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   deletion rates 的翻译结果: 查询用时:0.213秒
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deletion rates
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  缺失率
     p16 INK4a E1α and p19 ARF E1β deletion rates were 12 50%(2/16) and 6 25%(1/16) respectively,with total rate of exon 1α and exon 1β deletion 18 75%(3/16) in 16 premalignant lesions.
     在 16例癌前病变中发现p16 INK4aE1α和p19ARFE1β缺失的检出率分别为 12 5 0 % (2 16 )和 6 2 5 % (1 16 ) ; p16 INK4aE1α或 (和 )p19ARFE1β总缺失率为 18 75 % (3 16 )。
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     The correlation coefficient (r value)of mtDNA4977and mtDNA7436 deletion rates with LVEF is - 0.681 and - 0.675, respectively (p<0.05).
     mtDNA4977和mtDNA7436缺 失率与 LVEF的相关系数分别为-0.681和-0.675(P均<0.05)。
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     Results The deletion rates of RASSF1A mRNA expression were 42.4%(28/66), 15.2% (10/66), and 0 in the tumor tissues, tissues near tumor, and normal tissues respectively.
     结果RASSF1A mRNA在食管癌组织、近癌旁组织、癌旁正常组织中的表达缺失率分别为42·4%(28/66)、15·2%(10/66)、0(0/66)。
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     The deletion rates of RASSF1A mRNA expression in patients with lymph node metastasis was 61.1%, significantly higher than that of the patients without lymph node metastasis (20.0%, χ~2=11.323, P<0.01);
     淋巴结转移者食管癌组织中RASSF1A mRNA表达缺失率(61·1%)明显高于无淋巴结转移者(20·0%)(χ2=11·323,P<0·01);
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     The deletion rates of RASSF1A mRNA expression in the esophageal squamous cell carcinoma at the advanced stages (stages Ⅲ~Ⅳ) was 61.5%, significantly higher than that in the esophageal squamous cell carcinoma at the early stages (stages Ⅰ~Ⅱ, 30.0%, χ~2=6.417, P<0.01).
     晚期(Ⅲ~Ⅳ期)食管癌组织中RASSF1A mRNA表达缺失率(61·5%)明显高于早期(Ⅰ~Ⅱ期)(30·0%)(χ2=6·417,P<0·05);
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  “deletion rates”译为未确定词的双语例句
     Results The deletion rates of 3p and 9p were 14 29%(3/21),28 57%(6/21) in adjacent bronchial epithelial cells and 66 57%(14/21),80 95%(17/21) in lung cancer cells;
     结果 :3p、9p丢失在癌旁支气管上皮细胞中为14 2 9% (3/ 2 1)、2 8 5 7% (6 / 2 1) ; 在肺癌细胞中为 6 6 6 7% (14 / 2 1)、80 95 % (17/ 2 1)。
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     The deletion rates of p16 gene exon 2 were 34% i n NPC, Which were not detected in all the tumor-adjacent tissues(P<0.001);
     p16基因第二外显子缺失突变:鼻咽癌组中纯合缺失突变率34%,而相应的癌旁组织未检出(P<0.001);
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     The PTEN protein expression deletion rates in BTCC were significantly associated with histological grades and clinical stages.
     PTEN的表达随病理分级、临床分期的增高而明显下降。
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     The result shows that whatever insertion and deletion rates are, true scale-free structures would emerge, where the degree distributions obey a power law with an exponent of 3. It is the preferential attachment that essentially governs the scale-free structures.
     研究表明网络的无标度特征(幂律指数γ=3)本质上是因为链接的偏好特性,而与随机增加或删除节点或链接无明显关系.
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  相似匹配句对
     The Dr rates of E.
     coli的耐药性不同 ,尿中E .
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     The Deletion in Translation
     翻译中的除赘
短句来源
     The rates of increase of R。
     值增加的速率存在差异,前期R。
短句来源
     The p16 deletion rates were significantly higher in poorly differen tiated group.
     按组织学分级 ,中、低分化组 p1 6蛋白表达缺失率显著高于高分化组 (P <0 .0 5 )。
短句来源
     The positive rates of p16 gene deletion was closely correlated with histological grade (P<0.05).
     ( 2 ) p16基因缺损率的高低与组织学分级密切相关 (P <0 .0 5 )。
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  deletion rates
There was a surprisingly strong effect of even short sequence separations, with insertions of a few hundred base pairs exhibiting 10-fold reductions of deletion rates.
      
Deletion rates decreased over two orders of magnitude with increasing separation of up to 7 kb.
      
It has been recently suggested that the C-value paradox, the lack of an obvious association between organismal complexity and genome size, can result simply from biases in insertion and deletion rates-the DNA loss hypothesis.
      
The small increase over the wild-type level may be due to the already high deletion rates in the POL strain.
      
The myopodin deletion rates were similar among invasive, highly invasive, and relapsing cases and higher than for minimally invasive cancers.
      
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In the present study. 9 oligonucleotide primers were employed to amplify 9 pairs of DNA sequences of dystrophia gene using two-step multiplex polymerase chain reaction (mPCR). Furthermore, gene diagnosis was undertaken of 19 cases of Duchenne muscular dystrophy (DMD) and 2 cases of Becker muscular dystrophy. The findings showed that 8 cases of deletion were detected by 5 amplified primers with a relatively high incidence of deletion and 2 more cases of deletion were detected using the remaining...

