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991.
Kyle Bittinger Emily S Charlson Elizabeth Loy David J Shirley Andrew R Haas Alice Laughlin Yanjie Yi Gary D Wu James D Lewis Ian Frank Edward Cantu Joshua M Diamond Jason D Christie Ronald G Collman Frederic D Bushman 《Genome biology》2014,15(10)
Background
Fungi are important pathogens but challenging to enumerate using next-generation sequencing because of low absolute abundance in many samples and high levels of fungal DNA from contaminating sources.Results
Here, we analyze fungal lineages present in the human airway using an improved method for contamination filtering. We use DNA quantification data, which are routinely acquired during DNA library preparation, to annotate output sequence data, and improve the identification and filtering of contaminants. We compare fungal communities and bacterial communities from healthy subjects, HIV+ subjects, and lung transplant recipients, providing a gradient of increasing lung impairment for comparison. We use deep sequencing to characterize ribosomal rRNA gene segments from fungi and bacteria in DNA extracted from bronchiolar lavage samples and oropharyngeal wash. Comparison to clinical culture data documents improved detection after applying the filtering procedure.Conclusions
We find increased representation of medically relevant organisms, including Candida, Cryptococcus, and Aspergillus, in subjects with increasingly severe pulmonary and immunologic deficits. We analyze covariation of fungal and bacterial taxa, and find that oropharyngeal communities rich in Candida are also rich in mitis group Streptococci, a community pattern associated with pathogenic polymicrobial biofilms. Thus, using this approach, it is possible to characterize fungal communities in the human respiratory tract more accurately and explore their interactions with bacterial communities in health and disease.Electronic supplementary material
The online version of this article (doi:10.1186/s13059-014-0487-y) contains supplementary material, which is available to authorized users. 相似文献992.
Thomas Vanhercke Anna El Tahchy Qing Liu Xue‐Rong Zhou Pushkar Shrestha Uday K. Divi Jean‐Philippe Ral Maged P. Mansour Peter D. Nichols Christopher N. James Patrick J. Horn Kent D. Chapman Frederic Beaudoin Noemi Ruiz‐López Philip J. Larkin Robert C. de Feyter Surinder P. Singh James R. Petrie 《Plant biotechnology journal》2014,12(2):231-239
High biomass crops have recently attracted significant attention as an alternative platform for the renewable production of high energy storage lipids such as triacylglycerol (TAG). While TAG typically accumulates in seeds as storage compounds fuelling subsequent germination, levels in vegetative tissues are generally low. Here, we report the accumulation of more than 15% TAG (17.7% total lipids) by dry weight in Nicotiana tabacum (tobacco) leaves by the co‐expression of three genes involved in different aspects of TAG production without severely impacting plant development. These yields far exceed the levels found in wild‐type leaf tissue as well as previously reported engineered TAG yields in vegetative tissues of Arabidopsis thaliana and N. tabacum. When translated to a high biomass crop, the current levels would translate to an oil yield per hectare that exceeds those of most cultivated oilseed crops. Confocal fluorescence microscopy and mass spectrometry imaging confirmed the accumulation of TAG within leaf mesophyll cells. In addition, we explored the applicability of several existing oil‐processing methods using fresh leaf tissue. Our results demonstrate the technical feasibility of a vegetative plant oil production platform and provide for a step change in the bioenergy landscape, opening new prospects for sustainable food, high energy forage, biofuel and biomaterial applications. 相似文献
993.
Identity-by-descent probabilities are important for many applications in genetics. Here we propose a method for modeling the transmission of the haplotypes from the closest genotyped relatives along an entire chromosome. The method relies on a hidden Markov model where hidden states correspond to the set of all possible origins of a haplotype within a given pedigree. Initial state probabilities are estimated from average genetic contribution of each origin to the modeled haplotype while transition probabilities are computed from recombination probabilities and pedigree relationships between the modeled haplotype and the various possible origins. The method was tested on three simulated scenarios based on real data sets from dairy cattle, Arabidopsis thaliana, and maize. The mean identity-by-descent probabilities estimated for the truly inherited parental chromosome ranged from 0.94 to 0.98 according to the design and the marker density. The lowest values were observed in regions close to crossing over or where the method was not able to discriminate between several origins due to their similarity. It is shown that the estimated probabilities were correctly calibrated. For marker imputation (or QTL allele prediction for fine mapping or genomic selection), the method was efficient, with 3.75% allelic imputation error rates on a dairy cattle data set with a low marker density map (1 SNP/Mb). The method should prove useful for situations we are facing now in experimental designs and in plant and animal breeding, where founders are genotyped with relatively high markers densities and last generation(s) genotyped with a lower-density panel. 相似文献
994.
