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genotypes
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  基因型
    Quantitative Study on Blood C4 Level in Different Genotypes on Chinese Population
    中国人不同C4基因型时血中C4浓度的定量检测
短句来源
    The Dynamic Changes of the Protein during the Period of the Development of Wheat with Different Genotypes
    不同基因型小麦籽粒生育期蛋白质的动态变化
短句来源
    By using PCR plus nucleotide sequence analysis, the genotypes of the dominant L. interrogans serogroups in China were demonstrated.
    用PCR和核苷酸序列分析,了解中国流行的钩体主要血清群ompL1基因型
短句来源
    Routine genetic engineering technique was applied to construct the prokaryotic expression systems of genotypes ompL1/1 and ompL1/2, and Ni-NTA affinity chromatography was performed to extract the target recombinant products rOmpL1/1 and rOmpL1/2. Immune aurosol electron microscopy was selected to locate the position of OmpL1s on leptospiral envelope.
    采用常规基因工程技术构建ompL1/1和ompL1/2主要基因型原核表达系统,Ni-NTA亲和层析法提纯目的重组表达产物rOmpL1/1和rOmpL1/2。 采用胶体金免疫电镜技术,对OmpL1s进行膜定位。
短句来源
    There are two ompL1 genotypes of ompL1/1 and ompL1/2 in the dominant leptospiral serogroup in China. And remarkable differences of the nucleotide and putative amino acid sequence similarities between the two genotypes are present.
    中国流行的钩体主要血清群ompL1基因可有ompL1/1和ompL1/2两个基因型,两者核苷酸和氨基酸序列相似性之间有较明显的差异。
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    RESULTS For 85 strains,the total positive rate of plasmid-mediated AmpC genes was 32.9%,and the positive rates of DHA and ACT-1 genotypes were 29.4% and 3.5%,respectively.
    结果85株阴沟肠杆菌中,质粒AmpC酶基因阳性28株,阳性率32.9%,其中DHA和ACT-1基因阳性率分别为29.4%和3.5%;
短句来源
    METHODS: The genotypes of 90 Chinese Han in Guangdong and 104 Sherpas in Tibet were analyzed by sequence special primer polymerase chain reaction(SSP-PCR) sequencing the surfactant protein A gene.
    方法:应用序列特异性引物-聚合酶链反应(polymerase chain reac-tion-sequence specific primer,SSP-PCR)方法,对90名广东汉族人和104例西藏夏尔巴人SP-A基因进行检测。
短句来源
    Results In the 160 patients with CHB,genotype B was detected in 14 cases(8.7%),genotype C in 88 cases(55.0%),and mixed genotype of B and C in 51 cases(31.9%). 7 cases failed the genotyping(4.4%). Genotypes A,D,E and F were not found in the study.
    结果B型14例(8.7%),C型88例(55.0%),BC混合型51例(31.9%),未分型7例(4.4%),未发现A、D、E、F型。
短句来源
    Study on the association of estrogen receptor genotypes with bone mineral density in Chinese postmenopausal Han women in Beijing
    中国北京地区绝经后汉族妇女雌激素受体基因多态性与骨密度的相关性研究
短句来源
    Rapid determination of platelet alloantigen genotypes of HPA-1, 2, 3, 4, 5 systems by AS-PCR method
    快速AS-PCR技术用于血小板HPA-1,-2,-3,-4,-5抗原系统等位基因的分型
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  genotypes
The distributions of GNB3 C825T genotypes were CC (27.2%), TT (42.9%), and CT (29.9%) in the hypertensive subjects and CC (27.7%), TT (42.4%), CT (29.9%) in the normotensive subjects.
      
Further analysis shows that there is no association between C825T genotypes and age, body mass index (BMI), Glucose (GLU), Triglyceride (TG), Cholesterol (CHO), systolic blood pressure (SBP) and diastolic blood pressure (DBP).
      
Compared to individuals with EPHX1 rs1051741 CC or rs2234922 AA genotype in the drinkers, the risk of CBP in those carrying genotypes of EPHX1 rs1051741 CT+TT or rs2234922 AG+GG was decreased, respectively (P = 0.04, P >amp;lt; 0.01).
      
Karyotypic analysis on the metaphase plates from the root meristem demonstrated different genotypes.
      
