于植物基因工程领域。
Objective:To study on relationship between of BCR/ABL fusion gene expression and TCM syndrome classification in the patient of chronic myelogenous leukemia(CML).
目的：探讨慢性粒细胞白血病（CML）患者BCR/ABL融合基因表达与中医辨证分型的关系。
In this study, VP7 gene and CTB-VP7 fusion gene expression vectors were constructed, and a high-efficient genetic transfomation system of carrot(Daucus carota L. )
本实验以轮状病毒的VP7为目的基因，构建了VP7基因的表达载体和VP7-CTB融合表达载体；
Gene markers which are used to detect minimal residual disease(MRD)include fusion genes(FG), aberrant genes and some genes with high expression in leukemia disease.
残留白血病检测的基因标志可大致分为融合基因、变异基因和一些白血病中表达增高的基因。
The tyrosine kinases expressed by BCR-ABL fusion gene can cause cell proliferation, adhesion and survival natural change, several kinds of tumors can be caused by it.
BCR -ABL融合基因表达出的酪氨酸激酶能引起细胞增殖、黏附和生存性质的改变，导致多种肿瘤的产生。
Objective to detect SYT-SSX fusion gene transcripts in fresh-frozen synovial sarcoma specimens and analyze the correlation between histological phenotypes and SYT-SSX subtypes.
目的检测滑膜肉瘤新鲜冰冻标本中的SYT -SSX融合基因，分析融合基因亚型与病理表型之间的关系。
The specific chromosome and fusion gene are regarded as marker of leukemia, and helpful in leukemia diagnosis, evaluating prognosis, monitoring of treatment and minima residual leukemia.
特定的染色体和融合基因可作为白血病的标志物，对白血病的诊断、预后估计、监测治疗和微小残留白血病等方面具有一定的价值。
Objective To study the frequency and clinical significance of transloation, ets, leukemia-acute myeloblasticleukemia1 (TEL-AML1) fusion gene in children with acute lymphoblastic leukemia (ALL).
目的研究TEL-AML1融合基因在儿童急性淋巴细胞白血病（ALL）的发生率及其临床意义。
This study was aimed to explore the relationship of 6; 9 chromosome translocation with DEK-CAN fusion gene expression in patients with acute myeloid leukemia (AML) and its clinical significance.
本研究旨在探讨急性髓系白血病(aml)患者6；9染色体易位与DEK - CAN融合基因表达之间的关系及临床意义。
In 2007 a group of researchers discovered that the fusion of two normally independent genes, EML4 and ALK, into one aberrant gene seems to drive the formation of tumours.
2007年一个研究小组发现，两种普通基因(EML4和ALK)和一个异常化基因的融合能形成肿瘤。
After that, introducing weight gene, syncretized PID and fuzzy control's outputs by adding weight. At last, the result of fusion was output to object controlled.
之后引入加权因子，采用加权的方法将PID和模糊控制各自的输出进行融合，将融合的结果最后输出到被控对象上。
Conclusion The GRA7 gene may be expressed as a GST fusion protein in E. coli.
结论GRA7基因在大肠埃希菌中以gst融合蛋白的形式得到表达。
Objective: To clone and express the gene of human enterokinase light chain which would be used in the cleavage and purification of fusion proteins.
研究目的：克隆表达人肠激酶轻链编码基因，以期应用于融合蛋白的切割与纯化。
Aim: To express the whole length fusion protein of human IRGMa and prepare high quality rabbit anti-human immune-related gene guanosine triphosphate (IRGM) polyclonal antibody.
目的：表达人免疫相关鸟苷三磷酸酶基因(IRGM) a全长融合蛋白，制备高质量的兔抗人IRGM多克隆抗体。
Results: The CAT gene was cloned correctly and it's fusion protein was expressed in E.
结果：成功克隆了CAT的基因片段，并在大肠杆菌中得到其融合蛋白的表达。
Objective: to clone the gene of fructose binding protein BL0033 from Bifidobacterium longum NCC2705, and express and purify fusion protein GST-BL0033 in e.
目的：克隆长双歧杆菌ncc 2705株果糖结合蛋白bl 0033的基因，利用大肠杆菌表达GST -BL 0033融合蛋白并纯化。
The most commonly used gene delivery methods include: physical method, chemical methods, fusion method and gene gun etc.
目前基因转运方法有许多种，其中包括物理方法、化学方法，融合法，基因枪等。
Methods Based on the usefulness of gene fusion analysis for transcriptional analysis, two kinds of plasmids and integrant mutant strains were developed for the systemic study of PQS.
方法基于基因融合分析在转录研究中的实用性，构建了两种PQS相关对照质粒和整合突变株。
Objective: to detect the expression of the fusion epitopes gene of foot-and-mouth disease virus (FMDV) in vitro.
目的：在体外检测口蹄疫病毒融合表位基因的表达。
The principles, operation and applications of site-directed mutagenesis, gene fusion technology, and post-translational modification methods were introduced emphatically.
着重阐述了基因定点突变技术、基因融合技术和翻译修饰技术等新兴定点固定化技术的原理、特点和操作。
The principles, operation and applications of site-directed mutagenesis, gene fusion technology, and post-translational modification methods were introduced emphatically.
着重阐述了基因定点突变技术、基因融合技术和翻译修饰技术等新兴定点固定化技术的原理、特点和操作。
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