全文获取类型
收费全文 | 322079篇 |
免费 | 21679篇 |
国内免费 | 65篇 |
专业分类
343823篇 |
出版年
2021年 | 2690篇 |
2020年 | 2211篇 |
2019年 | 2516篇 |
2018年 | 5457篇 |
2017年 | 5159篇 |
2016年 | 6656篇 |
2015年 | 7634篇 |
2014年 | 8924篇 |
2013年 | 12399篇 |
2012年 | 14900篇 |
2011年 | 14965篇 |
2010年 | 10111篇 |
2009年 | 8131篇 |
2008年 | 12859篇 |
2007年 | 13124篇 |
2006年 | 12353篇 |
2005年 | 11514篇 |
2004年 | 11339篇 |
2003年 | 10733篇 |
2002年 | 10345篇 |
2001年 | 11213篇 |
2000年 | 10822篇 |
1999年 | 8607篇 |
1998年 | 2829篇 |
1997年 | 2509篇 |
1996年 | 2315篇 |
1995年 | 2159篇 |
1992年 | 6598篇 |
1991年 | 6727篇 |
1990年 | 6584篇 |
1989年 | 6470篇 |
1988年 | 6023篇 |
1987年 | 5562篇 |
1986年 | 5093篇 |
1985年 | 5382篇 |
1984年 | 4316篇 |
1983年 | 3537篇 |
1982年 | 2416篇 |
1979年 | 3882篇 |
1978年 | 2995篇 |
1977年 | 2752篇 |
1976年 | 2693篇 |
1975年 | 3223篇 |
1974年 | 3533篇 |
1973年 | 3509篇 |
1972年 | 3058篇 |
1971年 | 2915篇 |
1970年 | 2494篇 |
1969年 | 2424篇 |
1968年 | 2279篇 |
排序方式: 共有10000条查询结果,搜索用时 7 毫秒
141.
142.
143.
E M Melikhova I N Kurochkin S V Zaitsev S D Varfolomeev 《Analytical biochemistry》1988,175(2):507-515
A new method has been proposed for analysis of experimental data on ligand-receptor binding at equilibrium. This method makes it possible to detect heterogeneity of a receptor system in cases where the contribution of the high-affinity site to total binding is rather small and the problem of graphic discrimination of a model cannot be solved unambiguously by other methods. The difference method permits us to exclude experiments on measuring nonspecific binding. A computer program for analysis of ligand-receptor binding has been worked out in which the difference method and traditional methods of binding isotherm analysis are realized. Numerical modeling has shown that the best strategy in experimental data processing is the treatment of total binding isotherms by both the difference method and regression analysis, including the nonspecific binding constant as one of the regression parameters. 相似文献
144.
145.
146.
147.
Assessment of uncoupling activity of uncoupling protein 3 using a yeast heterologous expression system. 总被引:2,自引:0,他引:2
Uncoupling protein 3L, uncoupling protein 1 and the mitochondrial oxoglutarate carrier were expressed in Saccharomyces cerevisae. Effects on different parameters related to the energy expenditure were studied. Both uncoupling protein 3L and uncoupling protein 1 reduced the growth rate by 49% and 32% and increased the whole yeast O2 consumption by 31% and 19%, respectively. In isolated mitochondria, uncoupling protein 1 increased the state 4 respiration by 1.8-fold, while uncoupling protein 3L increased the state 4 respiration by 1.2-fold. Interestingly, mutant uncoupling protein 1 carrying the H145Q and H147N mutations, previously shown to markedly decrease the H+ transport activity of uncoupling protein 1 when assessed using a proteoliposome system (Bienengraeber et al. (1998) Biochem. 37, 3-8), uncoupled the mitochondrial respiration to almost the same degree as wild-type uncoupling protein 1. Thus, absence of this histidine pair in uncoupling protein 2 and uncoupling protein 3 does not by itself rule out the possibility that these carriers have an uncoupling function. The oxoglutarate carrier had no effect on any of the studied parameters. In summary, a discordance exists between the magnitude of effects of uncoupling protein 3L and uncoupling protein 1 in whole yeast versus isolated mitochondria, with uncoupling protein 3L having greater effects in whole yeast and a smaller effect on the state 4 respiration in isolated mitochondria. These findings suggest that uncoupling protein 3L, like uncoupling protein 1, has an uncoupling activity. However, the mechanism of action and/or regulation of the activity of uncoupling protein 3L is likely to be different. 相似文献
148.
149.
1. In rat kidney cortex, outer and inner medulla the development of activities of seven enzymes was investigated during postnatal ontogeny (10, 20, 30, 60 and 90 days of age). The enzymes were selected in such a manner, as to characterize most of the main metabolic pathways of energy supplying metabolism: hexokinase (glucose phosphorylation, HK), glycerol-3-phosphate dehydrogenase (glycerolphosphate metabolism or shunt, GPDH), triose phosphate dehydrogenase (glycolytic carbohydrate breakdown, TPDH), lactate dehydrogenase (lactate metabolism, LDH), citrate synthase (tricarboxylic acid cycle, aerobic metabolism, CS), malate NAD dehydrogenase (tricarboxylic acid cycle, intra-extra mitochondrial hydrogen transport, MDH) and 3-hydroxyacyl-CoA-dehydrogenase (fatty acid catabolism, HOADH). 2. The renal cortex already differs metabolically from the medullar structures on the 10th day of life. It displays a high activity of aerobic breakdown of both fatty acids and carbohydrates. Its metabolic capacity further increases up to the 30th day of life. 3. The outer medullar structure is not grossly different from the inner medulla on the 10th day of life. Further it differentiates into a highly aerobic tissue mainly able to utilize carbohydrates. It can, however, to some extent, also utilize fatty acids aerobically and produce lactate from carbohydrates anaerobically. 4. The inner medullar structure is best equipped to utilize carbohydrates by anaerobic glycolysis, forming lactate. This feature is already pronounced on the 10th day of life, its capacity increases to some extent during postnatal development, being highest between the 10th and the 60th day of life. 相似文献
150.
The time course of changes in the level of uncoupling protein mRNA when cold-acclimated mice were returned to a thermoneutral environment (33 degrees C) was examined using a cDNA probe. Upon deacclimation, there was a marked loss of uncoupling protein mRNA within 24 h, which precedes the loss of uncoupling protein from mitochondria. This loss of uncoupling protein mRNA was selective, since there was no change in the relative proportion of cytochrome c oxidase subunit IV mRNA or poly(A)+ RNA in total RNA. The results suggest that the decrease in the mitochondrial content of uncoupling protein during deacclimation is likely the result of turnover of existing protein, with very little replacement due to a lower level of its mRNA. 相似文献