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331.
We conducted an experiment on eastern fence lizards ( Sceloporus undulatus ) during August-September 1995 near Los Alamos, New Mexico, (1) to ascertain if lizards that were relocated short distances exhibited homing, (2) to investigate a possible barrier to movement, and (3) to determine the effect of translocating individuals from a transplant area on lizards in a recipient area. We relocated 15 of an estimated population of 39 (95% CI 36-45) lizards an average distance of 46 m. Fourteen of 15 translocated lizards returned to within 6.81 ( s  ̄x = 1.43) m of the original capture location. Movement distances did not vary ( F = 0.76; 1,53 df; P = 0.381) between resident and translocated lizards during the pretreatment period and did not vary for resident ( F = 2.86; 1,12 df; P = 0.1166), but varied between pretreatment and posttreatment periods for translocated ( F = 14.65, 1,7 df, P 0.0065) lizards. Translocated lizards did not affect the resighting probability of resident lizards ( F = 0.96; 1,14 df; P = 0.34), but this may be related to low power (1 — β = 0.15) and translocated lizards moving out of the area quickly. 相似文献
332.
The philosopher of chemistry Andrea Woody has recently published a wide-ranging article concerning the turn to practice in the philosophy of science. Her primary example consists of the use of different forms of representations by Lothar Meyer and Mendeleev when they presented their views on chemical periodicity. Woody believes that this distinction can cast light on various issues including why Mendeleev was able to make predictions while Meyer was not. Secondly, she claims that it can clarify the much-debated question concerning the relative values of prediction and accommodation of data in the way that the periodic system was accepted. Thirdly, Woody believes that such differences in the representation of periodicity can be used to argue for the explanatory nature of the periodic table in contrast with the more traditional view that the periodic table is not explanatory.This discussion examines each of these claims and argues that they need to be qualified and in some cases rejected. 相似文献
333.
Davidson EH 《Nature》2010,468(7326):911-920
Gene regulatory networks (GRNs) provide system level explanations of developmental and physiological functions in the terms of the genomic regulatory code. Depending on their developmental functions, GRNs differ in their degree of hierarchy, and also in the types of modular sub-circuit of which they are composed, although there is a commonly employed sub-circuit repertoire. Mathematical modelling of some types of GRN sub-circuit has deepened biological understanding of the functions they mediate. The structural organization of various kinds of GRN reflects their roles in the life process, and causally illuminates both developmental and evolutionary process. 相似文献
334.
Reich D Green RE Kircher M Krause J Patterson N Durand EY Viola B Briggs AW Stenzel U Johnson PL Maricic T Good JM Marques-Bonet T Alkan C Fu Q Mallick S Li H Meyer M Eichler EE Stoneking M Richards M Talamo S Shunkov MV Derevianko AP Hublin JJ Kelso J Slatkin M Pääbo S 《Nature》2010,468(7327):1053-1060
Using DNA extracted from a finger bone found in Denisova Cave in southern Siberia, we have sequenced the genome of an archaic hominin to about 1.9-fold coverage. This individual is from a group that shares a common origin with Neanderthals. This population was not involved in the putative gene flow from Neanderthals into Eurasians; however, the data suggest that it contributed 4-6% of its genetic material to the genomes of present-day Melanesians. We designate this hominin population 'Denisovans' and suggest that it may have been widespread in Asia during the Late Pleistocene epoch. A tooth found in Denisova Cave carries a mitochondrial genome highly similar to that of the finger bone. This tooth shares no derived morphological features with Neanderthals or modern humans, further indicating that Denisovans have an evolutionary history distinct from Neanderthals and modern humans. 相似文献
335.
The proteasome is the major ATP-dependent protease in eukaryotic cells, but limited structural information restricts a mechanistic understanding of its activities. The proteasome regulatory particle, consisting of the lid and base subcomplexes, recognizes and processes polyubiquitinated substrates. Here we used electron microscopy and a new heterologous expression system for the lid to delineate the complete subunit architecture of the regulatory particle from yeast. Our studies reveal the spatial arrangement of ubiquitin receptors, deubiquitinating enzymes and the protein unfolding machinery at subnanometre resolution, outlining the substrate's path to degradation. Unexpectedly, the ATPase subunits within the base unfoldase are arranged in a spiral staircase, providing insight into potential mechanisms for substrate translocation through the central pore. Large conformational rearrangements of the lid upon holoenzyme formation suggest allosteric regulation of deubiquitination. We provide a structural basis for the ability of the proteasome to degrade a diverse set of substrates and thus regulate vital cellular processes. 相似文献
336.
