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101.
This paper is concerned with a SIR model with saturated and periodic incidence rate and saturated treatment function. By using differential inequality technique, we employ a novel argument to show that the disease‐free equilibrium is globally exponentially stable. The obtained results improve and supplement existing ones. We also use numerical simulations to demonstrate our theoretical results. Copyright © 2015 John Wiley & Sons, Ltd.  相似文献   
102.
In the last 10 years, mesenchymal stem cells (MSCs) have emerged as a therapeutic approach to regenerative medicine, cancer, autoimmune diseases, and many more due to their potential to differentiate into various tissues, to repair damaged tissues and organs, and also for their immunomodulatory properties. Findings in vitro and in vivo have demonstrated immune regulatory function of MSCs and have facilitated their application in clinical trials, such as those of autoimmune diseases and chronic inflammatory diseases. There has been an increasing interest in the role of MSCs in allogeneic hematopoietic stem cell transplantation (HSCT), including hematopoietic stem cell engraftment and the prevention and treatment of graft-versus-host disease (GVHD), and their therapeutic potential has been reported in numerous clinical trials. Although the safety of clinical application of MSCs is established, further modifications to improve their efficacy are required. In this review, we summarize advances in the potential use of MSCs in HSCT. In addition, we discuss their use in clinical trials of the treatment of GVHD following HSCT, the immunomodulatory capacity of MSCs, and their regenerative and therapeutic potential in the field of HSCT.  相似文献   
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The amorphous aggregation of Aβ1‐40 peptide is addressed by using micromolding in capillaries. Both the morphology and the size of the aggregates are modulated by changing the contact angle of the sub‐micrometric channel walls. Upon decreasing the hydrophilicity of the channels, the aggregates change their morphology from small aligned drops to discontinuous lines, thereby keeping their amorphous structure. Aβ1‐40 fibrils are observed at high contact angles.  相似文献   
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The modelling of the spread of infectious disease is carried out for time t on a measure chain T. Our approach unifies the continuous case and the discrete case . The model is described by the integral equation
where x(t) represents the proportion of the population infected at time t, f(t,x(t)) denotes the proportion of the population newly infected per unit time, and τ is the length of time an individual remains infectious. Using the measure chain calculus, we shall develop criteria for the existence of a nontrivial and nonnegative periodic solution for the modelling equation. The criteria can be implemented numerically, for this we shall give an algorithm as well as illustrative examples.  相似文献   
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锌与疾病关系的探讨   总被引:8,自引:2,他引:6  
综述了锌与健康的关系,包括:锌的代谢,锌的主要功能,锌与疾病治疗等方面,参考文献16篇。  相似文献   
110.
This article reports the design and construction of a multiple-epitope foot and mouth disease virus (FMDV) antigen, designated as OAAT. This recombinant antigen consists of the structural protein VP1 genes from serotypes A and O FMDV, five major VP1 immunodominant epitopes from two genotypes of Asial serotype, and three Th2 epitopes originating from the nonstructural protein, three ABC gene and structural protein VP4 gene. Expressions of target gene from these plasmids in HeLa cells were verified by Western-blot. BALB/c mice were immunized intramuscularly with the DNA vaccines thrice every two weeks. We found that pA could induce simultaneously specific antibodies against serotypes A, Asial, and O FMDV. Compared to those of the controls, the spots of FMDV-specific IFN-7 and cytotoxic activity from mice immunized with pA were significantly increased, pA provided full protection in 2/4 guinea pigs from challenge with FMDV O/NY00 and Asial/YNBS/58, respectively. The results show that although pA did not give full protection in 100% immunized guinea pigs from challenge with type O and Asial FMDV, respectively, OAAT may be potential immunogen against FMDV and pA may be potential DNA vaccines against FMDV.  相似文献   
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