基于多系统综合控制的车辆侧翻稳定性研究

为提高车辆抗侧翻能力减小其侧翻的危险性，建立了11自由度整车侧翻模型。根据各系统侧翻控制权重及有效作用范围，提出一种基于转向、悬架和制动的多系统侧翻控制策略并设计了相关控制器。对系统单独控制及综合控制进行了仿真对比分析。结果表明，综合控制策略在提高车辆抗侧翻能力的同时也很好的改善了车辆侧向稳定性。     

高温变形过程中的动态再结晶类型识别

通过分析高温变形过程中伴随再结晶晶粒长大的内部位错密度变化,判别不同变形条件下动态再结晶过程的进行形式,研究动态再结晶形式对变形参数的依赖规律,发现：低温大应变速率下,高温变形过程中的再结晶形式以连续性动态再结晶为主;高温低应变速率下,以周期性动态再结晶为主.根据动态再结晶软化与加工硬化平衡,得到反映稳态流动时钛合金流动应力对变形参数的响应,建立具有实际物理意义描述钛合金稳态流动本构关系的Arrhenius型方程.通过热模拟压缩实验得到800~900℃,0.0005~10 s-1条件下的TC18钛合金高温变形流动应力应变曲线,验证动态再结晶形式的判据模型,并通过DMM耗散效率分布图分析模型的适用性.通过显微组织分析,研究不同变形参数下的高温变形过程中,不同动态再结晶形式对应的再结晶晶粒粗化/细化的特点.通过各变形条件下真应变？=0.8时的稳态应力验证得到的本构模型,并分析应变速率敏感系数的变化规律.     

Mitochondrial defects and hearing loss

The techniques of human molecular genetics have been rapidly applied to the study of hearing loss. These studies have implicated more than 60 loci as causes of nonsyndromic hearing loss. Mutations at more than a dozen nuclear genes have been demonstrated to cause hearing loss, and these have been covered in recent reviews. However, a perhaps unexpected feature of the molecular characterization of human hearing loss has been the occurrence of mutations in the mitochondrial DNA (mtDNA). The importance of mitochondrial function in hearing is emphasized by the recent discovery of mutations in a nuclear-encoded mitochondrial protein which results in hearing loss. This article reviews the current status of our knowledge of mtDNA mutations that have been shown to cause hearing loss, and the suggestion of potential molecular, cellular and tissue-specific pathophysiological mechanisms by which dysfunction of mitochondria may lead to a loss of hearing.     

Ein Beitrag zur Kenntnis von Lanatosid D

Summary A preparative method for the isolation of lanatoside D has been developed, and fundamental pharmacological characteristics of the pure compound have been established.The genuine glycoside has been converted to desacetyllanatoside D.     

The urokinase receptor and integrins in cancer progression

Enhanced levels of expression of urokinase receptor (uPAR) and certain integrins have been linked to cancer cell progression. This has classically been attributed to matrix degradation via the activation of the urokinase (uPA)/plasmin system and modulation of cell motility and survival through integrin engagement. More recently, uPAR has been shown to play multiple roles independent of protease activity. Specifically, uPAR has been shown to be intimately involved in the regulation of cell adhesion, migration and proliferation in part through interactions with other membrane partners, including integrins. The goal of this review is to summarize recent insights in the function of uPAR/integrin interactions, to provide a framework for understanding the importance of these interactions in the context of cancer, and to highlight its potential as a target for therapeutic intervention.     

Structural genomics for membrane proteins

Structure-based drug discovery has proven useful in improving and shortening the drug development process. The approach of structural genomics to study a large number of targets in parallel has been commonly applied to protein families and even whole genomes. Paradoxically, although membrane proteins represent the largest type of drug targets, up to 70% today, determination of their structure has been modest compared to that of soluble proteins. Because membrane proteins are important for drug discovery an emphasis has been placed on developing technologies and methods to determine membrane protein structures. Several structural genomics initiatives have been established, focusing on the structural biology of membrane proteins. Received 31 May 2006; received after revision 5 July 2006; accepted 9 August 2006     

Strategies for the inhibition of serine proteases

Serine proteases have been shown to play a multifarious role in health and disease. As a result, there has been considerable interest in the design and development of synthetic inhibitors of these enzymes. In view of their diverse roles in biological processing events, one of the great challenges in such endeavours has been the need to produce compounds with exquisite selectivity. Inhibitor design has been broadly guided by the use of either peptide- or heterocyclic-based compounds, designed to exploit the known substrate specificity characteristics of individual enzymes. This review describes the thinking and strategies employed in such efforts. Received 8 August 2000; received after revision 16 November 2000; accepted 17 November 2000     

Crustacean neuropeptides: structures, functions and comparative aspects.

