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171.
H. J. Wichers R. Wijnsma J. F. Visser TH. M. Malingré H. J. Huizing 《Plant Cell, Tissue and Organ Culture》1985,4(1):61-73
The endogenous synthesis of 3-(3,4-dihydroxyphenyl)-L-alanine (L-DOPA) by cell suspension cultures of Mucuna pruriens was found to be influenced by several environmental parameters. The nature of the nitrogen source as well as the concentration of nitrogen containing salts, sucrose and phosphate in the culture medium were found to affect the biosynthesis of L-DOPA. Addition of 2, 4-dichlorophenoxyacetic acid to the medium suppressed L-DOPA production; continuous illumination of the cultures had a strong beneficial effect on L-DOPA production. L-DOPA was accumulated intracellularly by the cell suspension cultures. These observations further demonstrate that for certain products of plant cell suspensions product synthesis can be manipulated by a proper selection of specified nutrients. 相似文献
172.
173.
Despite the growing interest to explore untapped microbial gene and protein diversity, no single platform has been able to acquire both gene and protein information from just a few cells. We present a microfluidic system that simultaneously performs on-chip capillary electrophoresis for protein analysis and whole genome amplification (WGA), and we demonstrate this by doing both for the same cohort of cyanobacterial cells. This technology opens avenues for studying protein profiles of precious environmental microbial samples and simultaneously accessing genomic information based on WGA. 相似文献
174.
Background
Feline infectious peritonitis (FIP) is a lethal immune-mediated disease caused by feline coronavirus (FCoV). Currently, no therapy with proven efficacy is available. In searching for agents that may prove clinically effective against FCoV infection, five analogous overlapping peptides were designed and synthesized based on the putative heptad repeat 2 (HR2) sequence of the spike protein of FCoV, and the antiviral efficacy was evaluated.Methods
Plaque reduction assay and MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) cytotoxicity assay were performed in this study. Peptides were selected using a plaque reduction assay to inhibit Feline coronavirus infection.Results
The results demonstrated that peptide (FP5) at concentrations below 20 μM inhibited viral replication by up to 97%. The peptide (FP5) exhibiting the most effective antiviral effect was further combined with a known anti-viral agent, human interferon-α (IFN-α), and a significant synergistic antiviral effect was observed.Conclusion
Our data suggest that the synthetic peptide FP5 could serve as a valuable addition to the current FIP prevention methods. 相似文献175.
Core/shell quantum dots (CdSe/Zns) conjugated with various nuclear localization signaling (NLS) peptides, which could facilitate the transportation of quantum dots across the plasma membrane into the nucleus, have been utilized to investigate the uptake mechanism of targeted delivery. Because of their brightness and photostability, it was possible to trace the trajectories of individual quantum dots in living cells using both confocal and total internal reflection microscopes. We found that, when the quantum dots were added to a cell culture, the peptide-coated quantum dots entered the cell nucleus while the uncoated quantum dots remained in the cytoplasm. At 8 nM, most of the peptide coated quantum dots were found in the cytoplasm due to aggregation. However, at a lower concentration (0.08 nM), approximately 25% of the NLS peptide-coated quantum dots entered the cell nucleus. We also found that some quantum dots without NLS coating could also enter the nucleus, suggesting that the size of the quantum dots may play an important role in such a process. 相似文献
176.
Chia-Ching Chen Fu-Shin Chueh Shu-Fen Peng Wen-Wen Huang Chang-Hai Tsai Fuu-Jen Tsai 《Bioscience, biotechnology, and biochemistry》2013,77(10):1912-1923
ABSTRACTCantharidin (CTD), a sesquiterpenoid bioactive substance, has been reported to exhibit anticancer activity against various types of cancer cells. The aim of the present study was to investigate the apoptosis effects and the underlying mechanisms of CTD on osteosarcoma U-2 OS cells. Results showed that CTD induced cell morphologic changes, reduced total viable cells, induced DNA damage, and G2/M phase arrest. CTD increased the production of reactive oxygen species and Ca2+, and elevated the activities of caspase-3 and ?9, but decreased the level of mitochondrial membrane potential. Furthermore, CTD increased the ROS- and ER stress-associated protein expressions and increased the levels of pro-apoptosis-associated proteins, but decreased that of anti-apoptosis-associated proteins. Based on these observations, we suggested that CTD decreased cell number through G2/M phase arrest and the induction of cell apoptosis in U-2 OS cells and CTD could be a potential candidate for osteosarcoma treatments. 相似文献
177.
