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991.
Oxido-pincer ligands with phenolate-groups [2,6-bis(2-methoxyphenyl)pyridine (LOMe2), 2,6-bis(2-hydroxyphenyl)-pyridine (LOH2), 2,6-bis-(2,4-dimethoxyphenyl)-pyridine (LOMe4)] coordinate to CuII forming binuclear complexes which can be easily and reliably converted into mononuclear species. Their physical properties were analysed using EPR, optical spectroscopy and (spectro-)electrochemical methods. The results were compared to those of related NiII complexes and discussed in view of Cu-containing metalloenzymes. Due to the ligands flexibility the CuII/CuI redox couple exhibits high reversibility, while the ligand-centred oxidation leads to highly reactive phenoxy radicals. Reduction of the LOH2 complex leads to sequential deprotonation. The ligand LOMe4 and the derived complexes show blue luminescence, which can be rationalised from its molecular structure (analysed by XRD). 相似文献
992.
Jenson Qi Wensheng Lang Edward Giardino Gary W. Caldwell Charles Smith Lisa K. Minor Andrew L. Darrow Gustaaf Willemsens Katharina DeWaepenaert Peter Roevens Joannes T. M. Linders Yin Liang Margery A. Connelly 《Journal of lipid research》2010,51(12):3559-3567
Acyl-CoA:diacylglycerol acyltransferase (DGAT) catalyzes the terminal step in triglyceride (TG) synthesis using diacylglycerol (DAG) and fatty acyl-CoA as substrates. In the liver, the production of VLDL permits the delivery of hydrophobic TG from the liver to peripheral tissues for energy metabolism. We describe here a novel high-content, high-throughput LC/MS/MS-based cellular assay for determining DGAT activity. We treated endogenous DGAT-expressing cells with stable isotope-labeled [13C18]oleic acid. The [13C18]oleoyl-incorporated TG and DAG lipid species were profiled. The TG synthesis pathway assay was optimized to a one-step extraction, followed by LC/MS/MS quantification. Further, we report a novel LC/MS/MS method for tracing hepatic TG synthesis and VLDL-TG secretion in vivo by administering [13C18]oleic acid to rats. The [13C18]oleic acid-incorporated VLDL-TG was detected after one-step extraction without conventional separation of TG and recovery by derivatizing [13C18]oleic acid for detection. Using potent and selective DGAT1 inhibitors as pharmacological tools, we measured changes in [13C18]oleoyl-incorporated TG and DAG and demonstrated that DGAT1 inhibition significantly reduced [13C18]oleoyl-incorporated VLDL-TG. This DGAT1-selective assay will enable researchers to discern differences between the roles of DGAT1 and DGAT2 in TG synthesis in vitro and in vivo. 相似文献
993.
Alpine ecosystems are, similar to arctic ecosystems, characterized by a very long snow season. Previous studies investigating arctic or alpine ecosystems have shown that winter CO2 effluxes can dominate the annual balance and that the timing and duration of the snow cover plays a crucial role for plant growth and phenology and might also influence the growing season ecosystem CO2 strength and dynamics. The objective of this study was to analyze seasonal and annual CO2 balances of a grassland site at an elevation of 2440 m a.s.l in the Swiss central Alps. We continuously measured the NEP using the eddy covariance method from June 2013 to October 2014, covering two growing seasons and one winter. We analyzed the influence of snow melt date on the CO2 exchange dynamics at this site, because snow melt differed about 24 days between the 2 years. To this end, we employed a process-based ecosystem carbon cycling model to disentangle the co-occurring effects of growing season length, environmental conditions during the growing season, and physiological/structural properties of the canopy on the ecosystem carbon balance. During the measurement period, the site was a net sink for CO2 although winter efflux contributed significantly to the total balance. The cumulative growing season NEP as well as mean and maximum daily CO2 uptake rates was lower during the year with the later snow melt, and the results indicated that the differences were mainly due to differing growing season lengths. 相似文献
994.
