全文获取类型
收费全文 | 8940篇 |
免费 | 641篇 |
国内免费 | 462篇 |
出版年
2024年 | 8篇 |
2023年 | 72篇 |
2022年 | 145篇 |
2021年 | 323篇 |
2020年 | 231篇 |
2019年 | 266篇 |
2018年 | 282篇 |
2017年 | 231篇 |
2016年 | 320篇 |
2015年 | 462篇 |
2014年 | 578篇 |
2013年 | 640篇 |
2012年 | 739篇 |
2011年 | 704篇 |
2010年 | 413篇 |
2009年 | 371篇 |
2008年 | 424篇 |
2007年 | 416篇 |
2006年 | 367篇 |
2005年 | 359篇 |
2004年 | 292篇 |
2003年 | 299篇 |
2002年 | 241篇 |
2001年 | 195篇 |
2000年 | 193篇 |
1999年 | 162篇 |
1998年 | 108篇 |
1997年 | 102篇 |
1996年 | 104篇 |
1995年 | 101篇 |
1994年 | 78篇 |
1993年 | 78篇 |
1992年 | 127篇 |
1991年 | 101篇 |
1990年 | 72篇 |
1989年 | 72篇 |
1988年 | 66篇 |
1987年 | 49篇 |
1986年 | 41篇 |
1985年 | 53篇 |
1984年 | 33篇 |
1983年 | 24篇 |
1982年 | 19篇 |
1981年 | 10篇 |
1979年 | 10篇 |
1978年 | 6篇 |
1977年 | 7篇 |
1971年 | 7篇 |
1970年 | 7篇 |
1966年 | 7篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
41.
42.
43.
44.
Absence of 7-acetyl taxol binding to unassembled brain tubulin 总被引:1,自引:0,他引:1
The effect of taxol on microtubule proteins at 0 degrees C is controversial. In order to determine if taxol is unable to bind to unassembled tubulin, as has been hypothesized, the binding of [3H]acetyl taxol has been studied using equilibrium microdialysis. Ac-taxol bound to microtubules at 37 degrees C and the binding remained stable when the temperature was lowered to 0 degrees C. Ac-taxol bound also at 0 degrees C to microtubules stabilized with rhazinilam. In contrast, there was no binding of Ac-taxol to unassembled tubulin, either free tubulin at 0 degrees C or tubulin, complexed with several microtubule poisons, at 0 and 37 degrees C. 相似文献
45.
J L Gu I D Goldfine J R Forsayeth P De Meyts 《Biochemical and biophysical research communications》1988,150(2):694-701
Two monoclonal antibodies to the insulin receptor, MA-5 and MA-20, unlike other monoclonal antibodies, do not mimick the accelerating effect of insulin on the dissociation of 125I-insulin from the receptors (negative cooperativity). On the contrary, MA-5 and MA-20 markedly slow down the dissociation rate. We show now that MA-5 and MA-20 are potent antagonists of the negative cooperativity induced by insulin, and reverse the insulin-induced acceleration whether added simultaneously with insulin or after insulin. The reversal of the insulin-induced acceleration is almost immediate. These data strengthen the concept therefore that the insulin-receptor complex has access to alternative conformational states that can be stabilized by ligand-induced site-site interactions. 相似文献
46.
