• 方法细胞内皮细胞取自小鼠肝脏

    Methods Hepatocytes and sinusoidal endothelial (se) cells were harvested from mouse liver.

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  • 结果边缘内皮细胞能吞噬消化、处理

    Results: the marginal sinus endothelial. cells possessed the function of phagocytosis, digestion and removing of carbon particles.

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  • 淋巴细胞成纤维细胞内皮细胞染色阳性。

    Lymphocyte, fibroblast and sinusoid endotheliocyte were stained positively.

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  • 结果VEGF组织表达有胞内皮细胞型;

    Results The expression types of VEGF in liver tissue were plasma type, sinusoid membrane type and sinusoid endothelial cells type.

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  • 结论内皮细胞毒症时肝组织细胞因子重要来源之一。

    Conclusions Liver sinusoidal endothelial cell is an important source of cytokine production in mice with sepsis.

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  • 目的为了进一步认识边缘内皮细胞屏障中的地位和作用

    Objective: To understand the function of splenic marginal sinus endothelial cells in blood spleen barrier.

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  • 目的研究内皮细胞损伤二甲基亚硝胺鼠肝纤维化形成中的作用

    Objective To study the role of hepatic sinusoidal endothelium injury during hepatic fibrogenesis induced by dimethylnitrosamine (DMN) in rats.

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  • 对照组比较,实验组大细胞内皮细胞变性坏死程度轻。

    Compared with the control group, the degenerative and necrotic degree of hepatocyte and sinusoidal endothelial cells was lighter in the experiment group.

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  • 本文内皮细胞其中重要作用及减轻这一损伤研究进展简要综述

    So, this article reviews the importance of endothelial cells in hepatic sinus and study progresses on the question tha…

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  • 番鸭呼孤病毒的主要细胞肝脏内的细胞、肝内皮细胞枯否细胞

    The target cells of MDRV were as follows, Liver cells, Endothelial of blood sinus, Kupffer's cells in Liver;

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  • 病理基础预处理毒性引起肝脏小叶3区内内皮细胞以及肝细胞损害所致

    The basis of pathology of vod is thought resulting from injury of hepatocytes and endodermis cells surrounding the central veins in zone3of the liver acinus by regimen-related toxicity.

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  • 目的探讨细胞粘附分子内皮细胞LSEC缺血再灌注损伤中的作用

    Objective:To investigate the role of granulocyte and adhesion molecules in the ischemia reperfusion injury of human liver sinusoidal endothelial cells(LSEC).

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  • 目的建立内皮细胞(sec)代分离培养方法研究生物学特性

    Objective To set up a method for the primary isolation and cultivation of rat sinusoidal endothelial cells (SEC), and study their biological characteristics.

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  • 结论D MN引起大鼠内皮细胞损伤及其表型改变可能是其诱导纤维化重要动机制之一。

    Conclusions the damage and phenotypic alteration of the hepatic sinusoidal endothelium may be a vital issue triggering the liver fibrosis induced by DMN.

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  • VEGF主要细胞分泌,其次内皮细胞贮脂细胞成肌纤维细胞单型细胞示阳性。

    VEGF was mainly secreted by hepatocytes, and was also positively expressed in liver sinusoid endothelial cells, fat-storing cells, myofibroblast and monomorphic nucleus cells.

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  • 应用一氧化氮基质蛋白酶抑制剂明显降低窦内皮细胞的损伤,表明一氧化氮基质蛋白酶缺血-再灌注损伤中重要介导物。

    The inhibitor for NO or for MMPs significantly reduced the LSEC IRI, suggesting that NO and MMPs are important mediators in the LSEC IRI.

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  • 星状细胞、成纤维细胞状隙内皮细胞肝内ctgf的重要来源。

    It can be concluded that CTGF was mainly produced in hepatic stellate cells, sinusoidal endothelial cells and fibroblasts.

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  • 目的研究门静脉高压症病人肝组织内血管内皮细胞凋亡及其微循环影响

    Objective To investigate the intrahepatic vascular and hepatic sinusoidal endothelial cell (SEC) apoptosis and its influence on hepatic microcirculation in patients with portal hypertension.

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  • 海绵状血管畸形由状扩张组成,内皮细胞物质细胞组成。

    There were endothelial cells , basal membrane like materials and pericytes in the walls of these blood sinus.

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  • 结论:肝内皮细胞体外培养条件下自发永生化

    Conclusions: in vitro sinusoid endothelial cells could spontaneously immortalize. Some biological characteristics of immortalized cells changed.

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  • 作为屏障中驻留的前细胞周围内皮细胞,骨前体统一成骨细胞壁龛状隙壁龛两个概念

    As pre-osteoblastic, peri-endothelial cells residing at the sinusoid wall, skeletal progenitors reconcile the notions of "osteoblastic" and "sinusoidal" niches with one another.

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  • CTGF表达主要集中于汇管区纤维化细胞成纤维细胞状隙内皮细胞染色常呈阳性

    CTGF was mainly expressed in portal tracts and fibrotic areas. Positive staining was observed in hepatic stellate cells, sinusoidal endothelial cells and fibroblasts.

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  • CTGF表达主要集中于汇管区纤维化细胞成纤维细胞状隙内皮细胞染色常呈阳性

    CTGF was mainly expressed in portal tracts and fibrotic areas. Positive staining was observed in hepatic stellate cells, sinusoidal endothelial cells and fibroblasts.

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