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   gingival fibroblast 的翻译结果: 查询用时:0.01秒
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gingival fibroblast
相关语句
  牙龈成纤维细胞
     RESULTS: Lanthanum chloride at 1×10-2mol/L can inhibit the proliferation of human gingival fibroblast, however, it can't inhibit the proliferation at 1×10-6,1×10-5,1×10-4,1×10-3mol/L.
     结果:1×10-2mol/L氯化镧能抑制人牙龈成纤维细胞的生长,1×10-6、1×10-5、1×10-4、1×10-3mol/L氯化镧对细胞生长无抑制作用。
     METHODS: Human gingival fibroblast was cultured in vitro, and MTT assay was used to analyse the effect of lanthanum chloride (1×10-6、1×10-5、1×10-4、1×10-3、1×10-2mol/L )on the proliferation of human gingival fibroblast.
     方法:体外培养人牙龈成纤维细胞,通过噻唑兰法(MTT法)检测6种浓度氯化镧(1×1016、1×10-5、1×10-4、1×10-3、1×10-2mol/L)对细胞的作用。
     Effect of Ti-Nb-Zr-Sn alloy on the biological behavior of gingival fibroblast
     Ti-Nb-Zr-Sn系合金对牙龈成纤维细胞生物学行为的影响
短句来源
     Comparison of production of interleukin-11(IL-11) and IL-6 in human gingival fibroblast stimulated with IL-1α
     IL-1α刺激人牙龈成纤维细胞产生IL-11和IL-6的比较研究
短句来源
     Study on Expression of Recombinant Plasmid PsecTaq2A-AMG for Human Amelogenin in Human Gingival Fibroblast.
     人釉原蛋白重组质粒Psec Taq2A-AMG在人牙龈成纤维细胞表达的研究
短句来源
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  “gingival fibroblast”译为未确定词的双语例句
     RESULTS: The cytotoxic effects in vitro of D-108 on various tumor cell lines (IC_ 50 : 0.22 to 2.19 mg·L~ -1 ) were more powerful than both human gingival fibroblast and marrow stromal cell (IC_ 50 : 5.55 and 3.57 mg·L~ -1 ).
     结果:D-108对肿瘤细胞的体外细胞毒作用(IC50:0.22~2.19mg·L-1)强于HGF及MSC(IC50分别为5.55、3.57mg·L-1)。
短句来源
     Ovarian epithelial cancer cell line SKOV 3(MUC 1 +) and normal human gingival fibroblast cell GF(MUC 1 -)were co cultured, then were infected by lentivirus.
     用磷酸钙沉淀法进行Anti MUC 1(ScFv)慢病毒包装 ,感染共培养的卵巢癌细胞SKOV 3(MUC 1+)和正常人成纤维细胞GF(MUC 1- ) ,荧光显微镜下观察感染效果。
短句来源
     These findings prompted us to investigate whether p38 MAPK signal pathway is involved in LPS-induced uPA expression in human gingival fibroblast.
     由此,我们认为,LPS对uPA表达的诱导作用很可能是通过p38 MAPK信号转导途径头现的。
短句来源
     RESULTS:IL-6 secreted by human gingival fibroblast was significantly inhibited by extracts from Chinese Nutgalls in a dose-dependent manner. When the concentration was higher than 50 μg/mL,extracts inhibited cell proliferation.
     结果 :五倍子水提取物可显著抑制内毒素诱导HGF分泌IL - 6水平 ,其作用在一定范围内呈浓度依赖性 ,同时当其浓度 >5 0 μg/mL时 ,可抑制HGF增殖。
短句来源
     Results:IL-6 secreted by human gingival fibroblast was significantly inhibited by Xi-payi mouth rinse in a dose dependent manner.
     结果:西帕依固龈液可显著抑制LPS诱导HGF分泌IL-6水平,其作用在一定范围内呈浓度依赖性。
短句来源
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  相似匹配句对
     Assessment of collagen degradation by human gingival fibroblast
     人牙龈成纤维细胞体外降解胶原能力的测定
短句来源
     The effect of lanthanum chloride on the proliferation of human gingival fibroblast
     氯化镧对人牙龈成纤维细胞增殖的影响
     A flexible gingival.
     本研究研制的一种柔性牙龈赝复材料。
短句来源
     (2) Fibroblast malignant
     (3)H_2O_2促进MNNG转化成纤维细胞恶性转化作用;
短句来源
     CRYOPRESERVATION OF FIBROBLAST BY VITRIFICATION
     成纤维细胞玻璃化保存的实验研究
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  gingival fibroblast
Growth and proliferation of the human gingival fibroblast cells on the surface of the materials was evaluated.
      
The growth properties of gingival fibroblast cultures from DS patients were more elevated than their ND age-matched controls.
      
Gingival fibroblast cultures from four patients with Down's Syndrome (DS) and periodontal disease were compared with four in vitro age-matched fibroblast cultures of handicapped subjects (ND) also affected by periodontitis.
      
Genetic control of variation in human gingival fibroblast proliferation rate
      
Human gingival fibroblast (hGF) cells reside in gingival tissues which are challenged frequently by oral bacteria.
      
