全文获取类型
收费全文 | 35213篇 |
免费 | 2877篇 |
国内免费 | 1867篇 |
专业分类
39957篇 |
出版年
2024年 | 70篇 |
2023年 | 398篇 |
2022年 | 938篇 |
2021年 | 1644篇 |
2020年 | 1045篇 |
2019年 | 1257篇 |
2018年 | 1234篇 |
2017年 | 874篇 |
2016年 | 1328篇 |
2015年 | 2034篇 |
2014年 | 2384篇 |
2013年 | 2569篇 |
2012年 | 3109篇 |
2011年 | 2775篇 |
2010年 | 1737篇 |
2009年 | 1439篇 |
2008年 | 1670篇 |
2007年 | 1523篇 |
2006年 | 1356篇 |
2005年 | 1150篇 |
2004年 | 1026篇 |
2003年 | 873篇 |
2002年 | 748篇 |
2001年 | 678篇 |
2000年 | 682篇 |
1999年 | 655篇 |
1998年 | 386篇 |
1997年 | 335篇 |
1996年 | 359篇 |
1995年 | 333篇 |
1994年 | 326篇 |
1993年 | 217篇 |
1992年 | 354篇 |
1991年 | 272篇 |
1990年 | 307篇 |
1989年 | 259篇 |
1988年 | 191篇 |
1987年 | 171篇 |
1986年 | 152篇 |
1985年 | 135篇 |
1984年 | 121篇 |
1983年 | 95篇 |
1982年 | 78篇 |
1981年 | 61篇 |
1979年 | 75篇 |
1978年 | 55篇 |
1977年 | 53篇 |
1975年 | 59篇 |
1974年 | 47篇 |
1973年 | 50篇 |
排序方式: 共有10000条查询结果,搜索用时 31 毫秒
991.
992.
Fei Huang Puiian Wong Jinglan Li Zheng Lv Liangliang Xu Genfu Zhu Mincong He Yiwen Luo 《Journal of cellular and molecular medicine》2022,26(13):3591
Osteoporosis is a bone disease that is caused by disorder of the skeletal microenvironment, and it characterized by a high disability rate and the occurrence of low energy fractures. Studies on osteoporosis and related treatment options have always been hot spots in the field of bone biology. In the past, the understanding of osteoporosis has been rather limited; research has only shown that osteoporosis involves the imbalance of bone resorption and bone formation, and recent studies have not provided cutting‐edge theories of the basic understanding of osteoporosis. Recent studies have shown crosstalk between bone and immune responses. RANKL, an essential factor for osteoclasts (OCs), is associated with the immune system. T helper (Th17)/regulatory T (Treg) cells are two different kinds of T cells that can self‐interact and regulate the differentiation and formation of OCs. Therefore, understanding the correlation between the skeletal and immune systems and further revealing the roles and the cooperation between RANKL and the Th17/Treg balance will help to provide new insights for the treatment of osteoporosis. 相似文献
993.
994.
ChaoChien Chang KeeChin Sia JiaFeng Chang ChiaMo Lin ChuenMao Yang ITa Lee Thi Thuy Tien Vo KuoYang Huang WeiNing Lin 《Journal of cellular and molecular medicine》2022,26(14):3850
Obesity is a world‐wide problem, especially the child obesity, with the complication of various metabolic diseases. Child obesity can be developed as early as the age between 2 and 6. The expansion of fat mass in child age includes both hyperplasia and hypertrophy of adipose tissue, suggesting the importance of proliferation and adipogenesis of preadipocytes. The changed composition of gut microbiota is associated with obesity, revealing the roles of lipopolysaccharide (LPS) on manipulating adipose tissue development. Studies suggest that LPS enters the circulation and acts as a pro‐inflammatory regulator to facilitate pathologies. Nevertheless, the underlying mechanisms behind LPS‐modulated obesity are yet clearly elucidated. This study showed that LPS enhanced the expression of cyclooxygenase‐2 (COX‐2), an inflammatory regulator of obesity, in preadipocytes. Pretreating preadipocytes with the scavenger of reactive oxygen species (ROS) or the inhibitors of NADPH oxidase or p42/p44 MAPK markedly decreased LPS‐stimulated gene expression of COX‐2 together with the phosphorylation of p47phox and p42/p44 MAPK, separately. LPS activated p42/p44 MAPK via NADPH oxidase‐dependent ROS accumulation in preadipocytes. Reduction of intracellular ROS or attenuation of p42/p44 MAPK activation both reduced LPS‐mediated COX‐2 expression and preadipocyte proliferation. Moreover, LPS‐induced preadipocyte proliferation and adipogenesis were abolished by the inhibition of COX‐2 or PEG2 receptors. Taken together, our results suggested that LPS enhanced the proliferation and adipogenesis of preadipocytes via NADPH oxidase/ROS/p42/p44 MAPK‐dependent COX‐2 expression. 相似文献
995.
