全文获取类型
收费全文 | 32555篇 |
免费 | 3035篇 |
国内免费 | 2455篇 |
专业分类
耳鼻咽喉 | 265篇 |
儿科学 | 261篇 |
妇产科学 | 337篇 |
基础医学 | 3824篇 |
口腔科学 | 503篇 |
临床医学 | 4762篇 |
内科学 | 4730篇 |
皮肤病学 | 251篇 |
神经病学 | 1763篇 |
特种医学 | 1091篇 |
外国民族医学 | 21篇 |
外科学 | 3008篇 |
综合类 | 5622篇 |
现状与发展 | 8篇 |
一般理论 | 2篇 |
预防医学 | 1861篇 |
眼科学 | 1198篇 |
药学 | 3638篇 |
28篇 | |
中国医学 | 1957篇 |
肿瘤学 | 2915篇 |
出版年
2024年 | 121篇 |
2023年 | 572篇 |
2022年 | 1511篇 |
2021年 | 1807篇 |
2020年 | 1381篇 |
2019年 | 1236篇 |
2018年 | 1144篇 |
2017年 | 1179篇 |
2016年 | 1025篇 |
2015年 | 1627篇 |
2014年 | 1913篇 |
2013年 | 1569篇 |
2012年 | 2385篇 |
2011年 | 2588篇 |
2010年 | 1547篇 |
2009年 | 1211篇 |
2008年 | 1634篇 |
2007年 | 1592篇 |
2006年 | 1640篇 |
2005年 | 1848篇 |
2004年 | 1015篇 |
2003年 | 879篇 |
2002年 | 804篇 |
2001年 | 681篇 |
2000年 | 670篇 |
1999年 | 782篇 |
1998年 | 551篇 |
1997年 | 518篇 |
1996年 | 404篇 |
1995年 | 374篇 |
1994年 | 307篇 |
1993年 | 216篇 |
1992年 | 236篇 |
1991年 | 216篇 |
1990年 | 196篇 |
1989年 | 144篇 |
1988年 | 148篇 |
1987年 | 106篇 |
1986年 | 102篇 |
1985年 | 66篇 |
1984年 | 29篇 |
1983年 | 24篇 |
1982年 | 11篇 |
1981年 | 19篇 |
1980年 | 9篇 |
1979年 | 8篇 |
排序方式: 共有10000条查询结果,搜索用时 16 毫秒
991.
992.
Ying Liang Fang Xie Xinyuan Tang Mei Wang Enmin Zhang Zhikai Zhang Hong Cai Yanhua Wang Xiaona Shen Hongqun Zhao Dongzheng Yu Lianxu Xia Rong Hai 《The American journal of tropical medicine and hygiene》2014,91(4):722-728
The Yersinia pestis chromosome contains a large variety and number of insert sequences that have resulted in frequent chromosome rearrangement events. To identify the chromosomal rearrangement features of Y. pestis strains from five typical plague foci in China and study spontaneous DNA rearrangements potentially stabilized in certain lineages of Y. pestis genomes, we examined the linking mode of locally collinear blocks (LCBs) in 30 Y. pestis strains by a polymerase chain reaction-based method. Our results suggest most strains have relatively stable chromosomal arrangement patterns, and these rearrangement characteristics also have a very close relationship with the geographical origin. In addition, some LCB linking modes are only present in specific strains. We conclude Y. pestis chromosome rearrangement patterns may reflect the genetic features of specific geographical areas and can be applied to distinguish Y. pestis isolates; furthermore, most of the rearrangement events are stable in certain lineages of Y. pestis genomes. 相似文献
993.
994.
Linyuan Wang Cynthia T. Luk Stephanie A. Schroer Alannah M. Smith Xie Li Erica P. Cai Herbert Gaisano Patrick E. MacDonald Zhenyue Hao Tak W. Mak Minna Woo 《Diabetologia》2014,57(9):1889-1898
Aims/hypothesis
Diabetes mellitus represents a significant burden on the health of the global population. Both type 1 and type 2 diabetes share a common feature of a reduction in functional beta cell mass. A newly discovered ubiquitination molecule HECT, UBA and WWE domain containing 1, E3 ubiquitin protein ligase (HUWE1 [also known as MULE or ARF-BP1]) is a critical regulator of p53-dependent apoptosis. However, its role in islet homeostasis is not entirely clear.Methods
We generated mice with pancreas-specific deletion of Huwe1 using a Cre-loxP recombination system driven by the Pdx1 promoter (Pdx1cre + Huwe1 fl/fl) to assess the in vivo role of HUWE1 in the pancreas.Results
Targeted deletion of Huwe1 in the pancreas preferentially activated p53-mediated beta cell apoptosis, leading to reduced beta cell mass and diminished insulin exocytosis. These defects were aggravated by ageing, with progressive further decline in insulin secretion and glucose homeostasis in older mice. Intriguingly, Huwe1 deletion provided protection against genotoxicity, such that Pdx1cre + Huwe1 fl/fl mice were resistant to multiple-low-dose-streptozotocin-induced beta cell apoptosis and diabetes.Conclusion/interpretation
HUWE1 expression in the pancreas is essential in determining beta cell mass. Furthermore, HUWE1 demonstrated divergent roles in regulating beta cell apoptosis depending on physiological or genotoxic conditions. 相似文献995.
Priscilla Mantik Minli Xie Harvey Wong Hank La Ronald W. Steigerwalt Uday Devanaboyina Geoffrey Ganem Danny Shih John A. Flygare Wayne J. Fairbrother Paroma Chakravarty David Russell Gilberto E. Fernandez Ajit S. Narang 《Journal of pharmaceutical sciences》2019,108(6):1934-1943
Solubilization of new chemical entities for toxicity assessment must use excipients that do not negatively impact drug pharmacokinetics and toxicology. In this study, we investigated the tolerability of a model freebase compound, GDC-0152, solubilized by pH adjustment with succinic acid and complexation with hydroxypropyl-β-cyclodextrin (HP-β-CD) to enable intravenous use. Solubility, critical micelle concentration, and association constant with HP-β-CD were determined. Blood compatibility and potential for hemolysis were assessed in vitro. Local tolerability was assessed after intravenous and subcutaneous injections in rats. A pharmacokinetic study was conducted in rats after intravenous bolus administration.GDC-0152 exhibited pH-dependent solubility that was influenced by self-association. The presence of succinic acid increased solubility in a concentration-dependent manner. HP-β-CD alone also increased solubility, but the extent of solubility enhancement was significantly lower than succinic acid alone. Inclusion of HP-β-CD in the solution of GDC-0152 improved blood compatibility, reduced hemolytic potential by ~20-fold in vitro, and increased the maximum tolerated dose to 80 mg/kg. 相似文献
996.
997.
998.
999.
1000.