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   4664篇
  免费   500篇
  国内免费   415篇
  2024年   12篇
  2023年   97篇
  2022年   82篇
  2021年   137篇
  2020年   195篇
  2019年   221篇
  2018年   208篇
  2017年   180篇
  2016年   185篇
  2015年   221篇
  2014年   284篇
  2013年   336篇
  2012年   229篇
  2011年   239篇
  2010年   203篇
  2009年   235篇
  2008年   255篇
  2007年   211篇
  2006年   228篇
  2005年   183篇
  2004年   169篇
  2003年   148篇
  2002年   146篇
  2001年   152篇
  2000年   117篇
  1999年   85篇
  1998年   116篇
  1997年   85篇
  1996年   76篇
  1995年   72篇
  1994年   60篇
  1993年   62篇
  1992年   48篇
  1991年   32篇
  1990年   34篇
  1989年   22篇
  1988年   17篇
  1987年   30篇
  1986年   20篇
  1985年   19篇
  1984年   22篇
  1983年   18篇
  1982年   25篇
  1981年   12篇
  1980年   9篇
  1979年   17篇
  1978年   5篇
  1977年   7篇
  1976年   6篇
  1974年   3篇
排序方式: 共有5579条查询结果,搜索用时 31 毫秒
981.
陈芳  陆永跃 《昆虫学报》2014,57(11):1253-1264
【目的】为了研究热激蛋白 Hsp70, Hsp70-4和Hsp90在棉花粉蚧Phenacoccus solenopsis抵抗逆温中的作用。【方法】在测序棉花粉蚧转录组的基础上,分析了该虫热激蛋白Hsp70基因家族的2个序列[Pshsp70(GenBank登录号为KJ909505)和Pshsp70-4(GenBank登录号为KJ909506)]和Hsp90基因家族的1个序列,[Pshsp90(GenBank登录号为KJ909507)],采用实时荧光定量 PCR(RT-qPCR)检测了在不同温度(18和32℃恒温, 37, 39, 41, 43和45℃热激1 h 后26℃恢复1 h)下棉花粉蚧不同发育阶段(2龄若虫、3龄若虫、雌成虫)3种热激蛋白基因的表达量。【结果】Pshsp70 cDNA序列包含1 923 bp的开放阅读框,编码641个氨基酸,理论分子量和等电点分别为70.9 kDa和5.65; Pshsp70-4 cDNA序列包含1 962 bp的开放阅读框,编码654个氨基酸,理论分子量和等电点分别为71.8 kDa和5.38;Pshsp90 cDNA序列包含2 172 bp的开放阅读框,编码724个氨基酸,理论分子量和等电点分别为83.5 kDa和4.93。Pshsp70 和Pshsp70-4均含有Hsp70基因家族高度保守的基序,Pshsp70编码的氨基酸序列与烟粉虱Bemisia tabaci和家蚕Bombyx mori等昆虫的Hsp70 的氨基酸序列一致性为 85%;Pshsp70-4编码的氨基酸序列与白蜡蚧Ericerus pela和点蜂缘蝽Riptortus pedestris等昆虫的Hsp70的氨基酸序列一致性高达95%;Pshsp90也含有Hsp90基因家族高度保守的基序,Pshsp90编码的氨基酸序列与赤拟谷盗Tribolium castaneum和东亚小花蝽Orius sauteri等昆虫的Hsp90 的氨基酸序列一致性为 87%。热激蛋白基因表达量分析结果表明,在18℃恒温条件下,粉蚧2龄若虫的3个PsHsps基因的mRNA相对表达量均比对照(26℃)低,在32℃恒温条件下,各龄期的Hsp70基因的相对表达量均显著高于对照。在37~45℃下热激1 h并在26℃下恢复1 h,棉花粉蚧3个龄期的3个热激蛋白PsHsps基因的相对表达量随温度的升高总体呈增加趋势,相关性分析表明,除Pshsp70-4在雌成虫中的表达量与热胁迫温度的相关系数为0.225外,各龄期中3个基因的表达量与温度的相关系数均大于0.6,显著相关;43℃和45℃胁迫下,各龄期的3个热激蛋白基因相对表达量均显著高于对照组(P<0.05)。【结论】棉花粉蚧热激蛋白基因的表达与温度呈正相关,在该虫应对高温中起着重要作用。  相似文献   
982.
