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   15785篇
  免费   1359篇
  国内免费   1970篇
  19114篇
  2024年   53篇
  2023年   282篇
  2022年   591篇
  2021年   910篇
  2020年   703篇
  2019年   822篇
  2018年   757篇
  2017年   560篇
  2016年   726篇
  2015年   1050篇
  2014年   1258篇
  2013年   1293篇
  2012年   1581篇
  2011年   1457篇
  2010年   921篇
  2009年   744篇
  2008年   838篇
  2007年   763篇
  2006年   625篇
  2005年   537篇
  2004年   400篇
  2003年   310篇
  2002年   284篇
  2001年   193篇
  2000年   181篇
  1999年   179篇
  1998年   125篇
  1997年   119篇
  1996年   125篇
  1995年   99篇
  1994年   92篇
  1993年   67篇
  1992年   85篇
  1991年   55篇
  1990年   57篇
  1989年   50篇
  1988年   37篇
  1987年   27篇
  1986年   28篇
  1985年   29篇
  1984年   15篇
  1983年   14篇
  1982年   13篇
  1981年   5篇
  1980年   4篇
  1979年   10篇
  1978年   4篇
  1976年   9篇
  1975年   8篇
  1971年   3篇
排序方式: 共有10000条查询结果,搜索用时 0 毫秒
101.
湛江棕囊藻对南美白对虾虾苗和多种鱼苗的毒性研究   总被引:3,自引:0,他引:3  
测定了湛江棕囊藻赤潮海水和棕囊藻(Phaeocystis globosa)对南美白对虾(Penaeus vannamei Boone)虾苗、青石斑鱼(Epinephelus awoara)、鲻鱼(Mugil cephalus)和尖吻鲈鱼(Latescal carifer)鱼苗的毒性。结果表明,棕囊藻对虾苗有一定的毒性,24 h LC50为1.0×109 cells L-1,去除囊泡液后的棕囊藻碎片对虾苗毒性较弱,细胞密度为1.0×109 cells L-1时,24 h虾苗的死亡率仅为10%,赤潮海水对虾苗无毒性;棕囊藻囊泡液对青石斑鱼有一定毒性,24 h LC50为囊泡液占海水总体积的10.9%,赤潮海水对青石斑鱼苗无毒性;棕囊藻对尖吻鲈鱼和鲻鱼鱼苗无毒性。  相似文献   
102.
拟南芥中的SIP1基因编码的蛋白与拟南芥盐胁迫应答中的关键蛋白SOS2存在互作关系,而NAC1为拟南芥中介导生长素信号促进其侧根发生的蛋白。本研究中我们将SIP1基因和NAC1正义基因以及SIP1基因和NAC1反义基因分别整合到一个经改造的具有2个35S启动子的可用于双基因表达的载体pFGC5941S中,构建了两个双基因表达载体pFGC5941S SIP1 NAC1 sense和pFGC5941S SIP1 NAC1 anti。并将这两个载体通过农杆菌介导的方法转化到野生型拟南芥中,共获得15株转基因植株。对这些转基因植株进行盐胁迫实验发现,在含75mmol·L-1 NaCl的MS培养基上,相比于野生型,pFGC5941S SIP1 NAC1 sense转基因植株主根增长,侧根数量明显增多,而pFGC5941S SIP1 NAC1 anti转基因植株长势与野生型苗相似。由此我们推测可能只有当SIP1和NAC1同时过表达时,才会促进盐胁迫下拟南芥侧根的发育。  相似文献   
103.
104.
Li  Wen-Ru  Ma  Yong-Kai  Shi  Qing-Shan  Xie  Xiao-Bao  Sun  Ting-Li  Peng  Hong  Huang  Xiao-Mo 《Applied microbiology and biotechnology》2018,102(17):7555-7564
Applied Microbiology and Biotechnology - Garlic oil can disrupt the quorum sensing (QS) pathways of the opportunistic pathogen Pseudomonas aeruginosa; however, the underlying mechanisms for this...  相似文献   
105.
Pi C  Liu J  Wang L  Jiang X  Liu Y  Peng C  Chen S  Xu A 《Journal of biotechnology》2007,128(1):184-193
Conotoxins are a diverse array of small peptides mostly with multiple disulfide bridges. These peptides become an increasing significant source of neuro-pharmacological probes and drugs as a result of the high selectivity for ion channels and receptors. Usually, the analogue of natural conotoxins is produced by means of chemical synthesis. Here, we present a simple and fast strategy of producing disulfide-rich conotoxins via recombinant expression. By fused with thioredoxin and His tag, a novel O-superfamily conotoxin lt7a was successfully expressed in Escherichia coli and purified, resulting in a high yield of recombinant lt7a about 6 mg/l. The purity of target protein is up to 95% as identified by HPLC results. Whole cell patch-clamp recording revealed that the new conotoxin blocked voltage-sensitive sodium channels in rat dorsal root ganglion neurons, indicating it might be a novel microO-conotoxin.  相似文献   
106.
