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   mrna gene 的翻译结果: 查询用时:0.181秒
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mrna gene
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  mrna基因
     Establishment of Fluorescent Quantitative RT-PCR Method for Detection of Expression of AFP mRNA Gene
     荧光定量RT-PCR检测AFP mRNA基因表达方法的建立
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     HLA-ABC mRNA gene fragment was positively detected.
     有少量HLA-ABC mRNA基因片断存在,未发现HLA-DR mRNA基因片断;
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     Effect of Qingfeikouhuye on β1 mRNA Gene Expression of Fibroblast Cells of Human Embryonic Lungs Induced by Adenovirus Types 3I and 7b
     清肺口服液对3I、7b型腺病毒感染人胚肺成纤维细胞TGF-β_1mRNA基因表达的影响
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     IL-6mRNA gene expression was observed by RT-PCR as early as 3 h after LPS stimuating.
     RT PCR方法检测显示LPS刺激后 3h即可见IL 6mRNA基因表达。
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     IL 6mRNA gene expression was observed by RT PCR as early as 3h after LPS stimulating.
     RT PCR方法检测显示LPS刺激后 3小时即可见IL 6mRNA基因表达。
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  “mrna gene”译为未确定词的双语例句
     The down regulation of iNOS mRNA gene expression at the level of transcription in the MC3T3 - E1 cells treated with 100 ng/mL IGF-Ⅱ might be one of the mechanisms to keep low NO levels.
     100 ng/mL IGF-Ⅱ在转录水平下调MC3T3-E1细胞iNOS基因的表达,可能是IGF-Ⅱ维持MC3T3-E1细胞低水平NO的机制之一。
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     Conclusion ASODN-EGF had remarkably antisense inhibition effect for HER-2 mRNA gene expression and transcription on SK-Br-3 cell.
     结论 ASODN-EGF具有抑制SK-Br-3细胞HER-2 mRNA转录和表达的作用。
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     IFNγ affects collagen α_1(Ⅰ) mRNA gene expression signals transduction pathway in rat hepatic stellate cells
     IFNγ影响肝星状细胞α_1(Ⅰ)mRNA表达信号的传递途径
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     Establishment of A Real Time Method for Detecting the Expression of BDNF mRNA Gene
     Real time RT-PCR定量检测BDNF mRNA表达水平方法的建立
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     Results Six differentially displayed genes were found. These genes were named C4M2, C1A1, A4M1, A1A2, G4A1, C7A2. Conclusion There were some differences between ACL and MCL at the level of mRNA gene expression.
     结果 :在ACL和MCL细胞之间找到 6个差异表达的基因 ,分别为C4M2 ,C1A1,A4M1,A1A2 ,G4A1,C7A2。
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     The mRNA of the gene was detected by RT-PCR.
     RT-PCR检测证明目的基因在mRNA水平上可有效表达;
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     Results There was expression of protamine mRNA gene in spermatozoon.
     结果精子中存在精核蛋白基因的mRNA;
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     Gene Migration
     迁徙的基因
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     -casein gene.
     -酪蛋白基因5'侧序列。
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  mrna gene
The most interesting finding was that on postnatal day 7 (P7), P14 and in the adult, but not on P0 or P3, a group of neurons in the lumbar ventral horn expressed the tenascin-C mRNA gene.
      
In conclusion, this method to visualize mRNA gene expression of steroidogenic enzymes, and especially expression of CYP11B2, has increased the knowledge of adrenal pathophysiology.
      
Dentin matrix protein (Dmp1) mRNA gene transcripts were identified by use of the reverse transcription polymerase chain reaction (RT-PCR) in the cells throughout the culture period.
      
Here, semi-quantitative (sq) PCR revealed a more pronounced elevation of mRNA gene expression in PDL-F after 6?h of stretch, when compared with 12?h.
      
The DNA fragment containing the mRNA gene for the large subunit of RuBP-carboxylase appears to belong to class 2.
      
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The accumulation of extracellular matrix is a prominent feature of progressive glomerulonephritisand glomerulosclerosis. The autocrine and paracrine of cytokines play a central role in the pathogenesisof glomerulonephritis and glomerulosclerosis.To evaluate the role of IL-1 on glomerulosclerosis, 1. we observed IL-1 and TGFβ mRNA ge-ne expression and cellular matrix accumulation during the development of glomerulosclerosis, 2. alsoeffect of rIL-1β on stimulating cultured MSc expressing IL-1 and TGFβ mRNA...

The accumulation of extracellular matrix is a prominent feature of progressive glomerulonephritisand glomerulosclerosis. The autocrine and paracrine of cytokines play a central role in the pathogenesisof glomerulonephritis and glomerulosclerosis.To evaluate the role of IL-1 on glomerulosclerosis, 1. we observed IL-1 and TGFβ mRNA ge-ne expression and cellular matrix accumulation during the development of glomerulosclerosis, 2. alsoeffect of rIL-1β on stimulating cultured MSc expressing IL-1 and TGFβ mRNA gene and producingcellular matrix were studied, 3. The influence of Dexamethasone (Dex.), Calcitonin generelated peptide(CGRP). Tamm-Horsfall glycoprotein (THP) on the suppression of IL-1 production and its increasingeffects on MSc proliferation was investigated.The exploration of both experimental and cellular studies indicates the IL-1 plays an impor-tant role in the development of glomerulosclerosis. These drugs antagonized IL-1 in MSc level whichmay stop the pathogenesis circle of MSc and IL-1.

