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991.
992.
Polypeptide variation in an N-CAM extracellular immunoglobulin-like fold is developmentally regulated through alternative splicing 总被引:11,自引:0,他引:11
The alternative splicing of a previously undiscovered 30 base exon confers a new level of polypeptide diversity on the N-CAM family of cell-surface glycoproteins. It results in the insertion of 10 amino acids into the fourth of five extracellular immunoglobulin-like folds. Each major size class of rat brain N-CAM mRNAs consists of members that contain or lack the exon. Furthermore, this splicing event is developmentally controlled: RNAs containing the inserted exon are expressed at extremely low levels (less than 3%) in embryonic brain but increase postnatally to 40%-45% of all N-CAM mRNAs in adult brain. Antibodies that recognize the alternative 10 amino acid segment react with a subset of N-CAM-expressing neurons in cultures of embryonic rat cells. 相似文献
993.
994.
Ferdinand Bohlmann Antoinette Suwita Harold Robinson Robert M. King 《Phytochemistry》1981,20(8):1887-1890
The investigation of Stylotrichium rotundifolium afforded the epoxide of β-sesquiphellandrene, a new derivative of geranylnerol and six guaianolides not isolated previously. Furthermore, two germacranolides also present in a Lasiolaena species and several known compounds were isolated. The structures were elucidated by detailed 1H NMR investigations. The chemotaxonomic situation is discussed briefly. 相似文献
995.
996.
Anne Weber Antoinette Hatzfeld André Guillouzo Fanny Schapira 《Biochemical and biophysical research communications》1979,86(1):6-13
Using the indirect immunoperoxidase technique with optical and electron microscopy, we have localized both fetal aldolases A and C from regenerating rat liver in Kupffer and endothelial cells (by contrast with the localization of aldolase B in hepatocytes only). These results have been confirmed by biochemical methods. The localization of the 3 aldolases differs widely from that observed in fast-growing hepatoma and suggests that control mechanisms of gene regulation are different in cancer and in liver regeneration. 相似文献
997.
998.
Decomposition of the intrinsic dynamics of proteins into collective motions among distant regions of the protein structure provides a physically appealing approach that couples the dynamics of the system with its functional role. The cellular functions of microtubules (an essential component of the cytoskeleton in all eukaryotic cells) depend on their dynamic instability, which is altered by various factors among which applied forces are central. To shed light on the coupling between forces and the dynamic instability of microtubules, we focus on the investigation of the response of the microtubule subunits (tubulin) to applied forces. We address this point by adapting an approach designed to survey correlations for the equilibrium dynamics of proteins to the case of correlations for proteins forced-dynamics. The resulting collective motions in tubulin have a number of functional implications, such as the identification of long-range couplings with a role in blocking the dynamic instability of microtubules. A fundamental implication of our study for the life of a cell is that, to increase the likelihood of unraveling of large cytoskeletal filaments under physiological forces, molecular motors must use a combination of pulling and torsion rather than just pulling. 相似文献
999.
1000.
A Biragyn M Surenhu D Yang P A Ruffini B A Haines E Klyushnenkova J J Oppenheim L W Kwak 《Journal of immunology (Baltimore, Md. : 1950)》2001,167(11):6644-6653
Chemokine receptors are differentially expressed on immature and mature dendritic cells (DC). Herein, we demonstrate for the first time that murine antimicrobial peptides beta-defensins 2 and 3 bind murine CCR6, similarly to inflammatory chemokine macrophage-inflammatory protein 3alpha, and they chemoattract bone marrow-derived immature, but not mature DC. Using various chemokines or defensins fused with nonimmunogenic tumor Ags, we studied their capacity to delivery Ags to subsets of immune cells to elicit antitumor immunity. We demonstrate that DNA immunizations with fusion constructs with beta-defensin 2 or inflammatory chemokines that target immature DC, but not homeostatic chemokines secondary lymphoid tissue chemokine, CCL21, or stromal cell-derived factor 1, CXCL12, which chemoattract mature DC, elicit humoral, protective, and therapeutic immunity against two different syngeneic lymphomas. 相似文献