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101.
M. Keith Wyatt Jen-Yue Tsai Sanghamitra Mishra Maria Campos Cynthia Jaworski Robert N. Fariss Steven L. Bernstein Graeme Wistow 《PloS one》2013,8(6)
Age-related macular degeneration (AMD) is a major cause of vision loss. It is associated with development of characteristic plaque-like deposits (soft drusen) in Bruch’s membrane basal to the retinal pigment epithelium (RPE). A sequence variant (Y402H) in short consensus repeat domain 7 (SCR7) of complement factor H (CFH) is associated with risk for “dry” AMD. We asked whether the eye-targeting of this disease might be related to specific interactions of CFH SCR7 with proteins expressed in the aging human RPE/choroid that could contribute to protein deposition in drusen. Yeast 2-hybrid (Y2H) screens of a retinal pigment epithelium/choroid library derived from aged donors using CFH SCR7 baits detected an interaction with EFEMP1/Fibulin 3 (Fib3), which is the locus for an inherited macular degeneration and also accumulates basal to macular RPE in AMD. The CFH/Fib3 interaction was validated by co-immunoprecipitation of native proteins. Quantitative Y2H and ELISA assays with different recombinant protein constructs both demonstrated higher affinity for Fib3 for the disease-related CFH 402H variant. Immuno-labeling revealed colocalization of CFH and Fib3 in globular deposits within cholesterol-rich domains in soft drusen in two AMD donors homozygous for CFH 402H (H/H). This pattern of labeling was quite distinct from those seen in examples of eyes with Y/Y and H/Y genotypes. The CFH 402H/Fib3 interaction could contribute to the development of pathological aggregates in soft drusen in some patients and as such might provide a target for therapeutic intervention in some forms of AMD. 相似文献
102.
Growth in relation to CO2-depletion and CO2-enrichment was investigated for the freshwater diatoms Asterionella formosa and Fragilaria crotonensis in batch cultures. Algal concentration and pH were measured during growth cycles, and inorganic carbon quantities determined by potentiometric Gran titrations and from pH-alkalinity relationships. After the primary growth with CO2-depletion and pH increase, successive CO2-enrichments induced further such cycles and produced a final three- to fivefold increase in algal biomass over that of unenriched controls. The extent of CO2-depletion, and pH rise, was greater in later cycles, indicative of some cellular adaptation. Values of pH reached 9·7 for Asterionella and 9·9 for Fragilaria. The lowest residual quantities of free CO2 were 0·1 and 0·03 μmol 1-1 for Asterionella and Fragilaria respectively, which were less than 0·05% of the corresponding residual quantities of total CO2. The primary limitation of CO2-uptake and growth was probably related to the concentration of free CO2, given the relative excess of other major nutrients (N, P, Si) in he media used. Limited of CO2-uptake could be restored without CO2 additions if the CO2 present was redistributed between its several forms (increasing free CO2) by the addition of strong acid, although growth was still restricted. Limitation of CO2-uptake, either by CO2-depletion or the addition of an inhibitor of photo-synthesis (DCMU), increased the sinking rate of Asterionella cells from 0·3 to 1 m day-1. The possible ecological implications of CO2-pH-growth and CO2-pH-buoyancy relationships are discussed, which may contribute to the frequent paucity of diatoms during summer in manv productive lakes. 相似文献
103.
Azoulay-Alfaguter I Yaffe Y Licht-Murava A Urbanska M Jaworski J Pietrokovski S Hirschberg K Eldar-Finkelman H 《The Journal of biological chemistry》2011,286(15):13470-13480
Glycogen synthase kinase-3 (GSK-3) is expressed as two isozymes α and β. They share high similarity in their catalytic domains but differ in their N- and C-terminal regions, with GSK-3α having an extended glycine-rich N terminus. Here, we undertook live cell imaging combined with molecular and bioinformatic studies to understand the distinct functions of the GSK-3 isozymes focusing on GSK-3α N-terminal region. We found that unlike GSK-3β, which shuttles between the nucleus and cytoplasm, GSK-3α was excluded from the nucleus. Deletion of the N-terminal region of GSK-3α resulted in nuclear localization, and treatment with leptomycin B resulted in GSK-3α accumulation in the nucleus. GSK-3α rapidly accumulated in the nucleus in response to calcium or serum deprivation, and accumulation was strongly inhibited by the calpain inhibitor calpeptin. This nuclear accumulation was not mediated by cleavage of the N-terminal region or phosphorylation of GSK-3α. Rather, we show that calcium-induced GSK-3α nuclear accumulation was governed by GSK-3α binding with as yet unknown calpain-sensitive protein or proteins; this binding was mediated by the N-terminal region. Bioinformatic and experimental analyses indicated that nuclear exclusion of GSK-3α was likely an exclusive characteristic of mammalian GSK-3α. Finally, we show that nuclear localization of GSK-3α reduced the nuclear pool of β-catenin and its target cyclin D1. Taken together, these data suggest that the N-terminal region of GSK-3α is responsible for its nuclear exclusion and that binding with a calcium/calpain-sensitive product enables GSK-3α nuclear retention. We further uncovered a novel link between calcium and nuclear GSK-3α-mediated inhibition of the canonical Wnt/β-catenin pathway. 相似文献
104.
