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In reaction-injection moldinga mixture of two or more reactive fluids is forced under high pressure into the mold cavity.Chemical reactions take place in the mold rapidly and the polymer solidifies.Various fibers such as glass,graphite,or boron may also be used to reinforce the materials.Structural foams are also produced by a similar methodusing an inert gasand resin mixture.The product consists of a rigid cellular(closed-cell)structure with a continuous solid skin as muchas 0.080 in.(2mm)in thickness.There are several methods for forming structural foams with density reductions as much as 40% from the solid structure.Because stiffness is proportional to the third power of the thickness of a part,for the same weight of material used,cellular structures are stiffer than solid plastics or metals.

在反应注射成型所夹杂的两个或两个以上的接触过程中,被迫在高压下进入模具cavity.chemical反应发生在模具迅速和聚合物solidifies.various纤维如玻璃,石墨,或硼可能也可以用来加强materials.structural泡沫也产生类似的方法利用惰性气体和树脂mixture.the产品构成的一个硬性蜂窝的结构与连续性固皮肤作为留言Muchas 0.080英寸( 2毫米),在thickness.there有几种方法,形成结构性的泡沫密度减少了四成之多,从固体structure.because刚度成正比第三力量厚度的一部分,为同样重量的使用材料,蜂窝结构更为严厉的比硬塑料或金属。

At the same time, some defects are pointed out: present fabrics are not properly applied, and most of looms can't produce woven perform whose property is similar in different directions. Their shearing strength are lower, utilization of mechanical properties are also smaller;Although three-dimensional braided composites is of excellent integrated structure, normal braided fiber is traveled from internal to external surface, which is passed through braider and becomes three-dimensional structure. If the external surface is cut or rubbed , it's possible for the fiber to break down. In addition , the shape of perform is easily changed after it's finished . To deal with respective shortcomings and highlight their own advantages, we're searching a new weaving method which is the combination between weaving and braiding .

但它们各自也具有许多缺点:目前机织物适应性不够,大多数织机还不能加工三维各向同性的机制预型件,材料剪切性能较低,力学性能利用率低;三维编织复合材料虽然具有良好的结构整体性,但常用的编织都是纤维从内表面穿到外表面,即穿过编织件的断面成三维结构,用这种方法制成的结构,如果外表面受到摩擦或切割损伤,就有可能导致结构的解体,此外编织结构的织物易变形,所以我们需要考虑一种新的结构,能同时发挥各自优势,又能同时克服二者缺点,这就是机织与编织结构相结合的方法。

The periostea of both experimental and control side of the mandibular ramus were taken and prepared, 2 of each 5 rabbits in a group were prepared for HE stain detection and 3 for proliferating cell nuclear antigen immunohistochemical detection.Results:1, The newly formed bone was detected on the lateral aspect of mandibular ramus after periosteal distraction. The bone was shaped like a hill. It looked very low and was full of holes at postoperative day 28. With the time of consolidation period lengthened, the newly formed bone matured gradually. X-ray examination showed the new bone shaped like a hill. The average values of new bone height at postoperative days 28,35,42 and 56 were 1.86 + 0.15mm, 2.29 + 0.29mm,3.19 + 0.13mm and 4.70 + 0.45mm. Histological examination of both HE stain and picricacid-fuchsin stain showed the increase in the number of osteoblasts and the change in the orientation of collagen fibers and bone trabecula. There were no significant differences between newly formed bone and original bone on the lateral aspect of mandibular ramus at postoperative day 56 histologically.2 Compared with the control side, the distracted periostea proliferated obviously under the microscope, and the number of periostealcells increased with satiation of cellular nuclear per unit area. The images of PCNA immunohistochemical stain of periosteum showed that the experimental periosteum proliferated obviously after distraction compared with the control side.

