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   1356篇
  免费   178篇
  国内免费   49篇
耳鼻咽喉   20篇
儿科学   106篇
妇产科学   19篇
基础医学   127篇
口腔科学   48篇
临床医学   116篇
内科学   363篇
皮肤病学   30篇
神经病学   33篇
特种医学   191篇
外科学   116篇
综合类   117篇
预防医学   104篇
眼科学   17篇
药学   77篇
中国医学   3篇
肿瘤学   96篇
  2024年   4篇
  2023年   16篇
  2022年   14篇
  2021年   27篇
  2020年   22篇
  2019年   12篇
  2018年   23篇
  2017年   44篇
  2016年   40篇
  2015年   35篇
  2014年   69篇
  2013年   74篇
  2012年   33篇
  2011年   30篇
  2010年   68篇
  2009年   72篇
  2008年   39篇
  2007年   77篇
  2006年   39篇
  2005年   29篇
  2004年   29篇
  2003年   13篇
  2002年   14篇
  2001年   35篇
  2000年   21篇
  1999年   26篇
  1998年   84篇
  1997年   70篇
  1996年   63篇
  1995年   53篇
  1994年   51篇
  1993年   52篇
  1992年   17篇
  1991年   9篇
  1990年   23篇
  1989年   29篇
  1988年   28篇
  1987年   16篇
  1986年   25篇
  1985年   21篇
  1984年   12篇
  1983年   14篇
  1982年   12篇
  1981年   6篇
  1980年   9篇
  1979年   6篇
  1978年   6篇
  1977年   7篇
  1976年   13篇
  1975年   9篇
排序方式: 共有1583条查询结果,搜索用时 15 毫秒
81.
82.
83.
84.
85.
86.

Background  

Despite extensive research, the five-year survival rate of oral squamous cell carcinoma (OSCC) patients has not improved. Effective treatment of OSCC requires the identification of molecular targets and signaling pathways to design appropriate therapeutic strategies. Several genes from the mTOR signaling pathway are known to be dysregulated in a wide spectrum of cancers. However, not much is known about the involvement of this pathway in tumorigenesis of OSCC. We therefore investigated the role of the tumor suppressor genes, TSC1 and TSC2, and other members of this pathway in tumorigenesis of OSCC.  相似文献   
87.
Interferon alpha (IFN-alpha) enhances the activity of 5-fluorouracil (5-FU) in the treatment of advanced colorectal cancer although the mechanism is not understood. We have investigated the effect of this combination on cellular immunity and compared this with standard therapy of 5-FU/L-leucovorin, in 24 patients with advanced colorectal cancer. This study has demonstrated an enhancement of the cellular immune response in patients given 5-FU/IFN-alpha with augmentation of natural killer (NK) cell function and abrogation of 5-FU-induced suppression of lymphokine-activated killer (LAK) cell activity.  相似文献   
88.
89.
Nasopharyngeal carriage of Haemophilus influenzae and Streptococcus pneumoniae was studied in 621 healthy Chinese children and 300 healthy Vietnamese children aged from 2 months to 5 years in Hong Kong. The carriage rate of H, influenzae type b in Vietnamese children was 1.3% (CI 0.04-2.63%); it was zero in Chinese. The carriage rate of non-typable H. influenzae was 5.8% (CI 1.4-7.6%) in Chinese and 65.4% (CI 58.9-69.8%) in Vietnamese. The carriage rates of S. pneumoniae were 10.8% (CI 8.3-13.2%) and 55.7% (CI 50.1-61.3%) in Chinese and Vietnamese children, respectively. Univariate and multivariate logistic regression analyses were performed to search for factors associated with differences in carriage rates of both H. influenzae and S. pneumoniae between Chinese and Vietnamese children. Although older age, smaller living area and parental smoking were associated with higher carriage rates, these could not explain the remarkably low carriage rates of both bacteria in Chinese children.  相似文献   
90.
Fragile X syndrome is the most common inherited cause of mental retardation. Early diagnosis is important not only for appropriate management of individuals but also to identify carriers who are unaware of their high risk of having an affected child. The disorder is associated with a cytogenetically visible fragile site (FRAXA) at Xq27.3, caused by amplification of a (CGG)n repeat sequence within the gene at this locus designated FMR1. Clinical and molecular studies have been undertaken to screen for fragile X syndrome in 154 children with moderate and severe learning difficulties of previously unknown origin. Southern blot analysis of peripheral blood showed the characteristic abnormally large (CGG)n repeat sequence associated with fragile X syndrome in four of the 154 children. The findings were confirmed by cytogenetic observation of the fragile site and by further molecular studies. The families of the affected children were offered genetic counselling and DNA tests to determine their carrier status. These findings show that there are still unrecognised cases of fragile X syndrome. Given the difficulty of making a clinical diagnosis and the implications for families when the diagnosis is missed, screening in high risk populations may be justified. The issues involved in screening all children in special schools for fragile X syndrome are discussed.  相似文献   
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