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991.
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肽核酸是一种寡核苷酸的类似物,它是由丹麦哥本哈根大学的Nielsen、Egholm等人首先发明合成的。肽核酸与传统的寡核苷酸相比,骨架结构发生了根要变化。肽核酸的电中性骨架有许多DNA所不具备的性质,例舅高灵敏度、高特异性、非盐依赖性等,从而使它成为一种优良的寡核苷酸的取代物,尤其是杂交检测领域。 相似文献
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两种五倍子蚜虫冬寄主藓类植物的光合特性及其与光照,温度和?… 总被引:3,自引:0,他引:3
The net photosynthesis of Thuidium cymbifolium and Chrysocladium retrorsum, two species of wintering host mosses for gullaphids, and its response to light, temperature and water content were measured with CI-301PS(CID Inc. USA) both in winter and spring. The photosynthetic capacity of Thuidium cymbifolium and Chrysocladium retrorsum was about 141 and 117 mumolCO2kg-1dw.s-1, respectively, and trended to increase from winter to spring. The light saturation point of these two mosses at 800-900 mumol.m-2.s-1 was much higher than that of many other mosses, and the compensation point ranged from 40 to 50 mumol.m-2.s-1. The temperature response curves of these two mosses were similar, with optium temperature ranging from 25 to 36 degrees C in spring, and from 20 to 30 degrees C in winter. When the temperature was below the freezing point(-15 to 0 degree C), they both maintained a distinct net photosynthesis, with the optimum water content ranging from 200 to 300(400)% dw. The photosynthesis started to be restrained evidently, when the water content declined to about 150% dw. The gas exchange ceased or became negative, when the water content was as low as 40-50% dw. It can be inferred that these two species might be both poikilothermal and poikilohydric organisms, but the resistibility of T. cymbifolium to intense light and high temperature was higher than that of C. retrorsum. 相似文献
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OBJECTIVE: The prognostic value of inflammation indexes in esophageal cancer was not established. In this study, therefore, both prognostic values of Glasgow prognostic score (GPS) and combination of platelet count and neutrophil lymphocyte ratio (COP-NLR) in patients with esophageal squamous cell carcinoma (ESCC) were investigated and compared. METHODS: This retrospective study included 375 patients who underwent esophagectomy for ESCC. The cancer-specific survival (CSS) was calculated by the Kaplan-Meier method, and the difference was assessed by the log-rank test. The GPS was calculated as follows: patients with elevated C-reactive protein (> 10 mg/l) and hypoalbuminemia (< 35 g/l) were assigned to GPS2. Patients with one or no abnormal value were assigned to GPS1 or GPS0, respectively. The COP-NLR was calculated as follows: patients with elevated platelet count (> 300 × 109/l) and neutrophil lymphocyte ratio (> 3) were assigned to COP-NLR2. Patients with one or no abnormal value were assigned to COP-NLR1 or COP-NLR0, respectively. RESULTS: The 5-year CSS in patients with GPS0, 1, and 2 was 50.0%, 27.0%, and 12.5%, respectively (P < .001). The 5-year CSS in patients with COP-NLR0, 1, and 2 was 51.8%, 27.0%, and 11.6%, respectively (P < .001). Multivariate analysis showed that both GPS (P = .003) and COP-NLR (P = .003) were significant predictors in such patients. In addition, our study demonstrated a similar hazard ratio (HR) between COP-NLR and GPS (HR = 1.394 vs HR = 1.367). CONCLUSIONS: COP-NLR is an independent predictive factor in patients with ESCC. We conclude that COP-NLR predicts survival in ESCC similar to GPS. 相似文献
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Rong-Guo Fu Tao Zhang Li Wang Yan Du Li-Ning Jia Jing-Jing Hou Gang-Lian Yao Xiao-Dan Liu Lei Zhang Ling Chen Bao-Song Gui Rong-Liang Xue 《PloS one》2014,9(1)
Objective
KCa3.1 channel participates in many important cellular functions. This study planned to investigate the potential involvement of KCa3.1 channel in premature senescence, myofibroblast phenotype transition and proliferation of mesangial cells.Methods & Materials
Rat mesangial cells were cultured together with TGF-β1 (2 ng/ml) and TGF-β1 (2 ng/ml) + TRAM-34 (16 nM) separately for specified times from 0 min to 60 min. The cells without treatment served as controls. The location of KCa3.1 channels in mesangial cells was determined with Confocal laser microscope, the cell cycle of mesangial cells was assessed with flow cytometry, the protein and mRNA expression of KCa3.1, α-smooth muscle actin (α-SMA) and fibroblast-specific protein-1 (FSP-1) were detected with Western blot and RT-PCR. One-way analysis of variance (ANOVA) and Student-Newman-Keuls-q test (SNK-q) were used to do statistical analysis. Statistical significance was considered at P<0.05.Results
Kca3.1 channels were located in the cell membranes and/or in the cytoplasm of mesangial cells. The percentage of cells in G0-G1 phase and the expression of Kca3.1, α-SMA and FSP-1 were elevated under the induction of TGF-β1 when compared to the control and decreased under the induction of TGF-β1+TRAM-34 when compared to the TGF-β1 induced (P<0.05 or P<0.01).Conclusion
Targeted disruption of KCa3.1 inhibits TGF-β1-induced premature aging, myofibroblast-like phenotype transdifferentiation and proliferation of mesangial cells. 相似文献996.
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