Lack of correlation between extensive accumulation of bisnucleoside polyphosphates and the heat-shock response in eukaryotic cells 总被引:4,自引:0,他引:4
G F Guédon G J Gilson J P Ebel N M Befort P M Remy 《The Journal of biological chemistry》1986,261(35):16459-16465
The accumulation in large amounts of bisnucleoside polyphosphates (Ap4X) after heat shock in Xenopus laevis oocytes or cultured hepatoma cells (HTC cells) is observed after exposure to temperatures of 45 degrees C or higher. The accumulation is a transient phenomenon, with the collapse in cellular ATP concentration severely affecting the rate of synthesis of Ap4X, allowing degrading activities to empty the pool of these compounds under prolonged heat shock. This accumulation of Ap4X to high levels, compared to the basic content, is only observed under conditions leading to irreversible damage, ultimately resulting in the death of the cell. It is shown that the increase in Ap4X after hyperthermia is due to the partial or almost complete inhibition of their degradation pathways, rather than to a stimulation of their rate of synthesis. Finally, the synthesis of heat-shock proteins could be observed under conditions which do not lead to important accumulation of Ap4X, therefore ruling out the possibility that these adenylylated nucleotides would behave as chemical signals ("alarmones") triggering the synthesis of heat-shock proteins. Nevertheless, on the basis of our earlier results (Guédon, G., Sovia, D., Ebel, J. P., Befort, D., and Remy, P. (1985) Embo J. 4, 3743-3749), it cannot be excluded that Ap4X might play a role in the regulation of the heat-shock response; this would, however, rely on variations in Ap4X concentrations which do not exceed a factor of 2. 相似文献
47.
48.
Occurrence of the methylisobutylxanthine-stimulated cyclic GMP binding protein in various rat tissues 总被引:1,自引:0,他引:1
J F Coquil G Brunelle J Guédon 《Biochemical and biophysical research communications》1985,127(1):226-231
A new type of cGMP binding protein, the activity of which is characteristically stimulated by methylisobutylxanthine, has been previously discovered in rat lung and platelets (Hamet, P. and Coquil, J.F. (1978) J. Cyclic Nucleotide Res. 4, 281-290). In the present study, we demonstrate the occurrence of this protein in soluble extracts of a variety of rat tissues fractionated by a DEAE-Sepharose chromatography. In several tissues (spleen, lung and brain) the binding activity of this protein was of the same order of magnitude as that of the cGMP-dependent protein kinase. 相似文献
49.
Complete complementary DNA of rat tyrosine aminotransferase messenger RNA. Deduction of the primary structure of the enzyme 总被引:11,自引:0,他引:11
T Grange C Guénet J B Dietrich S Chasserot M Fromont N Befort J Jami G Beck R Pictet 《Journal of molecular biology》1985,184(2):347-350
The primary structure of rat tyrosine aminotransferase (L-tyrosine:2-oxoglutarate aminotransferase; EC 2.6.1.5), a liver-specific enzyme involved in gluconeogenesis, has been deduced from the nucleotide sequence of a cloned full-length cDNA. The mRNA is 2362 nucleotides long (excluding the poly(A) tail) and codes for a polypeptide of 454 amino acids with a molecular weight of 50634. Unambiguous identification was obtained by comparison of this sequence with the amino acid sequences of several peptides obtained from the purified enzyme. 相似文献
50.
Opposite effects of two ligands for peripheral type benzodiazepine binding sites, PK 11195 and RO5-4864, in a conflict situation in the rat 总被引:7,自引:0,他引:7
J Mizoule A Gauthier A Uzan C Renault M C Dubroeucq C Guérémy G Le Fur 《Life sciences》1985,36(11):1059-1068
The effects of two drugs acting at the peripheral type benzodiazepine binding sites, PK 11195 and RO5-4864, were examined in shock-induced suppression of drinking in rats. These two compounds have opposite effects : RO5-4864 (3.1-1205 mg/kg i.p.) enhanced whereas PK 11195 (25-50 mg/kg i.p.) decreased the punished responding, and PK 11195 (6.25 mg/kg, a dose which did not alter the punished responding) blocked the proconflict action of RO5-4864 (6.25 and 12.5 mg/kg). The effects of RO5-4864 and PK 11195 were not antagonized by RO15-1788, a selective antagonist of the central benzodiazepine site. In addition, PK 11195 (6.25 mg/kg) did not reverse the proconflict effect of two beta-carbolines : beta-CEE and FG 7142. AS picrotoxin did not change the punished responding, these data imply that the effects of RO5-4864 and PK 11195 on the one hand and those of chlordiazepoxide and beta-carbolines on the other hand are differentially mediated and suggest that the peripheral type benzodiazepine binding sites are involved in this conflict model. 相似文献