全文获取类型
收费全文 | 1749篇 |
免费 | 95篇 |
国内免费 | 11篇 |
专业分类
耳鼻咽喉 | 9篇 |
儿科学 | 72篇 |
妇产科学 | 32篇 |
基础医学 | 270篇 |
口腔科学 | 54篇 |
临床医学 | 99篇 |
内科学 | 282篇 |
皮肤病学 | 25篇 |
神经病学 | 139篇 |
特种医学 | 29篇 |
外科学 | 192篇 |
综合类 | 38篇 |
一般理论 | 2篇 |
预防医学 | 174篇 |
眼科学 | 84篇 |
药学 | 206篇 |
中国医学 | 10篇 |
肿瘤学 | 138篇 |
出版年
2023年 | 19篇 |
2022年 | 34篇 |
2021年 | 58篇 |
2020年 | 30篇 |
2019年 | 40篇 |
2018年 | 55篇 |
2017年 | 38篇 |
2016年 | 49篇 |
2015年 | 48篇 |
2014年 | 78篇 |
2013年 | 99篇 |
2012年 | 107篇 |
2011年 | 122篇 |
2010年 | 86篇 |
2009年 | 77篇 |
2008年 | 102篇 |
2007年 | 91篇 |
2006年 | 94篇 |
2005年 | 84篇 |
2004年 | 65篇 |
2003年 | 83篇 |
2002年 | 51篇 |
2001年 | 54篇 |
2000年 | 31篇 |
1999年 | 40篇 |
1998年 | 22篇 |
1997年 | 10篇 |
1996年 | 7篇 |
1995年 | 11篇 |
1994年 | 7篇 |
1993年 | 10篇 |
1992年 | 19篇 |
1991年 | 16篇 |
1990年 | 12篇 |
1989年 | 11篇 |
1988年 | 17篇 |
1987年 | 11篇 |
1986年 | 11篇 |
1985年 | 11篇 |
1984年 | 13篇 |
1983年 | 3篇 |
1982年 | 3篇 |
1981年 | 3篇 |
1978年 | 2篇 |
1977年 | 2篇 |
1975年 | 2篇 |
1973年 | 3篇 |
1970年 | 3篇 |
1965年 | 2篇 |
1964年 | 2篇 |
排序方式: 共有1855条查询结果,搜索用时 0 毫秒
101.
Reliability of direct skin smear microscopy in leprosy 总被引:1,自引:0,他引:1
Skin smear direct microscopy is an important tool for diagnosis of leprosy. The study was planned to understand the reproducibility of skin smear reading by a trained technician. Skin smears were collected from known patients of leprosy from the field area. They were stained for acid fast bacilli following the standard cold staining procedure and were read following the Ridley scale. A sample of smears was re-examined on two occasions by the same technician, following blind procedure. There was a systematic under reading on the second occasion, which was attributed to the defective storage of the slides. However, the agreement between second and third examinations was very good (Concordance 81.34%, Kappa 0.74). The finding was confirmed on a repeat examination. It can be concluded that the Direct Skin Smear Microscopy is a reliable and reproducible technique under experimental conditions. 相似文献
102.
Social and physical environments and disparities in risk for cardiovascular disease: the healthy environments partnership conceptual model 总被引:4,自引:0,他引:4 下载免费PDF全文
Schulz AJ Kannan S Dvonch JT Israel BA Allen A James SA House JS Lepkowski J 《Environmental health perspectives》2005,113(12):1817-1825
The Healthy Environments Partnership (HEP) is a community-based participatory research effort investigating variations in cardiovascular disease risk, and the contributions of social and physical environments to those variations, among non-Hispanic black, non-Hispanic white, and Hispanic residents in three areas of Detroit, Michigan. Initiated in October 2000 as a part of the National Institute of Environmental Health Sciences' Health Disparities Initiative, HEP is affiliated with the Detroit Community-Academic Urban Research Center. The study is guided by a conceptual model that considers race-based residential segregation and associated concentrations of poverty and wealth to be fundamental factors influencing multiple, more proximate predictors of cardiovascular risk. Within this model, physical and social environments are identified as intermediate factors that mediate relationships between fundamental factors and more proximate factors such as physical activity and dietary practices that ultimately influence anthropomorphic and physiologic indicators of cardiovascular risk. The study design and data collection methods were jointly developed and implemented by a research team based in community-based organizations, health service organizations, and academic institutions. These efforts include collecting and analyzing airborne particulate matter over a 3-year period; census and administrative data; neighborhood observation checklist data to assess aspects of the physical and social environment; household survey data including information on perceived stressors, access to social support, and health-related behaviors; and anthropometric, biomarker, and self-report data as indicators of cardiovascular health. Through these collaborative efforts, HEP seeks to contribute to an understanding of factors that contribute to racial and socioeconomic health inequities, and develop a foundation for efforts to eliminate these disparities in Detroit. 相似文献
103.
Scaffolds of pure hydroxyapatite suitable for either direct clinical use or tissue-engineering applications were successfully produced via hydrothermal transformation of aragonite, obtained from fresh cuttlefish bones, at 200°C followed by sintering. Beyond low production cost, worldwide availability and natural–biological origin of raw materials, the produced scaffolds have ideal pore size and interconnectivity features suitable for supporting biological activities, such as bone tissue growth and vascularization. Bioactivity in vitro tests were excellent: (a) rapid and pronounced formation of hydroxyapatite occurred when the scaffolds were immersed in simulated body fluid (SBF), and (b) outstanding proliferation of osteoblasts was registered. The produced scaffolds can be machined and shaped very easily at any stage of processing. Therefore, these ceramic scaffolds can satisfy both bioactivity demands and the requirements for shaping of tailor-made individualized implants, especially for randomly damaged bones. 相似文献
104.
105.
106.
107.
108.
109.
Energy landscape of amyloidogenic peptide oligomerization by parallel-tempering molecular dynamics simulation: significant role of Asn ladder 下载免费PDF全文
Tsai HH Reches M Tsai CJ Gunasekaran K Gazit E Nussinov R 《Proceedings of the National Academy of Sciences of the United States of America》2005,102(23):8174-8179
Recent evidence suggests that amyloidogenic oligomers may be the toxic species in cell cultures. Thus, it is crucial to understand their structure and oligomerization mechanism in atomistic detail. By employing tens of fast central processing units and an advanced phase-space sampling algorithm, parallel-tempering molecular dynamics, we have explored the energy landscape of amyloidogenic peptide oligomerization in explicit water. A pentapeptide, DFNKF, derived from human calcitonin and its mutant, DFAKF, was simulated with a total simulation time of approximately 500 ns. The detailed oligomerization process of a DFNKF parallel beta-sheet formation at 300 K has been characterized. The assembly of a parallel beta-sheet from the amorphous state mainly occurs via a "bottleneck" channel where the interstrand Asn-Asn stacking is the major interaction. The interactions of Asn-Asn stacking include both backbone and side-chain hydrogen bonds. The Asn-Asn interactions work like "glue" by sticking the DFNKF strands together and assist the "on-pathway" oligomerization. The Asn-Asn stacking observed here is similar to the Asn ladder commonly found in globular beta-helix proteins. A control run shows that when Asn is mutated to Ala, the stability and population of the DFAKF parallel beta-sheet is decreased. Furthermore, our in vitro mutagenesis experiments show that the ability of DFAKF peptides to form amyloid fibrils is significantly reduced, in agreement with the simulations. Knowledge of the energy landscape of oligomerization may provide hints for rational drug design, preventing amyloid-associated diseases. 相似文献
110.