Michaluk P Kolodziej L Mioduszewska B Wilczynski GM Dzwonek J Jaworski J Gorecki DC Ottersen OP Kaczmarek L 《The Journal of biological chemistry》2007,282(22):16036-16041
Matrix metalloproteinase-9 has recently emerged as an important molecule in control of extracellular proteolysis in the synaptic plasticity. However, no synaptic targets for its enzymatic activity had been identified before. In this report, we show that beta-dystroglycan comprises such a neuronal activity-driven target for matrix metalloproteinase-9. This notion is based on the following observations. (i) Recombinant, autoactivating matrix metalloproteinase-9 produces limited proteolytic cleavage of beta-dystroglycan. (ii) In neuronal cultures, beta-dystroglycan proteolysis occurs in response to stimulation with either glutamate or bicuculline and is blocked by tissue inhibitor of metalloproteinases-1, a metalloproteinase inhibitor. (iii) Beta-dystroglycan degradation is also observed in the hippocampus in vivo in response to seizures but not in the matrix metalloproteinase-9 knock-out mice. (iv) Beta-dystroglycan cleavage correlates in time with increased matrix metalloproteinase-9 activity. (v) Finally, beta-dystroglycan and matrix metalloproteinase-9 colocalize in postsynaptic elements in the hippocampus. In conclusion, our data identify the beta-dystroglycan as a first matrix metalloproteinase-9 substrate digested in response to enhanced synaptic activity. This demonstration may help to understand the possible role of both proteins in neuronal functions, especially in synaptic plasticity, learning, and memory. 相似文献
105.
Our earlier paper has reported that Wharton's jelly is a reservoir of several peptide growth factors, including acidic and basic fibroblast growth factors (aFGF and bFGF, respectively). Both can be extracted by buffered salts solutions in the form of high molecular mass complexes, probably with a component(s) of the extracellular matrix. Both aFGF and bFGF from such extracts hardly penetrate 10% polyacrylamide gels during electrophoresis. Pre-treatment of Wharton's jelly with hyaluronidase slightly increased the extractability of aFGF, but did not affect the extractability of bFGF. In contrast, the pre-treatment of tissue homogenate with bacterial collagenase (2000 U/ml, 37 degrees C, 18 h) increased the extractability of bFGF. The presence of beta-mercaptoethanol in the extracting solutions increased the extractability of both FGFs, but did not release FGFs in their free form, despite reducing the molecular mass of the FGF-containing complexes. We conclude that both aFGF and bFGF are bound through disulphide bonds to a protein component of Wharton's jelly. We propose that ground substance composed mainly of collagen fibrils and hyaluronate molecules, which surrounds the cells of Wharton's jelly, prevents the access of the extracting solution to aFGF and bFGF. Although hyaluronate and collagen do not bind aFGF or bFGF directly, they may constitute a barrier which prevents the dispersion of FGFs in Wharton's jelly. Thus, the high concentration of FGFs around the cells of Wharton's jelly may facilitate the interaction of these factors with membrane receptors, thereby resulting in stimulation of cell division and differentiation, as well as of the synthesis of extracellular matrix components. 相似文献
106.
Jacek Hilszczański Tomasz Jaworski Radosław Plewa Nicklas Jansson 《Journal of Insect Conservation》2014,18(5):855-861
Many saproxylic insects have declined or became extinct, mainly due to habitat loss and fragmentation, and their survival increasingly depends on active conservation. Efforts to achieve this goal may be supported by the introduction of new methods, including creation of artificial habitats. Here we present results of studies on the use of wooden boxes mimicking tree cavities for an endangered saproxylic species, Osmoderma barnabita. Boxes were filled with the feeding substrate for larvae and installed on trees. Second and third-instar O. barnabita larvae were introduced in half of the boxes; the remaining ones were left uninhabited. Later inspection of boxes showed a high survival rate of introduced larvae, as well as successful breeding of a new generation inside the boxes. At the same time boxes were not colonized by the local population of O. barnabita, although other cetoniids did so. The co-occurring larvae of other cetoniids did not affect O. barnabita larvae. Thermal conditions inside boxes and natural tree cavities were almost identical and based on the results of our studies we conclude that wooden boxes may serve as temporary habitat for O. barnabita. They may be particularly useful in cases of destruction of species’ natural habitat, in restoration programs, and have the potential to act as a ‘stepping stones’ in cases of a lack of habitat continuity. 相似文献
107.