本文利用分子杂交技术研究了在系膜增殖性肾小球炎症硬化过程中白细胞介素1(IL-1)及转化生长因子β(TGFβ)基因表达及系膜细胞IL-1的自分泌和旁分泌作用与细胞外基质合成的关系;研究了3种药物对于系膜细胞产生IL-1的影响。结果证实IL-1和TGFβ在肾小球炎症硬化过程中起着重要作用。

The technology of nucleic acid in situ hybridization was used to study the effect of DDPH on PDGF mRNA gene expression of pulmonary artery SMC induced by the hypoxic bovine endothelium cell condition medium(HECCM).Experimental groups included normoxic, hypoxic serum free medium group(N,H group).normoxic,hypoxic endothelium cell conditional medium groups(NECCM,HECCM groups) and NECCM+DDPH,HECCM+DDPH group.Automatic image analysis showed that HECCM substantially enhanced the expression of PDGF+A and -B chain...

The technology of nucleic acid in situ hybridization was used to study the effect of DDPH on PDGF mRNA gene expression of pulmonary artery SMC induced by the hypoxic bovine endothelium cell condition medium(HECCM).Experimental groups included normoxic, hypoxic serum free medium group(N,H group).normoxic,hypoxic endothelium cell conditional medium groups(NECCM,HECCM groups) and NECCM+DDPH,HECCM+DDPH group.Automatic image analysis showed that HECCM substantially enhanced the expression of PDGF+A and -B chain mRNA(1.8 fold and 1.7 fold compared with N group;1.40 fold and 1.49 fold compared with NECCM group,respectively,P<0.01).HECCM+DDPH lowered the expression of PDGF-A and-B chain mRNA(0.73 fold and 0.65 fold compared with HECCM,with significant difference; but no difference was found when compared with NECCM).The results suggested that PDGF may be an autocrine growth factor of PASMC induced by HECCM and play an important role in the vascular structural remodeling of hypoxic pulmonary hypertension.DDPH could inhibit multiplication of PASMC induced by HECCM at the level of PDGF gene transcription.

利用地高辛标记的cDNA探针,原位检测DDPH[1-(2,6-二甲基苯氧基)-2-(3,4-二甲氧基苯乙胺基)丙烷酸盐]对缺氧内皮细胞条件培养液致猪PASMCPDGF基因表达的影响。实验分6组:常氧、低氧无血清培养液组(N、H组),常氧、低氧内皮细胞条件培养液组(NECCM、HECCM组),NECCM+DDPH、HECCM+DDPH组。用自动图像分析仪检测各组细胞PDGF-A和-B链杂交产物的平均光密度(OD)值。结果:HECCM组PDGF-A和-B链mRNA表达量分别是NECCM组的1.40、1.49倍(P<0.01),分别是N组的1.8倍、1.7倍(P<0.01),HECCM+DDPH组PDGF-A、-B链mRNA表达量分别为HECCM的0.73倍、0.65倍(P<0.01),与NECCM组相比,均无显著差异。提示DDPH在PDGF基因转录水平抑制HECCM诱导的PASMC的增殖。

On the basis of model of MCAO in spontaneously hypertensive rats (SHR), the changesof NOS activity and the NOS mRNA gene expression level were determined at different ischemictime points, and the effects of NO metabolism on ischemic brain edema by using extrinsicNOS inhibitor (L-NNA) were also explored. The results showed that the expression of NOS mRNA increased in the early ischemic phase, the activity of NOS after cerebral ischemia were significantly increased and the L-NNA can promote the brain...

On the basis of model of MCAO in spontaneously hypertensive rats (SHR), the changesof NOS activity and the NOS mRNA gene expression level were determined at different ischemictime points, and the effects of NO metabolism on ischemic brain edema by using extrinsicNOS inhibitor (L-NNA) were also explored. The results showed that the expression of NOS mRNA increased in the early ischemic phase, the activity of NOS after cerebral ischemia were significantly increased and the L-NNA can promote the brain edema. These resultssuggested that NO might have some protective effect on ischemic brain tissue in the early ischemicstage.

在SHR MCAO局灶脑缺血模型基础上,分别测定脑缺血后不同时限NOS活性变化及cNOS mRNA表达水平,并应用外源性NOS抑制剂L-NNA,观察NO代谢变化对脑缺血脑水肿的影响。结果发现脑缺血早期cNOS mRNA表达增加,NOS活性增高,L-NNA则促进脑水肿发生,提示NO在脑缺血早期可能具有保护作用。

 
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