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941.
Gender differences in immune capabilities suggest that sex hormones such as estrogens were involved in the regulation of the immunocompetence. Numerous studies also suggest that plasmacytoid dendritic cells (PDCs) play a pathogenic role in SLE. However, it is unclear whether estrogen can modulate the function of PDCs to influence the development of SLE. In the present study, PDCs from murine spleens were treated with 17β-estradiol (E2) and CpG respectively or both in vitro, then cell viability, costimulatory molecule expression, cytokine secretion of PDCs, as well as stimulatory capacity of PDCs to B cells were analyzed. Results showed that E2 and CpG increased the cell viability and costimulatory molecule expression on PDCs synergistically. Moreover, the intracellular and extracellular secretion of IFN-α was increased by E2 or E2 plus CpG. In addition, E2 and CpG also increased the stimulatory capacity of PDCs to B cells, and the viability of B cells was decreased after neutralizing IFN-α significantly. In the experiments in vivo, mice received daily s.c. injections of E2 and CpG respectively or both, then we found that the plasma concentration of IgM were elevated by E2 and CpG synergistically and the expression of IFN-α/β in spleens were noticeably increased by CpG plus E2 compared with the treatment of E2 or CpG only. This study indicates that E2 could exacerbate PDCs'' activation with CpG, which further activates B cells to upregulate susceptibility to autoantigens. IFN-α plays an important role in the stimulatory effect of PDCs on B cells. E2 stimulation of IFN-α production may result in female prevalence in autoimmune diseases such as SLE through activation of PDCs. This study provides novel evidence of relationship between estrogen and SLE and also sheds light on gender biases among SLE patients. 相似文献
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943.
Rui Cui Xiang-Lin Duan Gregory J. Anderson Ya-Tiao Qiao Peng Yu Zhong-Ming Qian Kunihiro Yoshida Shinichi Takeda Pei Guo Zhen-Ling Yang Yan-Zhong Chang 《Journal of trace elements in medicine and biology》2009,23(4):290-299
Aceruloplasminemia is an autosomal recessive disorder caused by mutations in the ceruloplasmin (CP) gene. It is characterized by iron accumulation in the brain and in visceral organs. However, little is known about the mechanism of iron transport in these regions. Adult CP null (CP−/−) mice show increased iron deposition in several regions of brain, such as the cerebellum and brainstem. In this study, we investigated the expression of the ceruloplasmin homolog hephaestin (Heph) in the brain of CP−/− mice as a function of age. In the cerebral cortex and caudate putamen of 80-week-old CP−/− mice, the expression of Heph increased significantly whilst iron levels remain normal [Patel BN, Dunn RJ, Jeong SY, Zhu Q, Julien JP, David S. Ceruloplasmin regulates iron levels in the CNS and prevents free radical injury. J Neurosci 2002;22(15):6578–6], indicating that Heph might compensate for the loss of CP. In contrast, the substantia nigra and cerebellum of 80-week-old CP−/− mice accumulate iron but do not express high levels or significant decrease of Heph, suggesting that Heph does not replace CP in these regions. These data suggest that Heph may compensate for the loss of CP in a region-specific manner. 相似文献
944.
The work presented in this paper demonstrates housing development as an application of ecological engineering on streamside. The study site consists of terrestrial, riverbank and aquatic zones, on which their correlation and effects were investigated. Interdisciplinary methods involving ecology, hydrology, environment and landscape were applied to achieve maximum benefits for humans and nature. A technical scheme for housing development was established and organized as a hierarchy structure, i.e. determination of problems, establishment of goals, designation of functions, production of plan, and development of designs. The designs and implementation of housing and land consisted of riverbank restoration, vegetation replanting, rainwater purification and landscape protection. Ecological benefit was to be the core of the housing project with consideration of social and economic benefits. 相似文献
945.
Spartina alterniflora, a species vegetating on inter-tidal flats that was introduced from the eastern coast of United States, has become a hot topic, focusing on its invasion within local species in the coastal zone of China. Impacts of S. alterniflora on the inter-tidal macrobenthos community in the Jiangsu coastland are addressed by comparing the macrobenthos characteristics in a mudflat and in a four-year-old Spartina salt marsh that had earlier been a mudflat. During the period October 2002–July 2003, we studied the distribution pattern and diversity of macrobenthos, and discussed their correlation with environmental factors caused by Spartina vegetation. The results showed that a total of 43 macrobenthos species were found, mainly consisting of Mollusca, Crustacea, and Annelida. Ten macrobenthos species were found in the Spartina salt marsh, and 36 species were found in the mudflat. Life forms and functional groups of macrobenthos in the Spartina salt marsh were obviously distrinct from that of the mudflat. The study showed that macrobenthos diversity in the Spartina salt marsh decreased, and the community structure altered obviously, whereas the biomass showed no differences in different seasons. Statistical analysis demonstrated that seasonal change of macrobenthos diversity in the Spartina salt marsh negatively related to content of sediment organic matter, total N, bulk density, height and biomass of Spartina vegetation, and positively related to the density of Spartina. All these differences suggested the obvious effects of the Spartina vegetation on the Jiangsu inter-tidal benthic macroinvertebrate ecology. Furthermore, the investigation also showed that the niche of the native macrobenthos living in the mudflat has been transferred down, seaward, due to the invasion of Spartina in our study site. 相似文献
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949.
Taruna Arora Rupa Padaki Ling Liu Agnes E. Hamburger Aaron R. Ellison Seth R. Stevens James S. Louie Tadahiko Kohno 《Cytokine》2009,45(2):124-131
There are currently two Food and Drug Administration-approved classes of biologic agents that target tumor necrosis factor-α (TNF-α): anti-TNF monoclonal antibodies (mAbs) (adalimumab and infliximab), and soluble TNF receptors (etanercept). This study examined the ability of the TNF antagonists to: (1) bind various polymorphic variants of cell surface-expressed Fc receptors (FcγRs) and the complement component C1q, and (2) mediate Ab-dependent cellular cytotoxicity (ADCC) and complement-mediated cytotoxicity (CDC) killing of cells expressing membrane-bound TNF (mTNF) in vitro. Both mAbs and the soluble TNF receptor demonstrated low-level binding to the activating receptors FcγRI, FcγRIIa, and FcγRIIIa, and the inhibitory receptor FcγRIIb, in the absence of exogenous TNF. However, upon addition of TNF, the mAbs, but not etanercept, showed significantly increased binding, in particular to the FcγRII and FcγRIII receptors. Infliximab and adalimumab induced ADCC much more potently than etanercept. In the presence of TNF, both mAbs bound C1q in in vitro assays, but etanercept did not bind C1q under any conditions. Infliximab and adalimumab also induced CDC in cells expressing mTNF more potently than etanercept. Differences in the ability to bind ligand and mediate cell death may account for the differences in efficacy and safety of TNF antagonists. 相似文献
950.
Advancing Cell Biology and Functional Genomics in Maize Using Fluorescent Protein-Tagged Lines 下载免费PDF全文