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Results: In the 120 cases, posterior nasal drip syndrome was found in 47 cases, acidophile bronchitis and cough variability asthma in 32 cases, gastroesophageal reflux diseases in 35 cases, hysteria in 2 cases and unknown cause in 4 cases.

结果:鼻后滴漏综合征47例,嗜酸细胞性支气管炎及咳嗽变异型哮喘32例,胃食管反流性咳嗽35例,癔病性病因2例,原因不明4例。98例患者3 7?

Results: In the 120 cases, posterior nasal drip syndrome was found in 47 cases, acidophile bronchitis and cough variability asthma in 32 cases, gastroesophageal reflux diseases in 35 cases, hysteria in 2 cases and unknown cause in 4 cases. After treatment, 98 cases were greatly improved in 3-7days, 106 patients felt obviously improved in 2 weeks, and 106 cases stopped taking medicine 1 week after the symptoms vanished.

结果:鼻后滴漏综合征47例,嗜酸细胞性支气管炎及咳嗽变异型哮喘32例,胃食管反流性咳嗽35例,癔病性病因2例,原因不明4例。98例患者3~7d内咳嗽明显好转,106例2周内自觉咳嗽明显好转,106例患者于咳嗽消失1周后停药,14例转入儿科及心理科。

Methods Tissue arrayer was used to create a 252-dot tissue microarray, consisting of 84 cases of malignant lymphomas arising in esophagus, stomach, intestines, thyroid, saliva gland , orbital cavity and lung, Seven cases of diffuse large B cell lymphomas,9 adenocarcinomas, 1 neuroendocrine tumor,1 squamous carcinoma, 6 T-cell lymphomas and 18 reactive lymphoid nodes were also included as control in the microarray.

建立包含84例MALT型淋巴瘤、7例弥漫性大B细胞淋巴瘤、9例腺癌、1例神经内分泌肿瘤、1例鳞癌、6例T细胞性非何杰金淋巴瘤和18例正常淋巴结共252点阵的组织芯片,应用免疫组织化学检测Ki-67、TopoⅡα、p53、Bcl-2、Bax、C-myc和Bcl-10在MALT型淋巴瘤中的表达情况。

There are three types of jaundice in adults and older children: haemolytic jaundice, hepatocellular jaundice and obstructive jaundice.

有三种类型的性黄疸在成人和年龄较大的儿童:溶血性黄疸,肝细胞性黄疸及梗阻性黄疸。

FUNGI Fungi are almost entirely multicellular, heterotrophic (deriving their energy from another organism, whether alive or dead), and usually having some cells with two nuclei multinucleate, as opposed to the more common one, or uninucleate per cell.

FUNGI Fungi是几乎完全地多细胞性,异养(获得他们的能量从另一个有机体,是否活或死)和通常有与二个中坚力量的有些细胞多核,与更加共同一个相对或者单核每个细胞。

During the development of dental germ, enamel matrix proteins secreted by epithelial root sheath could induce dental follicle cells to differentiate towards cementoblast and form acellular cementum finally on the surface of tooth root. Many researches of domestic and oversea scholars suggest that enamel matrix proteins could effectively induce periodontal regeneration, and the structure and function of this regenerated tissue are similar to healthy periodontal tissue. Moreover, the regeneration process is nearly the same to that of embryonic development of periodontal tissue.

自发现釉基质蛋白可诱使牙囊细胞向成牙骨质细胞方向分化并在根表面形成无细胞性牙骨质以来,国内外学者做了大量研究,结果表明釉基质蛋白能有效诱导牙周组织的再生,且这种再生组织的结构和功能更接近于健康的牙周组织,并且再生过程也与牙周组织的胚胎发育过程类似。

While symptoms may seem to improve almost immediately after surgery, it takes approximately 6-12 months before new vessels develop sufficiently. Diseases associated with moyamoya include sickle cell anemia, atherosclerosis, prior radiation therapy to the skull base in children, and less commonly neurofibromatosis, tuberous sclerosis, meningitis, retinitis pigmentosa, fibromuscular dysplasia, Down's syndrome and Fanconi's anemia.

手术之后几乎立即可以看到症状的好转,新的血供充分发展起来大概要花6-12月时间。moyamoya相关的疾病包括镰状细胞性贫血、动脉粥样硬化、颅底部放疗,不太常见的有神经纤维瘤病,结节性硬化、脑膜炎、色素性视网膜炎、纤维性肌发育不良、Down氏综合症和Fanconi's 贫血症

All of these patients underwent plain and contrast-enhancement CT scan. Results: Thirteen cases included 5 neurilemmomas (3 malignant cases included), 5 neurofibromas, 1 neuroblastoma, 1 ganglioneuroma, 1 malignant paraganglioma. In the 13 cases, 2 cases derived from plexus sacralis, 2 cases located in the pelvic peritoneal space, 6 cases located in the pelvic extrapentoneal space, and 3 cases located in the vesica extraperitoneal space.

结果:神经鞘瘤5例(其中恶性3例),神经纤维瘤5例,神经母细胞瘤1例,节细胞性神经瘤1例,恶性副节细胞瘤1例。2例起源于骶丛,经由骶孔向盆腔内生长;2例起源于盆腔,其中1例源于膀胱,1例位于膀胱直肠陷窝;直肠腹膜外间隙6例;膀胱腹膜外间隙3例。

Two cases of MFL also showed polypoid or nodular. It was composed of centrocytic/centroblastic cells.(4) Large multilobated nuclei lymphomas were seen in two cases.(5)Histiocytic in three cases.

MFL 2例亦呈息肉样或形成肿块,由中心细胞和中心母细胞组成,(4)大多叶核淋巴瘤2例,(5)组织细胞性3例。

Stupp R, Mason WP, van den Bent MJ, et al: Concomitant and adjuvant temozolomide and radiotherapy for newly diagnosed glioblastoma multiforme: conclusive results of a randomized phase III trial by the EORTC Brain and RT Groups and YCIC Clinical Trials Group.

星形细胞瘤则为5~10年。毛细胞性星形细胞瘤则为正常寿命。许多脑膜瘤[1]和垂体腺瘤[2]的病人一直没有症状。这些肿瘤被偶然发现,或在死于其它疾病后尸检发现肿瘤。

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