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   肝脏组织 的翻译结果: 查询用时:3.309秒
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      肝脏组织     
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  liver tissue
     As compared with the control group,in liver tissue,ratio of protein content (experimental group/control group) is 0. 60: 1. 00,ratio of DNA content is 0. 49: 1. 00;
     实验组与对照组相比,肝脏组织蛋白质含量比值为0.60∶1.00,DNA含量比值为0.49∶1.00;
短句来源
     Moreover,MDA contents in liver tissue were higher in LPS group than control and berberine treatment group,but there were no significant difference in SOD activity between berberine treatment and LPS group.
     此外,LPS组肝脏组织中MDA的含量明显高于对照组(P<0.01),而小檗碱防治组肝脏组织中MDA的含量低于LPS组(P<0.05),但小檗碱防治组肝组织中SOD活性与LPS组比较无显著差异。
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     Results The expression of COX-2 protein was detected in 25 of 41 HCC(61.0%),9 of 16 HCL(56.3%),and none of normal liver tissue.
     结果COX-2蛋白在肝细胞癌和肝硬化组织中的表达率分别为61.0%(25/41)和56.3%(9/16),正常肝脏组织中无表达,与以上各病变组织COX-2蛋白表达差异有显著性(P<0.05);
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     13. VIPR mRNA on human HSC and rat liver tissue was identified by RT-PCR.
     13.Rl’- PCR方法检测人HSC、肝脏组织VIPR的mRNA表达。
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     Experimental study on acoustic environment change in normal rabbit liver tissue with HL-1(Ⅱ)
     HL-1改变兔肝脏组织声学环境的实验研究(Ⅱ)
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  liver tissues
     The injury of Na_2SeO_4 and Na_2SeO_3 to the liver tissues of Rana nigromaculata tadpolesparaffin section of livers and HE dyeing are performed.
     Na_2SeO_4和Na_2SeO_3对黑斑蛙蝌蚪肝脏组织的损伤。
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     Methods:GGTⅠmRNA type A ,B , C and AFP mRNA of liver tissues, QSG-7701 and HepG2 cell line were checked by RT-PCR.
     方法:运用RT-PCR检测肝脏组织标本和人肝细胞株QSG-7701、人肝癌细胞株HepG2中GGTⅠmRNA A、B、C3种亚型和AFP mRNA的表达。
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     Results\ The relative mRNA expression of α 1a and α 1b AR subtype in liver tissues of cirrhotic patients (0.26±0.12,0.03±0.01) was significantly lower than that of controls (0.86±0.38, 0.23±0.10, P <0.01).
     结果 肝脏组织中α1a、α1bAR亚型的相对表达量对照组 (0 .86± 0 .38、0 .2 3± 0 .10 )均显著高于肝硬化组 (0 .2 6± 0 .12、0 .0 3± 0 .0 1,P <0 .0 1)。
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     Methods: Mouse PD-L1 cDNA was amplified by RT-PCR from total RNA of mouse liver tissues and was cloned into shuttle vector pSNAV1; the products were then transferred into BHK21 cells by lipofectamine and rAAV2-PD-L1 was screened out.
     方法:以鼠肝脏组织来源的总RNA为模板,应用RT-PCR扩增PD-L1 cDNA,克隆入穿梭质粒pSNAV1,脂质体法转染包装细胞BHK21,筛选获得重组病毒rAAV2-PD-L1。
短句来源
     Conclusion CYP2D1 mRNA expression level in hepatocarcinogenesis rat liver tissues is same to in normal rat ,CYP2D1 mRNA also can express in brain tissues and its level is lower in liver tissues.
     结论 肝癌大鼠的肝脏组织中有CYP2D1表达 ,其表达水平与正常组织一样 ,大脑组织中CYP2D1虽有表达 ,但是其表达水平明显低于肝脏组织
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  hepatic tissue
     Methods The total RNA was extracted from rat hepatic tissue. CYP2J3 gene was amplified by RT-PCR and OE-PCR,and cloned into the pcDNA 3.1(+) to form an eukaryotic expression vector.