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This investigation analyses the contents of prostaglandin E2(PGE2) 6-ketoprostaglandin F1a (6-k-PGF1a)and thromboxane B2(TXB2) in gingival fibroblast(GF) and periodontal ligament cell(PDLC) by microspectrophotometer. The results showed that the absorbance of PGE2 in GF was 0. 25±0. 03, the absorbance of 6-k-PGF1a was 0.20±0. 03, there were significant difference between PGE2 6-k-PGF1a and control group.The absorbance of PGE2. TXB2 and 6-k-PGF1a and control group. The absorbance of PGE2. TXB2 and 6-k-PGF1a...

This investigation analyses the contents of prostaglandin E2(PGE2) 6-ketoprostaglandin F1a (6-k-PGF1a)and thromboxane B2(TXB2) in gingival fibroblast(GF) and periodontal ligament cell(PDLC) by microspectrophotometer. The results showed that the absorbance of PGE2 in GF was 0. 25±0. 03, the absorbance of 6-k-PGF1a was 0.20±0. 03, there were significant difference between PGE2 6-k-PGF1a and control group.The absorbance of PGE2. TXB2 and 6-k-PGF1a and control group. The absorbance of PGE2. TXB2 and 6-k-PGF1a in PDLC each were 0. 20±0. 02、0. 16±0. 03 and 0.13±0.02. They were much bigger than control group(0. 07±0.01 ), which indicated prostaglandins in GF and PDLC can affect guided tissue regeneration and gingivitis degree, and there were important relationship between PG. in GF.PDLC and preiodontitis.

作者对体外培养的人牙龈成纤维细胞(GF)和牙周韧带细胞(PDLC)采用免疫组化ABC染色及显微分光光度法分析,测定GF和PDLC中前列腺素E2(PGE2)、6-酮一前列腺素F1a.(6-K-PGF1a)和血栓素B2(TXB2)含量,以探讨其与牙周炎的关系,结果表明GF的PGE2吸光度为0.25±0.03,6-K-PGF1a的吸光度为0.20±0.03,与对照组相比均有非常显著性差异;PDLC的吸光度分别为PGE20.21±0.02、TXB20.16±0.03和6-K-PGF1a0.13±0.02,与对照组相比均有非常显著性差异。表明GF和PDLC均可分泌一定量的PGE2、TXB2和6-K-PGF1a,但分泌的量略有差异,提示GF和PDLC可通过分泌PG,影响牙龈炎症变化和牙周组织再生。

Aim:SAM were examined for inhibitory effects on human gingival fibroblast. Methods: Using cell count and image pattern analysis. Results: SAM of Aa could inhibit division and proliferation and lead to increased cytoplasmic and nuclear area. Inhibitory effect was concenrtraition dependent, prounced difference of inhibitory percentage was observed at the concentration of 100 μg/ml compared with that of the control. Conclusions: SAM can inhibiti on the growth of human gingival fibroblast....

Aim:SAM were examined for inhibitory effects on human gingival fibroblast. Methods: Using cell count and image pattern analysis. Results: SAM of Aa could inhibit division and proliferation and lead to increased cytoplasmic and nuclear area. Inhibitory effect was concenrtraition dependent, prounced difference of inhibitory percentage was observed at the concentration of 100 μg/ml compared with that of the control. Conclusions: SAM can inhibiti on the growth of human gingival fibroblast.

目的:观察放线共生放线杆菌表面相关物质对人牙龈成纤维细胞的增殖抑制作用。方法:采用细胞计数法和图像分析法观察对人牙龈成纤维细胞的生长抑制作用。结果:此物质抑制作用明显,能抑制细胞的分裂、增殖,使细胞、细胞核面积增大,100mg/L对与对照组差别显著(P<0.05),且细胞无死亡现象。结论:此物质可明显抑制人牙龈成纤维细胞的生长、增殖,在牙周病病理变化过程中起重要作用

Aim:To evidence cemental matrix could stimulate human gingival fibroblast and human periodontal lagment cell to grow on root surface. Methods: Cell culture and cell counts. Results: Extracts of cemental matrix could stimulated human gingival fibroblast and human periodontal lagment cell to grow on root surface. Conclusions: Extracts of cemental matrix contain substances those stimulate human gingival fibroblast and human periodontal lagment cell to divide and grow on root ...

Aim:To evidence cemental matrix could stimulate human gingival fibroblast and human periodontal lagment cell to grow on root surface. Methods: Cell culture and cell counts. Results: Extracts of cemental matrix could stimulated human gingival fibroblast and human periodontal lagment cell to grow on root surface. Conclusions: Extracts of cemental matrix contain substances those stimulate human gingival fibroblast and human periodontal lagment cell to divide and grow on root surface; the extract of cemental matrix is more effective in promoting the attachment of humen periodontal ligament cell than doing the attachment of humen gingival fibroblast.

目的:证实牙骨质基质提取物可促进牙周结缔组织细胞在牙根表面上增殖。方法:用细胞培养法和增殖细胞记数法。结果:加入牙骨质基质提取物的实验组无论是牙龈成纤维细胞还是牙周膜细胞的增殖能力均有显著的提高。结论:牙骨质基质提取物可促进牙龈成纤维细胞和牙周膜成纤维细胞在牙根表面上的增殖,牙骨质基质提取物对牙龈成纤维细胞的促有丝分裂作用强于对牙周膜成纤维细胞的作用

 
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