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A V Ruiz G E Bisgard I B Tyson R F Grover J A Will 《Journal of applied physiology》1974,37(3):384-391
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A replacement material for autologous grafts for urinary tract reconstruction would dramatically reduce the complications of surgery for these procedures. However, acellular materials have not proven to work sufficiently well, and cell‐seeded materials are technically challenging and time consuming to generate. An important function of the urinary tract is to prevent urine leakage into the surrounding tissue—a function usually performed by the urothelium. We hypothesize that by providing an impermeable barrier in the acellular graft material, urine leakage would be minimized, as the urothelium forms in vivo. However, since urothelial cells require access to nutrients from the supporting vasculature, the impermeable barrier must degrade over time. Here we present the development of a novel biomaterial composed of the common degradable polymers, poly(ε‐caprolactone) and poly(L ‐lactic acid) and generated by electrospinning directly onto spin‐coated thin films. The composite scaffolds with thin films on the luminal surface were compared to their electrospun counterparts and commercially available small intestinal submucosa by surface analysis using scanning electron microscopy and by analysis of permeability to small molecules. In addition, the materials were examined for their ability to support urothelial cell adhesion, proliferation, and multilayered urothelium formation. We provide evidence that these unique composite scaffolds provide significant benefit over commonly used acellular materials in vitro and suggest that they be further examined in vivo. Biotechnol. Bioeng. 2011; 108:207–215. © 2010 Wiley Periodicals, Inc. 相似文献
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Tyson Vonderfecht Michael W. Cookson Thomas H. Giddings Jr. Christina Clarissa Mark Winey 《Molecular biology of the cell》2012,23(24):4766-4777
Centrins are a ubiquitous family of small Ca2+-binding proteins found at basal bodies that are placed into two groups based on sequence similarity to the human centrins 2 and 3. Analyses of basal body composition in different species suggest that they contain a centrin isoform from each group. We used the ciliate protist Tetrahymena thermophila to gain a better understanding of the functions of the two centrin groups and to determine their potential redundancy. We have previously shown that the Tetrahymena centrin 1 (Cen1), a human centrin 2 homologue, is required for proper basal body function. In this paper, we show that the Tetrahymena centrin 2 (Cen2), a human centrin 3 homologue, has functions similar to Cen1 in basal body orientation, maintenance, and separation. The two are, however, not redundant. A further examination of human centrin 3 homologues shows that they function in a manner distinct from human centrin 2 homologues. Our data suggest that basal bodies require a centrin from both groups in order to function correctly. 相似文献
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Five forms of thymidine kinase have been identified on isoelectric focusing gels of Physarum polycephalum supernatants. Their isoelectric points are 5.9, 6.4, 6.7, 6.9 and 7.1. All are inhibited by deoxythymidine 5′-triphosphate (dTTP). The activity of the pI 7.1 form does not change significantly during the cell cycle. The other four forms change in activity. About 1 h before metaphase the activity of the four more acidic forms is first detected. Their activity peaks during telophase, and by 1 h after metaphase there is a 50% decrease in activity of the 5.9 form. By 3 h after metaphase the activity of the 6.4 form has dropped more sharply than the activity of the 6.7 form. By 6 h after metaphase only the activity of the 6.9 form is present in significant amounts in addition to the 7.1 form. The activity of these new acidic forms probably accounts for the reported increase in total thymidine kinase activity during mitosis and early S phase. 相似文献
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Sec61p is required both for protein translocation and dislocation across the membrane of the endoplasmic reticulum (ER). However, the cellular role of the Sec61p homolog Ssh1p has not been clearly defined. We show that deltassh1 mutant cells have strong defects in both SRP-dependent and -independent translocation. Moreover, these cells were also found to be induced for the unfolded protein response and to be defective in dislocation of a misfolded ER protein. In addition, deltassh1 mutant cells rapidly became respiratory deficient. The other defects discussed above were suppressed in the respiratory-deficient state or under conditions where the rate of polypeptide translation was artificially reduced. These data identify Ssh1p as a component of a second, functionally distinct translocon in the yeast ER membrane. 相似文献