全文获取类型
收费全文 | 434篇 |
免费 | 0篇 |
国内免费 | 1篇 |
专业分类
系统科学 | 8篇 |
理论与方法论 | 1篇 |
现状及发展 | 85篇 |
研究方法 | 36篇 |
综合类 | 285篇 |
自然研究 | 20篇 |
出版年
2017年 | 3篇 |
2014年 | 3篇 |
2013年 | 3篇 |
2012年 | 17篇 |
2011年 | 38篇 |
2010年 | 8篇 |
2009年 | 2篇 |
2008年 | 20篇 |
2007年 | 15篇 |
2006年 | 15篇 |
2005年 | 13篇 |
2004年 | 10篇 |
2003年 | 15篇 |
2002年 | 12篇 |
2001年 | 25篇 |
2000年 | 21篇 |
1999年 | 9篇 |
1995年 | 3篇 |
1993年 | 1篇 |
1992年 | 15篇 |
1991年 | 6篇 |
1990年 | 6篇 |
1989年 | 2篇 |
1988年 | 4篇 |
1987年 | 7篇 |
1986年 | 7篇 |
1985年 | 10篇 |
1984年 | 4篇 |
1983年 | 3篇 |
1982年 | 4篇 |
1980年 | 7篇 |
1979年 | 1篇 |
1978年 | 11篇 |
1977年 | 5篇 |
1976年 | 8篇 |
1975年 | 5篇 |
1974年 | 5篇 |
1973年 | 6篇 |
1972年 | 4篇 |
1971年 | 13篇 |
1970年 | 20篇 |
1969年 | 5篇 |
1968年 | 10篇 |
1967年 | 10篇 |
1966年 | 6篇 |
1965年 | 4篇 |
1964年 | 3篇 |
1963年 | 2篇 |
1960年 | 1篇 |
1958年 | 1篇 |
排序方式: 共有435条查询结果,搜索用时 62 毫秒
231.
232.
Cathelicidins - a family of multifunctional antimicrobial peptides 总被引:12,自引:0,他引:12
One component of host defence at mucosal surfaces are epithelial-derived antimicrobial peptides. Cathelicidins are one family of antimicrobial peptides characterized by conserved pro-peptide sequences that have been identified in several mammalian species. LL-37/hCAP-18 is the only cathelicidin found in humans and is expressed in inflammatory and epithelial cells. Besides their direct antimicrobial function, cathelicidins have multiple roles as mediators of inflammation influencing diverse processes such as cell proliferation and migration, immune modulation, wound healing, angiogenesis and the release of cytokines and histamine. Finally, cathelicidin antimicrobial peptides qualify as prototypes of innovative drugs that may be used to treat infection and/or modulate the immune response. This review provides an overview of antimicrobial peptides of the cathelicidin family, the structures of their genes and peptides and their biological functions. 相似文献
233.
The effect of a phorbol ester upon the cholinergic regulation of potassium permeability in the rat submandibular gland 总被引:1,自引:0,他引:1
Acetylcholine releases calcium from cytoplasmic stores and permits an influx of calcium in salivary acinar cells. The resultant rise in [Ca2+]i causes an increase in potassium permeability which is an important part of the secretory response. We have investigated the effects of 12-0-tetradecanoyl phorbol-13-acetate, a potent activator of protein kinase C, upon this regulation of potassium permeability in superfused pieces of rat submandibular salivary gland. This compound inhibited the initial [Ca2+]o-independent component of the response of acetylcholine but had no effect upon the subsequent [Ca2+]o-dependent phase. This compound does not, therefore, appear to inhibit receptor-regulated calcium influx. 相似文献
234.
235.
236.
237.
238.
Résumé La lumière a un effet inhibiteur sur l'activité électrique tonique spontanée de l'épiphyse du rat, enregistrée dans l'obscurité. Les éléments photosensibles se trouvent au niveau des yeux. Le fait que la réponse a été bloquée par le chlorure de hexamethonium suggère qu'elle est transmise à l'épiphyse par les nerfs sympathiques postganglionnaires. 相似文献
239.
McClelland M Sanderson KE Clifton SW Latreille P Porwollik S Sabo A Meyer R Bieri T Ozersky P McLellan M Harkins CR Wang C Nguyen C Berghoff A Elliott G Kohlberg S Strong C Du F Carter J Kremizki C Layman D Leonard S Sun H Fulton L Nash W Miner T Minx P Delehaunty K Fronick C Magrini V Nhan M Warren W Florea L Spieth J Wilson RK 《Nature genetics》2004,36(12):1268-1274
Salmonella enterica serovars often have a broad host range, and some cause both gastrointestinal and systemic disease. But the serovars Paratyphi A and Typhi are restricted to humans and cause only systemic disease. It has been estimated that Typhi arose in the last few thousand years. The sequence and microarray analysis of the Paratyphi A genome indicates that it is similar to the Typhi genome but suggests that it has a more recent evolutionary origin. Both genomes have independently accumulated many pseudogenes among their approximately 4,400 protein coding sequences: 173 in Paratyphi A and approximately 210 in Typhi. The recent convergence of these two similar genomes on a similar phenotype is subtly reflected in their genotypes: only 30 genes are degraded in both serovars. Nevertheless, these 30 genes include three known to be important in gastroenteritis, which does not occur in these serovars, and four for Salmonella-translocated effectors, which are normally secreted into host cells to subvert host functions. Loss of function also occurs by mutation in different genes in the same pathway (e.g., in chemotaxis and in the production of fimbriae). 相似文献
240.
Tellides G Tereb DA Kirkiles-Smith NC Kim RW Wilson JH Schechner JS Lorber MI Pober JS 《Nature》2000,403(6766):207-211
Atherosclerosis and post-transplant graft arteriosclerosis are both characterized by expansion of the arterial intima as a result of the infiltration of mononuclear leukocytes, the proliferation of vascular smooth muscle cells (VSMCs) and the accumulation of extracellular matrix. They are also associated with the presence of the immunomodulatory cytokine interferon-gamma (IFN-gamma). Moreover, in mouse models of atheroma formation or allogeneic transplantation, the serological neutralization or genetic absence of IFN-gamma markedly reduces the extent of intimal expansion. However, other studies have found that exogenous IFN-gamma inhibits cultured VSMC proliferation and matrix synthesis, and reduces intimal expansion in response to mechanical injury. This discrepancy is generally explained by the idea that IFN-gamma either directly activates macrophages, or, by increasing antigen presentation, indirectly activates T cells within the lesions of atherosclerosis and graft arteriosclerosis. These activated leukocytes are thought to express the VSMC-activating cytokines and cell-surface molecules that cause the observed arteriosclerotic responses. Here we have inserted pig and human arteries into the aorta of immunodeficient mice, and we show that IFN-gamma can induce arteriosclerotic changes in the absence of detectable immunocytes by acting on VSMCs to potentiate growth-factor-induced mitogenesis. 相似文献