全文获取类型
收费全文 | 11641篇 |
免费 | 1123篇 |
出版年
2021年 | 148篇 |
2020年 | 99篇 |
2019年 | 110篇 |
2018年 | 168篇 |
2017年 | 143篇 |
2016年 | 262篇 |
2015年 | 467篇 |
2014年 | 483篇 |
2013年 | 614篇 |
2012年 | 745篇 |
2011年 | 674篇 |
2010年 | 467篇 |
2009年 | 424篇 |
2008年 | 561篇 |
2007年 | 527篇 |
2006年 | 492篇 |
2005年 | 505篇 |
2004年 | 497篇 |
2003年 | 441篇 |
2002年 | 437篇 |
2001年 | 234篇 |
2000年 | 248篇 |
1999年 | 210篇 |
1998年 | 153篇 |
1997年 | 140篇 |
1996年 | 114篇 |
1995年 | 131篇 |
1994年 | 107篇 |
1993年 | 116篇 |
1992年 | 173篇 |
1991年 | 175篇 |
1990年 | 174篇 |
1989年 | 164篇 |
1988年 | 140篇 |
1987年 | 160篇 |
1986年 | 139篇 |
1985年 | 126篇 |
1984年 | 134篇 |
1983年 | 94篇 |
1982年 | 74篇 |
1981年 | 90篇 |
1980年 | 65篇 |
1979年 | 99篇 |
1978年 | 54篇 |
1977年 | 93篇 |
1976年 | 64篇 |
1975年 | 61篇 |
1974年 | 58篇 |
1973年 | 74篇 |
1971年 | 62篇 |
排序方式: 共有10000条查询结果,搜索用时 78 毫秒
31.
32.
33.
34.
35.
36.
Elisabeth Hansson Ingemar Jacobson Richard Venema Åke Sellström 《Journal of neurochemistry》1980,34(3):569-573
Abstract: The lipophilic cation [3 H]triphenylrnethylphosphonium bromide ([3 H]TPMP+ ) was investigated as a measure of the membrane potential of synaptosomes. Conditions under which [3 H]TPMP+ achieved an equilibrium distribution were tested. The toxicity of TPMP has been studied relative to its inhibitory effects on [3 H]y-aminobutyric acid ([3 H]GABA) transport. In some experiments the distribution of 86 RbZ+ and [3 H]TPMP+ was changed upon incubation in the presence of elevated levels of K+ , ouabain, or KCN, or at 0°C in a way that would be expected from the membrane potential. In normal incubation conditions a membrane potential of ∼−60 mv was calculated. 相似文献
37.
R Ladenstein B Meyer R Huber H Labischinski K Bartels H D Bartunik L Bachmann H C Ludwig A Bacher 《Journal of molecular biology》1986,187(1):87-100
Heavy riboflavin synthase from Bacillus subtilis is an enzyme complex consisting of approximately three alpha-subunits (Mr 23.5 X 10(3)) and 60 beta-subunits (Mr 16 X 10(3)). The enzyme has been crystallized from phosphate buffer in a hexagonal crystal modification that belongs to space group P6(3)22. The asymmetric unit of the crystal cell contains ten beta-subunits. The structure of this unusual 10(6) Mr protein has been studied by small-angle X-ray scattering, electron microscopy of three-dimensional crystals, and crystallographic methods. The scattering curves can be interpreted in terms of a hollow sphere model with a ratio of inner and outer radius of 0.3:1. A diameter of 168 A was estimated from the scattering curves, in close agreement with electron microscopic studies. An aggregate with the stoichiometry beta 60, which was obtained by ligand-driven reaggregation of isolated beta-subunits, showed similar shape and dimensions, but a larger value for the ratio Ri/Ra. Electron micrographs of freeze-etched enzyme crystals showed approximately spherical molecules, which were arranged in hexagonal layers. The lattice constants found from the micrographs are in good agreement with the values derived from X-ray diffraction data. Rotation function calculations in Patterson space showed a set of peaks for 2-fold, 3-fold and 5-fold local rotation axes, accurately consistent with icosahedral symmetry and with the particle orientation A shown in the Appendix. The crystal packing can be described as follows: enzyme particles with icosahedral symmetry (point group 532) are located at points 32 of the hexagonal cell, corresponding to positions (0, 0, 0) and (0, 0, 1/2) on the 6-fold screw axes. From the data reported, it may be concluded that the enzyme structure can be described as an icosahedral capsid of 60 beta-subunits with the triangulation number T = 1. The alpha-subunits are located in the central core space of the capsid, but their spatial orientation is incompletely understood. 相似文献
38.
S. E. Franklin L. Young D. Watson A. Cigan T. Meyer L. A. Bulla Jr. 《Molecular genetics and genomics : MGG》1997,256(5):517-524
Various subspecies of the gram-positive bacterium Bacillus thuringiensis are known to produce a wide array of insecticidal crystal proteins (ICPs) upon sporulation. These ICPs act primarily on the brush border of midgut epithelial cells of susceptible larvae. Recently, a protein of 210?kDa, isolated from the midgut of Manduca sexta, has been demonstrated to bind the Cry1Ab toxin produced by B. thuringiensis subsp. berliner and is therefore postulated to be involved in mediating the toxicity of Cry1Ab. The cDNA encoding the 210?kDa protein, termed BT-R1 (Bacillus thuringiensis receptor-1), was recently cloned, and shows limited homology to the cadherin superfamily of proteins. Quite naturally, there is a great deal of interest in the characterization of BT-R 1 , the gene encoding the 210?kDa Cry1Ab binding protein. The studies presented here involve the use of various restriction fragments prepared from the cDNA encoding BT-R1 as probes of Southern blots bearing M. sexta genomic DNA cleaved with a variety of restriction endonucleases. These Southern blot data reveal that there are two discrete regions within the M. sexta genome which encode sequences homologous to BT-R1. On the basis of the signal intensities seen on Southern blots, it appears that only one of these genes encodes BT-R1, whereas the other is a closely related homologue. 相似文献
39.
40.
C Gerdemann C Eicken A Magrini H E Meyer A Rompel F Spener B Krebs 《Biochimica et biophysica acta》2001,1548(1):94-105
The amino acid sequences of two isozymes of catechol oxidase from sweet potatoes (Ipomoea batatas) were determined by Edman degradation of BrCN cleavage fragments of the native protein and by sequencing of amplified cDNA fragments. Sequence alignment and phylogenetic analysis of plant catechol oxidases revealed about 80% equidistance between the two I. batatas catechol oxidases and approximately 40--60% to catechol oxidases of other plants. When H(2)O(2) was applied as substrate the 39 kDa isozyme, but not the 40 kDa isozyme, showed catalase-like activity. The structure of the 40 kDa isozyme was modeled on the basis of the published crystal structure of the 39 kDa isozyme [T. Klabunde et al., Nat. Struct. Biol. 5 (1998) 1084]. The active site model closely resembled that of the 39 kDa isozyme determined by crystallography, except for a mutation of Thr243 (40 kDa isozyme) to Ile241 (39 kDa isozyme) close to the dimetal center. This residue difference affects the orientation of the Glu238/236 residue, which is thought to be responsible for the catalase-like activity of the 39 kDa isozyme for which a catalytic mechanism is proposed. 相似文献