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1.
2.
Prof. Dr. Vitaly G. Kuznetsov 《Facies》1996,34(1):151-157
Summary During the Early Permian deep-water basins existed in the southeastern part of the Russian craton. North and west of the Cis-Ural
foredeep and the Precaspian depression (micro-ocean) carbonate platforms were formed on a shallow-marine shelf during the
Asselian, Sakmarian and Early Artinskian. Reefs developed on the margin of these platforms along the slopes of the Cis-Ural
foredeep and the Precaspian depression. The reefs shifted platform ward in the eastern areas, due to the tectonic subsidence
of the platform margin and at the same time, prograded basinward in the south. Movements of continental blocks from the south
during the Late Artinskian and Kungurian caused the separation of the Early Permian basin of the Russian craton from the Palaeo-Tethys,
followed by evaporite sedimentation in the restricted basins.
The existence of source rocks (bituminous deep-water sediments), thick reservoir rocks (limestones and dolostones), evaporitic
seals and structural as well as stratigraphic traps are responsible for large productive gas and oil fields (e.g., Orenburg
field), some of which are distinctly associated with reef carbonates. 相似文献
3.
Deletion analysis of the SUP35 gene of the yeast Saccharomyces cerevisiae reveals two non-overlapping functional regions in the encoded protein 总被引:13,自引:0,他引:13
Michael D. Ter-Avanesyan Vitaly V. Kushnirov Adilya R. Dagkesamanskaya Svetlana A. Didichenko Yury O. Chernoff Sergey G. Inge-Vechtomov Vladimir N. Smirnov 《Molecular microbiology》1993,7(5):683-692
SUP35is an omnipotent suppressor gene of Saccharomyces cerevisiae coding for a protein consisting of a C-terminal part similar to the elongation factor EF-1α and a unique N-terminal sequence of 253 amino acids. Twelve truncated versions of the SUP35 gene were generated by the deletion of fragments internal to the coding sequence. Functional studies of these deletion mutants showed that: (i) only the EF-1α-like C-terminal part of the Sup35 protein is essential for the cell viability; (ii) overexpression of either the N-terminal part of the Sup35 protein or the full-length Sup35 protein decreases translational fidelity, resulting in omnipotent suppression and reduced growth of [psi+] strains; (iii) expression of the C-terminal part of the Sup35 protein generates an antisuppressor phenotype; and (iv) both the N- or C-terminal segments of the Sup35 protein can bind to 80S ribosomes. Thus, the data obtained define two domains within the Sup35 protein which are responsible for different functions. 相似文献
4.
Robert Lartey Soumitra Ghoshroy Joe Ho Vitaly Citovsky 《The Plant journal : for cell and molecular biology》1997,12(3):537-545
Tobamoviruses represent a well-characterized system used to examine viral infection, whereas Arabidopsis is a choice plant for most genetic experiments. It would be useful to combine both approaches into one experimental system for virus–plant interaction. Most tobamoviruses, however, are not pathogenic in Arabidopsis . Here, we describe infection of Arabidopsis by a recently discovered crucifer-infecting turnip vein clearing tobamovirus (TVCV). Using this system, we determined patterns and kinetics of viral local and systemic movement within Arabidopsis plants. Localization studies showed that the virus infects both vegetative and reproductive plant tissues. However, there may be a transport barrier between the seed coat and the embryo which virions cannot cross, preventing seed transmission of TVCV. The ability to move both locally and systemically in Arabidopsis , causing mild and fast-developing symptoms but allowing survival and fertility of the infected plants, distinguish TVCV infection of Arabidopsis as a model system to study virus–plant interaction. 相似文献
5.
Recent data on the proton-translocating activity of b cytochromes in chromatophores of purple bacteria and their arrangement in the photosynthetic redox chain are discussed. These data appear to support the concept of the b50 and b-90 cytochrome doublet spanning the membrane. Current schemes of H+ transport by b cytochromes are considered, and the scheme of H+ translocation by cytochrome b50 taking up H+ at the outer side of the membrane and a quinone delivering them from this cytochrome to the inner space of the chromatophore is favored as the most probable in the light of recent findings. This scheme is applicable both to Crofts' linear model of the redox chain and to Mitchell's Q cycle. Kinetic discrepancies between H+ uptake and cytochrome b50 reduction at high ambient redox potentials are interpreted in terms of a special, cytochrome b50-independent, yet Rieske FeS-protein-dependent mode of H+ transport. 相似文献
6.