In this article, an attempt is made to review the presently known, completely identified crustacean neuropeptides with regard to structure, function and distribution. Probably the most important progress has been made in the elucidation of a novel family of large peptides from the X-organ-sinus gland system which includes crustacean hyperglycemic hormone (CHH), putative molt-inhibiting hormone (MIH) and vitellogenesis (= gonad)-inhibiting hormone (VIH). These peptides have so far only been found in crustaceans. Renewed interest in the neurohemal pericardial organs has led to the identification of a number of cardioactive/myotropic neuropeptides, some of them unique to crustaceans. Important contributions have been made by immunocytochemical mapping of peptidergic neurons in the nervous system, which has provided evidence for a multiple role of several neuropeptides as neurohormones on the one hand and as local transmitters or modulators on the other. This has been corroborated by physiological studies. The long-known chromatophore-regulating hormones, red pigment concentrating hormone (RPCH) and pigment-dispending hormone (PDH), have been placed in a broader perspective by the demonstration of an additional role as local neuromodulators. The scope of crustacean neuropeptide research has thus been broadened considerably during the last years.     

Characterization and antithrombotic action of tissue plasminogen activator

An extractive fibrinolytic enzyme has been characterized and found to belong to the class of vascular plasminogen activators. The agent has been found to have an antithrombotic action in the rabbit.     

Fahraeus effect and Fahraeus-Lindqvist effect]

A series of experiments has been carried out on the flowing of suspended human erythrocytes into glass-tubes whose diameters varied between 30 mum and 1 mm. Thus, the Fahraeus and Fahraeus-Lindqvist effects emergence fields have been drawn, and it has been shown that, contrary to a widely admitted hypothesis, the Fahraeus effect does not account for the Fahraeus-Lindqvist effect.     

String theory and general methodology: A mutual evaluation

String theory has been the dominating research field in theoretical physics during the last decades. Despite the considerable time elapse, no new testable predictions have been derived by string theorists and it is understandable that doubts have been voiced. Some people have argued that it is time to give up since testability is wanting. But the majority has not been convinced and they continue to believe that string theory is the right way to go. This situation is interesting for philosophy of science since it highlights several of our central issues. In this paper we will discuss string theory from a number of different perspectives in general methodology. We will also relate the realism/antirealism debate to the current status of string theory. Our goal is two-fold; both to take a look at string theory from philosophical perspectives and to use string theory as a test case for some philosophical issues.     

Chromosome 17-linked dementias

Chromosome 17-linked dementias have been defined by linkage analysis. The most common of these syndromes has been estimated to be the cause of between 2 and 20% of all dementia and has alternately been called frontotemporal dementia, Pick's disease (without Pick bodies) and dementia lacking distinctive features [1 – 3]. The identification of the mutation responsible for these conditions in a group of clinically and pathologically heterogeneous disorders may allow us to gain broad insight into the processes of neurodegeneration.     

Crustacean neuropeptides: Structures,functions and comparative aspects

In this article, an attempt is made to review the presently known, completely identified crustacean neuropeptides with regard to structure, function and distribution. Probably the most important progress has been made in the elucidation of a novel family of large peptides from the X-organ-sinus gland system which includes crustacean hyperglycemic hormone (CHH), putative molt-inhibiting hormone (MIH) and vitellogenesis (=gonad)-inhibiting hormone (VIH). These peptides have so far only been found in crustaceans. Renewed interest in the neurohemal pericardial organs has led to the identification of a number of cardioactive/myotropic neuropeptides, some of them. unique to crustaceans. Important contributions have been made by immunocytochemical mapping of peptidergic neurons in the nervous system, which has provided evidence for a multiple role of several neuropeptides as neurohormones on the one hand and as local transmitters or modulators on the other. This has been corroborated by physiological studies. The long-known chromatophore-regulating hormones, red pigment concentrating hormone (RPCH) and pigment-dispending hormone (PDH), have been placed in a broader perspective by the demonstration of an additional role as local neuromodulators. The scope of crustacean neuropeptide research has thus been broadened considerably during the last years.     