结果:骨膜牵张成骨的实验研究南京医科大学硕{学位论文l、骨膜牵张后,可见下领升支外侧的骨皮质上有新骨形成,新骨呈山峰状凸起,术后第28天的新生骨较低平,多孔隙,随着固定时间的延长,新骨逐渐成熟;下领升支前后向切线位X线投照显示新骨呈山峰样隆起;经测量,术后第28、35、42和56天组平均新生骨厚度分别为x.86士0.15mm、2.29士0.29mm、3.19士0.13mm和4.70 土0.45mm;脱钙骨组织的HE染色和不脱钙骨组织的苦味酸一品红染色的组织学观察均显示了新生骨在成骨细胞数量上的增长,以及胶原纤维和骨小梁排列方向上的变化,术后第56天的新生骨在组织学上与原升支骨组织已无明显区别。2、HE染色显示,与对照组相比较,实验侧骨膜增生明显,细胞间排列紧密,单位面积内骨膜细胞数增多,细胞核饱满;骨膜PCNA 免疫组化染色显示,与对照侧相比较,实验侧骨膜在牵张后出现了明显的增生迹象,PCNA阳性细胞分布紧密,单位面积内阳性细胞数较对照组多,靠近骨表面的骨膜中的阳性细胞数更多而且分布更为紧密。

Methods Employing cholera toxin B-subunit combined horseradish peroxidase retrograde tracing technique and cholera toxin B-subunit combined colloid goldretrograde tracing with calcitonin gene-related peptideimmunohistochemical double-labeled staining technique,the innervation of musculus sacrococcygeus ventralis medialisin rats was studied.

大鼠骶尾腹内侧肌又称荐尾腹侧中肌(musculus sacrococcygeus ventralis medialis)或屈尾短肌,是位于盆腔后壁、骶椎前方的一对梭形肌肉,属尾肌群,因其功能似乎仅为屈尾,故至今尚未引起人们的注意,而与该肌位置关系较密切的会阴肌因在某些运动神经元疾患时仍可保持其正常生理功能而一直受到神经工作者的关注,尤其是近年来有诸多文献报道了会阴肌的神经支配、相关神经元的细胞构筑、神经递质和神经调质的分布以及纤维联系特点[1~10],藉以探讨运动神经元疾病的神经病理学。

In rat esophagus, the positive varicosities and fibres could be observed in the circular muscle layer and the muscularis mucosae layer at 21st day before birth. With the development of rat digestive tract, neurokinin A-immunoreactivity positive nerves could be observed gradually in the epithelium, submucosa, longitudinal muscle layer, myenteric plexus and submucosal plexes, while mature nerve fibres could be seen at one month after birth. 2. In rat stomach, the positive reaction of NKA initially happened in the myenteric plexus at the 14th day of embryo, and then appeared on circular muscles, longitudinal muscles, submucosal, muscularis mucosae, lamina propria and epithelium. 30 days after birth, expression of NKA is same as seen in adaulthood. 3. In rat small intestinal, the NKA-IR could first be found in the myenteric plexus of the duodenum, jejunum and ileum at 14th , 15th and 17th day before birth respectively. Then the NKA-IR occurred in the longitudinal muscle layer, circular muscle layer, intestinal villus, intestinal gland, muscularis mucosae, submucosa, submucosal plexes, mucosa plexus and deep muscular plexus.

结果 1、在食管,于胚胎21天的粘膜肌层和环肌层内观察到神经激肽A免疫阳性膨体纤维,出生后,随幼鼠的生长发育,相继在上皮,粘膜下层,纵肌层、肌间丛、粘膜下丛有NKA-IR表达,30天时已和成年鼠相似;2、在胃,首先于胚胎14天的肌间丛出现NKA-IR的表达,随发育相继在环肌、纵肌,粘膜下层、粘膜肌、固有膜及上皮内出现NKA-IR的表达,30天时具备成年鼠的分布特征;3、在小肠,分别于胚胎14、15、17天的十二指肠、空肠和回肠的肌间丛处出现NKA-IR的表达,随发育相继出现在纵肌、环肌、绒毛、小肠腺周、粘膜肌、粘膜下层、粘膜下丛、粘膜丛、深肌丛。

Production of Creping paper and handchief paper increases very rapidly, which ask for good sopping properties, softness, appearance and strength.what more, the thin paper and straw fiber instead of cotton fiber will be development trend for decreasing cost. Therefore, we do a lot of studies on the raw material, process, equipment and chemicals in order to solve three practical problems. Firstly, decreasing beating degree, shorting beating time and saving energy. Secondly, ensuring papermaking normally and improving productive. Finally, increasing the paper brightness, softness and sopping properties.