     方法提取大鼠肝脏组织总RNA,采用逆转录聚合酶链反应(RT-PCR)和重叠延伸聚合酶链反应(OE-PCR)扩增大鼠CYP2 J3基因,克隆入真核表达载体pcDNA 3.1(+)。
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     ③ Contents of triglyceride(TG)and malondialdehyde(MDA) in hepatic tissue and concentrations of TG and free fatty acid(FFA) in serum;
     ③测定肝脏组织甘油三酯(TG)、丙二醛(MDA)、以及血清中TG、游离脂肪酸(FFA)生化指标的含量变化;
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     The expression of adipose tissue aromatase and blood E 2 level were significantly higher in OVX+EA+T group than in OVX+EA group (P< 0.05), but there was no significant change in hepatic tissue aromatase.
     OVX+EA+T大鼠脂肪组织芳香化酶蛋白表达和血 E2 水平 ,比 OVX+EA显著升高 (P<0 .0 5 ) ,但肝脏组织的酶蛋白表达无明显改变。
短句来源
     ④Activities of CYP1A1 (7-ethoxyl isoxazole O-deethylase,EROD), CYP2E1 (aniline hydroxylase, ANH) and CYP3Al(erythromycin N-demethylase,ERD) in rat hepatic tissue using enzymatic methods;
     ④酶学测定大鼠肝脏组织CYP4501A1(7-乙氧基异恶唑0-脱乙基酶,EROD)活性; CYP4502E1(苯胺羟化酶,ANH)活性;
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     Hepatic tissue (0.1g) was procured before warm ischemia and 0.5,1,2 and 3 h after reperfusion in WI group,before and after IPC and 0.5,1,2 and 3 h after reperfusion in IPC group. The expression of eNOS and iNOS mRNA was detected by fluorescence-quantitating-PCR.
     WI组于缺血前、再灌注后0.5、1、2、3 h,IPC组于IPC前、IPC结束时、再灌注后0.5、1、2及3 h分别切取肝脏组织约0.1 g,用荧光定量PCR法检测其内皮型NOS(eNOS)mRNA和诱导型NOS(iNOS) mRNA。
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  hepatic tissues
     For the MDA concentration, it decreased in hepatocarcinoma tissue following ischemia and reperfusion until 7d(21.59±0.59). In contrast, the increasing of that in normal hepatic tissues was marked after reperfusion for 0 min to 7d(29.04±1.43) and kept at higher level than that before ischemia (18.26±0.43).
     从缺血再灌注开始至7d肿瘤组织的MDA含量下降(21.59±0.59),而肝脏组织缺血再灌注后0min至7d(29.04±1.43),MDA含量明显升高,均高于缺血再灌注前水平(18.26±0.43)。
短句来源
     In the experimental group, the postive rate of CD44V6 in the gastric and ovaria n tissues were 63.2% and 42.1%, In the control group, the postive rate of CD44V6 in the gastric and hepatic tissues were 70% and 60%, the two groups has no obv ious difference(P>0.05).
     肝脏转移组胃癌组织和肝脏组织的CD44V6阳性率分别为70%和60%,卵巢转移组胃癌组织和卵巢转移组织CD44V6阳性率分别为63.2%和42.1%,两组差异无显著性(P>0.05)。
短句来源
     In addition to the examination of Superoxide Dismutase (SOD) and malondialdehyde (MDA), the apoptotic changes in the hepatocarcinoma and its contiguous area and normal hepatic tissues were observed by HE staining.
     取肿瘤组织、癌周组织和肝脏组织,除测定肿瘤组织和肝脏组织超氧化物歧化酶(SOD)、丙二醛(MDA)的含量外,还对肿瘤组织、癌周组织及肝脏组织进行了HE染色。
短句来源
     METHODS: The experiment was performed at the Laboratory of Cardiology, Tongji Hospital from September 2004 to February 2005. Total RNA was extracted from hepatic tissues of rats to form CYP2J3CDNA by reverse transcription reaction and obtain A and B fragments of CYP2J3 gene, totally 1 228 bp and 345 bp, respectively by polymerase chain reaction (PCR) amplification.