Functional investigations of exercising muscle: a noninvasive magnetic resonance spectroscopy-magnetic resonance imaging approach

Muscle fatigue, which is defined as the decline in muscle performance during exercise, may occur at different sites along the pathway from the central nervous system through to the intramuscular contractile machinery. Historically, both impairment of neuromuscular transmission and peripheral alterations within the muscle have been proposed as causative factors of fatigue development. However, according to more recent studies, muscle energetics play a key role in this process. Intramyoplasmic accumulation of inorganic phosphate (P_i) and limitation in ATP availability have been frequently evoked as the main mechanisms leading to fatigue. Although attractive, these hypotheses have been elaborated on the basis of experimental results obtained in vitro, and their physiological relevance has never been clearly demonstrated in vivo. In that context, noninvasive methods such as 31-phosphorus magnetic resonance spectroscopy and surface electromyography have been employed to understand both metabolic and electrical aspects of muscle fatigue under physiological conditions. Mapping of muscles activated during exercise is another interesting issue which can be addressed using magnetic resonance imaging (MRI). Exercise-induced T2 changes have been used in order to locate activated muscles and also as a quantitative index of exercise intensity. The main results related to both issues, i.e. the metabolic and electrical aspects of fatigue and the MRI functional investigation of exercising muscle, are discussed in the present review.Received 4 September 2003; received after revision 4 December 2003; accepted 22 December 2003     

蓄压式燃气发生器内弹道分析与预计

针对我国姿态控制和轨道控制液体火箭发动机推进荆输送系统，围绕蓄压式燃气发生器内弹道预计开展研究。探讨了喷管在超临界状态和亚临界状态下其内部燃气流动的变化规律；分析了燃气发生器工作结束后在对流换热和稳态导热条件下燃气发生器和储气瓶内高温燃气与外界环境的换热过程；编写了内弹道计算程序，在试验论证的基础上，表明该程序可初步预计蓄压式燃气发生器内弹道性能。     

Primordial chemistry and enzyme evolution in a hot environment

Ever since the publication of Darwin’s Origin of Species, questions have been raised about whether enough time has elapsed for living organisms to have reached their present level of complexity by mutation and natural selection. More recently, it has become apparent that life originated very early in Earth’s history, and there has been controversy as to whether life originated in a hot or cold environment. This review describes evidence that rising temperature accelerates slow reactions disproportionately, and to a much greater extent than has been generally recognized. Thus, the time that would have been required for primordial chemistry to become established would have been abbreviated profoundly at high temperatures. Moreover, if the catalytic effect of a primitive enzyme (like that of modern enzymes) were to reduce a reaction’s heat of activation, then the rate enhancement that it produced would have increased as the surroundings cooled, quite aside from changes arising from mutation (which is itself highly sensitive to temperature). Some nonenzymatic catalysts of slow reactions, including PLP as a catalyst of amino acid decarboxylation, and the Ce^IV ion as a catalyst of phosphate ester hydrolysis, have been shown to meet that criterion. The work reviewed here suggests that elevated temperatures collapsed the time required for early evolution on Earth, furnishing an appropriate setting for exploring the vast range of chemical possibilities and for the rapid evolution of enzymes from primitive catalysts.     

Radioautographic analysis of retinofugal projections in the primitive bony fish Polypterus senegalus C.]

Retinofugal pathways of Polypterus senegalus C. have been examined by means of the radioautographic method. Contralaterally the retina projects to the hypothalamus, thalamus, pretectum and tectum. An important ipsilateral component has been observed. No retinal projection to the mesencephalic tegmentum has been identified. Comparing the primary optic system of Polypterus with that of other body Fish, indicates that this species possesses a combination of characteristics which are both actinopterygian and sarcopterygian. The significance of this mozaic arrangement is discussed.     

Somatic chromosomes of Indian burrowing toad,Uperodon globulosum (Gunther) (Anura; Amphibia)

Summary Somatic chromosome complements of the Indian burrowing toad,Uperodon globulosum, have been described for the first time. The 2n number is 26 (NF=52) in both the sexes. No heteromorphism in relation to sex chromosome pair has been recorded. Deviations from 2n number (2n=10–28) have been noticed in the cells of different specimens. The result has been compared withU. systoma.Acknowledgment. Sincere thanks are due to Prof. P. K. Ghosh, Hooghly Mohsin College and to Dr A. K. Roy of the same college for encouragement. Thanks are due to Mr Bipul Kumar Das for his help during collection of specimen.     

Molecular parasitology: progress towards the development of vaccines for malaria, filariasis, and schistosomiasis

Advances in molecular biology have allowed for the identification of potential vaccine candidates against several parasitic diseases. Antigens from various life stages of Plasmodium and Schistosoma species and filarial worms have been cloned, sequenced and tested as vaccines. Results to date in animal models have been promising. Modest levels of protection against experimental human malaria have been obtained using both sporozoite and blood-stage antigens. However, a greater understanding of the mechanisms which lead to immunity against parasites is required before effective vaccines can be developed.