全文获取类型
收费全文 | 163970篇 |
免费 | 6878篇 |
国内免费 | 61篇 |
专业分类
170909篇 |
出版年
2021年 | 1082篇 |
2020年 | 988篇 |
2019年 | 931篇 |
2018年 | 3149篇 |
2017年 | 3009篇 |
2016年 | 5281篇 |
2015年 | 9080篇 |
2014年 | 8846篇 |
2013年 | 9900篇 |
2012年 | 10015篇 |
2011年 | 6996篇 |
2010年 | 5246篇 |
2009年 | 4350篇 |
2008年 | 4618篇 |
2007年 | 4345篇 |
2006年 | 4352篇 |
2005年 | 9618篇 |
2004年 | 8433篇 |
2003年 | 6337篇 |
2002年 | 3705篇 |
2001年 | 3109篇 |
2000年 | 2249篇 |
1999年 | 2886篇 |
1998年 | 1000篇 |
1992年 | 2793篇 |
1991年 | 2808篇 |
1990年 | 2830篇 |
1989年 | 2832篇 |
1988年 | 2637篇 |
1987年 | 2515篇 |
1986年 | 2270篇 |
1985年 | 2395篇 |
1984年 | 1709篇 |
1983年 | 1376篇 |
1982年 | 921篇 |
1981年 | 838篇 |
1979年 | 1722篇 |
1978年 | 1253篇 |
1977年 | 1094篇 |
1976年 | 1069篇 |
1975年 | 1446篇 |
1974年 | 1609篇 |
1973年 | 1579篇 |
1972年 | 1464篇 |
1971年 | 1394篇 |
1970年 | 1327篇 |
1969年 | 1394篇 |
1968年 | 1281篇 |
1967年 | 1195篇 |
1966年 | 1027篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
101.
102.
F Krizsa Z Borbényi E Arokszállásy I Cserháti 《Folia haematologica (Leipzig, Germany : 1928)》1980,107(4):683-687
The thrombopoietic serum activity was examined in rats during thrombocytopenia produced by bleeding or after treatment with antithrombocyte serum (ATS). 6 hours after both treatments the thrombopoietic activity of the serum, i.e. its content of thrombopoietin, is increased. After the ATS treatment of nephrectomized animals a similar increase of thrombopoietic activity as in normal animals could be achieved. In contrast to that, no similar increase of thrombopoietic activity was observed in nephrectomized animals after blood loss. According to the results of the authors the increase of thrombopoietic activity produced by different stimuli can be attributed to different mechanisms. 相似文献
103.
G Kh Goldshte?ne I B Tsorin G G Chichkanov 《Biulleten' eksperimental'no? biologii i meditsiny》1986,101(2):177-179
The experiments on rats with a 3-day myocardial infarction caused by the left coronary artery ligation have shown that multiple lidocaine and pyromecaine injections according to a given scheme decrease the size of the necrosis area. Drug effects were not related to their action on the blood supply of the ischemic area. 相似文献
104.
R V Balasiavichius A I Dagis A I Tole?kis A K Prashkiavichius 《Biulleten' eksperimental'no? biologii i meditsiny》1985,99(3):294-296
The influence of malate and cytochrome c on fatty acid oxidation under control and ischemic conditions was investigated. In the medium without malate, cytochrome did not make fatty acid oxidation decreased during ischemia return to normal. Oxidation in the media containing malate and cytochrome did not differ from control only when it was measured after preliminary oxidation of endogenous substrates. The ratio of palmitoyl-CoA and palmitoyl carnitine to the respiration rates at state 3 was unchanged at 60 min ischemia. Apparently, no changes in carnitine acyltransferase playing a role in oxidation of palmitoyl-CoA took place. Thus, the decrease of fatty acid oxidation at early periods of ischemia is largely caused by a reduction in the content of cytochrome c and intermediates of Krebs cycle in the mitochondria. 相似文献
105.
106.