N. E. El-Wakeil K. T. Awadallah H. TH. Farghaly A. -A.M. Ibrahim Z. A. Ragab 《Archives Of Phytopathology And Plant Protection》2013,46(5):340-348
Abstract Pediobius furvus (Gahan) (Eulophidae: Hymenoptera) was recorded as a new pupal parasitoid (gregarious endo-parasitoid) of Sesamia cretica pupae (Led.) in El-Noubaria region (El-Beheira Governorate), Egypt. This study was conducted in maize and sorghum fields in El-Beheira and Giza Governorates in Egypt during 1994 and 1995. The percentage parasitism was 8.4 and 15.4% in August and September, respectively. The number of parasitoids emerging from one pupa ranged from 28 to 222. It has been concluded that this new species is a gregarious endo-parasitoid that pupates inside its host. Pediobius furvus has a high reproductive ability, which may afford mass production and enable mass release of the parasitoid to control S. cretica in maize fields. 相似文献
178.
A single lineage of r2 retrotransposable elements is an active, evolutionarily stable component of the Drosophila rDNA locus 总被引:1,自引:0,他引:1
R2 elements are non-long-terminal-repeat (non-LTR) retrotransposons that
insert specifically in the 28S rRNA genes of many insects. Previous reports
concerning this element in the genus Drosophila have suggested that R2
elements are absent from many species of this genus, particularly those
species from the subgenus Drosophila. In this report, we present an
extensive study of the distribution and evolution of R2 elements in
Drosophila. A PCR survey of 59 species from 23 species groups of the two
major Drosophila subgenera found that R2 elements are present in all but
two species of the melanogaster species subgroup. Phylogenetic analysis
based on partial nucleotide sequences of R2 elements from 23 species
demonstrates that the relationships of R2 elements are congruent with those
of the Drosophila species phylogeny, suggesting that these elements have
been vertically inherited since the divergence of this genus some 60 MYA.
Sequence variation between different copies of R2 elements within each
species was less than 0.16%, indicating that these elements are undergoing
concerted evolution similar to that of the 28S genes. Several properties of
the R2 sequences suggest that these elements depend on retrotransposition
in addition to simple recombination to remain within the rDNA locus: the
rates of synonymous substitutions averaged 4.8 times the rate of
replacement substitutions, 82 of 83 R2 copies partially sequenced contained
intact open reading frames, and, finally, length variation associated with
the poly(A) 3' tails indicated that many R2 copies are the direct result of
retrotransposition.
相似文献
179.
180.
Thiostrepton interacts covalently with Rpt subunits of the 19S proteasome and proteasome substrates
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Cristinel Sandu Nagaranjan Chandramouli Joseph Fraser Glickman Henrik Molina Chueh‐Ling Kuo Nikolay Kukushkin Alfred L. Goldberg Hermann Steller 《Journal of cellular and molecular medicine》2015,19(9):2181-2192
Here, we report a novel mechanism of proteasome inhibition mediated by Thiostrepton (Thsp), which interacts covalently with Rpt subunits of the 19S proteasome and proteasome substrates. We identified Thsp in a cell‐based high‐throughput screen using a fluorescent reporter sensitive to degradation by the ubiquitin–proteasome pathway. Thiostrepton behaves as a proteasome inhibitor in several paradigms, including cell‐based reporters, detection of global ubiquitination status, and proteasome‐mediated labile protein degradation. In vitro, Thsp does not block the chymotrypsin activity of the 26S proteasome. In a cell‐based IκBα degradation assay, Thsp is a slow inhibitor and 4 hrs of treatment achieves the same effects as MG‐132 at 30 min. We show that Thsp forms covalent adducts with proteins in human cells and demonstrate their nature by mass spectrometry. Furthermore, the ability of Thsp to interact covalently with the cysteine residues is essential for its proteasome inhibitory function. We further show that a Thsp modified peptide cannot be degraded by proteasomes in vitro. Importantly, we demonstrate that Thsp binds covalently to Rpt subunits of the 19S regulatory particle and forms bridges with a proteasome substrate. Taken together, our results uncover an important role of Thsp in 19S proteasome inhibition. 相似文献