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All of the families were white and from the United States, Canada or England, and they all had at least two members with generalized vitiligo and at least one with another autoimmune disease (autoimmune thyroid disease, latent autoimmune diabetes in adults, rheumatoid arthritis, psoriasis, pernicious anemia, systemic lupus erythematosus or Addison's disease). Investigators at St.

所有的家庭都是来自美国、加拿大或英国的白人家庭,这些家庭中至少有两名成员患有白癜风典型症状,并且至少有一名成员患有另外一种自身免疫性疾病(如:自身免疫性甲状腺疾病,潜伏性自身免疫性糖尿病的成人,类风湿关节炎,牛皮癣,恶性贫血,系统性红斑狼疮或艾迪生氏病)。

Using the theories of probability, algebra and spectral theory comprehensively, we investigate some related characteristics of logic functions in cryptography: Firstly, we introduce m order generalized s - correlation immunity of Boolean vector functions and prove that the higher order generalized ε- correlation immunity can guarantee the lower order generalized ε- correlation immunity. Then by applying decomposition formula of joint distribution of Boolean random vectors, we give a spectrum criterion of m order generalized e - correlation immunity of Boolean vector functions. Furthermore, we show that the algebraic degree of m order generalized e - correlation immune Boolean vector functions is not restricted by the correlation immune orders.

本文主要运用概率论的思想和方法,并结合代数学和频谱理论的相关知识,对密码学中逻辑函数的有关性质进行了研究,主要包括以下三个方面的内容:首先,对布尔向量函数的相关免疫性进行了拓展,给出了k维布尔向量函数m阶广义ε-相关免疫的概念,证明了布尔向量函数的高阶广义ε-相关免疫性蕴含低阶广义ε-相关免疫性,并根据布尔随机向量联合分布分解式得到了布尔向量函数m阶广义ε-相关免疫的一个谱判别条件,还说明了m阶广义ε-相关免疫布尔向量函数的代数次数不受相关免疫阶数的制约。

These diseases can occur together in defined syndromes with distinct pathophysiology and characteristics: autoimmune polyendocrine syndrome I, autoimmune polyendocrine syndrome II, and the immunodysregulation polyendocrinopathy enteropathy X-linked syndrome.

这些疾病可以与一些有不同病生理和特征的确定的综合症一起发生:多发性自身免疫性内分泌综合征1型,多发性自身免疫性内分泌综合征2型,免疫调节不能性多发性内分泌腺X-连锁肠病综合征。

The Pathological changes of immune vasculitis were analyzed by hematoxylin and eosin staining, elastic fibers staining and electron microscopy.

目的 分析丹参酮ⅡA对免疫性血管炎、血小板及凝血活性的影响,探讨其抗血小板、抗凝及降低免疫性血管炎炎症反应的机理。

Results Among 234 cases,38 patients (16.2%) had complicated with autoimmune diseases,which usually were rheumatoid arthritis (31.6%) and ulcerative colitis (26.3%). The rate of transforming to leucocythemia in MDS patients complicated with autoimmune disease is not more than that in MDS patients without autoimmune disease,but the median lifetime decreased.

结果 234例MDS患者中38例并发自身免疫性疾病,占162%;MDS并发自身免疫性疾病以类风湿关节炎(316%)和溃疡性结肠炎(263%)常见;MDS并发自身免疫性疾病者比无自身免疫性疾病者其转白率并不增加,但中位生存期缩短。

METHODS: Three different MBP peptides(MBP68 86, 87 99, and the non encephalitogenic peptide 110 128) were synthesized and administrated nasally to Lewis rat on day 11, 10, 9, 8 and 7 prior to immunization with the guinea pig MBP + CFA, which was used to induce EAE.

实验性自身免疫性脑脊髓炎(experimental autoimmune encephalomyelitis, EAE)是一种可致中枢神经系统瘫痪的自身免疫性疾病,为人类多发性硬化(multiple sclerosis, MS)的实验动物模型。

Thymus and autoimmunity: production of CD4+CD25+ naturally anergic and suppressive T cell as a key funtion of the thymus in maintaining immunologic selftolerance.

在人、大鼠和小鼠中有大约3%-10%的CD4+CD8-单阳性胸腺细胞共表达CD25表面分子,这些细胞能够阻止包括自身免疫性胃炎、自身免疫性小肠炎和自身免疫性糖尿病等在内的多种自身免疫性疾病的形成和发展[8-10]。

Especially, the nonlinearity bounds of functions with balancedness, with correlation-immunity, or with balanced correlation-immunity are discussed respectively. Using the relationship between nonlinearity and the order of correlation-immune, one upper bound of nonlinearity of correlation-immune functions is obtained.

尤其对满足平衡性、相关免疫性和同时满足平衡相关免疫性函数的非线性度的界分别进行了研究,利用非线性度和相关免疫阶之间的关系,给出相关免疫函数非线性度的一种新的上界。

Immune thrombocytopenic purpura is an autoimmune disorder characteriezed by a low platelet count and mucocutaneous bleeding. Some research shows that the cytokines network disorder result from the abnormal level of cytokine play an important role in the pathogenesis of ITP.

免疫性血小板减少性紫癜是一种以血小板减少和皮肤粘膜出血为特征的自身免疫性疾病,研究表明细胞因子水平的异常导致的细胞因子网络失衡在ITP发病中具有重要作用。

For raising the accuracy of the diagnasis ancl treatinemt of ALH We realised of 86 patients with diagnosis of Autoimmune liver disease, strictly defined by the criteria for diagnosis of autoimmune hepatitis or the results of liver histology, and tested its biochemical, serological, histological results. AIH patients were main women female 75 cases, male 11 cases, main in 40 - 60 years old ,AIH characterized by a flare of ALT, AST, elevated immunoglobulin G,γ-immunoglobulin: ALP, IgG, and presence of antinuclear antibody (81.5%); moderate or severe periportal or periseptal lymphocytic piecemeal necrosis.

为提高对自身免疫性肝炎的诊治水平,采用国际自身免疫性肝炎小组新修订的描述性诊断标准和计分系统,对符合诊断的患者进行临床、生化、病理特点分析。86例AIH患者,女75例,男11例,高发年龄为40~60岁,其中Ⅰ型80例(93.020k),Ⅱ型3例(3.49%);Ⅲ型3例(3.49%);肝功能生化检查表现为肝炎样改变;实验室检查主要表现为高γ球蛋白血症,高IgG、ALP、γ-GT及甘油三酯增高,81.5%患者抗核抗体阳性:病理改变以界板性肝炎,浆细胞浸润为主,78%的患者对免疫抑制剂治疗效佳。

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然而,要让一个真正的引用,你需要提供详细的个人和财务信息。