全文获取类型
收费全文 | 3263篇 |
免费 | 225篇 |
出版年
2021年 | 31篇 |
2020年 | 16篇 |
2019年 | 27篇 |
2018年 | 28篇 |
2017年 | 27篇 |
2016年 | 42篇 |
2015年 | 75篇 |
2014年 | 84篇 |
2013年 | 209篇 |
2012年 | 125篇 |
2011年 | 153篇 |
2010年 | 107篇 |
2009年 | 90篇 |
2008年 | 165篇 |
2007年 | 171篇 |
2006年 | 146篇 |
2005年 | 142篇 |
2004年 | 170篇 |
2003年 | 165篇 |
2002年 | 149篇 |
2001年 | 110篇 |
2000年 | 142篇 |
1999年 | 93篇 |
1998年 | 31篇 |
1997年 | 32篇 |
1996年 | 42篇 |
1995年 | 32篇 |
1994年 | 45篇 |
1993年 | 43篇 |
1992年 | 69篇 |
1991年 | 74篇 |
1990年 | 60篇 |
1989年 | 52篇 |
1988年 | 48篇 |
1987年 | 35篇 |
1986年 | 40篇 |
1985年 | 47篇 |
1984年 | 45篇 |
1983年 | 26篇 |
1982年 | 29篇 |
1981年 | 38篇 |
1980年 | 23篇 |
1979年 | 20篇 |
1978年 | 27篇 |
1977年 | 19篇 |
1976年 | 18篇 |
1975年 | 15篇 |
1973年 | 18篇 |
1972年 | 11篇 |
1967年 | 13篇 |
排序方式: 共有3488条查询结果,搜索用时 168 毫秒
971.
Suematsu N Okamoto K Isohashi F 《Journal of chromatography. B, Analytical technologies in the biomedical and life sciences》2003,790(1-2):239-244
An overview of the purification of an oligomeric enzyme, an extramitochondrial acetyl-coenzyme A hydrolase from rat liver, is presented. The enzyme has been purified to homogeneity using two successive size-exclusion chromatography runs, first for the monomeric and second for the oligomeric form of the enzyme. The sequential gel-filtration steps efficiently removed the contaminants of any molecular size, first of different size from that of the monomeric form of the enzyme (K(av)=0.47 on Superdex 200) and second of different size from that of the oligomeric form (K(av)=0.33), allowing us to purify the enzyme in high purity. This strategy provides an excellent model for purifying many other oligomeric proteins including key enzymes or allosteric enzymes regulating metabolism. 相似文献
972.
Okamoto K Isohashi F 《Journal of chromatography. B, Analytical technologies in the biomedical and life sciences》2003,797(1-2):367-371
In this report, we describe a new purification method for activated recombinant glucocorticoid receptor (GR) utilizing a cation-exchanger (Mono S) at pH8.4. This method is based upon a new finding that activated GR binds to both Mono Q and Mono S columns at the same pH. This method enables us to purify recombinant GR within 3 h. The purified GR represents more than 97% of the eluted proteins. Purified recombinant GR is able to bind specifically to a DNA fragment containing the glucocorticoid response element. Recombinant GR has no tag sequence that can be utilized for purification. Thus, this separation method is also applicable to purification of native GR. 相似文献
973.
Kuhara T Ohdoi C Ohse M van Kuilenburg AB van Gennip AH Sumi S Ito T Wada Y Matsumoto I 《Journal of chromatography. B, Analytical technologies in the biomedical and life sciences》2003,792(1):107-115
A rapid yet reliable chemical diagnosis for dihydropyrimidine dehydrogenase (DHPD) deficiency, and possibly dihydropyrimidinase (DHP) deficiency in cancer patients, prior to therapy with pyrimidine analogues such as 5-fluorouracil, is desired for prevention of severe side-effects by these drugs. We have reported the basic separation and quantitation technology for pyrimidine metabolites using gas chromatography-mass spectrometry. A proposal to use the number (n) of standard deviations (SD) above the normal mean, as the index of the excessive urinary excretion of the metabolites appears not to be commonly used. When used, the values were too small, such as two or three, even in genetic disorders. Here, we applied the method to 11 urine specimens from proven cases including two DHP carriers and proved how specific the method is, because "n"-values were markedly large for thymine (T), uracil (U) and/or dihydrothymine (DHT) and dihydrouracil (DHU). In three cases with DHPD deficiency, two were siblings, one with symptoms and the other without, n was 12 for T and 5.9 for U, and 5-hydroxymethyluracil was distinctly detected. These values indicate that the nature of genetic mutation relates closely to the degree of metabolite accumulation in pyrimidine disorders. In six patients with DHP deficiency, n was 8.4-12 for DHT and 7.2-11 for DHU. Many mutations are known for both genes and the assay of residual enzyme activity may be time-consuming or invasive especially for those with DHP deficiency. Thus, this noninvasive yet comprehensive urinalysis has great value for those without a family history, as the first trial, before DNA or the enzyme assay. Our findings again raise the question whether the metabolic block really causes the symptoms found in pyrimidine disorders. 相似文献
974.