沈征涛  施斌  王宝军  姜洪涛 《生态学报》2013,33(10):3011-3019
土壤有机质转化对温度变化的响应,是气候变暖与全球碳循环关系中的核心问题.掌握土壤有机质对温度变化的响应规律,对准确评价气候变暖背景下,全球土壤有机质的转化至关重要.综述了国内外大量研究成果,对基质成分、基质损耗、测试方法、微生物、水分含量等因素,对土壤有机质转化与温度关系的影响机理与影响规律以及Q10的变化规律进行了探讨.提出稳定有机质与不稳定有机质温度敏感性异同问题,应作为土壤有机质转化与温度关系中的核心问题进行深入研究.同时通过分析,提出室内短期培养是首选测试方法.分析认为微生物生长温度曲线与微生物呼吸之间不存在必然联系,而在过低和过高之间,水分含量是否会影响土壤呼吸,有待进一步试验验证.提出随着城市热岛效应这一环境问题的加剧,研究及评价更大温度区间内的城市土壤有机质对温度变化的响应规律十分重要.  相似文献   
983.
Higher temperatures caused by future climate change will bring more frequent heat stress events and pose an increasing risk to global wheat production. Crop models have been widely used to simulate future crop productivity but are rarely tested with observed heat stress experimental datasets. Four wheat models (DSSAT‐CERES‐Wheat, DSSAT‐Nwheat, APSIM‐Wheat, and WheatGrow) were evaluated with 4 years of environment‐controlled phytotron experimental datasets with two wheat cultivars under heat stress at anthesis and grain filling stages. Heat stress at anthesis reduced observed grain numbers per unit area and individual grain size, while heat stress during grain filling mainly decreased the size of the individual grains. The observed impact of heat stress on grain filling duration, total aboveground biomass, grain yield, and grain protein concentration (GPC) varied depending on cultivar and accumulated heat stress. For every unit increase of heat degree days (HDD, degree days over 30 °C), grain filling duration was reduced by 0.30–0.60%, total aboveground biomass was reduced by 0.37–0.43%, and grain yield was reduced by 1.0–1.6%, but GPC was increased by 0.50% for cv Yangmai16 and 0.80% for cv Xumai30. The tested crop simulation models could reproduce some of the observed reductions in grain filling duration, final total aboveground biomass, and grain yield, as well as the observed increase in GPC due to heat stress. Most of the crop models tended to reproduce heat stress impacts better during grain filling than at anthesis. Some of the tested models require improvements in the response to heat stress during grain filling, but all models need improvements in simulating heat stress effects on grain set during anthesis. The observed significant genetic variability in the response of wheat to heat stress needs to be considered through cultivar parameters in future simulation studies.  相似文献   
984.
985.
热休克反应是机体中一个重要的内源性保护机制,但其对TNF-α诱导的单核/巨噬细胞迁移有无影响目前尚不清楚.采用酶联免疫吸附实验观察TNF-α(20μg/L)刺激RAW264.7巨噬细胞4h后炎症因子IL-1β、IL-6、IL-15的表达情况;Western blot验证热休克预处理诱导热休克蛋白表达的增加;利用细胞趋化实验观察热休克预处理(42℃,1h)对TNF-α所致巨噬细胞迁移的影响.研究发现,TNF-α可明显促进RAW264.7细胞株中IL-1β、IL-6、IL-15等炎症因子的释放;热休克预处理诱导热休克蛋白HSP70、HSP90、HSP25表达增加;细胞趋化实验发现TNF-α处理的RAW264.7细胞迁移能力较正常对照组明显增强,而热休克预处理组巨噬细胞的迁移能力较单纯TNF-α处理组明显减弱.上述结果表明,热休克预处理抑制TNF-α所致巨噬细胞的迁移.  相似文献   
986.
