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   基因诊断 的翻译结果: 查询用时:0.052秒
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基因诊断     
相关语句
  gene diagnosis
     Application of Bcl I and ST14 Site in Gene Diagnosis of Hemophilia A
     Bcl I及ST14位点在血友病A基因诊断中的应用
短句来源
     Gene diagnosis of MJD/SCA3 based on fragment analysis with capillary electrophoresis
     基于毛细管电泳片段分析的MJD/SCA3基因诊断
短句来源
     Gene Diagnosis of Hemophilia A by Polymorphism of St14 (DXS52) VNTR
     应用St14(DXS52)位点VNTR多态进行甲型血友病基因诊断
短句来源
     Results The results of gene diagnosis in 50 cases of FSHD patients were that the EcoRⅠ-BlnⅠ/p13E-11 fragment size ranged 10~33.5 kb [mean (17.70±6.628) kb]. Different patients belonging to the same family had the same result of gene diagnosis.
     结果50名FSHD患者的基因诊断结果为EcoRⅠ+BlnⅠ/p13E-11DNA片段大小介于10 ̄33.5kb,平均(17.70±6.628)kb,其中同一家系中不同患者的基因诊断结果相同。
短句来源
     Amp FLP Analysis on D5S436 Locus and Its Application to Linkage Analysis in Gene Diagnosis of Asthma
     D5S436位点的Amp-FLP分析及其在哮喘基因诊断中的应用
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  genetic diagnosis
     A Study of Genetic Diagnosis on HSV-1, HSV-2, EBV and HCMV
     HSV-1,HSV-2,EBV和HCMV的基因诊断研究
短句来源
     Genetic Diagnosis of 46,XX True Hermaphroditism
     46,XX真两性畸形的基因诊断
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     Conclusion: KG8、AC2.5 and SM7 are highly polymorphic and can be used in genetic diagnosis of Uygur PKD1 gene.
     结论 KG8、AC2 .5、SM7均为高度多态的遗传标记 ,可用于维吾尔族PKD1的连锁基因诊断
短句来源
     Mitochondrial tRNA ̄(Leu(UUR)) gene mutation diabetes mellitus──the estimated prevalence, clinical features and the approach for genetic diagnosis
     线粒体tRNA~(Leu(UUR))基因突变糖尿病──患病率估测、临床特点及基因诊断途径
短句来源
     The constructed allele-specific PCR of CD26(G→A) mutation can be a fast, effective, economic detecting way for genetic diagnosis and prenata diagnosis of β-thalassemia.
     作者建立的检测CD26(G→A)突变的等位基因特异性PCR可作为β-地中海贫血基因诊断和产前基因诊断的一种快速、有效、经济的直接检测方法。
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  gene diagnoses
     The Research of DNA Biosensor for Gene Diagnoses
     DNA生物传感器在“基因诊断”中的实验研究
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     the data might be used for gene diagnoses and for population genetic researches.
     实验数据对X染色体特异性STR的群体遗传学研究及一些X连锁遗传病的基因诊断有重要意义。
短句来源
     Clinical analysis and gene diagnoses of four patients in one family of Huntington disease
     舞蹈病一家系临床分析及基因诊断
短句来源
     [Objective] To investigate the mutations of WD gene in exon 18 and exon 14, and provide information for gene diagnoses.
     目的了解中国人肝豆状核变性(WD)患者基因第18、第14外显子的突变情况,为掌握该病的突变特点并进行基因诊断提供依据。
短句来源
     Using Single-Chip Computer to Detect Fluorescence and Achieve Gene Diagnoses
     用单片机荧光检测实现医学基因诊断
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  gene diagnose
     It can be applied prospectively in life science research, such as gene expression, gene diagnose and gene polymorphism etc.
     基因芯片技术是近年来发展起来的一项新技术 ,在生命科学研究中有着广泛的应用前景 ,可用于基因测序、基因表达、基因诊断、基因多态性分析等研究。
短句来源
     The Study on the Gene Diagnose、Molecular Genotype and Resistance Mechanisms of Systemic Candida
     深部念珠菌的基因诊断、分子分型及耐药机制研究
短句来源
     [Objective] : To study the expression of PTEN, EGFR and P16 in astrocytoma ,combining the expression of 53, Ki-67 LI, histological grading and tumor size, to make clear the relationship between the biomarks and astrocytoma,and to provide the valuable information to gene diagnose and prognosis in astrocytoma.
     [目的]:本课题通过研究PTEN、EGFR、P16蛋白在星形细胞瘤中的表达,并结合肿瘤组织学分级、肿瘤大小、年龄及Ki-67、P53蛋白表达进行分析,旨在探讨星形细胞瘤的发生发展机制,从而为星形细胞瘤的基因诊断、基因治疗、评估预后提供理论依据。
短句来源
     With the implement of Human Genome Plan, gene diagnose has become an important area of molecular biology and biomedical research.
     随着人类基因组计划(HGP)的实施,基因诊断已经成为分子生物学和生物医学研究中的重要领域。
短句来源
     miRNA has great meaning to the study of gene function, gene diagnose and therapyas well as the development of new medicine.
     miRNA的研究,对基因功能的研究、疾病的基因诊断、治疗和新药物的研发都具有很重要的意义。
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  gene diagnosis
This STR would be able to be regarded as a novel genetic marker which can increase the genetic map accuracy in this chromosome region and improve the gene diagnosis on some genetic diseases located in chromosome 14q24.3 band.
      
Gene diagnosis of phenylketonuria by capillary electrophoresis in a novel nongel sieving polymer solution
      
Gene diagnosis and family linkage analysis of phenylketonuria (PKU) was performed as an application.
      
Using the cDNA microarray to analyze of human ovarian cancer cell line gene expression profile difference will help the gene diagnosis, treatment and protection.
      
So it could be made gene diagnosis with Bcl I RFLP in family C and D.
      
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  genetic diagnosis
The short report will be focused on the genetic basis and possible mechanisms of tumorigenesis, common types of cancer, the importance of genetic diagnosis of cancer, and the methodology of cancer genetic diagnosis.
      
Preimplantation genetic diagnosis for Down syndrome pregnancy
      
Definition of the problem: Preimplantation genetic diagnosis (PGD) is a new technique to test the in-vitro embryo for genetic disorders.
      
Our inquiry focuses on the textual, visual and musical elements that are used in two short television features on preimplantation genetic diagnosis.
      
A genetic diagnosis allows relatives to undergo predictive testing and helps to streamline surgical and screening recommendations for patients and their relatives.
      
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