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   近端肾小管上皮细胞 的翻译结果: 查询用时:1.469秒
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近端肾小管上皮细胞     
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  proximal tubular epithelial cells
     Inhibition of CTGF and ECM Expression in Human Renal Proximal Tubular Epithelial Cells by pBSHH1 Plasmid Vector Mediated CTGF shRNA
     pBSHH1质粒载体介导CTGF shRNA抑制TGF-β_1诱导的人近端肾小管上皮细胞CTGF及ECM的表达
短句来源
     Specific shRNA Suppress the Expression of Toll Like Receptor 4 in Human Proximal Tubular Epithelial Cells
     特异性shRNA抑制人近端肾小管上皮细胞Toll样受体4的表达
短句来源
     Inhibiting cubilin gene expression in human proximal tubular epithelial cells by plasmid-mediated siRNA
     质粒表达型siRNA对人近端肾小管上皮细胞cubilin表达的抑制作用
短句来源
     Human serum albumin stimulates osteopontin and CD44 expression in human renal proximal tubular epithelial cells
     人血清白蛋白对近端肾小管上皮细胞骨调素和CD44表达的影响
短句来源
     Effect of baicalein on high glucose-induced expression of extracellular matrix and transforming growth factor β1 in proximal tubular epithelial cells
     黄芩素对高糖诱导近端肾小管上皮细胞外基质及转化生长因子β1表达的影响
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  proximal tubular epithelial cell
     Objective To explore the effect of transforming growth factor β_1 (TGF-β_1) on expression of paxillin(Pax) in human kidney proximal tubular epithelial cell line (HKC cells) in different phases.
     目的探讨重组人类转化生长因子β1(rhTGF-β1)对人近端肾小管上皮细胞(HKC)桩蛋白(Pax)表达时相的影响。
短句来源
     Objective To investigate the effect of transforming growth factor-β1 (TGF-β1) on the activity of connective tissue growth factor(CTGF) gene promoter in human renal proximal tubular epithelial cell line HK-2. Methods The regulation fragment of 5' flanking region of human CTGF gene was linked to pGL3-Basic vector.
     目的探讨转化生长因子β1(TGF-β1)对人近端肾小管上皮细胞系HK-2中结缔组织生长因子(CTGF)基因启动子活性的调控作用,以及丝裂原激活蛋白激酶(MAPK)途径对该生长因子作用的影响。
短句来源
     Methods Human proximal tubular epithelial cell line (HK-2) was cultured in vitro, untreated HK-2 cells were acted as normal control group. HK-2 cells were then stimulated by Ang Ⅱ for 1-24 hours (Ang Ⅱ stimulation group),so that optimal dosage and duration could be chosen.
     方法体外培养人近端肾小管上皮细胞系(HK-2),以未处理HK-2细胞为正常对照,以 AII刺激HK-2细胞(AngⅡ组),选择合成TSP1和TGF-β1最佳刺激浓度和时间。
短句来源
     Methods:Human proximal tubular epithelial cell line HK-2 was pre-treated with AA-I(2.5 mg/L)for 4 hours. Cells were then treated with or without A&A for additional 44 hours. Cell apoptosis was evaluated by using FACS.
     方法:以体外培养的人近端肾小管上皮细胞系(HK-2)为研究对象,在AA-I(2.5 mg/L)刺激细胞4 h后,给予A&A药物血清并使细胞继续生长至48 h,应用流式细胞仪分析细胞DNA含量了解细胞凋亡情况;
短句来源
     To investigate if tumor necrosis factor-alpha (TNF-α) could induce NRK-52E cells, a rat renal proximal tubular epithelial cell line, up-regulating expression of fractalkine, one of chemokines, and if the induced effect appear time- and dose-dependent, and at the same time to investigate if the expression of fractalkine in renal tubular epithelial cells mediate macrophages chemotaxis.
     【目的】探讨肿瘤坏死因子-α(TNF-α)诱导大鼠近端肾小管上皮细胞株NRK-52E上调表达趋化因子fractalkine的时间和剂量效应,并观察肾小管上皮细胞fractalkine表达是否介导了对巨噬细胞的趋化作用。
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  proximal renal tubular epithelial cell
     Objective To investigate the expression of programmed death ligand-1 (PD-L1) in the cultured human proximal renal tubular epithelial cell HK2 under the stimulation of IFN-γ.
     目的 了解培养的人近端肾小管上皮细胞株HK2细胞程序性死亡配体 (PD L1)的表达及其影响因素。
短句来源
  renal proximal tubular cell
     METHODS: Conditioned medium(M-CM) of human peripheral blood MO/MAC was collected and added to HK-2,a human renal proximal tubular cell line. After incubation with M-CM for 24 hours,HK-2 cells were detected for DNA synthesis by -TdR incorporation,osteopontin (OPN) and α-smooth muscle actin (α-SMA) expression by Western blot,and fibronectin(FN) secretion by ELISA.
     方法 :应用正常人外周血M -CM刺激人近端肾小管上皮细胞 (HK - 2 ) ,以[3 H]-TdR掺入法检测HK - 2细胞DNA合成、Westernblot法检测骨桥蛋白 (OPN)和α -平滑肌肌动蛋白 (α -SMA)表达、间接抑制ELISA法检测纤连蛋白 (FN)分泌。
短句来源
     Objective To observe whether local aldosterone (ALDO) may be synthesized by hum an renal proximal tubular cell lines (HKC) and investigate whether endothelin-1 (ET-1) has effects on the production of local ALDO.
     目的 观察人近端肾小管上皮细胞能否合成组织醛固酮(ALDO),以及内皮素-1 (ET-1)对该作用的影响。
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      proximal tubular epithelial cells
    Silencing of Bak Ameliorates Apoptosis of Human Proximal Tubular Epithelial Cells by Escherichia coli-Derived Shiga Toxin 2
          