975.
Yamagishi S Inagaki Y Okamoto T Amano S Koga K Takeuchi M Makita Z 《The Journal of biological chemistry》2002,277(23):20309-20315
Advanced glycation end products (AGE) have been implicated in the pathogenesis of glomerulosclerosis in diabetes. However, their involvement in the development of the early phase of diabetic nephropathy has not been fully elucidated. We investigated the effects of AGE on growth and on vascular endothelial growth factor (VEGF) and monocyte chemoattractant protein-1 (MCP-1) expression in human cultured mesangial cells. We prepared three immunochemically distinct AGE by incubating bovine serum albumin (BSA) with glucose, glyceraldehyde, or glycolaldehyde. When human mesangial cells were cultured with various types of AGE-BSA, viable cell numbers as well as DNA syntheses were significantly decreased. All of the AGE-BSA were found to significantly increase p53 and Bax protein accumulations and subsequently induce apoptotic cell death in mesangial cells. An antioxidant, N-acetylcysteine, significantly prevented the AGE-induced apoptotic cell death in mesangial cells. Human mesangial cells stimulated prostacyclin production by co-cultured glomerular endothelial cells. Furthermore, various types of AGE-BSA were found to up-regulate the levels of mRNAs for VEGF and stimulate the secretion of VEGF and MCP-1 proteins in mesangial cells. The results suggest that AGE disturbed glomerular homeostasis by inducing apoptotic cell death in mesangial cells and elicited hyperfiltration and microalbuminuria by stimulating the secretion of VEGF and MCP-1 proteins, thereby being involved in the pathogenesis of the early phase of diabetic nephropathy. 相似文献
976.
Role of adiponectin in preventing vascular stenosis. The missing link of adipo-vascular axis 总被引:93,自引:0,他引:93
Matsuda M Shimomura I Sata M Arita Y Nishida M Maeda N Kumada M Okamoto Y Nagaretani H Nishizawa H Kishida K Komuro R Ouchi N Kihara S Nagai R Funahashi T Matsuzawa Y 《The Journal of biological chemistry》2002,277(40):37487-37491
Obesity is more linked to vascular disease, including atherosclerosis and restenotic change, after balloon angioplasty. The precise mechanism linking obesity and vascular disease is still unclear. Previously we have demonstrated that the plasma levels of adiponectin, an adipose-derived hormone, decreases in obese subjects, and that hypoadiponectinemia is associated to ischemic heart disease. In current the study, we investigated the in vivo role of adiponectin on the neointimal thickening after artery injury using adiponectin-deficient mice and adiponectin-producing adenovirus. Adiponectin-deficient mice showed severe neointimal thickening and increased proliferation of vascular smooth muscle cells in mechanically injured arteries. Adenovirus-mediated supplement of adiponectin attenuated neointimal proliferation. In cultured smooth muscle cells, adiponectin attenuated DNA synthesis induced by growth factors including platelet-derived growth factor, heparin-binding epidermal growth factor (EGF)-like growth factor (HB-EGF), basic fibroblast growth factor, and EGF and cell proliferation and migration induced by HB-EGF. In cultured endothelial cells, adiponectin attenuated HB-EGF expression stimulated by tumor necrosis factor alpha. The current study suggests an adipo-vascular axis, a direct link between fat and artery. A therapeutic strategy to increase plasma adiponectin should be useful in preventing vascular restenosis after angioplasty. 相似文献
977.
