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排序方式: 共有136条查询结果,搜索用时 15 毫秒
41.
Kristina J. Brunjes Warren B. Ballard Mary H. Humphrey Fielding Harwell Nancy E. McIntyre Paul R. Krausman Mark C. Wallace 《西北部美国博物学家》2011,69(1)
Information about the ecology of sympatric male deer is limited, which may influence management strategies for these species. We estimated home-range and core-area sizes and overlap, and survival of sympatric male desert mule deer ( Odocoileus hemionus eremicus ) and white-tailed deer ( Odocoileus virginianus ) in west central Texas. We captured 18 males of each species, fitted them with radio-collars, and monitored them for mortality from 2000 through 2003. We calculated home ranges for 7 males of each species in 2001 and 2002. Home-range sizes of mule deer (8.8 km 2 ) and white-tailed deer (7.4 km 2 ) were similar. Interspecific home-range overlap was less common than intraspecific overlap. Mean annual survival was 0.76 (SE = 0.04) for mule deer and 0.80 (SE = 0.06) for white-tailed deer. The high degree of home-range overlap and similar survival between the 2 deer species suggest that management targeting only 1 species may be unfeasible. 相似文献
42.
Warren J. Blumenfeld 《Journal of Classification》2011,28(1):6-6
Reviewers
Guest Reviewers, Journal of Classification Volume 28(1) 2011, Special Issue 相似文献43.
Identification of an actin-binding protein from Dictyostelium as elongation factor 1a 总被引:30,自引:0,他引:30
Indirect evidence has implicated an interaction between the cytoskeleton and the protein synthetic machinery. Two recent reports have linked the elongation factor 1a (EF-1a) which is involved in protein synthesis, with the microtubular cytoskeleton. In situ hybridization has, however, revealed that the messages for certain cytoskeletal proteins are preferentially associated with actin filaments. ABP-50 is an abundant actin filament bundling protein of native relative molecular mass 50,000 (50K) isolated from Dictyostelium discoideum. Immunofluorescence studies show that ABP-50 is present in filopodia and other cortical regions that contain actin filament bundles. In addition, ABP-50 binds to monomeric actin in the cytosol of unstimulated cells and the association of ABP-50 with the actin cytoskeleton is regulated during chemotaxis. Through complementary DNA sequencing and subsequent functional analysis, we have identified ABP-50 as D. discoideum EF-1a. The ability of EF-1a to bind reversibly to the actin cytoskeleton upon stimulation could provide a mechanism for spatially and temporally regulated protein synthesis in eukaryotic cells. 相似文献
44.
Intracellular transport. Vesicular consumption 总被引:1,自引:0,他引:1
45.
Homology between Streptomyces genes coding for synthesis of different polyketides used to clone antibiotic biosynthetic genes 总被引:5,自引:0,他引:5
F Malpartida S E Hallam H M Kieser H Motamedi C R Hutchinson M J Butler D A Sugden M Warren C McKillop C R Bailey 《Nature》1987,325(6107):818-821
Many important antibiotics such as tetracyclines, erythromycin, adriamycin, monensin, rifamycin and avermectins are polyketides. In their biosynthesis, multifunctional synthases catalyse iterated condensation of thio-esters derived from acetate, propionate or butyrate to yield aliphatic chains of varying length and carrying different alkyl substituents. Subsequent modifications, including aromatic or macrolide ring closure or specific methylations or glycosylations, generate further chemical diversity. It has been suggested that, if different polyketide synthases had a common evolutionary origin, cloned DNA coding for one synthase might be used as a hybridization probe for the isolation of others. We show here that this is indeed possible. Study of a range of such synthase genes and their products should help to elucidate what determines the choice and order of condensation of different residues in polyketide assembly, and might yield, by in vitro recombination or mutagenesis, synthase genes capable of producing novel antibiotics. Moreover, because genes for entire antibiotic pathways are usually clustered in Streptomyces, cloned polyketide synthase genes are valuable in giving access to groups of linked biosynthetic genes. 相似文献
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48.
ColE1 plasmid mobility and relaxation complex. 总被引:20,自引:0,他引:20
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50.
Blumenfeld I Clayton CE Decker FJ Hogan MJ Huang C Ischebeck R Iverson R Joshi C Katsouleas T Kirby N Lu W Marsh KA Mori WB Muggli P Oz E Siemann RH Walz D Zhou M 《Nature》2007,445(7129):741-744
The energy frontier of particle physics is several trillion electron volts, but colliders capable of reaching this regime (such as the Large Hadron Collider and the International Linear Collider) are costly and time-consuming to build; it is therefore important to explore new methods of accelerating particles to high energies. Plasma-based accelerators are particularly attractive because they are capable of producing accelerating fields that are orders of magnitude larger than those used in conventional colliders. In these accelerators, a drive beam (either laser or particle) produces a plasma wave (wakefield) that accelerates charged particles. The ultimate utility of plasma accelerators will depend on sustaining ultrahigh accelerating fields over a substantial length to achieve a significant energy gain. Here we show that an energy gain of more than 42 GeV is achieved in a plasma wakefield accelerator of 85 cm length, driven by a 42 GeV electron beam at the Stanford Linear Accelerator Center (SLAC). The results are in excellent agreement with the predictions of three-dimensional particle-in-cell simulations. Most of the beam electrons lose energy to the plasma wave, but some electrons in the back of the same beam pulse are accelerated with a field of approximately 52 GV m(-1). This effectively doubles their energy, producing the energy gain of the 3-km-long SLAC accelerator in less than a metre for a small fraction of the electrons in the injected bunch. This is an important step towards demonstrating the viability of plasma accelerators for high-energy physics applications. 相似文献