Andrey A. Rosenkranz Sergey V. Yachmenev David A. Jans Natalya V. Serebryakova Vitaly I. Murav''ev Reiner Peters Alexander S. Sobolev 《Experimental cell research》1992,199(2):323-329
A soluble construct consisting of a plasmid carrying the gene of the SV40 large T-antigen and an insulin-poly-L-lysine conjugate is able to selectively transfect PLC/PRF/5 human hepatoma cells which possess insulin receptors. Transfection can be efficiently competed by excess free insulin. To examine intracellular transport of the construct, it was fluorescently labeled and its accumulation on and in cells visualized by video-enhanced microscopy and quantitative confocal laser scanning microscopy. After 2 h at 37 degrees C, the labeled construct was found predominantly in intracellular acidic compartments, with a substantial portion of fluorescence localized both near and in the cell nucleus. Binding, endocytosis, and nuclear localization of the labeled conjugate could all be competed by excess free insulin, thus indicating that entry of the conjugate into cells was specifically mediated by the insulin receptor. 相似文献
7.
Vitaly A Selivanov Pedro Vizán Faustino Mollinedo Teresa WM Fan Paul WN Lee Marta Cascante 《BMC systems biology》2010,4(1):135
Background
Metabolic flux profiling based on the analysis of distribution of stable isotope tracer in metabolites is an important method widely used in cancer research to understand the regulation of cell metabolism and elaborate new therapeutic strategies. Recently, we developed software Isodyn, which extends the methodology of kinetic modeling to the analysis of isotopic isomer distribution for the evaluation of cellular metabolic flux profile under relevant conditions. This tool can be applied to reveal the metabolic effect of proapoptotic drug edelfosine in leukemia Jurkat cell line, uncovering the mechanisms of induction of apoptosis in cancer cells. 相似文献8.
Expression of the recombinant antibacterial peptide sarcotoxin IA in Escherichia coli cells 总被引:5,自引:0,他引:5
Skosyrev VS Kulesskiy EA Yakhnin AV Temirov YV Vinokurov LM 《Protein expression and purification》2003,28(2):350-356
Sarcotoxin IA is an antibacterial peptide that is secreted by a meat-fly Sarcophaga peregrina larva in response to a hypodermic injury or bacterial infection. This peptide is highly toxic against a broad spectrum of both Gram-positive and Gram-negative bacteria and lethal to microbes even at nanomolar concentrations. However, research needs as well as its potential use in medicine require substantial amounts of highly purified sarcotoxin. Because heterologous expression systems proved to be inefficient due to sarcotoxin sensitivity to intracellular proteases, here we propose the biosynthesis of sarcotoxin precursors in Escherichia coli cells that are highly sensitive to the mature peptide. To optimize its biosynthesis, sarcotoxin was translationally fused with proteins highly expressed in E. coli. A fusion partner and the position of sarcotoxin in the chimeric polypeptide were crucial for protecting the sarcotoxin portion of the fusion protein from proteolysis. Released after chemical cleavage of the fusion protein and purified to homogeneity, sarcotoxin displayed antibacterial activity comparable to that previously reported for the natural peptide. 相似文献
9.
Elizabeth Howard Vitaly Citovsky 《BioEssays : news and reviews in molecular, cellular and developmental biology》1990,12(3):103-108
Single-stranded DNA-protein complex (T-complex) is proposed to mediate T-DNA transfer from Agrobacterium to plant cells. A novel model for transfer is presented which incorporates features of both bacterial conjugation and viral infection. Specific protein components of the T-complex, its ultrastructure and possible functions in the plant cell are discussed. 相似文献
10.
Andriy I. Vovk Lyudmyla A. Kononets Vsevolod Yu. Tanchuk Sergiy O. Cherenok Andriy B. Drapailo Vitaly I. Kalchenko Valery P. Kukhar 《Bioorganic & medicinal chemistry letters》2010,20(2):483-487
Inhibition of Yersinia protein tyrosine phosphatase by calix[4]arene mono-, bis-, and tetrakis(methylenebisphosphonic) acids as well as calix[4]arene and thiacalix[4]arene tetrakis(methylphosphonic) acids have been investigated. The kinetic studies revealed that some compounds in this class are potent competitive inhibitors of Yersinia PTP with inhibition constants in the low micromolar range. The binding modes of macrocyclic phosphonate derivatives in the enzyme active center have been explained using computational docking approach. The results obtained indicate that calix[4]arenes are promising scaffolds for the development of inhibitors of Yersinia PTP. 相似文献