全文获取类型
收费全文 | 108121篇 |
免费 | 21192篇 |
国内免费 | 6374篇 |
出版年
2024年 | 113篇 |
2023年 | 965篇 |
2022年 | 2276篇 |
2021年 | 4498篇 |
2020年 | 4644篇 |
2019年 | 6824篇 |
2018年 | 6755篇 |
2017年 | 6184篇 |
2016年 | 7287篇 |
2015年 | 8784篇 |
2014年 | 9507篇 |
2013年 | 10375篇 |
2012年 | 9256篇 |
2011年 | 8371篇 |
2010年 | 7047篇 |
2009年 | 5577篇 |
2008年 | 5114篇 |
2007年 | 4256篇 |
2006年 | 3657篇 |
2005年 | 3155篇 |
2004年 | 2696篇 |
2003年 | 2439篇 |
2002年 | 2072篇 |
2001年 | 1846篇 |
2000年 | 1628篇 |
1999年 | 1513篇 |
1998年 | 857篇 |
1997年 | 849篇 |
1996年 | 811篇 |
1995年 | 703篇 |
1994年 | 701篇 |
1993年 | 515篇 |
1992年 | 715篇 |
1991年 | 620篇 |
1990年 | 506篇 |
1989年 | 375篇 |
1988年 | 350篇 |
1987年 | 282篇 |
1986年 | 193篇 |
1985年 | 244篇 |
1984年 | 156篇 |
1983年 | 147篇 |
1982年 | 108篇 |
1981年 | 79篇 |
1980年 | 66篇 |
1979年 | 78篇 |
1978年 | 71篇 |
1977年 | 48篇 |
1976年 | 49篇 |
1973年 | 53篇 |
排序方式: 共有10000条查询结果,搜索用时 31 毫秒
761.
我们用免疫胶体金色埋前标记技术和免疫荧光技术研究了人胚肺细胞(HEL)内,人巨细胞病毒(HCMV-AD_(169))对单纯疱疹病毒1型(HSV-ⅠSM_(44))抗原表达的影响,旨在探讨在细胞这一微生境内,一病毒对另一病毒可能发生的影响。电镜下计数HSV-1组和HCMV HSV-1组特异性结合金颗粒数得HSV-1组为657个,HCMV HSV-1组的总数为283个。t检验P<0.01,差别非常显著。并且HSV-1组细胞的胞浆中的病毒颗粒,比HCMV HSV-1组明显多。荧光显微镜下:HSV-1组阳性细胞数为689个HCMV HSV-1组只有484个,经poisson分布u检验,P<0.01,差别非常显著。免疫荧光实验还表明:HSV-1组,抗血清在1:320时仍有荧光清晰的阳性细胞,而HCMV HSV-1组,抗血清在1:160时,却无荧光阳性细胞。细胞病变效应(CPE)动态观察显示:HSV-1组8小时即有细胞病变,24小时蔓延整个单层;而HCMV HSV-1组超感染14小时才有细胞病变。24小时约有75%细胞受累。结果表明HCMV对HSV-1的抗原表达有明显的抑制作用。对抑制作用的可能机理及其在分子生态学中的意义,进行了讨论。 相似文献
762.
763.
764.
棉铃虫雄蛾触角的毛形感器对其性信息素组分及类似物的反应 总被引:39,自引:8,他引:31
本文用单细胞电反应的记录方法,测定了棉铃虫Heliothis armigera Hubner雄蛾触角的毛形感器对其性信息素组分及雌蛾腹部提取物的反应,发现顺-11-十六碳烯醛和顺-9-十六碳烯醛能引起反应。对前者发放大脉冲,对后者发放小脉冲,对雌蛾腹部提取物发放大、小两种脉冲,但以大脉冲为主。 相似文献
765.
氯化镧对玉米根切段钾离子外渗影响的动力学研究 总被引:9,自引:0,他引:9
研究了氯化镧对玉米(Zea mays L.)“京早8号”根切段细胞膜透性及质子分泌的影响,并用动力学方法研究了钾离子外渗过程的变化。氯化镧处理可降低外渗液的电导率及K~ 和糖的外渗量,使质子分泌活动增强。用动力学方法分析玉米根切段K~ 外渗过程的结果表明:(1)应用于K~ 吸收研究的数学模型也能适应于K~ 外渗的研究;(2)在LaCl_3和(或)CaCl_2存在的条件下,最大吸收速度(V_(max))升高,而米氏常数(K_m)没有变化;(3)在LaCl_3和(或)CaCl_2存在的条件下,K~ 外渗量降低是由于最大吸收速度(V_(max))升高所致。 相似文献
766.
