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增殖细胞
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  proliferating cell
    A quantitative study of microvascular density and proliferating cell ratio in buccal mucosa squamous cell carcinoma
    颊粘膜鳞癌微血管密度与增殖细胞比率的定量研究
短句来源
    Quantitative Study of Microvascular Density and Proliferating Cell Ratio in Oral Squamous Cell Carcinoma
    口腔鳞癌血管密度与增殖细胞比率关系的研究
短句来源
    Immunohistochemical study was applied to explore clinicopathologic characteristic and behavior and expression of c-erbB-2 oncogene , proliferating cell nuclear antigen(PCNA) and mutant p53 protein in malignant myoepithelioma(MME) of salivary glands .
    本研究采用免疫组化技术探讨癌基因c-erbB-2、增殖细胞抗原(PCNA)与抑癌基因p53在涎腺恶性肌上皮瘤(MME)中的表达与临床病理的特点。
短句来源
    By the ABC enzyme labelling method we studied the microvascular density and proliferating cell ratio in buccal mucosa squamous cell carcimoma (BMSCC) and in normal buccal tissues quantitatively.
    用ABC酶标法定量分析了颊癌内微血管密度和增殖细胞比率,其与正常组织的差别及参考价值。
短句来源
    Objective Todiscuss the relation between microvascular density and proliferating cell ratio in oral squamous cell carcinoma.
    目的 探讨口腔鳞癌血管密度与增殖细胞比率的相关性。
短句来源
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  proliferating cells
    The distribution of proliferating cells, corresponds to the area where the microvascular density is high, mainly in the periphery and basal parts of cancer nests.
    研究结果表明,微血管密度改变和增殖细胞比例变化均反映了肿瘤组织的恶性特征。 增殖细胞分布区域与颊癌内微血管密集增生区域相一致,主要分布在肿瘤周边部和癌巢的基底部;
短句来源
    Results:The distributions of apoptotic cells and proliferating cells were abnormal and their densities significantly increased in epithelium adjacent to carcinoma compared with normal regions;
    结果 :与正常区域相比较 ,癌旁上皮中凋亡细胞及增殖细胞分布异常且细胞密度增高 ;
短句来源
    Tumor areas showed that apoptotic cells decreased and proliferating cells increased significantly.
    肿瘤组织中 ,凋亡细胞明显减少 ,增殖细胞明显增多。
短句来源
    CONCLUSION Significantly increased proliferating cells and their activities are observed in maxilla after suture expansion which implies suture expansion can improve the growth and development of maxilla.
    结论:缝牵张过程中,上颌骨周围骨缝增殖细胞数和活跃程度明显增加,提示缝牵张可促进上颌骨生长发育。
短句来源
  “增殖细胞”译为未确定词的双语例句
    Methods 23 examples of radicular cysts were immunohistochemically analyzed for the distribution of Langerhans, cell and proliferative activity as indicated by positivity for S-100 and Ki-67 respectively.
    方法收集23例经组织病理学确诊的根尖囊肿石蜡标本,分别进行增殖细胞标记Ki-67和郎格罕细胞标记S-100的免疫组化染色,观察根尖囊肿衬里上皮的细胞增殖及其与郎格罕细胞分布的关系。
短句来源
    Methods: Cell culture and cell counts.
    方法:用细胞培养法和增殖细胞记数法。
短句来源
    Methods The expression of Fas,Fas Ligand(FasL),caspase-3 and bcl-2 proteins,as well as cell proliferation marker Ki67,were examined immunohistochemically in 39 ameloblastomas. TUNEL method was used to detect the apoptotic cells in 11 cases.
    方法采用免疫组化方法观察39例经典型成釉细胞瘤中凋亡相关蛋白Fas、Fas配体(Fas Ligand,FasL)、caspase-3和bcl-2及增殖细胞标记Ki67的表达,采用TUNEL法检测11例成釉细胞瘤中的凋亡细胞。
短句来源
    Methods The number of cell proliferation (Ki67) and apoptosis (AI) was observed in 10 normal oral epithelial,48 epithelial dysplasia and 42 SCC by immunohistochemical and TUNEL evaluation.
    方法 采用免疫组织化学S -P法和原位末端标记法检测 10例正常口腔粘膜上皮、48例异常增生上皮和 42例鳞癌组织中增殖细胞数和凋亡数。
短句来源
    The apoptosis index and PCNA count were significantly higher in malignant salivary gland tumors than in pleomorphic adenoma (P<0.05).
    结果 恶性涎腺肿瘤的凋亡细胞指数和增殖细胞指数明显高于多形性腺瘤 (P <0 0 5 )。
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  proliferating cell
Special attention is given to the regulation of excision repair by different proteins-proliferating cell nuclear antigen (PCNA), p53, and proteasome.
      
Synthesis with eukaryotic DNA polymerases α, δ, and ε involves various replication factors, including the replication protein A, replication factor C, proliferating cell nuclear antigen, etc.
      