Arathy D. S. Nair Chuanmin Cheng Deborah C. Jaworski Lloyd H. Willard Michael W. Sanderson Roman R. Ganta 《PloS one》2014,9(10)
Ehrlichia chaffeensis, transmitted from Amblyomma americanum ticks, causes human monocytic ehrlichiosis. It also infects white-tailed deer, dogs and several other vertebrates. Deer are its reservoir hosts, while humans and dogs are incidental hosts. E. chaffeensis protein expression is influenced by its growth in macrophages and tick cells. We report here infection progression in deer or dogs infected intravenously with macrophage- or tick cell-grown E. chaffeensis or by tick transmission in deer. Deer and dogs developed mild fever and persistent rickettsemia; the infection was detected more frequently in the blood of infected animals with macrophage inoculum compared to tick cell inoculum or tick transmission. Tick cell inoculum and tick transmission caused a drop in tick infection acquisition rates compared to infection rates in ticks fed on deer receiving macrophage inoculum. Independent of deer or dogs, IgG antibody response was higher in animals receiving macrophage inoculum against macrophage-derived Ehrlichia antigens, while it was significantly lower in the same animals against tick cell-derived Ehrlichia antigens. Deer infected with tick cell inoculum and tick transmission caused a higher antibody response to tick cell cultured bacterial antigens compared to the antibody response for macrophage cultured antigens for the same animals. The data demonstrate that the host cell-specific E. chaffeensis protein expression influences rickettsemia in a host and its acquisition by ticks. The data also reveal that tick cell-derived inoculum is similar to tick transmission with reduced rickettsemia, IgG response and tick acquisition of E. chaffeensis. 相似文献
108.
Jaworski JP Krebs SJ Trovato M Kovarik DN Brower Z Sutton WF Waagmeester G Sartorius R D'Apice L Caivano A Doria-Rose NA Malherbe D Montefiori DC Barnett S De Berardinis P Haigwood NL 《PloS one》2012,7(2):e31464
To obtain proof of concept for HIV vaccines, we generated recombinant multimeric particles displaying the HIV-1 Envelope (Env) third hypervariable region (V3) as an N-terminal fusion protein on the E2 subunit of the pyruvate dehydrogenase complex of Geobacillus stearothermophilus. The E2 scaffold self-assembles into a 60-mer core that is 24 nm in diameter, with a molecular weight of 1.5 MDa, similar to a virus like particle with up to 60 copies of a heterologous protein accessible on the surface. Env(V3)-E2 multimers were tested alone and in combination with Env(gp160) DNA in mice and rabbits. Following two or more co-immunizations with Env(V3)-E2 and Env gp160 DNA, all 18 rabbits developed potent autologous neutralizing antibodies specific for V3 in six weeks. These neutralizing antibodies were sustained for 16 weeks without boosting, and comparable responses were obtained when lipopolysaccharide, a contaminant from expression in E. coli, was removed. Co-immunizations of Env(V3)-E2 and DNA expressing gp160 elicited moderate CD8-specific responses and Env-specific antibodies in mice. Co-immunization with DNA and E2 was superior to individual or sequential vaccination with these components in eliciting both neutralizing antibodies in rabbits and CD8(+) T cell responses in mice. Co-immunization with DNA and multimeric E2 scaffolds appears to offer a highly effective means of eliciting rapid, specific, and sustained immune responses that may be a useful approach for other vaccine targets. 相似文献
109.
Seefeld MA Miller WH Newlander KA Burgess WJ Payne DJ Rittenhouse SF Moore TD DeWolf WE Keller PM Qiu X Janson CA Vaidya K Fosberry AP Smyth MG Jaworski DD Slater-Radosti C Huffman WF 《Bioorganic & medicinal chemistry letters》2001,11(17):2241-2244
An SAR study of a screening lead has led to the identification of 2,9-disubstituted 1,2,3,4-tetrahydropyrido[3,4-b]indoles as inhibitors of Staphylococcus aureus enoyl acyl carrier protein reductase (FabI). 相似文献
110.
Sylvain Charlat Anne Duplouy Emily A Hornett Emily A Dyson Neil Davies George K Roderick Nina Wedell Gregory DD Hurst 《BMC evolutionary biology》2009,9(1):64-9