首页 | 本学科首页   官方微博 | 高级检索  
文章检索
  按 检索   检索词:      
出版年份:   被引次数:   他引次数: 提示:输入*表示无穷大
  收费全文   1680篇
  免费   145篇
  国内免费   2篇
耳鼻咽喉   2篇
儿科学   111篇
妇产科学   47篇
基础医学   252篇
口腔科学   25篇
临床医学   156篇
内科学   276篇
皮肤病学   36篇
神经病学   115篇
特种医学   153篇
外科学   163篇
综合类   75篇
预防医学   150篇
眼科学   29篇
药学   130篇
中国医学   1篇
肿瘤学   106篇
  2022年   8篇
  2021年   19篇
  2020年   13篇
  2019年   18篇
  2018年   37篇
  2017年   35篇
  2016年   25篇
  2015年   44篇
  2014年   43篇
  2013年   64篇
  2012年   76篇
  2011年   87篇
  2010年   82篇
  2009年   50篇
  2008年   76篇
  2007年   63篇
  2006年   60篇
  2005年   61篇
  2004年   46篇
  2003年   36篇
  2002年   52篇
  2001年   44篇
  2000年   34篇
  1999年   36篇
  1998年   36篇
  1997年   40篇
  1996年   38篇
  1995年   43篇
  1994年   35篇
  1993年   48篇
  1992年   41篇
  1991年   29篇
  1990年   33篇
  1989年   30篇
  1988年   38篇
  1987年   25篇
  1986年   27篇
  1985年   30篇
  1984年   18篇
  1983年   15篇
  1982年   17篇
  1981年   16篇
  1980年   14篇
  1979年   11篇
  1978年   11篇
  1977年   17篇
  1976年   24篇
  1975年   11篇
  1973年   11篇
  1966年   7篇
排序方式: 共有1827条查询结果,搜索用时 15 毫秒
1.
Cidofovir is an acyclic nucleoside phosphonate with broad-spectrum activity against DNA viruses, including human papilloma virus (HPV). However, data on the efficacy of cidofovir in an immunosuppressive setting remain contradictory. We report for the first time on the promotion of the healing of recalcitrant warts in a patient with myelodysplastic syndrome with intravenous cidofovir treatment.  相似文献   
2.
Fracture of the metatarsal head is uncommon, and reports of isolated osteochondral fracture of the metatarsal head are rare. Because of the distal location of the fracture, it is difficult to achieve and maintain reduction, and potential complications include avascular necrosis and subchondral fatigue fracture. The authors present a case of an osteochondral fracture in a 40-year-old man, which was treated by open reduction and internal fixation with a single twist-off screw, with good results 12 months postoperatively.  相似文献   
3.
4.
5.
6.
7.
Experimental columnar metaplasia in the canine oesophagus   总被引:7,自引:0,他引:7  
Regeneration of canine oesophageal mucosa was studied under basal conditions and in the presence of gastro-oesophageal reflux. In normal circumstances mucosal defects in the oesophagus regenerate by squamous epithelium. In the presence of gastro-oesophageal reflux of either acid or a combination of acid and bile, regeneration was frequently by columnar epithelium (Barrett's oesophagus). This columnar regeneration was not seen with bile reflux alone. By the use of squamous barriers to proximal migration of columnar epithelium in the stomach, it was demonstrated that columnar re-epithelialization may occur from cells intrinsic to the oesophagus and is not dependent on proximal migration of cardiac columnar epithelium. The cell of origin of this epithelium may be located in oesophageal gland ducts and is likely to be a multipotential stem cell since the regenerated columnar epithelium may contain goblet and parietal cells not normally found in the oesophagus. This epithelium is morphologically distinct on mucin histochemistry from cardiac columnar epithelium. These findings support the concept that Barrett's epithelium is metaplastic.  相似文献   
8.
The receptor tyrosine kinase (RTK) Ret is activated by the formation of a complex consisting of ligands such as glial cell line-derived neurotrophic factor (GDNF) and glycerophosphatidylinositol-anchored coreceptors termed GFRalphas. During activation, Ret translocates into lipid rafts, which is critical for functional responses to GDNF. We found that Ret was rapidly ubiquitinated and degraded in sympathetic neurons when activated with GDNF, but, unlike other RTKs that are trafficked to lysosomes for degradation, Ret was degraded predominantly by the proteasome. After GDNF stimulation, the majority of ubiquitinated Ret was located outside of lipid rafts and Ret was lost predominantly from nonraft membrane domains. Consistent with the predominance of Ret degradation outside of rafts, disruption of lipid rafts in neurons did not alter either the GDNF-dependent ubiquitination or degradation of Ret. GDNF-mediated survival of sympathetic neurons was inhibited by lipid raft depletion, and this inhibitory effect of raft disruption on GDNF-mediated survival was reversed if Ret degradation was blocked via proteasome inhibition. Therefore, lipid rafts sequester Ret away from the degradation machinery located in nonraft membrane domains, such as Cbl family E3 ligases, thereby sustaining Ret signaling.  相似文献   
9.
10.
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号