全文获取类型
收费全文 | 9570篇 |
免费 | 856篇 |
国内免费 | 3篇 |
出版年
2023年 | 53篇 |
2022年 | 104篇 |
2021年 | 187篇 |
2020年 | 122篇 |
2019年 | 157篇 |
2018年 | 178篇 |
2017年 | 192篇 |
2016年 | 322篇 |
2015年 | 496篇 |
2014年 | 552篇 |
2013年 | 673篇 |
2012年 | 740篇 |
2011年 | 671篇 |
2010年 | 441篇 |
2009年 | 379篇 |
2008年 | 557篇 |
2007年 | 564篇 |
2006年 | 529篇 |
2005年 | 476篇 |
2004年 | 476篇 |
2003年 | 441篇 |
2002年 | 444篇 |
2001年 | 97篇 |
2000年 | 78篇 |
1999年 | 103篇 |
1998年 | 115篇 |
1997年 | 80篇 |
1996年 | 86篇 |
1995年 | 74篇 |
1994年 | 57篇 |
1993年 | 74篇 |
1992年 | 67篇 |
1991年 | 52篇 |
1990年 | 41篇 |
1989年 | 45篇 |
1988年 | 39篇 |
1987年 | 36篇 |
1986年 | 38篇 |
1985年 | 39篇 |
1984年 | 46篇 |
1983年 | 40篇 |
1982年 | 40篇 |
1981年 | 36篇 |
1980年 | 28篇 |
1979年 | 31篇 |
1978年 | 37篇 |
1977年 | 26篇 |
1976年 | 39篇 |
1974年 | 20篇 |
1973年 | 23篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
971.
Wright J Bellissimi E de Hulster E Wagner A Pronk JT van Maris AJ 《FEMS yeast research》2011,11(3):299-306
Acetic acid tolerance of Saccharomyces cerevisiae is crucial for the production of bioethanol and other bulk chemicals from lignocellulosic plant-biomass hydrolysates, especially at a low pH. This study explores two evolutionary engineering strategies for the improvement of acetic acid tolerance of the xylose-fermenting S. cerevisiae RWB218, whose anaerobic growth on xylose at pH 4 is inhibited at acetic acid concentrations >1 g L(-1) : (1) sequential anaerobic, batch cultivation (pH 4) at increasing acetic acid concentrations and (2) prolonged anaerobic continuous cultivation without pH control, in which acidification by ammonium assimilation generates selective pressure for acetic acid tolerance. After c. 400 generations, the sequential-batch and continuous selection cultures grew on xylose at pH≤4 with 6 and 5 g L(-1) acetic acid, respectively. In the continuous cultures, the specific xylose-consumption rate had increased by 75% to 1.7 g xylose g(-1) biomass h(-1) . After storage of samples from both selection experiments at -80 °C and cultivation without acetic acid, they failed to grow on xylose at pH 4 in the presence of 5 g L(-1) acetic acid. Characterization in chemostat cultures with linear acetic acid gradients demonstrated an acetate-inducible acetic acid tolerance in samples from the continuous selection protocol. 相似文献
972.
973.
The spread of infectious diseases fundamentally depends on the pattern of contacts between individuals. Although studies of contact networks have shown that heterogeneity in the number of contacts and the duration of contacts can have far-reaching epidemiological consequences, models often assume that contacts are chosen at random and thereby ignore the sociological, temporal and/or spatial clustering of contacts. Here we investigate the simultaneous effects of heterogeneous and clustered contact patterns on epidemic dynamics. To model population structure, we generalize the configuration model which has a tunable degree distribution (number of contacts per node) and level of clustering (number of three cliques). To model epidemic dynamics for this class of random graph, we derive a tractable, low-dimensional system of ordinary differential equations that accounts for the effects of network structure on the course of the epidemic. We find that the interaction between clustering and the degree distribution is complex. Clustering always slows an epidemic, but simultaneously increasing clustering and the variance of the degree distribution can increase final epidemic size. We also show that bond percolation-based approximations can be highly biased if one incorrectly assumes that infectious periods are homogeneous, and the magnitude of this bias increases with the amount of clustering in the network. We apply this approach to model the high clustering of contacts within households, using contact parameters estimated from survey data of social interactions, and we identify conditions under which network models that do not account for household structure will be biased. 相似文献
974.
