全文获取类型
收费全文 | 12317篇 |
免费 | 783篇 |
国内免费 | 8篇 |
专业分类
13108篇 |
出版年
2024年 | 22篇 |
2023年 | 49篇 |
2022年 | 155篇 |
2021年 | 234篇 |
2020年 | 131篇 |
2019年 | 207篇 |
2018年 | 298篇 |
2017年 | 245篇 |
2016年 | 426篇 |
2015年 | 620篇 |
2014年 | 756篇 |
2013年 | 809篇 |
2012年 | 1077篇 |
2011年 | 1061篇 |
2010年 | 666篇 |
2009年 | 508篇 |
2008年 | 803篇 |
2007年 | 696篇 |
2006年 | 628篇 |
2005年 | 570篇 |
2004年 | 578篇 |
2003年 | 465篇 |
2002年 | 367篇 |
2001年 | 357篇 |
2000年 | 327篇 |
1999年 | 228篇 |
1998年 | 90篇 |
1997年 | 78篇 |
1996年 | 50篇 |
1995年 | 49篇 |
1994年 | 38篇 |
1993年 | 29篇 |
1992年 | 84篇 |
1991年 | 54篇 |
1990年 | 45篇 |
1989年 | 49篇 |
1988年 | 28篇 |
1987年 | 29篇 |
1986年 | 21篇 |
1985年 | 24篇 |
1984年 | 13篇 |
1983年 | 15篇 |
1982年 | 13篇 |
1981年 | 12篇 |
1980年 | 11篇 |
1979年 | 9篇 |
1978年 | 15篇 |
1975年 | 13篇 |
1974年 | 11篇 |
1970年 | 6篇 |
排序方式: 共有10000条查询结果,搜索用时 0 毫秒
991.
992.
Ji JE Kim SK Ahn KH Choi JM Jung SY Jung KM Jeon HJ Kim DK 《Prostaglandins & other lipid mediators》2011,94(3-4):88-95
Ceramide has been suggested to function as a mediator of exocytosis in response to the addition of a calcium ionophore from PC12 cells. Here, we show that although cell-permeable C(6)-ceramide or a calcium ionophore alone did not increase either the degranulation of serotonin or the release of arachidonic acid (AA) from RBL-2H3 cells, their combined effect significantly stimulated these processes in a time- and dose-dependent manner. This effect was inhibited by the presence of an exogenous calcium chelator and significantly suppressed by the CERK inhibitor (K1) and phospholipase A(2) (PLA(2)) inhibitors. Moreover, cytosolic PLA(2) GIVA (cPLA(2) GIVA) siRNA-transfected RBL-2H3 cells showed a lower level of serotonin release than scramble siRNA-transfected cells. Little is known about the regulation of degranulation proximal to the activation of cytosolic phospholipase A(2) GIVA, the initial rate-limiting step in RBL-2H3 cells. In this study, we suggest that CERK, ceramide-1-phosphate, and PLA(2) are involved in degranulation in a calcium-dependent manner. Inhibition of p44/p42 mitogen-activated protein kinase partially decreased the AA release, but did not affect degranulation. Furthermore, treatment of the cells with AA (ω-6, C20:4), not linoleic acid (ω-6, C18:2) or α-linolenic acid (ω-6, C18:3), induced degranulation. Taken together, these results suggest that ceramide is involved in mast cell degranulation via the calcium-mediated activation of PLA(2). 相似文献
993.
Hsing CH Lin MC Choi PC Huang WC Kai JI Tsai CC Cheng YL Hsieh CY Wang CY Chang YP Chen YH Chen CL Lin CF 《PloS one》2011,6(3):e17598
Background
Anesthetic propofol has immunomodulatory effects, particularly in the area of anti-inflammation. Bacterial endotoxin lipopolysaccharide (LPS) induces inflammation through toll-like receptor (TLR) 4 signaling. We investigated the molecular actions of propofol against LPS/TLR4-induced inflammatory activation in murine RAW264.7 macrophages.Methodology/Principal Findings
Non-cytotoxic levels of propofol reduced LPS-induced inducible nitric oxide synthase (iNOS) and NO as determined by western blotting and the Griess reaction, respectively. Propofol also reduced the production of tumor necrosis factor-α (TNF-α), interleukin (IL)-6, and IL-10 as detected by enzyme-linked immunosorbent assays. Western blot analysis showed propofol inhibited LPS-induced activation and phosphorylation of IKKβ (Ser180) and nuclear factor (NF)-κB (Ser536); the subsequent nuclear translocation of NF-κB p65 was also reduced. Additionally, propofol inhibited LPS-induced Akt activation and phosphorylation (Ser473) partly by reducing reactive oxygen species (ROS) generation; inter-regulation that ROS regulated Akt followed by NF-κB activation was found to be crucial for LPS-induced inflammatory responses in macrophages. An in vivo study using C57BL/6 mice also demonstrated the anti-inflammatory properties against LPS in peritoneal macrophages.Conclusions/Significance
These results suggest that propofol reduces LPS-induced inflammatory responses in macrophages by inhibiting the interconnected ROS/Akt/IKKβ/NF-κB signaling pathways. 相似文献994.