Antonia Torcasio Katharina J?hn Maarten Van Guyse Pieter Spaepen Andrea E. Tami Jos Vander Sloten Martin J. Stoddart G. Harry van Lenthe 《PloS one》2014,9(5)
Exposure to microgravity causes loss of lower body bone mass in some astronauts. Low-magnitude high-frequency loading can stimulate bone formation on earth. Here we hypothesized that low-magnitude high-frequency loading will also stimulate bone formation under microgravity conditions. Two groups of six bovine cancellous bone explants were cultured at microgravity on a Russian Foton-M3 spacecraft and were either loaded dynamically using a sinusoidal curve or experienced only a static load. Comparable reference groups were investigated at normal gravity. Bone structure was assessed by histology, and mechanical competence was quantified using μCT and FE modelling; bone remodelling was assessed by fluorescent labelling and secreted bone turnover markers. Statistical analyses on morphometric parameters and apparent stiffness did not reveal significant differences between the treatment groups. The release of bone formation marker from the groups cultured at normal gravity increased significantly from the first to the second week of the experiment by 90.4% and 82.5% in response to static and dynamic loading, respectively. Bone resorption markers decreased significantly for the groups cultured at microgravity by 7.5% and 8.0% in response to static and dynamic loading, respectively. We found low strain magnitudes to drive bone turnover when applied at high frequency, and this to be valid at normal as well as at microgravity. In conclusion, we found the effect of mechanical loading on trabecular bone to be regulated mainly by an increase of bone formation at normal gravity and by a decrease in bone resorption at microgravity. Additional studies with extended experimental time and increased samples number appear necessary for a further understanding of the anabolic potential of dynamic loading on bone quality and mechanical competence. 相似文献
995.
Birds which must learn their species-specific song need a means for choosing the appropriate song model. As individual Bengalese Finch ♂♂ have distinctive songs and song elements it is possible to determine a juvenile's choice of song models from within a restricted population. The results suggest that after an early period of learning from several models, juveniles preferentially copy the song of their father. 相似文献
996.
997.
Gonzalo P. Solis Yvonne Radon Emily Sempou Katharina Jechow Claudia A. O. Stuermer Edward Málaga-Trillo 《PloS one》2013,8(7)
Analyses of cultured cells and transgenic mice expressing prion protein (PrP) deletion mutants have revealed that some properties of PrP -such as its ability to misfold, aggregate and trigger neurotoxicity- are controlled by discrete molecular determinants within its protein domains. Although the contributions of these determinants to PrP biosynthesis and turnover are relatively well characterized, it is still unclear how they modulate cellular functions of PrP. To address this question, we used two defined activities of PrP as functional readouts: 1) the recruitment of PrP to cell-cell contacts in Drosophila S2 and human MCF-7 epithelial cells, and 2) the induction of PrP embryonic loss- and gain-of-function phenotypes in zebrafish. Our results show that homologous mutations in mouse and zebrafish PrPs similarly affect their subcellular localization patterns as well as their in vitro and in vivo activities. Among PrP’s essential features, the N-terminal leader peptide was sufficient to drive targeting of our constructs to cell contact sites, whereas lack of GPI-anchoring and N-glycosylation rendered them inactive by blocking their cell surface expression. Importantly, our data suggest that the ability of PrP to homophilically trans-interact and elicit intracellular signaling is primarily encoded in its globular domain, and modulated by its repetitive domain. Thus, while the latter induces the local accumulation of PrPs at discrete punctae along cell contacts, the former counteracts this effect by promoting the continuous distribution of PrP. In early zebrafish embryos, deletion of either domain significantly impaired PrP’s ability to modulate E-cadherin cell adhesion. Altogether, these experiments relate structural features of PrP to its subcellular distribution and in vivo activity. Furthermore, they show that despite their large evolutionary history, the roles of PrP domains and posttranslational modifications are conserved between mouse and zebrafish. 相似文献
998.