In the present study. 9 oligonucleotide primers were employed to amplify 9 pairs of DNA sequences of dystrophia gene using two-step multiplex polymerase chain reaction (mPCR). Furthermore, gene diagnosis was undertaken of 19 cases of Duchenne muscular dystrophy (DMD) and 2 cases of Becker muscular dystrophy. The findings showed that 8 cases of deletion were detected by 5 amplified primers with a relatively high incidence of deletion and 2 more cases of deletion were detected using the remaining 4 amplified primers. The deletion rate of 9 primers using two-step mPCR was 47. 2% of the patients examined, suggesting that about 90% of patients with gene deletion were delected. The results of the experiment show that two step mPCR can be used in the gene diagnosis of DMD/BMD. This method is not only simple, convenient and rapid, but also free radioisotope interforence. Therefore, this method may be of importance for rapid diagnosis of DMD/BMD.

作者应用分子生物学技术,用9组寡核苷酸引物分两步多重聚合酶链反应(mPCR扩增dystrophia基因的9对DNA序列。对19例Duchenne型肌营养不良(DMD)和2例Becker型肌营养不良(BMD)进行基国诊断。首先用缺失率较高的5对引物扩增,检出缺失者8例,再用4对引物扩增,检出缺夫者2例。这样,9 对引物多重PCR总缺失率占受检患者的47.2%,表明可检测出90%左右有基因缺失的患者。实验结果提示,两步多重PCR可用于DMD和(或)BMD的基因诊断。此法简便,快速又免除了使用同位素的困扰,不失为一种对DMD和(或)BMD快速诊断的好方法。

Abstract In the present study,9 oligonucleotide primers were employed to amplify 9 pairs of DNA sequences of dystrophin gene using the two-step multiplex polymerase chain reaction(mPCR)Furthennore,gene diagnosis were undertaken in 36 cases of Duchenne muscular dystrophy and 4 cases of Becker muscular dystrophy,The findings showed that 17 cases of deletiori were detected by 5 ampli-fied primers with a relatively high incidence of deletion and 2 more cases of deletion were detected using the remaining...

Abstract In the present study,9 oligonucleotide primers were employed to amplify 9 pairs of DNA sequences of dystrophin gene using the two-step multiplex polymerase chain reaction(mPCR)Furthennore,gene diagnosis were undertaken in 36 cases of Duchenne muscular dystrophy and 4 cases of Becker muscular dystrophy,The findings showed that 17 cases of deletiori were detected by 5 ampli-fied primers with a relatively high incidence of deletion and 2 more cases of deletion were detected using the remaining 4 amplified primers.The deletion rate of 9 primers using two-step mPC R was 47.5%of the patients examined,suggesting that about 79.1%of patients with gene deletion were detected.The resuIts of the experiment show that two-step mPCR can be used in the gene diagnosis of DMD/BMD.

应用分子生物学技术,用9组寡核苷酸引物分两步多重聚合酶链反应(mPCR)扩增dystrophin基因的9段脱氧核糖核酸(DNA)序列。对36例DMD和4例BMD进行基因诊断。首先用缺失率较高的5对引物扩增,检出缺失者17例,再用4对引物扩增,检出缺失者2例。这样,9对引物多重PCR总缺失率占受检患者的47.5%,表明此法可检测出79.1%左右有基因缺失的患者。实验结果提示,两步多重PCR可用于DMD/BMD的基因诊断。文中从DMD/BMD的临床表型与基因缺失的关系上进行了比较、探讨。

in the present study,9 exon-containing DNA segments of dystrophin gene with 9 sets of oligonucleotide primers by two-step multiplex polymerase chain reaction (mPCR) were amplified. Subsequently,gene analysis was performed in 36 cases of Duchenne mascular dystroply (DMD) and 4 cases of Becker muscular dystrophy(BMD). The findings showed that 17 cases of deletion were detected by using the first 5 sets of primers with a relatively high incidence of deletion detection and 2 more cases of deletion...

in the present study,9 exon-containing DNA segments of dystrophin gene with 9 sets of oligonucleotide primers by two-step multiplex polymerase chain reaction (mPCR) were amplified. Subsequently,gene analysis was performed in 36 cases of Duchenne mascular dystroply (DMD) and 4 cases of Becker muscular dystrophy(BMD). The findings showed that 17 cases of deletion were detected by using the first 5 sets of primers with a relatively high incidence of deletion detection and 2 more cases of deletion were detected by using the remaining 4 sets of primers. The total deletion rate detected by mPCR with 9 cases of primers was 47. 5% of the patients examined,suggesting that about 79. 1% of the patients with gene deletion could be detected. Thus,as a preliminary screening, the two-step mPCR can be used in the gene diagnosis of DMD/BMD. The method is not only simple, convenient and rapid,but also free from radiosotope trouble.

Two-stepmultiplexpolymerasechainreactionforgenediagnosisofprogressivepseudohypertrophicmusculardystrophy¥TanQingrong(谭庆荣);WuB...

 
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