de Medina P Paillasse MR Ségala G Khallouki F Brillouet S Dalenc F Courbon F Record M Poirot M Silvente-Poirot S 《Chemistry and physics of lipids》2011,(6):432-437
Tamoxifen is one of the major drugs used for the hormonotherapy of estrogen receptor positive breast cancers. However, its therapeutic efficacy can be limited by acquired resistance and tumor recurrence can occur after several years of treatment. Tamoxifen is known as the prototypical modulator of estrogen receptors, but other targets have been identified that could account for its pharmacology. In particular, tamoxifen binds with high affinity to the microsomal antiestrogen binding site (AEBS) and inhibits cholesterol esterification at therapeutic doses. We have recently shown that the AEBS was a hetero-oligomeric complex composed of 3β-hydroxysterol-Δ(8)-Δ(7)-isomerase and 3β-hydroxysterol-Δ(7)-reductase, that binds different structural classes of ligands, including selective estrogen receptor modulators, several sigma receptor ligands, poly-unsaturated fatty acids and ring B oxysterols. We established a link between the modulation of cholesterol metabolism by tamoxifen and other AEBS ligands and their capacity to induce breast cancer cell differentiation, apoptosis and autophagy. Moreover, we showed that the AEBS carries out cholesterol-5,6-epoxide hydrolase activity and established that cholesterol-5,6-epoxide hydrolase is a new target for tamoxifen and other AEBS ligands. Finally in this review, we report on recent data from the literature showing how the modulation of cholesterol and oxysterol metabolism can be linked to the antitumor and chemopreventive properties of tamoxifen, and give new perspectives to improve the clinical outcome of the hormonotherapy of breast cancers. 相似文献
995.
Akhmetzhanov AR Grognard F Mailleret L 《Evolution; international journal of organic evolution》2011,65(11):3113-3125
The interplay between individual adaptive life histories and populations dynamics is an important issue in ecology. In this context, we considered a seasonal consumer-resource model with nonoverlapping generations. We focused on the consumers decision-making process through which they maximize their reproductive output via a differential investment into foraging for resources or reproducing. Our model takes a semi-discrete form, and is composed of a continuous time within-season part, similar to a dynamic model of energy allocation, and of a discrete time part, depicting the between seasons reproduction and mortality processes. We showed that the optimal foraging-reproduction strategies of the consumers may be "determinate" or "indeterminate" depending on the season length. More surprisingly, it depended on the consumers population density as well, with large densities promoting indeterminacy. A bifurcation analysis showed that the long-term dynamics produced by this model were quite rich, ranging from both populations' extinction, coexistence at some season-to-season equilibrium or on (quasi)-periodic motions, to initial condition-dependent dynamics. Interestingly, we observed that any long-term sustainable situation corresponds to indeterminate consumers' strategies. Finally, a comparison with a model involving typical nonoptimal consumers highlighted the stabilizing effects of the optimal life histories of the consumers. 相似文献
996.
Navarro-Sastre A Tort F Stehling O Uzarska MA Arranz JA Del Toro M Labayru MT Landa J Font A Garcia-Villoria J Merinero B Ugarte M Gutierrez-Solana LG Campistol J Garcia-Cazorla A Vaquerizo J Riudor E Briones P Elpeleg O Ribes A Lill R 《American journal of human genetics》2011,(5):656-667
We report on ten individuals with a fatal infantile encephalopathy and/or pulmonary hypertension, leading to death before the age of 15 months. Hyperglycinemia and lactic acidosis were common findings. Glycine cleavage system and pyruvate dehydrogenase complex (PDHC) activities were low. Homozygosity mapping revealed a perfectly overlapping homozygous region of 1.24 Mb corresponding to chromosome 2 and led to the identification of a homozygous missense mutation (c.622G > T) in NFU1, which encodes a conserved protein suggested to participate in Fe-S cluster biogenesis. Nine individuals were homozygous for this mutation, whereas one was compound heterozygous for this and a splice-site (c.545 + 5G > A) mutation. The biochemical phenotype suggested an impaired activity of the Fe-S enzyme lipoic acid synthase (LAS). Direct measurement of protein-bound lipoic acid in individual tissues indeed showed marked decreases. Upon depletion of NFU1 by RNA interference in human cell culture, LAS and, in turn, PDHC activities were largely diminished. In addition, the amount of succinate dehydrogenase, but no other Fe-S proteins, was decreased. In contrast, depletion of the general Fe-S scaffold protein ISCU severely affected assembly of all tested Fe-S proteins, suggesting that NFU1 performs a specific function in mitochondrial Fe-S cluster maturation. Similar biochemical effects were observed in Saccharomyces cerevisiae upon deletion of NFU1, resulting in lower lipoylation and SDH activity. Importantly, yeast Nfu1 protein carrying the individuals' missense mutation was functionally impaired. We conclude that NFU1 functions as a late-acting maturation factor for a subset of mitochondrial Fe-S proteins. 相似文献
997.