Anne Katharina Jäger Brigitte Schottländer Ulla Wagner Smitt Ulf Nyman 《Plant cell reports》1993,12(9):517-520
Cell cultures from different species of the genus Thapsia (Apiaceae) have been investigated. In one 4-yearold line of T. garganica L. spontaneous somatic embryogenesis up to the globular stage occurred in a suspension culture containing 1 mg l–12,4-dichlorophenoxyacetic acid (2,4-D). Also callus cultures of this line, previously maintained on a medium containing 1 mg l–1 2,4-D, when transferred to various media deprived of 2,4-D, produced somatic embryos that developed into plantlets. Cell culture, embryos and regenerated organs were analysed for their content of thapsigargins. The undifferentiated cell culture did not synthezise thapsigargins, but was found to produce a yet unidentified compound not present in planta. White embryos in the pre-cotyledonary stage did not synthezise thapsigargins either, but when the embryos developed to the cotyledonary stage and became green, the synthesis started. Regenerated roots and shoots also contained thapsigargins.Abbreviations BAP
Benzylaminopurine
- 2,4-D
2,4-Dichlorophenoxyacetic acid
- EtOAc
ethyl acetate
- FDA
fluorescein diacetate
- IAA
Indole-3-acetic acid
- IBA
indole-3-butyric acid
- 2-iP
2-isopentenyladenine
- NAA
1-Napthaleneacetic acid 相似文献
999.
Katharina Miebach Maurice Finger Alexandra Maria Katarina Scherer Constantin Alexander Maaß Jochen Büchs 《Biotechnology and bioengineering》2023,120(8):2199-2213
H2-producing microorganisms are a promising source of sustainable biohydrogen. However, most H2-producing microorganisms are anaerobes, which are difficult to cultivate and characterize. While several methods for measuring H2 exist, common H2 sensors often require oxygen, making them unsuitable for anaerobic processes. Other sensors can often not be operated at high gas humidity. Thus, we applied thermal conductivity (TC) sensors and developed a parallelized, online H2 monitoring for time-efficient characterization of H2 production by anaerobes. Since TC sensors are nonspecific for H2, the cross-sensitivity of the sensors was evaluated regarding temperature, gas humidity, and CO2 concentrations. The systems' measurement range was validated with two anaerobes: a high H2-producer (Clostridium pasteurianum) and a low H2-producer (Phocaeicola vulgatus). Online monitoring of H2 production in shake flask cultivations was demonstrated, and H2 transfer rates were derived. Combined with online CO2 and pressure measurements, molar gas balances of the cultivations were closed, and an anaerobic respiration quotient was calculated. Thus, insight into the effect of medium components and inhibitory cultivation conditions on H2 production with the model anaerobes was gained. The presented online H2 monitoring method can accelerate the characterization of anaerobes for biohydrogen production and reveal metabolic changes without expensive equipment and offline analysis. 相似文献
1000.
Christian Plas Katharina Wimmer Peter Holubar Diethard Mattanovich Herbert Danner Eveline Jelinek Hanna Harant Rudolf Braun 《Applied microbiology and biotechnology》1993,38(6):820-823
During experiments investigating the purification of waste gas a bacterium capable of using carbon disulphide (CS2) als sole energy source was isolated. It could be identified as a Thiobacillus sp.; however, the species remains unclear. Both the properties of T. thioparus and T. thiooxidans have been observed. Since the organism could be used for removing CS2 in the environment, the degradation kinetics have been investigated by different methods. Substrate concentrations of up to 100 mg CS2·l–1 were oxidized at maximum rates of 2.5 mg CS2·g–1 protein·min–1 at pH 7.0 and at 30°C. CS2 levels above 150 mg CS2·l–1 caused termination of degradative activity.
Correspondence to: Ch. Plas 相似文献