987.
Small heat shock proteins (sHsps) were found to exhibit efficient chaperone-like activities under stress conditions although their native structures are severely disturbed. Here, using an alternative approach (site-directed mutagenesis), we obtained two structurally and functionally distinct Mycobacterium tuberculosis Hsp16.3 single-site mutant proteins. The G59W mutant protein (with Gly59 substituted by Trp) is capable of exhibiting efficient chaperone-like activity even under non-stress conditions although its secondary, tertiary, and quaternary structures are very different from that of the wild type protein. By contrast, the G59A mutant protein (with Gly59 substituted by Ala) resembles with the wild type protein in structure and function. These observations suggest that the Gly59 of the Hsp16.3 protein is critical for its folding and assembly. In particular, we propose that the exhibition of chaperone-like activity for Hsp16.3 does not require its intact (native) structures but requires the disturbance of its native structures (i.e., the native structure-disturbed Hsp16.3 retains its chaperone-like activity or even becomes more active). In addition, the behavior of such an active mutant protein (G59W) also strongly supports our previous suggestion that Hsp16.3 exhibits chaperone-like activity via oligomeric dissociation.  相似文献   
988.
Heat shock proteins act as molecular chaperones, facilitating protein folding in cells of living organisms. Their role is particularly important in parasites because environmental changes associated with their life cycles place a strain on protein homoeostasis. Not surprisingly, some heat shock proteins are essential for the survival of the most virulent malaria parasite, Plasmodium falciparum . This justifies the need for a greater understanding of the specific roles and regulation of malarial heat shock proteins. Furthermore, heat shock proteins play a major role during invasion of the host by the parasite and mediate in malaria pathogenesis. The identification and development of inhibitor compounds of heat shock proteins has recently attracted attention. This is important, given the fact that traditional antimalarial drugs are increasingly failing, as a consequence of parasite increasing drug resistance. Heat shock protein 90 (Hsp90), Hsp70/Hsp40 partnerships and small heat shock proteins are major malaria drug targets. This review examines the structural and functional features of these proteins that render them ideal drug targets and the challenges of targeting these proteins towards malaria drug design. The major antimalarial compounds that have been used to inhibit heat shock proteins include the antibiotic, geldanamycin, deoxyspergualin and pyrimidinones. The proposed mechanisms of action of these molecules and the pathways they inhibit are discussed.  相似文献   
989.
作为生态系统稳定性维持的一个重要因素,火对泥炭地优势植物泥炭藓(Sphagnum)孢子库的影响尚不清楚.以采自长白山区泥炭地的泥炭土和3种泥炭藓的成熟孢子为实验材料,室内模拟火烧,以此设置不同温度水平(20、40、60或100℃,持续0.5、1、2、4或10 min),对泥炭藓孢子进行热激处理,经萌发实验后,研究火烧高温对孢子萌发率的影响.结果显示,火烧期间各层土温随深度而递减,表层泥炭可达300℃的极端高温,而1 cm深温度仅为70℃,体现出泥炭土良好的热缓冲性;40℃的热激可使锈色泥炭藓(S.fuscum)与中位泥炭藓(S.magellanicum)孢子萌发率提高20%与50%;60℃的热激使尖叶泥炭藓(S.capillifolium)孢子的萌发率提高1倍;100℃热激对3种泥炭藓孢子萌发则有强烈的抑制作用.研究表明,泥炭藓孢子耐受高温的能力有限,但土壤中的孢子凭借泥炭的良好热缓冲性,可以躲避火烧高温造成的致命伤害,适度的热激甚至能提高其萌发力,对其在火后的建植及种群的长存可能有重要意义.  相似文献   
990.
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