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epithelial相关的网络例句

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与 epithelial 相关的网络例句 [注:此内容来源于网络,仅供参考]

However, in 2 cases with intestinal tuberculosis, another chronic inflammatory disease of the large bowel, reticulum cells and countless neutrophilic leucocytes were seen in both cases , and plasma cells , atypical epithelial cells, and multinucleated giant cells in one case, In 7cases with amebic colitis countless neutrophilic leucocytes were seen in 2 cases (28.6%), plasma cells, reticulum cells, atypical epithelial cells, and multinucleated giant cells in one case (14.3%) respectively.

然而,在肠结核(另一种大肠慢性感染疾病)2例中,网状细胞和无数嗜中性白细胞在2例中均可见,浆细胞、网状细胞何多核巨噬细胞仅在1例中可见。在7例变形虫结肠炎中,2例无数嗜中性白细胞可见,浆细胞、网状细胞、不规则上皮细胞和多核巨噬细胞分别在1例中可见。

Special staining methods, such as Masson and the Van Gieson staining were used to study the distribution of collogen fibers and elastic fibers. ResultsBy HE staining, the subepithelial connective tissues and vessels in the pterygium were more prominent than normal conjunctival tissues. An amorphous subepithelial superficial hyalinized zone and coarse eosinophilic granular materials were observed in the pterygia, but they were not found in normal conjunctival specimens. Coarse fibers were visible only in the deeper subepithelial connective tissues of pterygial samples. With Masson′s staining, the dense staining of collagen fibers was also more prominent in the pterygium than in the subepithelial connective tissues of normal conjunctiva. Abnormal collagen fibers were visible in the deeper sub-epithelial connective tissues of pterygial samples. With Van Gieson staining, abnormal collagen fibers were visible in the deeper subepithelial connective tissues. Dark coarse elastic fibers were found in the abnormal fibers only in the subepithelial deep connective tissues of pinguecula in the pterygia but not in the conjunctiva. With immunohistochemistry staining, MMP-3 was strong in the pterygial epithelium, moderate in fibroblast and absent from pterygial vascular walls. LN was strongly expressed in the blood vessel wall, moderately in the epithelial basement membrane and absent from the entire stroma.

结果HE染色:翼状胬肉组织上皮下基质中存在结缔组织的增生和血管形成;基质浅层存在一无定形物质透明区及粗糙的颗粒样嗜酸性物质,在翼状胬肉体部深层基质中存在粗糙的纤维组织;正常球结膜组织细胞排列整齐;基质为疏松结缔组织,胶原纤维平行排列,其间可见成纤维细胞,散在少量中性粒细胞、毛细血管;Masson染色:翼状胬肉浅层基质中存在致密的胶原纤维染色,深层基质中的胶原纤维存在变性样改变;VG染色:翼状胬肉组织深层基质中存在大量变性的胶原纤维,其间夹杂黑色的弹性纤维;免疫组化染色法:MMP-3在翼状胬肉上皮细胞中呈强表达,成纤维细胞中呈中等强度表达,血管内皮细胞中未见表达;LN在血管壁中呈强表达,在上皮细胞基底膜中呈中等强度表达,在整个基质中未见明显表达;col Ⅲ在整个翼状胬肉基质中呈强表达。

The pured mammary epithelial cell line could be obtained by 2~3 passages. 2.Using RPMI1640 containing 10黃, 100IU/ml Penicillin and 100IU/ml Streptomycin as basic media, several different growth factors such as insulin, hydrocortisone, insulin-like growth factor, EGF and so on, were added and selected to culture goat mammary epithelial cells.

以RPMI1640 为基础培养液,山羊乳腺上皮细胞在含血清、双抗的同时,添加氢化考的松、Insulin、IGF-1、E2、EGF 及ITS 的不同组合,以细胞生长群体倍增值为参考标准,评估不同组合的生物活性因子对山羊乳腺上皮细胞生长的影响。

The pured mammary epithelial cell line could be obtained by 2~3 passages. 2.Using RPMI1640 containing 10%FCS, 100IU/ml Penicillin and 100IU/ml Streptomycin as basic media, several different growth factors such as insulin, hydrocortisone, insulin-like growth factor, EGF and so on, were added and selected to culture goat mammary epithelial cells.

