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   8553篇
  免费   508篇
  国内免费   1526篇
  2023年   184篇
  2022年   231篇
  2021年   262篇
  2020年   263篇
  2019年   338篇
  2018年   351篇
  2017年   252篇
  2016年   229篇
  2015年   220篇
  2014年   500篇
  2013年   600篇
  2012年   352篇
  2011年   466篇
  2010年   371篇
  2009年   421篇
  2008年   440篇
  2007年   532篇
  2006年   406篇
  2005年   349篇
  2004年   237篇
  2003年   259篇
  2002年   232篇
  2001年   193篇
  2000年   169篇
  1999年   119篇
  1998年   102篇
  1997年   94篇
  1996年   123篇
  1995年   86篇
  1994年   86篇
  1993年   78篇
  1992年   94篇
  1991年   115篇
  1990年   77篇
  1989年   72篇
  1988年   58篇
  1987年   53篇
  1986年   73篇
  1985年   94篇
  1984年   171篇
  1983年   140篇
  1982年   171篇
  1981年   117篇
  1980年   149篇
  1979年   137篇
  1978年   113篇
  1977年   110篇
  1976年   73篇
  1975年   50篇
  1974年   56篇
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
971.
Syndecan-4 core protein is composed of extracellular, transmembrane, and cytoplasmic domains. The cytoplasmic domain functions in transmitting signals into the cell through the protein kinase C alpha (PKCα) pathway. The glycosaminoglycan (GAG) and N-linked glycosylated (N-glycosylated) chains attached to the extracellular domain influence cell proliferation. The current study investigated the function of syndecan-4 cytoplasmic domain in combination with GAG and N-glycosylated chains in turkey muscle cell proliferation, differentiation, fibroblast growth factor 2 (FGF2) responsiveness, and PKCα membrane localization. Syndecan-4 or syndecan-4 without the cytoplasmic domain and with or without the GAG and N-glycosylated chains were transfected or co-transfected with a small interfering RNA targeting syndecan-4 cytoplasmic domain into turkey muscle satellite cells. The overexpression of syndecan-4 mutants increased cell proliferation but did not change differentiation. Syndecan-4 mutants had increased cellular responsiveness to FGF2 during proliferation. Syndecan-4 increased PKCα cell membrane localization, whereas the syndecan-4 mutants decreased PKCα cell membrane localization compared to syndecan-4. However, compared to the cells without transfection, syndecan-4 mutants increased cell membrane localization of PKCα. These data indicated that the syndecan‐4 cytoplasmic domain and the GAG and N-glycosylated chains are critical in syndecan-4 regulating satellite cell proliferation, responsiveness to FGF2, and PKCα cell membrane localization.  相似文献   
972.
Miller JJ  Delwiche CF  Coats DW 《Protist》2012,163(5):720-745
Amoebophrya is a syndinian parasite that kills harmful bloom forming algae. Previously uncharacterized ultrastructural aspects of infection and development were elucidated. The biflagellate dinospore has two mitochondria, electron-dense bodies, striated strips, trichocysts, and a nucleus with peripherally condensed chromatin. After finding an Akashiwo sanguinea host and adhering to its surface, the parasite penetrates the host surface, apparently using a microfilament based motility and electron-dense bodies within a microtubular basket in the process of parasitophorous vacuole membrane formation. After entering the host nucleus, possibly by a similar mechanism used to enter the host cell, the parasite cytosol expanded substantially prior to mitosis. From 12-36 hours mitochondria were inconspicuous but present. Chromatin condensation was variable. By 36 hours post-infection, parasites had multiple nuclei, a microtubule-supported cytopharynx, and were beginning to form a fully internal mastigocoel. By 48 hours, the characteristic "beehive" appearance was apparent with flagella projecting into a fully developed mastigocoel. The cytoplasm contained trichocysts, elongated mitochondria, and nuclei with peripherally condensed chromatin. Although Amoebophrya lacks an apical complex, its electron-dense bodies show functional similarities to apicomplexan rhoptries. Its lack of permanently condensed chromosomes, but compact dinospore chromatin, supports the idea that dinoflagellate permanently condensed chromosomes may be a remnant of a parasitic ancestor with a compact dispersal stage.  相似文献   
973.