Effects of Genotypes at the Unspecific Esterase (Est) and Leucine Aminopeptidase (Lap) Loci on the Temporal Dynamics of Morpholo
      
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Analysis of genotype and haplotype detemined by polymorphic restriction endonuclease site in β-globin gene cluster is the basis of prenatal diagnosis for β-thalassemias. By application of 3 gene probes in relation to β-globin gene cluster and Southern blotting, there are 5 restriction polymorphic sites in clusters of Chinese.Linking these polymorphic sites,we obtained 9 genotypes which were composed of 7 haplotypes. Among them, the frequency of thetwo types +----and + +---is 61%, so they are predominant...

Analysis of genotype and haplotype detemined by polymorphic restriction endonuclease site in β-globin gene cluster is the basis of prenatal diagnosis for β-thalassemias. By application of 3 gene probes in relation to β-globin gene cluster and Southern blotting, there are 5 restriction polymorphic sites in clusters of Chinese.Linking these polymorphic sites,we obtained 9 genotypes which were composed of 7 haplotypes. Among them, the frequency of thetwo types +----and + +---is 61%, so they are predominant in Chinese β-globingene cluster.

β珠蛋白基因多态性限制酶位点所组成的基因型和单体型的分析,是进行β地中海贫血产前诊断的基础。本文用Southern印迹杂交法,借助于与β珠蛋白基因簇有关的3个基因探针,分析了β珠蛋白基因簇内5个多态性位点,根据对这些多态性位点的连锁分析获得了9个正常中国人的基因型。这18个单基因型是由7种单体型组成的。其中+----及++---两型占61%,是我国β珠蛋白基因簇单体型的主要形式。

By means of analysing Hind Ⅲ restriction fragments length polymorphism on ,human zeta-globin gene mapping,genotypes of a nondeletion patient and his family were detected,prenatal diagnosis for the fetus at risk for the same disease was successfully made within the first three months of pregnancy The fetus'genotype is (aa/aaT).

利用ζ珠蛋白基因的限制性内切酶HindⅢ特异片段长度多态性分析,鉴别了一个非缺失型HbH病患儿及其父母的单体型,并对该家系正在妊娠中的重型HbH危险胎儿进行了早期产前诊断,确定其基因型为(αα/αα~T)。

A survey of Hb Bart's in 470 cord blood samples at birth from Guangxi province was reported. An incidence of α-thalassemia of 16.4% was obtained from 77 positives, with Hb Bart's ranging 0.86~92. 0%. The DNAs from wbc of positives were digested by Bam H I, EcoR I or Hind Ⅲ and detected by α or ζ-globin gene probe for gene mapping. In 35 of 77 samples with Hb Bart's ranging from 0.86~16.6%, one α-glcbin gene deletion was noticed. In 39 of 77 samples with Hb Bart's ranging from 3.2~35.2%, two α-globin gene deletion...

A survey of Hb Bart's in 470 cord blood samples at birth from Guangxi province was reported. An incidence of α-thalassemia of 16.4% was obtained from 77 positives, with Hb Bart's ranging 0.86~92. 0%. The DNAs from wbc of positives were digested by Bam H I, EcoR I or Hind Ⅲ and detected by α or ζ-globin gene probe for gene mapping. In 35 of 77 samples with Hb Bart's ranging from 0.86~16.6%, one α-glcbin gene deletion was noticed. In 39 of 77 samples with Hb Bart's ranging from 3.2~35.2%, two α-globin gene deletion were found. The relations between Hb Bart's level in cord blood and α-thala-ssemia genotypes were discussed.

于南宁市及其近郊10所医院随机取新生儿脐血470例,发现Hb Bart′s,阳性的77例(16.4%),以α-及ζ-珠蛋白基因探针作DNA图谱分析表明,缺失一个α-基因的35例,缺失两个α-基因的39例,缺失四个α-基因的1例。两例Hb Bart′s阳性和随机选择的20例阴性脐血DNA图谱完全正常。认为脐血Hb Bart′s含量与α-珠蛋白基因缺失的程度有一定关系,单纯缺失一个α-基因的脐血 Hb Bart′s含量<3.2%;单纯缺失两个α-基因的脐血 Hb Bart′8含量在3.2%~8.0%之间。提出非缺失型α-地贫占α-地贫的37.7%,它可能造成部份病例不符合以上分析。

 
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