Ameur A Stewart JB Freyer C Hagström E Ingman M Larsson NG Gyllensten U 《PLoS genetics》2011,7(3):e1002028
Somatic mutations of mtDNA are implicated in the aging process, but there is no universally accepted method for their accurate quantification. We have used ultra-deep sequencing to study genome-wide mtDNA mutation load in the liver of normally- and prematurely-aging mice. Mice that are homozygous for an allele expressing a proof-reading-deficient mtDNA polymerase (mtDNA mutator mice) have 10-times-higher point mutation loads than their wildtype siblings. In addition, the mtDNA mutator mice have increased levels of a truncated linear mtDNA molecule, resulting in decreased sequence coverage in the deleted region. In contrast, circular mtDNA molecules with large deletions occur at extremely low frequencies in mtDNA mutator mice and can therefore not drive the premature aging phenotype. Sequence analysis shows that the main proportion of the mutation load in heterozygous mtDNA mutator mice and their wildtype siblings is inherited from their heterozygous mothers consistent with germline transmission. We found no increase in levels of point mutations or deletions in wildtype C57Bl/6N mice with increasing age, thus questioning the causative role of these changes in aging. In addition, there was no increased frequency of transversion mutations with time in any of the studied genotypes, arguing against oxidative damage as a major cause of mtDNA mutations. Our results from studies of mice thus indicate that most somatic mtDNA mutations occur as replication errors during development and do not result from damage accumulation in adult life. 相似文献
975.
The major replicative DNA polymerases of S. cerevisiae (Pols α, δ, and ?) incorporate substantial numbers of ribonucleotides into DNA during DNA synthesis. When these ribonucleotides are not removed in vivo, they reside in the template strand used for the next round of replication and could potentially reduce replication efficiency and fidelity. To examine if the presence of ribonucleotides in a DNA template impede DNA synthesis, we determined the efficiency with which Pols α, δ, and ? copy DNA templates containing a single ribonucleotide. All three polymerases can replicate past ribonucleotides. Relative to all-DNA templates, bypass of ribo-containing templates is slightly reduced, to extents that depend on the identity of the ribo and the sequence context in which it resides. Bypass efficiencies for Pols δ and ? were increased by increasing the dNTP concentrations to those induced by cellular stress, and in the case of Pol ?, by inactivating the 3'-exonuclease activity. Overall, ribonucleotide bypass efficiencies are comparable to, and usually exceed, those for the common oxidative stress-induced lesion 8-oxo-guanine. 相似文献
976.
977.
Holleboom AG Karlsson H Lin RS Beres TM Sierts JA Herman DS Stroes ES Aerts JM Kastelein JJ Motazacker MM Dallinga-Thie GM Levels JH Zwinderman AH Seidman JG Seidman CE Ljunggren S Lefeber DJ Morava E Wevers RA Fritz TA Tabak LA Lindahl M Hovingh GK Kuivenhoven JA 《Cell metabolism》2011,14(6):811-818
Genome-wide association studies have identified GALNT2 as a candidate gene in lipid metabolism, but it is not known how the encoded enzyme ppGalNAc-T2, which contributes to the initiation of mucin-type O-linked glycosylation, mediates this effect. In two probands with elevated plasma high-density lipoprotein cholesterol and reduced triglycerides, we identified a mutation in GALNT2. It is shown that carriers have improved postprandial triglyceride clearance, which is likely attributable to attenuated glycosylation of apolipoprotein (apo) C-III, as observed in their plasma. This protein inhibits lipoprotein lipase (LPL), which hydrolyses plasma triglycerides. We show that an apoC-III-based peptide is a substrate for ppGalNAc-T2 while its glycosylation by the mutant enzyme is impaired. In addition, neuraminidase treatment of apoC-III which removes the sialic acids from its glycan chain decreases its potential to inhibit LPL. Combined, these data suggest that ppGalNAc-T2 can affect lipid metabolism through apoC-III glycosylation, thereby establishing GALNT2 as a lipid-modifying gene. 相似文献
978.
