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91.
Preliminary study of female-targeted semiochemical baits for the western corn rootworm in Europe 总被引:1,自引:0,他引:1
M. Tóth J. Vuts I. Szarukán I. Juhász F. Manajlovics 《Journal of Applied Entomology》2007,131(6):416-419
Abstract: In recent years emphasis of semiochemical research on the western corn rootworm (WCR) ( Diabrotica v. virgifera LeConte, Coleoptera, Chrysomelidae) shifted towards the development of more female-specific lures. Through identifying volatile compounds from maize silk, Hammack (J. Chem. Ecol., 27, 2001,1373) claimed that some combinations of the newly identified compounds were more powerful in attracting females than the conventional floral baits (based on 4-methoxycinnamaldehyde). Earlier we found that the newly developed 'hat' trap design (KLP) when baited with the floral bait was especially suitable for the capture of female WCR. Encouraged by this we set out to compare efficiency of female-targeted Diabrotica baits. None of the treatments tested captured females in higher percentage than the conventional WCR floral bait (4-methoxycinnamaldehyde + indole). The combination of β -ionone + methyl salicylate + β -caryophyllene (attractant found to be more female-specific in the USA previously) was not more attractive for females than unbaited controls. No other treatment produced significantly higher female percentages than the conventional floral bait. However, the conventional bait caught far more beetles than any of the other treatments. Electroantennographic responses from male or female antennae were very similar, suggesting that all 27 floral compounds tested were perceived similarly by the two sexes. The only exception was β -ionone, to which females were slightly more responsive. It seemed that among the other compounds none showed potential for the development of a more female-specific lure. In conclusion, so far the most efficient female-targeted trap-bait combination for WCR in Europe is the conventional floral attractant applied in KLP traps. 相似文献
92.
Different plant species produce a variety of terpenoid indole alkaloids, which are of interest as plant defensive secondary metabolites and as valuable pharmaceuticals. Although significant progress has been made, the mechanisms regulating the levels of this important class of compounds require continued elucidation. Previous precursor feeding studies have indicated that alkaloid accumulation can be improved during the exponential growth phase of hairy root cultures through enhanced tryptophan availability. To test this relationship, transgenic hairy root cultures of Catharanthus roseus were established with a glucocorticoid-inducible promoter controlling the expression of an Arabidopsis feedback-resistant anthranilate synthase alpha subunit. Enzyme assays demonstrated that the Arabidopsis alpha subunit is compatible with the native beta subunit and that anthranilate synthase activity is more resistant to tryptophan inhibition in induced than in uninduced extracts. The metabolic effects of expressing the feedback-resistant anthranilate synthase alpha subunit were also dramatic. Over a 6-day induction period during the late exponential growth phase, tryptophan and tryptamine specific yields increased from almost undetectable levels to 2.5 mg/g dry weight and from 25 microg/g to 267 microg/g dry weight, respectively. The greater than 300-fold increase in tryptophan levels observed in these studies under certain induction conditions compares favorably with the fold increases obtained in previous constitutive expression studies. Despite the large increases in tryptophan and tryptamine, the levels of most terpenoid indole alkaloids were not significantly altered, with the exception of lochnericine, which increased 81% after a 3-day induction period. These results suggest that terpenoid indole alkaloid levels are tightly controlled. 相似文献
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John C. Marecki Suja Aarattuthodiyil Alicia K. Byrd Narsimha R. Penthala Peter A. Crooks Kevin D. Raney 《Bioorganic & medicinal chemistry letters》2019,29(3):430-434
The hepatitis C virus (HCV) represents a substantial threat to human health worldwide. The virus expresses a dual-function protein, NS3 having both protease and RNA helicase activities that are essential for productive viral replication and sustained infections. While viral protease and polymerase inhibitors have shown great successes in treating chronic HCV infections, drugs that specifically target the helicase activity have not advanced. A robust and quantitative 96-well plate-based fluorescent DNA unwinding assay was used to screen a class of indole thio-barbituric acid (ITBA) analogs using the full-length, recombinant HCV NS3, and identified three naphthoyl-containing analogs that efficiently inhibited NS3 helicase activity in a dose-dependent manner, with observed IC50 values of 21–24?µM. Standard gel electrophoresis helicase assays using radiolabeled duplex DNA and RNA NS3 substrates confirmed the inhibition of NS3 unwinding activity. Subsequent anisotropy measurements demonstrated that the candidate compounds did not disrupt NS3 binding to nucleic acids. Additionally, the rate of ATP hydrolysis and the protease activity were also not affected by the inhibitors. Thus, these results indicate that the three ITBA analogs containing N-naphthoyl moieties are the foundation of a potential series of small molecules capable of inhibiting NS3 activity via a novel interaction with the helicase domain that prevents the productive unwinding of nucleic acid substrates, and may represent the basis for a new class of therapeutic agents with the potential to aid in the treatment and eradication of hepatitis C virus. 相似文献
97.
This review describes the different plant transformation techniques, including guided infection with Agrobacterium tumefaciens and A. rhizogenes, particle bombardment and protoplast fusion, that have been attempted to create transgenic Catharanthus roseus (L.) G. Don cell cultures, hairy roots and whole plants. The review also focuses on the different approaches used to manipulate
and improve secondary metabolite yields in various culture systems, with special attention to the most relevant results achieved.
Finally, under future perspectives, the authors propose several approaches which would likely be implemented with this species,
to try to boost the accumulation of the anti-tumour agents, vinblastine and vincristine. Some comments on how the future of
the genetic manipulation of medicinal plants may proceed aiming at achieving higher secondary metabolite yields are also given. 相似文献
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Hai‐Yang Wang Ru‐Xia Wang Yan‐Xia Zhao Ke Liu Feng‐Ling Wang Jing‐Yong Sun 《化学与生物多样性》2015,12(8):1256-1262
Three new isomeric monoterpene indole alkaloids, naucleofficines I–III ( 1 – 3 , resp.) were isolated from the stems (with bark) of Nauclea officinalis. Their structures were elucidated on the basis of spectroscopic methods and single‐crystal diffraction analyses. The cytotoxic activities of 1 – 3 against human colon cancer, human gastric cancer, and human hepatoma cells were also investigated. 相似文献
100.
We have established Catharanthus roseus hairy root cultures transgenic for the rol ABC genes from T(L)-DNA of the agropine-type Agrobacterium rhizogenes strain A4. The rol ABC hairy root lines exhibit a wild-type hairy root syndrome in terms of growth and morphology on solid medium. However, they differ from wild-type hairy root lines in that they more frequently have excellent adaptability to liquid medium and do not appear to form calli during cultivation. Moreover, they do not produce detectable levels of mannopine and agropine which, in contrast, are often synthesized abundantly in wild-type hairy root lines. The absence of these opines does not appear to cause the rol ABC lines to have higher levels of terpenoid indole alkaloids than wild-type hairy root lines. Unlike wild-type lines, rol ABC lines produce very similar levels of total alkaloids despite wide variations in individual alkaloid contents. This work demonstrates that the three genes rol ABC are sufficient to induce high-quality hairy roots in Catharanthus roseus. 相似文献