    Enzymehistochemistry demonstrated that lactate dehydrogenase (LDH) activity in proximal tubular epithelial cells increased but succino dehydrogenase (SDH) activity decreased.
          
    The proximal tubular epithelial cells were cultured in vitro under different conditions.
          
    Our results showed that under different conditions, there were no significant differences in the proliferation of proximal tubular epithelial cells 12 h and 24 h after the culuture (P>amp;gt;0.05).
          
    The proliferation of proximal tubular epithelial cells showed a significant change 96 h after the culture and the cellular proliferation induced by hepatocyte growth factor (HGF) was very active (P>amp;lt;0.05).
          
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      proximal tubular epithelial cell
    The present study was undertaken to determine the role of the ERK activation in H2O2-induced apoptosis of renal epithelial cells using opossum kidney (OK) cells, an established proximal tubular epithelial cell line.
          
    This study was carried out to investigate the effect of aristolochic acid I (AAI) on DNA damage and cell cycle in porcine proximal tubular epithelial cell lines (LLC-PK1 cells).
          
    In the current study, we investigated the oxalate-induced injury and up-regulation of monocyte-chemoattractant protein-1 (MCP-1) in HK-2 cells, a proximal tubular epithelial cell line derived from normal human kidney.
          
    Methods: The mouse lymphocytic leukemia cell line L1210 and pig kidney proximal tubular epithelial cell line LLC-PK1 were used as neoplastic and normal cells, respectively.
          
    This study investigates the potential of an immortalized human proximal tubular epithelial cell line, HK-2, to serve as a representative model for low level exposures of the human kidney to arsenic.
          
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      proximal tubule epithelial cells
    The pig proximal tubule epithelial cells (LLC-PK1 cells) were cryopreserved in hypoxic UW solution (Ar-UW group) or standard UW solution (UW group) at 4°C for 48 h.
          
    We exposed human renal proximal tubule epithelial cells (huRPTECs) to different concentrations of TGF-β1, IL-1α, IL-10, or methionine and measured total Hcy (tHcy) in culture supernatants.
          
    Histopathological examination showed that the necrosis score in the proximal tubule epithelial cells and average apoptitic cell numbers in the CP group were higher than those in the CP+HBO and HBO groups (P>amp;lt;0.05).
          
    There was no statistical difference between the CP+HBO group and the HBO group in terms of necrosis score in the proximal tubule epithelial cells and the percentage of distal tubules containing hyaline casts in the lumen.
          
    Increased functional load on mouse kidney proximal tubule epithelial cells causes changes in nucleolar 3-D architecture
          
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