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纤维细胞

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Methods HPDLFs were primary cultured from tissue explants, and the cells of the 5th to 8th passages were used after immunohistochemical identification of keratin and vimentin expressions. The cells were divided into 5 groups and treated with TP at 1, 0.5, 0.25, 0.125, and 0.0625 mg/ml, respectively, with another group without TP treatment as the blank control group. Cell counting and MTT colorimetric assay were performed to assess the cell proliferation, and flow cytometry was employed to determine the DNA content of the HPDLFs.

采用组织块培养法培养原代人牙周膜成纤维细胞并传代,经免疫组化SABC法检测角蛋白和波形丝蛋白鉴定,取5~8代细胞用于实验;按茶多酚不同浓度分1mg/ml、0.5mg/ml、0.25mg/ml、0.125mg/ml、0.0625mg/ml组和空白对照组,采用细胞计数法、MTT法检测细胞增殖情况,流式细胞术检测细胞DNA含量。

Tumor cells grew actively in the tumor tissues of the control group. Prodrug therapy group: small amount of tumor cells were denatured vacuously,others were infiltrated by lympholeukocyte,and the growth of tumor cells were surspressed.Prodrug themochemotherapy group: what we can see that tumor cells were denatured vacuously, mesoplasts crinkled, cellular boundary disappered, only a small number of tumor cells remained, fibroblast were seen scatteredly, tumor cells were invaded by a lot of lympholeukocyte and eosinophilic granulocyte. Normal liver tissues, stomach tissues, lung tissues, pancreas tissues, small intestine tissues, large intestine tissues showed normal shape.

对照组肿瘤组织见肿瘤细胞生长活跃;前药治疗组肿瘤组织见有少量细胞空泡变性,少量淋巴细胞浸润,肿瘤细胞生长受到抑制;前药热疗组肿瘤组织可见肿瘤细胞空泡变性,细胞核皱缩,边集甚至消失,仅残留少量肿瘤细胞,并可见散在的成纤维细胞,大量淋巴细胞和嗜酸性粒细胞浸润;3组裸鼠正常肝组织、胃、肺、胰腺、小肠、大肠组织均呈正常形态学,无病理性损伤改变。

Xenopus laevis Tadpole (1) Xenopus laevis Tadpole was capable of lens regeneration, which originated from the outer cornea.(2)The days of lens regeneration of Xenopus laevis Tadpole was earlier than Bufo Raddei Strauch Tadpole, The rate of regeneration of Xenopus laevis Tadpole was higher than Bufo Raddei Strauch Tadpole.(3)During Xenopus laevis lens regeneration the outer cornea cells proliferated, in the elongating cells the mitochondria became complicated and in the columnar cells the cisternal dilating of endoplasmic reticulum was ubiquity.

非洲爪蟾蝌蚪(1)再生晶状体来源于外角膜;(2)晶状体再生较花背蟾蜍蝌蚪晶状体再生时期早,再生率高;(3)电镜观察发现再生前期外角膜增殖,观察到晶状体上皮细胞和伸长细胞(进一步发育为晶状体纤维细胞),伸长细胞中线粒体形状各异随着进一步的分化,细胞器逐渐消失;分化过程中晶状体上皮细胞粗面内质网增多,并且内质网扩张普遍存在。

METHODS: We assessed the number of fibrocytes in bronchial biopsy specimens and peripheral blood from subjects with mild-to-severe refractory asthma versus healthy control subjects.

我们评估了轻-重度难治性哮喘患者气道活检标本和外周血中成纤维细胞的数量,同时通过体外实验,探讨了调控纤维细胞向气道平滑肌移行的可能机制。

RESULTS Expression rate of MHCI antigen of cultured smooth muscle cells and fibroblast was(88.7±4.3)%,(84.8±2.0)%respectively;and that of the revived smooth muscle cells and fibroblasts of aortic homografts after cryopreservation was(89.4±3.5)%,(81.9±2.7)%respectively.

结果 正常培养的大鼠主动脉平滑肌细和成纤维细胞MHCⅠ类抗原表达的阳性率分别为(88.7±4.3)%和(84.8±2.0)%;液氮低温保存的大鼠主动脉平滑肌和成纤维细胞在复苏后MHCⅠ类抗原表达的阳性率分别为(89.4±3.5)%和(81.9±2.7)%。

RESULTS Expression rate of MHCI antigen of cult ured smooth muscle cells and fibroblast was (88.7±4.3)%,(84.8±2.0)%respectively; and th at of the revived smooth muscle cells and fibroblasts of aortic homografts after cryoprese rvation was (89.4±3.5)%,(81.9±2.7)%respectively.

结果正 常培养的大鼠主动脉平滑肌细和成纤维细胞MHC Ⅰ类抗原表达的阳性率分别为(88.7±4.3)%和(84.8±2.0)%;液氮低温保存的大鼠主动脉平滑肌和成纤维细胞在复苏后MHC Ⅰ类抗原表达的阳性率分别为(89.4±3.5)%和(81.9±2.7)%。

Seed-flax variety CI. 2446 was planted at four different dates (Oct. 5, Oct 20, Nov. 5, Nov. 20) and four different densities (2250, 1800, 1350 and 900 plants/m^2) to study the effects on the fiber cell development at different growing stages. All traits, except the phloem thickness, of fiber cell showed no significant difference among different sowing densities.

以种子用亚麻CI2446为材料,分四种植期(10月5日,10月20日、11月5日、11月20日)及四种密度(2250、1800、1350、900株/平方公尺),以探讨其对种子用亚麻在不同生育期间纤维细胞发育之影响,由结果得知播种密度除对靱皮部厚度有显著差异外,对纤维细胞之其他性状影响并不显著。

Since an excessive cell growth is considered as the main pathological event, cell proliferation model occupy most of the animal models, and these cells include retinal pigment epithelial cell, fibroblast cell, cartilage cell and vascular endothelial cell.

由于PVR的主要病理变化是细胞的过度增生,因而动物模型多以细胞增生模型为主,细胞种类有视网膜色素上皮细胞、成纤维细胞、软骨细胞、血管内皮细胞等。

Materials and Methods: the HPDLFs were isolated and cultured in vitro from healthy premolars of orthodontic patients, which were 10~14 years old.

材料和方法:取材自临床上10~14岁青少年需要拔除的健康的正畸牙,在体外分离、培养并纯化人牙周膜成纤维细胞,建立人牙周膜成纤维细胞有限细胞系。

MATERIALS: Basic fibroblast growth factor freeze-dry powder (50 mg/ampoule) was thoroughly dissolved with ddH2O to prepare 5 g/L bFGF solution.

材料:取碱性成纤维细胞生长因子冻干粉(50 mg/支),ddH20彻底溶解,制成含碱性成纤维细胞生长因子 5 g/L的溶液。

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