塔里木河下游柽柳灌丛地上生物量估测   总被引:4,自引:0,他引:4  
根据划分的柽柳灌丛大、中、小等级,在塔里木河下游英苏至喀尔达依区段进行地表采样、称重,采用统计相关法对柽柳年龄及地径关系进行分析,构建柽柳直立枝与单丛地上生物量估测模型,对模型精度进行检验,筛选最佳模型,并对模型估测值与实测值进行卡方检验。结果表明:(1)输水后柽柳新萌直立枝地径随年龄增加而增大,但输水前柽柳萌生直立枝的地径随年龄增加未呈现规律性变化。在地下水条件非一致性的干旱荒漠区,柽柳地径大小不能作为判断其年龄的依据。(2)根据柽柳标准枝和灌丛因子实测数据,用一元线性函数、幂函数、指数函数、对数函数4种函数进行柽柳直立枝生物量估测模型拟合结果表明,幂函数w=2.007(d2 h)0.837估测模型最优,其总体估测精度达89.92%。(3)以冠幅面积单变量、冠幅周长与丛高双变量构建的柽柳单丛生物量估测模型的精度分别为78.95%和80.09%。(4)以全收获法实测数据为真值对估测模型进行精度检验,柽柳冠幅面积为自变量模型的估测精度为80.54%,柽柳冠幅周长和丛高估测模型的精度为66.85%。(5)对柽柳单株及单丛生物量模型估测值与实测值进行卡方检验结果表明两者之间无显著差异。研究认为,由于柽柳冠幅在高分辨遥感数据上容易获取,柽柳冠幅面积估测模型在传统生物量估测和遥感生物量估测都具有实用价值。  相似文献   
974.
以1B/1R类K型不育系K3314A及其保持系3314B,非1B/1R类K型不育系732A及其保持系732B,YS温敏雄性不育小麦A3017为材料,提取不同温度处理下各时期小穗的总RNA进行反转录,对AY914051和AY660990两个目标基因进行半定量PCR和电泳分析,测定其在小麦中的表达变化趋势,以分析其与这几种不育系的育性相关关系,探讨这几种不育小麦败育的关键发育时期。结果表明,除AY914051基因在2种保持系3314B和732B中表达量变化不大之外,其它均有明显差异;2个目标基因与这几种雄性不育系的败育有关,但与育性相关程度不同,不育系两个目的基因的表达受温度变化影响程度明显大于保持系。由实验结果推测,1B/1R类K型不育系、非1B/1R类K型不育系和YS温敏雄性不育系的败育关键时期为单核期或单核期至二核期之间;温度差异可能会导致YS温敏雄性不育系的育性相关基因表达时期错位,错位后的表达差异积累可能最终导致其败育。  相似文献   
975.
测定了大耳猬血清及尿中多种无机离子和尿素氮等指标,并应用免疫组织化学方法观察了AQP1、AQP2在肾脏的表达.大耳猬血清钠、氯含量较高;而尿液中以钾、钠、氯及尿素氮含量较高.尿液中主要离子浓度高于血清,较为浓缩,尿素氮、钾排泄能力较强.AQP1免疫反应阳性表达于近曲小管上皮和髓袢细段,AQP2主要表达于集合管上皮细胞.因此,AQP1、AQP2可能在大耳猬肾脏水重吸收及尿液浓缩过程中具有重要作用.  相似文献   
976.
灌溉对孕穗期冬小麦农田温度的影响   总被引:2,自引:0,他引:2  
余卫东  成林 《生态学杂志》2012,31(7):1701-1706
灌溉是抵御和减轻冬小麦晚霜冻危害的有效措施之一。针对黄淮地区2010年4月的一次强降温过程,通过郑州农业气象观测站的灌溉防霜试验,对比分析了冬小麦孕穗期田间空气温度和土壤温度特征。结果表明:在外界环境温度下降时,灌溉可以提高田间最低气温0.1~0.6℃,增温效应主要集中在地上5cm处,灌溉可减少气温≤0℃的持续时间1~2h;对土壤温度的影响随着深度而存在差异,0cm土壤温度以增加为主,5~20cm土壤以降温效应为主;灌溉减小了气温和0~5cm土壤温度的变异系数和平均相对变率,而增大了10~20cm土壤温度的变异系数和相对变率;灌溉引起的温度差异只在15和20cm土壤处比较显著,其余各层温度差异并不明显。  相似文献   
977.
The WAVE regulatory complex (WRC), consisting of WAVE, Sra, Nap, Abi, and HSPC300, activates the Arp2/3 complex to control branched actin polymerization in response to Rac activation. How the WRC is assembled in vivo is not clear. Here we show that Nudel, a protein critical for lamellipodia formation, dramatically stabilized the Sra1-Nap1-Abi1 complex against degradation in cells through a dynamic binding to Sra1, whereas its physical interaction with HSPC300 protected free HSPC300 from the proteasome-mediated degradation and stimulated the HSPC300-WAVE2 complex formation. By contrast, Nudel showed little or no interactions with the Sra1-Nap1-Abi1-WAVE2 and the Sra1-Nap1-Abi1-HSPC300 complexes as well as the mature WRC. Depletion of Nudel by RNAi led to general subunit degradation and markedly attenuated the levels of mature WRC. It also abolished the WRC-dependent actin polymerization in vitro and the Rac1-induced lamellipodial actin network formation during cell spreading. Therefore, Nudel is important for the early steps of the WRC assembly in vivo by antagonizing the instability of certain WRC subunits and subcomplexes.  相似文献   
978.