Welsh WF Orosz JA Carter JA Fabrycky DC Ford EB Lissauer JJ Prša A Quinn SN Ragozzine D Short DR Torres G Winn JN Doyle LR Barclay T Batalha N Bloemen S Brugamyer E Buchhave LA Caldwell C Caldwell DA Christiansen JL Ciardi DR Cochran WD Endl M Fortney JJ Gautier TN Gilliland RL Haas MR Hall JR Holman MJ Howard AW Howell SB Isaacson H Jenkins JM Klaus TC Latham DW Li J Marcy GW Mazeh T Quintana EV Robertson P Shporer A Steffen JH Windmiller G Koch DG Borucki WJ 《Nature》2012,481(7382):475-479
Most Sun-like stars in the Galaxy reside in gravitationally bound pairs of stars (binaries). Although long anticipated, the existence of a 'circumbinary planet' orbiting such a pair of normal stars was not definitively established until the discovery of the planet transiting (that is, passing in front of) Kepler-16. Questions remained, however, about the prevalence of circumbinary planets and their range of orbital and physical properties. Here we report two additional transiting circumbinary planets: Kepler-34 (AB)b and Kepler-35 (AB)b, referred to here as Kepler-34 b and Kepler-35 b, respectively. Each is a low-density gas-giant planet on an orbit closely aligned with that of its parent stars. Kepler-34 b orbits two Sun-like stars every 289?days, whereas Kepler-35 b orbits a pair of smaller stars (89% and 81% of the Sun's mass) every 131?days. The planets experience large multi-periodic variations in incident stellar radiation arising from the orbital motion of the stars. The observed rate of circumbinary planets in our sample implies that more than ~1% of close binary stars have giant planets in nearly coplanar orbits, yielding a Galactic population of at least several million. 相似文献
337.
Rett syndrome is an X-linked autism spectrum disorder. The disease is characterized in most cases by mutation of the MECP2 gene, which encodes a methyl-CpG-binding protein. Although MECP2 is expressed in many tissues, the disease is generally attributed to a primary neuronal dysfunction. However, as shown recently, glia, specifically astrocytes, also contribute to Rett pathophysiology. Here we examine the role of another form of glia, microglia, in a murine model of Rett syndrome. Transplantation of wild-type bone marrow into irradiation-conditioned Mecp2-null hosts resulted in engraftment of brain parenchyma by bone-marrow-derived myeloid cells of microglial phenotype, and arrest of disease development. However, when cranial irradiation was blocked by lead shield, and microglial engraftment was prevented, disease was not arrested. Similarly, targeted expression of MECP2 in myeloid cells, driven by Lysm(cre) on an Mecp2-null background, markedly attenuated disease symptoms. Thus, through multiple approaches, wild-type Mecp2-expressing microglia within the context of an Mecp2-null male mouse arrested numerous facets of disease pathology: lifespan was increased, breathing patterns were normalized, apnoeas were reduced, body weight was increased to near that of wild type, and locomotor activity was improved. Mecp2(+/-) females also showed significant improvements as a result of wild-type microglial engraftment. These benefits mediated by wild-type microglia, however, were diminished when phagocytic activity was inhibited pharmacologically by using annexin V to block phosphatydilserine residues on apoptotic targets, thus preventing recognition and engulfment by tissue-resident phagocytes. These results suggest the importance of microglial phagocytic activity in Rett syndrome. Our data implicate microglia as major players in the pathophysiology of this devastating disorder, and suggest that bone marrow transplantation might offer a feasible therapeutic approach for it. 相似文献
338.
Everitt AR Clare S Pertel T John SP Wash RS Smith SE Chin CR Feeley EM Sims JS Adams DJ Wise HM Kane L Goulding D Digard P Anttila V Baillie JK Walsh TS Hume DA Palotie A Xue Y Colonna V Tyler-Smith C Dunning J Gordon SB;GenISIS Investigators;MOSAIC Investigators Smyth RL Openshaw PJ Dougan G Brass AL Kellam P 《Nature》2012,484(7395):519-523
The 2009 H1N1 influenza pandemic showed the speed with which a novel respiratory virus can spread and the ability of a generally mild infection to induce severe morbidity and mortality in a subset of the population. Recent in vitro studies show that the interferon-inducible transmembrane (IFITM) protein family members potently restrict the replication of multiple pathogenic viruses. Both the magnitude and breadth of the IFITM proteins' in vitro effects suggest that they are critical for intrinsic resistance to such viruses, including influenza viruses. Using a knockout mouse model, we now test this hypothesis directly and find that IFITM3 is essential for defending the host against influenza A virus in vivo. Mice lacking Ifitm3 display fulminant viral pneumonia when challenged with a normally low-pathogenicity influenza virus, mirroring the destruction inflicted by the highly pathogenic 1918 'Spanish' influenza. Similar increased viral replication is seen in vitro, with protection rescued by the re-introduction of Ifitm3. To test the role of IFITM3 in human influenza virus infection, we assessed the IFITM3 alleles of individuals hospitalized with seasonal or pandemic influenza H1N1/09 viruses. We find that a statistically significant number of hospitalized subjects show enrichment for a minor IFITM3 allele (SNP rs12252-C) that alters a splice acceptor site, and functional assays show the minor CC genotype IFITM3 has reduced influenza virus restriction in vitro. Together these data reveal that the action of a single intrinsic immune effector, IFITM3, profoundly alters the course of influenza virus infection in mouse and humans. 相似文献
339.
340.