This is done by forming complexes of polymerase δ or ? with proliferating cell nuclear antigen (PCNA) and replication factors RP-A and RF-C.
      
The endothelium proliferation was evaluated using antibodies to proliferating cell nuclear antigen.
      
The obtained data indicate an important role of cardiomyocyte polyploidy and of activation of the proliferating cell nuclear antigen in development of myocardial hypertrophy in patients with OHCMP.
      
更多          
  proliferating cells
In a culture, the stem cells form spheroids consisting of depigmented and proliferating cells.
      
Different distributions of proliferating cells in retinal pigment epithelium have been revealed in adult amphibians (newt, axolotl, and Xenopus).
      
Proliferating cells were also localized in the ciliary marginal zone of the retina in all studied amphibians, particularly, in the axolotl.
      
An increased pool of proliferating cells in the corneal epithelium was observed both in the affected and intact areas.
      
The phenotypic variabilities of vegetative proliferating cells and those germinated from endospores and cystlike refractory cells were different.
      
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By the ABC enzyme labelling method we studied the microvascular density and proliferating cell ratio in buccal mucosa squamous cell carcimoma (BMSCC) and in normal buccal tissues quantitatively. These two parameters in BMSCC are 208% and 335% ( P <0.05) respectively which are distinctly higher than those of the normal buccal tissues, indicating malignant features of the carcinoma. The distribution of proliferating cells, corresponds to the area where the microvascular density is high, mainly in the periphery...

By the ABC enzyme labelling method we studied the microvascular density and proliferating cell ratio in buccal mucosa squamous cell carcimoma (BMSCC) and in normal buccal tissues quantitatively. These two parameters in BMSCC are 208% and 335% ( P <0.05) respectively which are distinctly higher than those of the normal buccal tissues, indicating malignant features of the carcinoma. The distribution of proliferating cells, corresponds to the area where the microvascular density is high, mainly in the periphery and basal parts of cancer nests. There is a dependent relationship between them, showing a linear positive correlation statistically. The results confirm that angiogenesis and cancer cell proliferation promote each other. They are two important indexes of the local biological behavior of BMSCC and are very important to predict the malignant potential and to evaluate therapeutic effect for BMSCC

用ABC酶标法定量分析了颊癌内微血管密度和增殖细胞比率,其与正常组织的差别及参考价值。颊癌内这二个指标均明显高于正常颊部组织,分别为后者的208%(P<0.05)和335%(P<0.05)。研究结果表明,微血管密度改变和增殖细胞比例变化均反映了肿瘤组织的恶性特征。增殖细胞分布区域与颊癌内微血管密集增生区域相一致,主要分布在肿瘤周边部和癌巢的基底部;二者间存在密切的依存关系,呈直线正相关。经统计学处理,其直线回归方程为Y=20.0801+1.3044X(r=0.9680,P<0.01)。本研究证明颊癌内血管生成与癌细胞增殖相互促进,是颊癌生物学行为表达的二个重要指标,对判断颊癌的发展和疗效评价有重要意义。

Objective In order to study cellular dynamicfeatures in carcinoma and premalignancy originated inepithelial tissue.Methods The golden hamster pouch premalignant model with dimethylbenzanthracence (DMBA) smeared was established by Salley and detected with flow cytometry (FCM) binding to bromodeoxyuridine (BRDU), 30 Syrian golden hamsters were grouped and done contrast study.Results The cellular lesions were aggravated gradually along with extention of smeared...

Objective In order to study cellular dynamicfeatures in carcinoma and premalignancy originated inepithelial tissue.Methods The golden hamster pouch premalignant model with dimethylbenzanthracence (DMBA) smeared was established by Salley and detected with flow cytometry (FCM) binding to bromodeoxyuridine (BRDU), 30 Syrian golden hamsters were grouped and done contrast study.Results The cellular lesions were aggravated gradually along with extention of smeared DMBA microstopically.FCM detective results demonstrated that the detective rate of Sporiod cell between contrast and smeared group had significant difference.Even though mild dysplsia presented microscopically FCM detective result and significant difference.Conclusion The study suggests that golden hamster cheek pouch premalignancy has cellular dynamicfeatures of dysplasia.

目的研究口腔上皮组织癌和癌前病变的细胞动力学变化特征。方法采用Saley的DMBA涂布诱导法,建立金地鼠颊囊癌前病变模型,并用溴脱氧尿苷流式细胞动力学检测方法,对30只叙利亚种金地鼠进行分组对照研究。结果涂药组光镜下的细胞病变程度随涂药时间延长而逐渐加重,而空白对照组无变化;FCM检测显示涂药组与对照组在S期阳性细胞检出率存在显著差异。即使在光镜下表现为轻度不典型增生时,FCM检测结果也有显著差别。结论金地鼠颊囊癌前病变具有细胞异常增殖的细胞动力学特征

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...

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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