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81.
以研究不连续面的变形特性为目的,采用双曲线函数作为描迷不连续面剪切位移曲线的本构式,讨论了表征剪切位移曲线形态的关键因素,即:公式中的系数A,B.根据系数A,B的物理意义,分析了它们与垂直应力比、不连续面的起伏角i以及不连续面的剪切面积之间的关系.同时,又将双曲线函数的模拟曲线与试验曲线进行了比较.由于模拟曲线能较为正确地描述初始剪切刚度以及峰值剪应力,使它能较为理想地表现剪切位移曲线,进而使该定量的评价方法具有实际的使用价值. 相似文献
82.
Summary In the rabbit jejunum, the elevation of temperature within the range of 25–37°C diminished the sensitivity to noradrenaline (NA) for both the relaxation and amplitude inhibition. The relaxation by NA was mainly mediated via adrenergic -receptors at 25, 30 or 37°C. The amplitude inhibition was mediated via -receptors at 37°C, and both - and -receptors at 30 or 25°C. 相似文献
83.
84.
Loss of the autophagy protein Atg16L1 enhances endotoxin-induced IL-1beta production 总被引:1,自引:0,他引:1
Saitoh T Fujita N Jang MH Uematsu S Yang BG Satoh T Omori H Noda T Yamamoto N Komatsu M Tanaka K Kawai T Tsujimura T Takeuchi O Yoshimori T Akira S 《Nature》2008,456(7219):264-268
Systems for protein degradation are essential for tight control of the inflammatory immune response. Autophagy, a bulk degradation system that delivers cytoplasmic constituents into autolysosomes, controls degradation of long-lived proteins, insoluble protein aggregates and invading microbes, and is suggested to be involved in the regulation of inflammation. However, the mechanism underlying the regulation of inflammatory response by autophagy is poorly understood. Here we show that Atg16L1 (autophagy-related 16-like 1), which is implicated in Crohn's disease, regulates endotoxin-induced inflammasome activation in mice. Atg16L1-deficiency disrupts the recruitment of the Atg12-Atg5 conjugate to the isolation membrane, resulting in a loss of microtubule-associated protein 1 light chain 3 (LC3) conjugation to phosphatidylethanolamine. Consequently, both autophagosome formation and degradation of long-lived proteins are severely impaired in Atg16L1-deficient cells. Following stimulation with lipopolysaccharide, a ligand for Toll-like receptor 4 (refs 8, 9), Atg16L1-deficient macrophages produce high amounts of the inflammatory cytokines IL-1beta and IL-18. In lipopolysaccharide-stimulated macrophages, Atg16L1-deficiency causes Toll/IL-1 receptor domain-containing adaptor inducing IFN-beta (TRIF)-dependent activation of caspase-1, leading to increased production of IL-1beta. Mice lacking Atg16L1 in haematopoietic cells are highly susceptible to dextran sulphate sodium-induced acute colitis, which is alleviated by injection of anti-IL-1beta and IL-18 antibodies, indicating the importance of Atg16L1 in the suppression of intestinal inflammation. These results demonstrate that Atg16L1 is an essential component of the autophagic machinery responsible for control of the endotoxin-induced inflammatory immune response. 相似文献
85.