Kenyon NJ van der Vliet A Schock BC Okamoto T McGrew GM Last JA 《American journal of physiology. Lung cellular and molecular physiology》2002,282(3):L540-L545
Mice deficient in inducible nitric oxide synthase (iNOS; C57Bl/6Ai-[KO]NOS2 N5) or wild-type C57Bl/6 mice were exposed to 1 part/million of ozone 8 h/night or to filtered air for three consecutive nights. Endpoints measured included lavagable total protein, macrophage inflammatory protein (MIP)-2, matrix metalloproteinase (MMP)-9, cell content, and tyrosine nitration of whole lung proteins. Ozone exposure caused acute edema and an inflammatory response in the lungs of wild-type mice, as indicated by significant increases in lavage protein content, MIP-2 and MMP-9 content, and polymorphonuclear leukocytes. The iNOS knockout mice showed significantly greater levels of lung injury by all of these criteria than did the wild-type mice. We conclude that iNOS knockout mice are more susceptible to acute lung damage induced by exposure to ozone than are wild-type C57Bl/6 mice and that protein nitration is associated with the degree of inflammation and not dependent on iNOS-derived nitric oxide. 相似文献
978.
Damaged epithelia regenerated by bone marrow-derived cells in the human gastrointestinal tract 总被引:36,自引:0,他引:36
Okamoto R Yajima T Yamazaki M Kanai T Mukai M Okamoto S Ikeda Y Hibi T Inazawa J Watanabe M 《Nature medicine》2002,8(9):1011-1017
Studies have shown that bone marrow cells have the potential to differentiate into a variety of cell types. Here we show that bone marrow cells can repopulate the epithelia of the human gastrointestinal tract. Epithelial cells of male donor origin were distributed in every part of the gastrointestinal tract of female bone marrow transplant recipients. Donor-derived epithelial cells substantially repopulated the gastrointestinal tract during epithelial regeneration after graft-versus-host disease or ulcer formation. Regeneration of gastrointestinal epithelia with donor-derived cells in humans shows a potential clinical application of bone marrow-derived cells for repairing severely damaged epithelia, not only in the gastrointestinal tract but also in other tissues. 相似文献
979.
Rapid PCR-based method which can determine both phenotype and genotype of Lactococcus lactis subspecies 总被引:2,自引:0,他引:2
A highly efficient, rapid, and reliable PCR-based method for distinguishing Lactococcus lactis subspecies (L. lactis subsp. lactis and L. lactis subsp. cremoris) is described. Primers complementary to positions in the glutamate decarboxylase gene have been constructed. PCR analysis with extracted DNA or with cells of different L. lactis strains resulted in specific fragments. The length polymorphism of the PCR fragments allowed a clear distinction of the L. lactis subspecies. The amplified fragment length polymorphism with the primers and the restriction fragment length polymorphism of the amplified products agreed perfectly with the identification based on genotypic and phenotypic analyses, respectively. Isolates from cheese starters were investigated by this method, and amplified fragments of genetic variants were found to be approximately 40 bp shorter than the typical L. lactis subsp. cremoris fragments. 相似文献
980.
Contribution of IL-18 to Th1 response and host defense against infection by Mycobacterium tuberculosis: a comparative study with IL-12p40 总被引:4,自引:0,他引:4
Kinjo Y Kawakami K Uezu K Yara S Miyagi K Koguchi Y Hoshino T Okamoto M Kawase Y Yokota K Yoshino K Takeda K Akira S Saito A 《Journal of immunology (Baltimore, Md. : 1950)》2002,169(1):323-329
The present study was conducted to critically determine the protective role of IL-18 in host response to Mycobacterium tuberculosis infection. IL-18-deficient (knockout (KO)) mice were slightly more prone to this infection than wild-type (WT) mice. Sensitivity of IL-12p40KO mice was lower than that of IL-12p40/IL-18 double KO mice. IFN-gamma production caused by the infection was significantly attenuated in IL-18KO mice compared with WT mice, as indicated by reduction in the levels of this cytokine in sera, spleen, lung, and liver, and its synthesis by spleen cells restimulated with purified protein derivatives. Serum IL-12p40 level postinfection and its production by peritoneal exudate cells stimulated with live bacilli were also significantly lower in IL-18KO mice than WT mice, suggesting that attenuated production of IFN-gamma was secondary to reduction of IL-12 synthesis. However, this was not likely the case, because administration of excess IL-12 did not restore the reduced IFN-gamma production in IL-18KO mice. In further studies, IL-18 transgenic mice were more resistant to the infection than control littermate mice, and serum IFN-gamma level and its production by restimulated spleen cells were increased in the former mice. Taken together, our results indicate that IL-18 plays an important role in Th1 response and host defense against M. tuberculosis infection although the contribution was not as profound as that of IL-12p40. 相似文献