Ronald E. Crump Ching-I Huang Simon E. F. Spencer Paul E. Brown Chansy Shampa Erick Mwamba Miaka Kat S. Rock 《PLoS neglected tropical diseases》2022,16(7)
Gambiense human African trypanosomiasis (gHAT) has been targeted for elimination of transmission (EoT) to humans by 2030. Whilst this ambitious goal is rapidly approaching, there remain fundamental questions about the presence of non-human animal transmission cycles and their potential role in slowing progress towards, or even preventing, EoT. In this study we focus on the country with the most gHAT disease burden, the Democratic Republic of Congo (DRC), and use mathematical modelling to assess whether animals may contribute to transmission in specific regions, and if so, how their presence could impact the likelihood and timing of EoT.By fitting two model variants—one with, and one without animal transmission—to the human case data from 2000–2016 we estimate model parameters for 158 endemic health zones of the DRC. We evaluate the statistical support for each model variant in each health zone and infer the contribution of animals to overall transmission and how this could impact predicted time to EoT.We conclude that there are 24/158 health zones where there is substantial to decisive statistical support for some animal transmission. However—even in these regions—we estimate that animals would be extremely unlikely to maintain transmission on their own. Animal transmission could hamper progress towards EoT in some settings, with projections under continuing interventions indicating that the number of health zones expected to achieve EoT by 2030 reduces from 68/158 to 61/158 if animal transmission is included in the model. With supplementary vector control (at a modest 60% tsetse reduction) added to medical screening and treatment interventions, the predicted number of health zones meeting the goal increases to 147/158 for the model including animal transmission. This is due to the impact of vector reduction on transmission to and from all hosts. 相似文献
996.
997.
Jianping Hu Yiting Zhang Shenglan Yi Chaokui Wang Xinyue Huang Su Pan Jinglu Yang Gangxiang Yuan Sisi Tan Hong Li 《International journal of biological sciences》2022,18(11):4545
Dendritic cells (DCs) are the major antigen-presenting cells and play an important role in autoimmune uveitis. Emerging evidence suggests that bile acids (BAs) regulate DCs maturation. However, the underlying mechanisms by which BAs regulate the function of DCs still need to be clarified. Here, we demonstrate that lithocholic acid (LCA) inhibits the production of pro-inflammatory cytokines and the expression of surface molecules in bone marrow-derived dendritic cells (BMDCs). LCA attenuates the severity of EAU by modulating the maturation of splenic CD11C+MHCIIhigh DCs. Notably, Takeda G-protein coupled receptor 5 (TGR5) deficiency partially reverses the inhibitory effect of LCA on DCs in vitro and in vivo. TGR5 activation also downregulates the NF-κB and MAPK pathways by inhibiting glutathione production and inducing oxidative stress in DCs, which leads to apoptosis and autophagy in DCs. In addition, LCA or INT-777 treatment increases the TGR5 expression in monocyte-derived dendritic cells (MD-DCs) of patients with active BD, whereas both LCA and TGR5 agonists inhibit the activation of MD-DCs. These results suggest that LCA and TGR5 agonists might be potential therapeutic drugs for the treatment of autoimmune uveitis. 相似文献
998.
深黄被孢霉高产脂变株的选育及其发酵的研究 总被引:33,自引:0,他引:33
以深黄被孢霉(Mortierellaisabellina)AS3.3410为出发菌株,经紫外线,硫酸二乙酯和亚硝基胍复合诱变处理,选育成功高产脂深黄被抱霉M018变株,其摇瓶培养菌体油脂含量达65.6%,比出发菌株提高133%。60m3罐三级发酵培养菌体油脂含量高达79.2%,生物量达37.8g/L.气相色谱分析表明变株M018r-亚麻酸的含量比出发菌株提高了53%。连续传代试验表明M018是一稳定的变株。该变株油脂合成的最佳碳源为葡萄糖,最佳氮源为酵母膏,最佳C/N为 相似文献
999.
1000.
Terrence Tsz-Tai Yuen Jasper Fuk-Woo Chan Bingpeng Yan Cynthia Cheuk-Ying Shum Yuanchen Liu Huiping Shuai Yuxin Hou Xiner Huang Bingjie Hu Yue Chai Chaemin Yoon Tianrenzheng Zhu Huan Liu Jialu Shi Jinjin Zhang Jian-Piao Cai Anna Jinxia Zhang Jie Zhou Feifei Yin Shuofeng Yuan Bao-Zhong Zhang Hin Chu 《International journal of biological sciences》2022,18(12):4714
The Coronavirus Disease 2019 (COVID-19) pandemic caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the biggest public health challenge the world has witnessed in the past decades. SARS-CoV-2 undergoes constant mutations and new variants of concerns (VOCs) with altered transmissibility, virulence, and/or susceptibility to vaccines and therapeutics continue to emerge. Detailed analysis of host factors involved in virus replication may help to identify novel treatment targets. In this study, we dissected the metabolome derived from COVID-19 patients to identify key host factors that are required for efficient SARS-CoV-2 replication. Through a series of metabolomic analyses, in vitro, and in vivo investigations, we identified ATP citrate lyase (ACLY) as a novel host factor required for efficient replication of SARS-CoV-2 wild-type and variants, including Omicron. ACLY should be further explored as a novel intervention target for COVID-19. 相似文献