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   10603篇
  免费   1158篇
  国内免费   1331篇
  2024年   20篇
  2023年   262篇
  2022年   252篇
  2021年   389篇
  2020年   378篇
  2019年   443篇
  2018年   376篇
  2017年   410篇
  2016年   432篇
  2015年   421篇
  2014年   498篇
  2013年   650篇
  2012年   422篇
  2011年   460篇
  2010年   437篇
  2009年   560篇
  2008年   532篇
  2007年   600篇
  2006年   478篇
  2005年   442篇
  2004年   371篇
  2003年   341篇
  2002年   325篇
  2001年   304篇
  2000年   305篇
  1999年   278篇
  1998年   232篇
  1997年   227篇
  1996年   204篇
  1995年   230篇
  1994年   190篇
  1993年   184篇
  1992年   178篇
  1991年   171篇
  1990年   135篇
  1989年   127篇
  1988年   95篇
  1987年   104篇
  1986年   84篇
  1985年   84篇
  1984年   67篇
  1983年   37篇
  1982年   72篇
  1981年   54篇
  1980年   56篇
  1979年   46篇
  1978年   33篇
  1977年   20篇
  1976年   25篇
  1973年   18篇
排序方式: 共有10000条查询结果,搜索用时 46 毫秒
21.
22.
Abstract. Southern Appalachian high-elevation outcrops harbour six regionally rare Northern Appalachian taxa usually considered relicts of a Pleistocene alpine flora. For five of the six taxa, minimum elevation in the south was 367–1113 m higher than in the north. While habitats compared between the two regions share only 9% of their total flora, individual plots had up to 70% of their species occurring in the opposite region. The northern affinity of southern outcrops increased with elevation, slope steepness, soil Cu, B and SO4 and decreased with potential solar radiation and soil Na. As a result, communities above 1600 m on felsic bedrock, and above 1350 m on mafic bedrock, were most northern in composition. Northern affinity of southern outcrops also increased with latitude, which may partly result from closer geographic proximity to past communities that provided progenitors for the current northern flora. Northern treeless habitats increased in southern affinity with increased slope steepness, perennial seepage, vegetation height, shade, soil pH, Al, Mn, Na and decreased elevation and organic matter. As a result, northern outcrop communities below treeline were most similar to those on southern outcrops. This suggests that southern outcrop vegetation may be more similar to Pleistocene outcrop vegetation than to Pleistocene alpine vegetation. Partial constrained ordination showed that while compositional differences between the Northern and Southern Appalachian habitats were largely explained by environmental differences, there was a significant component of residual variation explained by north or south position that was unrelated to environment. These residual compositional differences may result from historical influences on community structure involving stochastic extinction and colonization processes.  相似文献   
23.
24.
Drug resistance is a critical obstacle to effective treatment in patients with chronic myeloid leukemia. To understand the underlying resistance mechanisms in response to imatinib mesylate (IMA) and adriamycin (ADR), the parental K562 cells were treated with low doses of IMA or ADR for 2 months to generate derivative cells with mild, intermediate, and severe resistance to the drugs as defined by their increasing resistance index. PulseDIA-based (DIA [data-independent acquisition]) quantitative proteomics was then employed to reveal the proteome changes in these resistant cells. In total, 7082 proteins from 98,232 peptides were identified and quantified from the dataset using four DIA software tools including OpenSWATH, Spectronaut, DIA-NN, and EncyclopeDIA. Sirtuin signaling pathway was found to be significantly enriched in both ADR-resistant and IMA-resistant K562 cells. In particular, isocitrate dehydrogenase (NADP(+)) 2 was identified as a potential drug target correlated with the drug resistance phenotype, and its inhibition by the antagonist AGI-6780 reversed the acquired resistance in K562 cells to either ADR or IMA. Together, our study has implicated isocitrate dehydrogenase (NADP(+)) 2 as a potential target that can be therapeutically leveraged to alleviate the drug resistance in K562 cells when treated with IMA and ADR.  相似文献   
25.
26.
植物叶片功能性状能够响应环境条件的变化,反应了植物对环境的适应策略。当前,针对藤本植物叶片功能性状地理格局及其环境驱动力的研究较少。以国家重点保护植物永瓣藤(Monimopetalum chinense)为研究对象,对其分布区内11个种群的15个叶片功能性状进行测量,并结合气候、土壤因子来解释叶性状变异。比较叶片性状在局域和区域尺度上的种内变异程度,利用多元逐步回归分析环境因子对叶性状的影响。结果表明,在局域尺度上,永瓣藤叶功能性状变异系数介于3.0%-22.5%,其中,叶面积变异程度最大,叶片碳含量变异最小。永瓣藤叶片形状随纬度上升而变得宽且圆。叶片磷含量相对较低,永瓣藤的生长可能受到了磷限制。土壤与气候因子是叶片性状的重要驱动因素,解释了25%-97%的叶片性状变异。在温度和水分充足的情况下,永瓣藤叶片趋向于的慢速生长的保守策略。总体来说,永瓣藤叶片功能性状通过一定的种内变异和性状组合,并与气候、土壤因子相互作用,适应当前的环境条件。  相似文献   
27.
Abstract The diapause of two populations of Trichogramma evanescens Westwood (T. evanescens A and T. evanescens B), collected from different Iranian insect pests, was studied. T. evunescens A in the eggs of Corcyra cephalonica was easily induced to stable diapause with constant 8°C, 15 % and fluctuating temperature (11–23) C -11C. T. evanescens B could not be induced to diapause with the same temperatural regime and host. The experiments showed that the host of maternal generations and the ability of avoiding super-parasitism may play an important role in intraspecific variation of T. evunescens in diapause induction.  相似文献   
28.
The environmental conditions to which juvenile barnacle geese (Branta leucopsis) were exposed during growth were found to affect their body size at fledging as well as their final adult body size. Small juveniles showed compensatory growth from the time of fledging up to one year of age, but this did not fully compensate the differences in body size that were established before fledging. The variation in protein content in plants eaten during growth could probably explain the observed body size differences, sometimes of more than 10%, between different categories of adult geese. Our results imply that one cannot infer selection on morphological characters from differences between samples of adult birds from different localities or from different cohorts within a population, without first showing that environmental conditions during growth do not affect the development of the characters under study.  相似文献   
29.
30.
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