In this overview to biomedical computing in the cloud, we discussed two primary ways to use the cloud (a single instance or cluster), provided a detailed example using NGS mapping, and highlighted the associated costs. While many users new to the cloud may assume that entry is as straightforward as uploading an application and selecting an instance type and storage options, we illustrated that there is substantial up-front effort required before an application can make full use of the cloud's vast resources. Our intention was to provide a set of best practices and to illustrate how those apply to a typical application pipeline for biomedical informatics, but also general enough for extrapolation to other types of computational problems. Our mapping example was intended to illustrate how to develop a scalable project and not to compare and contrast alignment algorithms for read mapping and genome assembly. Indeed, with a newer aligner such as Bowtie, it is possible to map the entire African genome using one m2.2xlarge instance in 48 hours for a total cost of approximately $48 in computation time. In our example, we were not concerned with data transfer rates, which are heavily influenced by the amount of available bandwidth, connection latency, and network availability. When transferring large amounts of data to the cloud, bandwidth limitations can be a major bottleneck, and in some cases it is more efficient to simply mail a storage device containing the data to AWS (http://aws.amazon.com/importexport/). More information about cloud computing, detailed cost analysis, and security can be found in references. 相似文献
979.
Vidar Selås Geir A. Sonerud Olav Hjeljord Lars Erik Gangsei Helge B. Pedersen Erik Framstad Tor Kristian Spidsø Øystein Wiig 《European Journal of Wildlife Research》2011,57(3):523-535
The plant stress hypothesis states that plant stress factors other than herbivory improve herbivore performance due to changes
in the content of nutritive or defensive compounds in the plants. In Norway, the bilberry (Vaccinium myrtillus) is important forage for the bank vole (Myodes glareolus) in winter and for the moose (Alces alces) in summer and autumn. The observed peaks in bank vole numbers after years with high production of bilberries are suggested
to be caused by increased winter survival of bank voles due to improved forage quality. High production of bilberries should
also lead to higher recruitment rates in moose in the following year. We predict, however, that there is an increasing tendency
for a 1-year delay of moose indices relative to vole indices with decreasing summer temperatures, because low temperatures
prolong the period needed by plants to recover in the vole peak year, and thus positively affect moose reproduction also in
the succeeding year. In eight out of nine counties in south-eastern Norway, there was a positive relationship between the
number of calves observed per female moose during hunting and a bilberry seed production index or an autumn bank vole population
index. When dividing the study area into regions, there was a negative relationship between a moose-vole time-lag index and
the mean summer temperature of the region. These patterns suggest that annual fluctuations in the production of bilberries
affect forage quality, but that the effect on moose reproduction also depends on summer temperatures. 相似文献
980.
Dukes MJ Ramachandra R Baudoin JP Gray Jerome W de Jonge N 《Journal of structural biology》2011,174(3):552-562
Three-dimensional (3D) maps of proteins within the context of whole cells are important for investigating cellular function. However, 3D reconstructions of whole cells are challenging to obtain using conventional transmission electron microscopy (TEM). We describe a methodology to determine the 3D locations of proteins labeled with gold nanoparticles on whole eukaryotic cells. The epidermal growth factor receptors on COS7 cells were labeled with gold nanoparticles, and critical-point dried whole-mount cell samples were prepared. 3D focal series were obtained with aberration-corrected scanning transmission electron microscopy (STEM), without tilting the specimen. The axial resolution was improved with deconvolution. The vertical locations of the nanoparticles in a whole-mount cell were determined with a precision of 3nm. From the analysis of the variation of the axial positions of the labels we concluded that the cellular surface was ruffled. To achieve sufficient stability of the sample under electron beam irradiation during the recording of the focal series, the sample was carbon coated. A quantitative method was developed to analyze the stability of the ultrastructure after electron beam irradiation using TEM. The results of this study demonstrate the feasibility of using aberration-corrected STEM to study the 3D nanoparticle distribution in whole cells. 相似文献