以RPMI1640 为基础培养液,山羊乳腺上皮细胞在含血清、双抗的同时,添加氢化考的松、Insulin、IGF-1、E2、EGF 及ITS 的不同组合,以细胞生长群体倍增值为参考标准,评估不同组合的生物活性因子对山羊乳腺上皮细胞生长的影响。

Primary culture of goat mammary gland cells could be derived by outgrowth of migrating cells from fragment of tissue. Fibroblast and epithelial cells could be pured according to their different sensibility to trypsin. Complex cultures treated by 0.25% trypsin in Hanks' for 5~7min at 37℃, the dispersed cells were mainly fibroblasts,then the rest treated by 0.15% trypsin-0.02% EDTA in Hanks'for 5~8min at 37℃, the majority cells harvested were mammary epithelial cells.

用组织块培养法可获得良好的山羊乳腺细胞原代培养物;培养的山羊乳腺成纤维细胞比上皮细胞对胰蛋白酶更敏感,据此可在传代过程中将二者分离纯化,获得纯细胞系;混合培养物先用0.25%胰蛋白酶在37℃消化5~7min 所收集的细胞主要为成纤维细胞;再加0.15%胰蛋白酶-0.02鞹A 消化液在37℃继续消化5~6min 所回收的细胞绝大多数为上皮细胞,经过2~3 代,即可得到纯化的乳腺上皮细胞系。

Primary culture of goat mammary gland cells could be derived by outgrowth of migrating cells from fragment of tissue. Fibroblast and epithelial cells could be pured according to their different sensibility to trypsin. Complex cultures treated by 0.25% trypsin in Hanks' for 5~7min at 37℃, the dispersed cells were mainly fibroblasts,then the rest treated by 0.15% trypsin-0.02% EDTA in Hanks'for 5~8min at 37℃, the majority cells harvested were mammary epithelial cells.

用组织块培养法可获得良好的山羊乳腺细胞原代培养物;培养的山羊乳腺成纤维细胞比上皮细胞对胰蛋白酶更敏感,据此可在传代过程中将二者分离纯化,获得纯细胞系;混合培养物先用0.25%胰蛋白酶在37℃消化5~7min 所收集的细胞主要为成纤维细胞;再加0.15%胰蛋白酶-0.02%EDTA 消化液在37℃继续消化5~6min 所回收的细胞绝大多数为上皮细胞,经过2~3 代,即可得到纯化的乳腺上皮细胞系。

FN have barrier action to tumor cell. Lower or absence of EN expression may play a role to judge prognosis in epithelial carcinoma ovary. Positive of EN expression symptomatize good prognosis in epithelial carcinoma of ovary.

FN对肿瘤细胞有屏障作用,FN表达降低或缺失可作为判定上皮性卵巢癌预后的指标之一,上皮性卵巢癌FN阳性表达是预后较好的指标之一。

FN have barrier action to tumor cell.Lower or absence of FN expression may play a role to judge prognosis in epithelial carcinoma ovary.Positive of FN expression symptomatize good prognosis in epithelial carcinoma of ovary.

FN对肿瘤细胞有屏障作用,FN表达降低或缺失可作为判定上皮性卵巢癌预后的指标之一,上皮性卵巢癌FN阳性表达是预后较好的指标之一。

Effects of Simvastatin on the Transdifferentiation of Renal Tubular Epithelial Cells Induced with High Glucose UANG Xiao-xia,KE Chang-bin,ZHANG Qing-hong,ZHANG Jian-e*(Department of Nephrology;Department of Anesthesia,Taihe Hospital,Yunyang Medical College,Shiyan,Hubei 442000,China)Abstract:Objective To investigate the effects of simvastatin in renal tubular epithelial cells transdifferentiation induced with high glucose.

作者:黄晓霞,柯昌斌,张庆红,张建鄂*作者单位:郧阳医学院附属太和医院肾病内科;麻醉科,湖北十堰 442000 目的:观察辛伐他汀对高糖诱导的肾小管上皮细胞转分化的作用。

Methods Both in vitro and in vivo models of ventilator-induced lung injury were used. Alveolar epithelial cells were stretched in vitro to mimic the lung injury in VILI. Rats were ventilated at large tidal volume to produce ventilator-induced lung injury in vivo. A total of 23 inflammatory cytokines were screened with micro gene array in stretched alveolar epithelial cells.

方法通过呼吸机诱导肺损伤的体内及体外模型,将分离的肺泡上皮细胞于体外拉长,利用基因微阵列技术分析并筛选出上调的炎性细胞因子,之后给予大鼠呼吸机机械通气,留取血清标本,测量这些细胞因子在血清中是否上调。

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