We have previously shown that a loss of stromal Cav-1 is a biomarker of poor prognosis in breast cancers. Mechanistically, a loss of Cav-1 induces the metabolic reprogramming of stromal cells, with increased autophagy/mitophagy, mitochondrial dysfunction and aerobic glycolysis. As a consequence, Cav-1-low CAFs generate nutrients (such as L-lactate) and chemical building blocks that fuel mitochondrial metabolism and the anabolic growth of adjacent breast cancer cells. It is also known that a loss of Cav-1 is associated with hyperactive TGF-β signaling. However, it remains unknown whether hyperactivation of the TGF-β signaling pathway contributes to the metabolic reprogramming of Cav-1-low CAFs. To address these issues, we overexpressed TGF-β ligands and the TGF-β receptor I (TGFβ-RI) in stromal fibroblasts and breast cancer cells. Here, we show that the role of TGF-β in tumorigenesis is compartment-specific, and that TGF-β promotes tumorigenesis by shifting cancer-associated fibroblasts toward catabolic metabolism. Importantly, the tumor-promoting effects of TGF-β are independent of the cell type generating TGF-β. Thus, stromal-derived TGF-β activates signaling in stromal cells in an autocrine fashion, leading to fibroblast activation, as judged by increased expression of myofibroblast markers, and metabolic reprogramming, with a shift toward catabolic metabolism and oxidative stress. We also show that TGF-β-activated fibroblasts promote the mitochondrial activity of adjacent cancer cells, and in a xenograft model, enhancing the growth of breast cancer cells, independently of angiogenesis. Conversely, activation of the TGF-β pathway in cancer cells does not influence tumor growth, but cancer cell-derived-TGF-β ligands affect stromal cells in a paracrine fashion, leading to fibroblast activation and enhanced tumor growth. In conclusion, ligand-dependent or cell-autonomous activation of the TGF-β pathway in stromal cells induces their metabolic reprogramming, with increased oxidative stress, autophagy/mitophagy and glycolysis, and downregulation of Cav-1. These metabolic alterations can spread among neighboring fibroblasts and greatly sustain the growth of breast cancer cells. Our data provide novel insights into the role of the TGF-β pathway in breast tumorigenesis, and establish a clear causative link between the tumor-promoting effects of TGF-β signaling and the metabolic reprogramming of the tumor microenvironment.  相似文献   
979.
Although hydrogen peroxide (H2O2) and nitric oxide (NO) can act as an upstream signaling molecule to modulate the dynamic microtubule cytoskeleton during the defense responses to Verticillium dahliae (VD) toxins in Arabidopsis, it is not known the relationship between these two signaling molecules. Here, we show that VD-toxin-induced NO accumulation was dependent on prior H2O2 production, NO is downstream of H2O2 in the signaling process, and that H2O2 acted synergistically with NO to modulate the dynamic microtubule cytoskeleton responses to VD-toxins in Arabidopsis.  相似文献   
980.
当前,全球能源系统的主体是"碳基能源"——石油和煤等。这些不可再生的资源已日渐枯竭,而且大量使用会破坏地球生态系统。因此,用"氢基能源"逐步取代"碳基能源"已成为发达国家能源战略的首选目标,有的国家甚至将这一目标定在本世纪中叶。对于中国等发展中国家,大力开发生物质能等新的可再生"碳基能源",同时加速发展"氢基能源",争取提前进入氢能时代,才能实现可持续发展,甚至跨越式发展。制氢技术包括非生物制氢和生物制氢。非生物制氢目前已小量生产和应用,生物制氢的研究也有相当长的时间,其中影响生物制氢进入实用的主要因素是能耗和生产成本过高。因此,如果作为一个孤立的技术系统,生物制氢只能作为战略性项目。首先介绍了生物制氢的主要原理、目前限制生物制氢产业化的关键限制因子;提出了从系统论的原理出发,通过技术集成,突破生物制氢成本的"瓶颈",达到环保和资源利用的双重目的,使其提前实用化;最后,重点阐述了以海水为介质的高盐有机废水的生物制氢技术的研究进展,尤其介绍我国在相关方面的研究进展。  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