全文获取类型
收费全文 | 4223篇 |
免费 | 381篇 |
国内免费 | 27篇 |
专业分类
耳鼻咽喉 | 20篇 |
儿科学 | 128篇 |
妇产科学 | 58篇 |
基础医学 | 692篇 |
口腔科学 | 278篇 |
临床医学 | 366篇 |
内科学 | 798篇 |
皮肤病学 | 88篇 |
神经病学 | 247篇 |
特种医学 | 398篇 |
外科学 | 369篇 |
综合类 | 13篇 |
一般理论 | 2篇 |
预防医学 | 280篇 |
眼科学 | 12篇 |
药学 | 311篇 |
中国医学 | 1篇 |
肿瘤学 | 570篇 |
出版年
2023年 | 23篇 |
2022年 | 17篇 |
2021年 | 59篇 |
2020年 | 44篇 |
2019年 | 64篇 |
2018年 | 77篇 |
2017年 | 54篇 |
2016年 | 83篇 |
2015年 | 74篇 |
2014年 | 105篇 |
2013年 | 148篇 |
2012年 | 204篇 |
2011年 | 170篇 |
2010年 | 135篇 |
2009年 | 112篇 |
2008年 | 170篇 |
2007年 | 162篇 |
2006年 | 156篇 |
2005年 | 168篇 |
2004年 | 170篇 |
2003年 | 169篇 |
2002年 | 184篇 |
2001年 | 154篇 |
2000年 | 144篇 |
1999年 | 138篇 |
1998年 | 139篇 |
1997年 | 107篇 |
1996年 | 128篇 |
1995年 | 99篇 |
1994年 | 79篇 |
1993年 | 83篇 |
1992年 | 81篇 |
1991年 | 73篇 |
1990年 | 93篇 |
1989年 | 108篇 |
1988年 | 59篇 |
1987年 | 70篇 |
1986年 | 48篇 |
1985年 | 63篇 |
1984年 | 61篇 |
1983年 | 45篇 |
1982年 | 42篇 |
1981年 | 35篇 |
1980年 | 43篇 |
1979年 | 27篇 |
1978年 | 28篇 |
1977年 | 28篇 |
1976年 | 26篇 |
1975年 | 24篇 |
1974年 | 11篇 |
排序方式: 共有4631条查询结果,搜索用时 15 毫秒
1.
2.
3.
Needle-localized breast biopsy: why do we fail? 总被引:10,自引:0,他引:10
4.
Genotyping of Chlamydia trachomatis in Urine Specimens Will Facilitate Large Epidemiological Studies 总被引:4,自引:0,他引:4
下载免费PDF全文
![点击此处可从《Journal of clinical microbiology》网站下载免费的PDF全文](/ch/ext_images/free.gif)
Servaas A. Morr Robert Moes Irene Van Valkengoed Joan P. Boeke Jacques T. M. van Eijk Chris J. L. M. Meijer Adriaan J. C. Van den Brule 《Journal of clinical microbiology》1998,36(10):3077-3078
The serovars of Chlamydia trachomatis-positive urine specimens (n = 81; as detected by PCR and ligase chain reaction) were successfully analyzed in 94% of cases by omp1 PCR-based RFLP analysis. The use of urine specimens and this simple and sensitive typing method will greatly facilitate epidemiological studies of C. trachomatis serovar distribution in asymptomatic C. trachomatis infections in both females and males. 相似文献
5.
6.
Carrier-mediated transport in the hepatic distribution and elimination of drugs, with special reference to the category of organic cations 总被引:1,自引:0,他引:1
D K Meijer W E Mol M Müller G Kurz 《Journal of pharmacokinetics and biopharmaceutics》1990,18(1):35-70
Carrier-mediated transport of drugs occurs in various tissues in the body and may largely affect the rate of distribution and elimination. Saturable translocation mechanisms allowing competitive interactions have been identified in the kidneys (tubular secretion), mucosal cells in the gut (intestinal absorption and secretion), choroid plexus (removal of drug from the cerebrospinal fluid), and liver (hepatobiliary excretion). Drugs with quaternary and tertiary amine groups represent the large category of organic cations that can be transported via such mechanisms. The hepatic and to a lesser extent the intestinal cation carrier systems preferentially recognize relatively large molecular weight amphipathic compounds. In the case of multivalent cationic drugs, efficient transport only occurs if large hydrophobic ring structures provide a sufficient lipophilicity-hydrophilicity balance within the drug molecule. At least two separate carrier systems for hepatic uptake of organic cations have been identified through kinetic and photoaffinity labeling studies. In addition absorptive endocytosis may play a role that along with proton-antiport systems and membrane potential driven transport may lead to intracellular sequestration in lysosomes and mitochondria. Concentration gradients of inorganic ions may represent the driving forces for hepatic uptake and biliary excretion of drugs. Recent studies that aim to the identification of potential membrane carrier proteins indicate multiple carriers for organic anions, cations, and uncharged compounds with molecular weights around 50,000 Da. They may represent a family of closely related proteins exhibiting overlapping substrate specificity or, alternatively, an aspecific transport system that mediates translocation of various forms of drugs coupled with inorganic ions. Consequently, extensive pharmacokinetic interactions can be anticipated at the level of uptake and secretion of drugs regardless of their charge. 相似文献
7.
Ketai LH; Williamson MR; Telepak RJ; Levy H; Koster FT; Nolte KB; Allen SE 《Radiology》1994,191(3):665
8.
We studied a possible acinar heterogeneity in the transport of organic cations, using rhodamine B as model compound. Employing perfusions of isolated rat livers in the ante- and retrograde mode and quantitative fluorescence microscopy, Zones 1 and 3 were shown to be equally efficient in taking up rhodamine B. Ten minutes after injection in an antegrade perfusion, 95% of the dose was localized in the portal half of the acinus. Fifty minutes later, however, the amount of rhodamine B in Zone 1 had been reduced to 23%; 30 and 31% were in Zones 2 and 3, respectively, and the medium concentration was doubled. Thus, unchanged rhodamine B appeared to be transported downstream within the liver, either via the medium or directly from cell to cell, finally resulting in a relatively higher rhodamine B concentration in Zone 3. To obtain additional data, we designed a perfusion setup in which the zones could be studied separately. In both zones, the amount excreted into the medium was about 30 times the amount excreted into bile. Intracellular sequestration of rhodamine B and the rate constant for sinusoidal secretion were higher in Zone 3, while the sinusoidal uptake rates were equal; biliary excretion was higher in Zone 1. Acinar distribution changed with time because rhodamine B, primarily accumulated in Zone 1, was secreted into the sinusoids and taken up again by downstream cells. The finally higher rhodamine B concentration in Zone 3 was caused by a zonal heterogeneity in intracellular sequestration and sinusoidal secretion of rhodamine B. 相似文献
9.
Ingestion of Staphylococcus aureus, Staphylococcus epidermidis, and Escherichia coli by human peritoneal mesothelial cells.
下载免费PDF全文
![点击此处可从《Infection and immunity》网站下载免费的PDF全文](/ch/ext_images/free.gif)
C E Visser J J Brouwer-Steenbergen I L Schadee-Eestermans S Meijer R T Krediet R H Beelen 《Infection and immunity》1996,64(8):3425-3428
In the present study we examined whether mesothelial cells can ingest and digest bacteria. The results showed that all strains were ingested. Ingested staphylococci proliferated abundantly, and only a few were digested. Escherichia coli, however, was digested during the first 8 h, whereafter the mesothelial cells disintegrated and proliferation of bacteria could be observed. The clinical implications of these findings are discussed. 相似文献
10.