     方法:实验于2004-09/2005-02在同济医院心血管实验室完成。 提取大鼠肝脏组织总RNA,通过逆转录反应形成CYP2J3CDNA,采用聚合酶链反应扩增出CYP2J3基因A和B两片段,全长分别是1228bp和345bp。
短句来源
     [WT5HZ]Results[WT5”FZ] The relative mRNA expression of α 1a adrenoceptor subtype in the hepatic tissues was significantly lower in the cirrhotic patients (0 26±0 12) than in the controls(0 86±0 38, P <0 01).
     结果 肝脏组织中α1a肾上腺素受体亚型的相对表达量 :对照组 0 86± 0 38显著高于肝硬化组 0 2 6± 0 12 (P <0 0 1) ;
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  liver tissue
Antioxidant activity of melatonin and some new melatonin analogue indole derivatives were investigated, using lipid peroxidation and superoxide anion radical scavenger activity assays, in rat liver tissue homogenate.
例句来源      
Insulin-like growth factor-1 and IGFBP-3 mRNA in the liver tissue was detected by RT-PCR.
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The number of eggs in liver tissue was reduced by 36.8%, 43.2%, and 46.1%, respectively.
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Development of liver pathology was accompanied by adipose dystrophy, fibrosis, and an increase of triglycerides and lipid peroxidation products in the liver tissue.
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And a clue to the function ofEDRF1 has been found from confirmation of high levels ofEDRF1 mRNA in differentiated K562 and human fetal liver tissue.
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  liver tissues
Spotty necrosis occurred in some local liver tissues.
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Hepatic steatosis, lobular inflammation, hepatocytic ballooning and fibrosis were presented widespread in NAFLD liver tissues.
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Regulatory Effects of Essential and Nonessential Amino Acids on Organotypic Cultures of Spleen and Liver Tissues
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The protein expression profiles of liver tissues were acquired by fluorescence two-dimensional difference gel electrophoresis (2D DIGE) that incorporated a pooled internal standard and reverse fluorescent labeling method.
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Paraffine embedded tissue sections from placental and liver tissues from each case were evaluated by histopathology, immunohistochemistry, nested PCR and commercial quantitative Real-time PCR.
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  hepatic tissue
The overall amounts of both phospholipids and gangliosides increased appreciably in the subcutaneously growing hepatoma (in contrast to the intrahepatically growing tumor) in comparison to the control hepatic tissue.
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INOS and eNOS were not detected in normal hepatic tissue.
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The Michaelis-Menten constant for glycerol was not different from the values found in hepatic tissue.
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The rate of metabolism of testosterone in histologically normal hepatic tissue was as high as in cirrhotic tissue, while the rate of metabolism in fatty liver was lower.
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The main pathogenetic factor is obviously the functioning hepatic tissue, reflected by the galactose elimination capacity (r=0.666;P>amp;lt;0.01; theophylline clearance vs galactose elimination capacity).
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  hepatic tissues
Capability and extent of xylitol metabolism in vitro was studied in a variety of non-hepatic tissues of rats, using enzymatic and isotopic methods.
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A single dose of 30 mg/kg (~30% LD50) endosulfan significantly (p>amp;lt;0.001) increased the TBARS and, hence, the lipid peroxidation in cerebral and hepatic tissues of rats.
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The same doses caused a significant alteration in glutathione redox status of cerebral and hepatic tissues, where total glutathione and oxidized glutathione were measured by an enzymatic cycling procedure.
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Thiobarbituric acid reactive species (TBARS) (an estimate of lipid peroxidation / free radical formation) was measured in renal and hepatic tissues.
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The influence of point injection therapy on hepatic tissues and SOD in rats with MNNG-induced chronic atrophic gastritis
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