Changes in the duration and size of the vulnerable period of the myocardium in the presence of respiratory changes were studied in acute experiments on rats. The limits of the vulnerable period were determined by directly stimulating the heart during ventilation via the enlarged respiratory dead space, during hyperventilation and during heart failure. In the control group (normal ventilation without enlargement of the dead space), the vulnerable period lasted 5.7 +/- 0.76 ms. During ventilation via the enlarged dead space, hypercapnic hypoxaemia developed and the vulnerable period was markedly prolonged (18.55 +/- 5.29 ms) by a shift of its inner limit to the left. Hyperventilation caused normoxic to hyperoxic hypocapnia and markedly reduced the duration of the vulnerable period (8.17 +/- 2.21 and 9.31 +/- 2.38 ms respectively). The vulnerable period lengthened the most in heart failure (25.46 +/- 3.93), mainly as a result of a shift of its outer limit. In all the experimental groups there was a shift of the vulnerable period to the right, which was fastest in hypercapnic hypoxaemia and slowest in hyperoxic hypocapnia. The administration of Inderal (3 mg/kg i.p.) or Arfonad (50 mg/kg i.p.) markedly shortened the vulnerable period during hypercapnic hypoxaemia (9.87 +/- 2.78 and 9.32 +/- 2.16 ms respectively), but did not block the shift. Lengthening of the vulnerable period during hypercapnic hypoxaemia was probably due to activation of sympathetic nerves via beta-adrenergic receptors. 相似文献
107.
The production of L-lysine fromDL-α-amino-ε-caprolactam (DL-ACL) by new strains producingL-α-amino-ε-caprolactamase and aminocaprolactam racemase is described. Optimal conditions for hydrolysis ofL-ACL byCryptococcus sp. and for racemization of ACL by cells of a strain isolated in nature and identified asPseudomonas sp. were determined. Synthesis ofL-α-amino-ε-caprolactamase is induced byDL-ACL orL-lysine with the same effectivity. A positive effect of phosphates (potassium salts) on reduction of the induction lag was
detected, the synthesis of this enzyme was found to be repressed by glucose and some possibilities of the reversion of this
repressive effect were demonstrated. Under conditions optimal for the production of both enzymes a quantitative theoretical
conversion of 10 % aqueousDL-ACL toL-lysine by a mixture of native cells in a mass ratio of 1: 2 (producer of ACL-hydrolase to producer of ACL-racemase) occurred
in 8 h at 40 °C and pH 8.0 相似文献
108.
109.
Claus Rueffler Johan A. J. Metz Tom J. M. Van Dooren 《Journal of mathematical biology》2013,66(1-2):225-279
We analyze long-term evolutionary dynamics in a large class of life history models. The model family is characterized by discrete-time population dynamics and a finite number of individual states such that the life cycle can be described in terms of a population projection matrix. We allow an arbitrary number of demographic parameters to be subject to density-dependent population regulation and two or more demographic parameters to be subject to evolutionary change. Our aim is to identify structural features of life cycles and modes of population regulation that correspond to specific evolutionary dynamics. Our derivations are based on a fitness proxy that is an algebraically simple function of loops within the life cycle. This allows us to phrase the results in terms of properties of such loops which are readily interpreted biologically. The following results could be obtained. First, we give sufficient conditions for the existence of optimisation principles in models with an arbitrary number of evolving traits. These models are then classified with respect to their appropriate optimisation principle. Second, under the assumption of just two evolving traits we identify structural features of the life cycle that determine whether equilibria of the monomorphic adaptive dynamics (evolutionarily singular points) correspond to fitness minima or maxima. Third, for one class of frequency-dependent models, where optimisation is not possible, we present sufficient conditions that allow classifying singular points in terms of the curvature of the trade-off curve. Throughout the article we illustrate the utility of our framework with a variety of examples. 相似文献
110.
Summary A male fetus of a pregnancy known to be at risk for X-linked mental retardation with fragile site Xq27 was found to be affected by demonstrating the marker X-chromosome in five of 180 (2.8%) of metaphases derived from amniocytes cultured in medium 199. The results were confirmed in fetal lymphocytes (25 of 86 metaphases, i.e. 29%), and fetal fibroblasts (five of 100 metaphases when cultured in medium 199, and 14 of 100 after exposure to methotrexate for 43 h).This work was supported in part by a research grant from the Deutsche Forschungsgemeinschaft 相似文献