皱纹卫生纸和纸巾纸是近来发展较快的生活用纸,由于它们要求具有好的吸水性和柔软度,对纸页的外观和强度也有较高的要求,同时为了降低成本,纸张向薄型化和以草类纤维替代棉纤维的方向发展,因此各厂对使用的原料、工艺、设备、化学助剂等进行了大量的研究,其目的是为了解决在实际生产中存在的三个问题:第一,降低打浆度,缩短打浆时间,节约能源;第二,保证纸张抄造正常,提高纸机生产能力;第三,提高纸张白度、柔软度、吸水性。

Detail Contents: Genetic disorders -- Immune deficiencies -- Breast cancer -- Colon cancer -- Melanoma -- Cystic fibrosis -- Hemophilia -- Liver disease -- Cardiovascular disease -- Muscular dystrophy -- Alzheimer's disease -- Parkinson's disease -- Huntington's disease -- Viruses: the cornerstone of gene therapy -- Viruses are living crystals -- Viral genomes may be RNA or DNA -- Viruses evolved from plasmids -- Viruses know how to infect cells -- The virus as a gene vehicle -- Viruses used in gene therapy -- Ashi DeSilva: a promising start -- Clinical trials defined -- Cells of the immune system -- Adenosine deaminase -- Preliminary research -- Clinical procedure for ADA gene therapy -- The DeSilva clinical trial -- Jesse Gelsinger: down to earth -- Ornithine transcarbamylase -- Preliminary research -- Clinical procedure for OTC gene therapy -- The Gelsinger clinical trial -- The investigation -- Concluding remarks -- Future prospects -- Safer vehicles -- Reducing immune rejection of the vector -- Improved risk assessment -- Redesigning human anatomy and physiology -- Ethics of gene therapy -- The Belmont report -- Clinical trials -- Physiological enhancement -- Cosmetic applications -- Legal issues -- Regulatory agencies -- The Gelsinger legal trial -- International regulation -- Resource center -- Eucaryote cell primer -- Recombinant DNA primer -- The human genome project -- X-linked severe combined immunodeficiency (SCID-X1)-- Alzheimer's disease -- Huntington's disease.

细节内容︰遗传疾病-免疫的缺乏-乳腺癌-结肠癌-黑瘤-囊性纤维变性-血友症-肝疾病-心血管疾病-肌营养不良-早老性痴呆病-帕金森疾病-亨廷顿疾病-病毒︰基础的基因治疗-病毒在活著水晶--病毒的基因可能是RNA或者DNA --病毒从plasmids被逐步形成--病毒知道怎样感染细胞--作为一辆基因车辆的病毒--基因治疗使用的病毒-Ashi DeSilva︰有希望开始-临床试验确定--细胞的这免疫系统-Adenosine deaminase-初步研究-临床程式给埃达基因治疗--这DeSilva临床试验-婕西Gelsinger︰到地球-Ornithine transcarbamylase-初步研究-临床程式给OTC基因治疗-- Gelsinger临床试验-调查-达成评论-前景-更安全的车辆--矢量的降低免疫的拒绝-改进风险估计-重新设计人解剖学和生理学--伦理学的基因治疗-那些贝拉蒙特报告-临床试验-生理提升-美容应用-法律问题-协调机构-- Gelsinger 合法审讯-国际管理-资源中心人物-Eucaryote信元第一-Recombinant DNA 入门--人类基因工程-- X 连结的严重的结合的免疫缺陷(SCID-X1)-早老性痴呆病--亨廷顿的疾病。

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