998.
Rodrigo Gonzalez-Valencia Armando Sepulveda-Jauregui Karla Martinez-Cruz Jorge Hoyos-Santillan Luc Dendooven Frederic Thalasso 《Hydrobiologia》2014,721(1):9-22
The literature concerning methane (CH4) emissions from temperate and boreal lakes is extensive, but emissions from tropical and subtropical lakes have been less documented. In particular, methane emissions from Mexican lakes, which are often polluted by anthropogenic carbon and nutrient inputs, have not been reported previously. In this work, methane emissions from six Mexican lakes were measured, covering a broad range of organic inputs, trophic states, and climatic conditions. Methane emissions ranged from 5 to 5,000 mg CH4 m?2 day?1. Water samples from several depths in each lake were analyzed for correlation between water quality indicators and methane emissions. Trophic state and water quality indexes were most strongly correlated with methane fluxes. The global methane flux from Mexican freshwater lakes was estimated to be approximately 1.3 Tg CH4 year?1, which is about 20% of methane and 4.4% of total national greenhouse gas emissions. Data for untreated wastewater releases to the environment gave an emission factor of 0.19 kg CH4 kg?1 of Biochemical Oxygen Demand, which is superior to that previously estimated by the IPCC for lake discharges. Thus, the large volume of untreated wastewater in Mexico implies higher methane emission than previously estimated. 相似文献
999.
Kushol Gupta Troy Brady Benjamin M. Dyer Nirav Malani Young Hwang Frances Male Robert T. Nolte Liping Wang Emile Velthuisen Jerry Jeffrey Gregory D. Van Duyne Frederic D. Bushman 《The Journal of biological chemistry》2014,289(30):20477-20488
HIV-1 replication in the presence of antiviral agents results in evolution of drug-resistant variants, motivating the search for additional drug classes. Here we report studies of GSK1264, which was identified as a compound that disrupts the interaction between HIV-1 integrase (IN) and the cellular factor lens epithelium-derived growth factor (LEDGF)/p75. GSK1264 displayed potent antiviral activity and was found to bind at the site occupied by LEDGF/p75 on IN by x-ray crystallography. Assays of HIV replication in the presence of GSK1264 showed only modest inhibition of the early infection steps and little effect on integration targeting, which is guided by the LEDGF/p75·IN interaction. In contrast, inhibition of late replication steps was more potent. Particle production was normal, but particles showed reduced infectivity. GSK1264 promoted aggregation of IN and preformed LEDGF/p75·IN complexes, suggesting a mechanism of inhibition. LEDGF/p75 was not displaced from IN during aggregation, indicating trapping of LEDGF/p75 in aggregates. Aggregation assays with truncated IN variants revealed that a construct with catalytic and C-terminal domains of IN only formed an open polymer associated with efficient drug-induced aggregation. These data suggest that the allosteric inhibitors of IN are promising antiviral agents and provide new information on their mechanism of action. 相似文献
1000.
Alexandra Duverger Frank Wolschendorf Joshua C. Anderson Frederic Wagner Alberto Bosque Takao Shishido Jennifer Jones Vicente Planelles Christopher Willey Randall Q. Cron Olaf Kutsch 《Journal of virology》2014,88(1):364-376
Despite the clinical relevance of latent HIV-1 infection as a block to HIV-1 eradication, the molecular biology of HIV-1 latency remains incompletely understood. We recently demonstrated the presence of a gatekeeper kinase function that controls latent HIV-1 infection. Using kinase array analysis, we here expand on this finding and demonstrate that the kinase activity profile of latently HIV-1-infected T cells is altered relative to that of uninfected T cells. A ranking of altered kinases generated from these kinome profile data predicted PIM-1 kinase as a key switch involved in HIV-1 latency control. Using genetic and pharmacologic perturbation strategies, we demonstrate that PIM-1 activity is indeed required for HIV-1 reactivation in T cell lines and primary CD4 T cells. The presented results thus confirm that kinases are key contributors to HIV-1 latency control. In addition, through mutational studies we link the inhibitory effect of PIM-1 inhibitor IV (PIMi IV) on HIV-1 reactivation to an AP-1 motif in the CD28-responsive element of the HIV-1 long terminal repeat (LTR). The results expand our conceptual understanding of the dynamic interactions of the host cell and the latent HIV-1 integration event and position kinome profiling as a research tool to reveal novel molecular mechanisms that can eventually be targeted to therapeutically trigger HIV-1 reactivation. 相似文献