995.
Yong Chae Lim Jed Johnson Zhengzheng Fei Yun Wu Dave F. Farson John J. Lannutti Hae Woon Choi L. James Lee 《Biotechnology and bioengineering》2011,108(1):116-126
Experimental investigations aimed at assessing the effectiveness of femtosecond (FS) laser ablation for creating microscale features on electrospun poly(ε‐caprolactone) (PCL)/gelatin nanofiber tissue scaffold capable of controlling cell distribution are described. Statistical comparisons of the fiber diameter and surface porosity on laser‐machined and as‐spun surface were made and results showed that laser ablation did not change the fiber surface morphology. The minimum feature size that could be created on electrospun nanofiber surfaces by direct‐write ablation was measured over a range of laser pulse energies. The minimum feature size that could be created was limited only by the pore size of the scaffold surface. The chemical states of PCL/gelatin nanofiber surfaces were measured before and after FS laser machining by attenuated total reflectance Fourier transform infrared (ATR‐FTIR) spectroscopy and X‐ray photoelectron spectroscopy (XPS) and showed that laser machining produced no changes in the chemistry of the surface. In vitro, mouse embryonic stem cells (mES cells) were cultured on as‐spun surfaces and in laser‐machined microwells. Cell densities were found to be statistically indistinguishable after 1 and 2 days of growth. Additionally, confocal microscope imaging confirmed that spreading of mES cells cultured within laser‐machined microwells was constrained by the cavity walls, the expected and desired function of these cavities. The geometric constraint caused statistically significant smaller density of cells in microwells after 3 days of growth. It was concluded that FS laser ablation is an effective process for microscale structuring of these electrospun nanofiber tissue scaffold surfaces. Biotechnol. Bioeng. 2011; 108:116–126. © 2010 Wiley Periodicals, Inc. 相似文献
996.
Hwang IK Yoo KY Yoo DY Choi JW Lee CH Choi JH Yoon YS Won MH 《Cellular and molecular neurobiology》2011,31(5):669-674
Cyclic AMP (cAMP) response element-binding protein (CREB) is involved in memory, learning, and synaptic transmission. In this
study, we observed changes of phosphorylated CREB (pCREB) immunoreactivity and its protein levels as well as brain-derived
neurotrophic factor (BDNF) levels in the hippocampal dentate gyrus at postnatal (P) 1, 7, 14, and 21 in mice. In addition,
we also investigated pCREB expression in doublecortin (DCX, a marker for neuronal progenitors) immunoreactive neuroblasts
at P21. pCREB immunoreaction at P1 was detected in most of cells in the dentate gyrus, thereafter pCREB immunoreactivity was
decreased in all the layers of the dentate gyrus with time, however, strong pCREB immunoreactivity was shown in cells confined
to the subgranular zone of the dentate gyrus at P21. In this group, many pCREB immunoreactive cells were co-localized with
DCX immunoreactive neuroblasts. In addition, pCREB protein levels were decreased with age, showing that their levels were
very low at P21, while BDNF protein levels were increased with age. These results suggest that pCREB may play important roles
in functional maturity of granule cells in mice. 相似文献
997.
The exchange of HTO with aerial portions of the soybean was studied under a variety of conditions. When fed to a lone leaf or leaflet in a saturated air atmosphere (all other leaves and the growing point having been excised), the HTO profile virtually ceases at a distance of 2 cm from the feeding chamber in the photosynthetic plant, but is greater and more extensive in the unilluminated plant. The differences are accentuated when roots are excised. Under these latter conditions the photosynthetic T-fixed gradient virtually disappears. 相似文献
998.
999.
1000.
Na Na Kim Hyun Suk Shin Heum Gi Park Jehee Lee Gyung-Suk Kil Cheol Young Choi 《Biotechnology and Bioprocess Engineering》2014,19(2):250-256
Light quality is a significant environmental factor that influences photosynthetic pigments in cyanobacteria. In the present study, we illuminated the marine cyanobacteria Synechococcus sp. with white (350 ~ 700 nm), red (630 nm), green (530 nm), and blue (450 nm) light emitting diodes (LEDs) and measured pigment levels (chlorophyll, carotenoid, and phycobiliprotein) and expression of photosynthesis-related genes (pebA, psbB, and psaE). The amount of photosynthetic pigments (total pigments, chlorophyll, and phycobiliproteins) was higher in the green and blue LED groups than in the white and red LED groups after 8 days of culture. The cells were prepared in a 1.5 mL solution for the analysis of the total pigments, chlorophyll, and carotenoid, and in a 2 mL for analysis of phycobiliproteins. The mRNA expression levels of pebA and psbB significantly increased after 8 days of cultivation under green and blue light, while the mRNA expression levels of psaE decreased. These results indicate that green and blue light increase the accumulation of photosynthetic pigments. In contrast red light induced mRNA expression of psaE and stimulated cell growth in Synechococcus sp. 相似文献