白刺属植物的分类学及系统学研究   总被引:34,自引:0,他引:34  
在回顾白刺属(NitrariaL)研究历史的基础上,对全球所产白刺属的12种植物作了详细的考证和系统整理。根据果皮结构及演化趋势,花粉形态及分布区等方面的研究资料,探讨了属内种间的系统发育,提出了属下的分类系统,在此系统下编制出分组及分种检索表。根据其地理分布,绘制了白刺属植物的中国及世界分布图。  相似文献   
107.
人心肌肌球蛋白轻链1的克隆,表达纯化和单抗制备   总被引:2,自引:2,他引:2  
报道了中国人心肌肌球蛋白轻链1cDNA的核苷酸序列,并由此推算的氨基酸序列。与国外发表的人心肌肌球蛋白轻链的氨基酸序列比较,发现有两处差异,即在24位,由谷氨酸变为丙氨酸,则从98位起至101位有4个氨基酸序列的连续差异,即由天冬酰胺-精氨酸-丝氨酸-赖氨酸变为赖氨酸-脯氨酸-精氨酸-谷氨酰妥,推测可能是由于人种差异而引起的。利用该cDNA在大肠杆菌内的表达产物,已获得一株高效的抗中国人心肌肌球蛋  相似文献   
108.
Aging process in mammals is associated with a decline in amplitude and a long period of circadian behaviors which are regulated by a central circadian regulator in the suprachiasmatic nucleus (SCN) and local oscillators in peripheral tissues. It is unclear whether enhancing clock function can retard aging. Using fibroblasts expressing per2::lucSV and senescent cells, we revealed cycloastragenol (CAG), a natural aglycone derivative from astragaloside IV, as a clock amplitude enhancing small molecule. CAG could activate telomerase to antiaging, but no reports focused on its effects on circadian rhythm disorders in aging mice. Here we analyze the potential effects of CAG on d -galactose-induced aging mice on the circadian behavior and expression of clock genes. For this purpose, CAG (20 mg/kg orally), was administered daily to d -galactose (150 mg/kg, subcutaneous) mice model of aging for 6 weeks. An actogram analysis of free-running activity of these mice showed that CAG significantly enhances the locomotor activity. We further found that CAG increase expressions of per2 and bmal1 genes in liver and kidney of aging mouse. Furthermore, CAG enhanced clock protein BMAL1 and PER2 levels in aging mouse liver and SCN. Our results indicated that the CAG could restore the behavior of circadian rhythm in aging mice induced by d -galactose. These data of present study suggested that CAG could be used as a novel therapeutic strategy for the treatment of age-related circadian rhythm disruption.  相似文献   
109.
A purified polysaccharide ACDP-2 was isolated from water extract of the stems of Cistanche deserticola. Chemical and spectroscopic analyses indicated that ACDP-2 is a highly branched arabinogalactan polymer that composes of linked d-galactopyranose and d-glucopyranose, which contains predominantly a branching point at the 6-carbon. The branched side-chains compose of terminal-, 1,5-, and 1,3,5-linked arabinofuranosyl residues. ACDP-2 showed an effect in stimulating the immune response, which when applied onto the cultured mouse lymphocytes induced the cell proliferation in a dose-dependent manner.  相似文献   
110.
RNA can interact with RNA-binding proteins(RBPs), mRNA, or other non-coding RNAs(ncRNAs) to form complex regulatory networks. High-throughput CLIP-seq, degradome-seq, and RNA-RNA interactome sequencing methods represent powerful approaches to identify biologically relevant ncRNA-target and protein-ncRNA interactions. However, assigning ncRNAs to their regulatory target genes or interacting RNA-binding proteins(RBPs) remains technically challenging. Chemical modifications to mRNA also play important roles in regulating gene expression. Investigation of the functional roles of these modifications relies highly on the detection methods used. RNA structure is also critical at nearly every step of the RNA life cycle. In this review, we summarize recent advances and limitations in CLIP technologies and discuss the computational challenges of and bioinformatics tools used for decoding the functions and regulatory networks of ncRNAs. We also summarize methods used to detect RNA modifications and to probe RNA structure.  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