Galagan JE Calvo SE Cuomo C Ma LJ Wortman JR Batzoglou S Lee SI Baştürkmen M Spevak CC Clutterbuck J Kapitonov V Jurka J Scazzocchio C Farman M Butler J Purcell S Harris S Braus GH Draht O Busch S D'Enfert C Bouchier C Goldman GH Bell-Pedersen D Griffiths-Jones S Doonan JH Yu J Vienken K Pain A Freitag M Selker EU Archer DB Peñalva MA Oakley BR Momany M Tanaka T Kumagai T Asai K Machida M Nierman WC Denning DW Caddick M Hynes M Paoletti M Fischer R Miller B Dyer P Sachs MS Osmani SA Birren BW 《Nature》2005,438(7071):1105-1115
The aspergilli comprise a diverse group of filamentous fungi spanning over 200 million years of evolution. Here we report the genome sequence of the model organism Aspergillus nidulans, and a comparative study with Aspergillus fumigatus, a serious human pathogen, and Aspergillus oryzae, used in the production of sake, miso and soy sauce. Our analysis of genome structure provided a quantitative evaluation of forces driving long-term eukaryotic genome evolution. It also led to an experimentally validated model of mating-type locus evolution, suggesting the potential for sexual reproduction in A. fumigatus and A. oryzae. Our analysis of sequence conservation revealed over 5,000 non-coding regions actively conserved across all three species. Within these regions, we identified potential functional elements including a previously uncharacterized TPP riboswitch and motifs suggesting regulation in filamentous fungi by Puf family genes. We further obtained comparative and experimental evidence indicating widespread translational regulation by upstream open reading frames. These results enhance our understanding of these widely studied fungi as well as provide new insight into eukaryotic genome evolution and gene regulation. 相似文献
86.
Gene expression in spermiogenesis 总被引:10,自引:0,他引:10
Germ cells convey parental genes to the next generation, and only germ cells perform meiosis, which is a mechanism that preserves the parental genes. The fusion of the products of germ cell meiosis, the haploid sperm and egg, creates the next generation. Sperm are the haploid germ cells that contribute genes to the egg. In preparation for this, the haploid round spermatids produced by meiosis undergo drastic morphological changes to become sperm. During this process of spermiogenesis, the nuclear form of the haploid germ cell takes shape, the mitochondria are rearranged in a specific manner, the flagellum develops and the acrosome forms. Spermatogenesis is supported by precise and orderly regulation of gene expression during the changes in chromatin structure, when protamine replaces histone. In this report, we summarize the molecular mechanisms involved in spermiogenesis.Received 2 September 2004; received after revision 7 October 2004; accepted 7 October 2004 相似文献
87.
Myocardial infarction might result from the interactions of multiple genetic and environmental factors, none of which can cause disease solely by each of themselves. Although molecular biological studies revealed that a number of proteins are possibly involved in its pathogenesis, little, if any genetic findings have been reported so far. To reveal genetic backgrounds of myocardial infarction, we performed a large-scale, case-control association study using 92,788 gene-based single-nucleotide polymorphism (SNP) markers. We have identified functional SNPs within the lymphotoxin-α gene (LTA) located on chromosome 6p21 that conferred susceptibility to myocardial infarction. Furthermore, we could identify galectin-2 protein as a binding partner of LTA protein. The association study further revealed that a functional SNP in LGALS2 encoding galectin-2, which led to altered secretion of LTA, also indicated a risk of myocardial infarction. A combined strategy of genetic and molecularcellular biological approaches may be useful in clarifying pathogenesis of common diseases.Received 7 March 2005; received after revision 22 April 2005; accepted 25 April 2005 相似文献
88.
The modification of neutrophils with amino group blocking reagents of different chemical specificities showed that dansyl chloride caused inhibition of chemotaxis without suppression of random movement. Dansylated neutrophils, like control cells, ingested bacteria. Neither the stimulated cyanide-insensitive respiration, nor lactate production during phagocytosis, was affected significantly by dansylation as compared with the inhibition of directed movement. 相似文献
89.
T. Yamashita Y. Tanaka T. Horigome E. Fujikawa 《Cellular and molecular life sciences : CMLS》1979,35(8):1054-1056
Summary Modification of polymorphonuclear neutrophils by a series of maleimide derivatives with various degrees of lipophilicity and hydrophilicity indicated that hydrophilic reagents had little effect on chemotaxis, whereas the degree of the inhibitory effect of lipophilic reagents on the chemotaxis was parallel to the degree of their lipophilicity.This work was supported in part by a grant-in-aid for Scientific Research (No.267043) from the Ministry of Education, Science and Culture, Japan, awarded to T.Y. 相似文献
90.
Summary A treadmill was improved so as to eliminate foot and tail injuries in small test-animals. The improvement was inexpensive and easily fabricated by the researchers. 相似文献