【目的】为齐整小核菌代谢工程研究建立高效的转录单元组装系统。【方法】通过应用Golden Gate技术,以mobius assembly为基础,分别设计并构建DNA元件标准化接口改造、单转录单元组装、应用质粒(多转录单元)组装等功能的载体,从而形成一套完整的多转录单元组装系统。【结果】构建了2个用于DNA元件标准化接口改造的Level 0载体,4个用于单转录单元组装的Level 1载体,4个用于应用质粒组装的Level 2载体和13个应用质粒组装的辅助质粒。然后应用此系统为齐整小核菌组装了若干经过标准化接口改造的DNA元件质粒、单转录单元质粒和硬葡聚糖相关基因的功能分析质粒。所构建的最终应用质粒可以同时适用于齐整小核菌的根癌农杆菌介导转化法、电穿孔转化法和原生质体转化法。【结论】此质粒系统具有强大的DNA设计、组装和容纳能力,为未来齐整小核菌代谢工程和功能基因组学研究提供了高效的质粒构建技术平台。 相似文献
767.
768.
Qihe Tang Wanli Li Zhengwei Wang Zhixiang Dong Xijie Li Jiali Li Qi Huang Zhe Cao Wei Gong Yazhou Zhao Minzeng Wang Jun Guo 《Environmental microbiology》2023,25(10):2020-2031
Honeybee (Apis mellifera) ingestion of toxic nectar plants can threaten their health and survival. However, little is known about how to help honeybees mitigate the effects of toxic nectar plant poisoning. We exposed honeybees to different concentrations of Bidens pilosa flower extracts and found that B. pilosa exposure significantly reduced honeybee survival in a dose-dependent manner. By measuring changes in detoxification and antioxidant enzymes and the gut microbiome, we found that superoxide dismutase, glutathione-S-transferase and carboxylesterase activities were significantly activated with increasing concentrations of B. pilosa and that different concentrations of B. pilosa exposure changed the structure of the honeybee gut microbiome, causing a significant reduction in the abundance of Bartonella (p < 0.001) and an increase in Lactobacillus. Importantly, by using Germ-Free bees, we found that colonization by the gut microbes Bartonella apis and Apilactobacillus kunkeei (original classification as Lactobacillus kunkeei) significantly increased the resistance of honeybees to B. pilosa and significantly upregulated bee-associated immune genes. These results suggest that honeybee detoxification systems possess a level of resistance to the toxic nectar plant B. pilosa and that the gut microbes B. apis and A. kunkeei may augment resistance to B. pilosa stress by improving host immunity. 相似文献
769.
Siyuan Zhang Jinhong Kan Xin Liu Yao Wu Mingyang Zhang Jinqing Ou Juan Wang Lin An Defeng Li Li Wang Xiu-Jie Wang Rongxiang Fang Yantao Jia 《Molecular Plant Pathology》2023,24(4):359-373
Chemical signal-mediated biological communication is common within bacteria and between bacteria and their hosts. Many plant-associated bacteria respond to unknown plant compounds to regulate bacterial gene expression. However, the nature of the plant compounds that mediate such interkingdom communication and the underlying mechanisms remain poorly characterized. Xanthomonas campestris pv. campestris (Xcc) causes black rot disease on brassica vegetables. Xcc contains an orphan LuxR regulator (XccR) which senses a plant signal that was validated to be glucose by HPLC-MS. The glucose concentration increases in apoplast fluid after Xcc infection, which is caused by the enhanced activity of plant sugar transporters translocating sugar and cell-wall invertases releasing glucose from sucrose. XccR recruits glucose, but not fructose, sucrose, glucose 6-phosphate, and UDP-glucose, to activate pip expression. Deletion of the bacterial glucose transporter gene sglT impaired pathogen virulence and pip expression. Structural prediction showed that the N-terminal domain of XccR forms an alternative pocket neighbouring the AHL-binding pocket for glucose docking. Substitution of three residues affecting structural stability abolished the ability of XccR to bind to the luxXc box in the pip promoter. Several other XccR homologues from plant-associated bacteria can also form stable complexes with glucose, indicating that glucose may function as a common signal molecule for pathogen–plant interactions. The conservation of a glucose/XccR/pip-like system in plant-associated bacteria suggests that some phytopathogens have evolved the ability to utilize host compounds as virulence signals, indicating that LuxRs mediate an interkingdom signalling circuit. 相似文献
770.
Henipaviruses and lyssaviruses target nucleolar treacle protein and regulate ribosomal RNA synthesis
Stephen M. Rawlinson Tianyue Zhao Katie Ardipradja Yilin Zhang Patrick F. Veugelers Jennifer A. Harper Cassandra T. David Vinod Sundaramoorthy Gregory W. Moseley 《Traffic (Copenhagen, Denmark)》2023,24(3):146-157
The nucleolus is a common target of viruses and viral proteins, but for many viruses the functional outcomes and significance of this targeting remains unresolved. Recently, the first intranucleolar function of a protein of a cytoplasmically-replicating negative-sense RNA virus (NSV) was identified, with the finding that the matrix (M) protein of Hendra virus (HeV) (genus Henipavirus, family Paramyxoviridae) interacts with Treacle protein within nucleolar subcompartments and mimics a cellular mechanism of the nucleolar DNA-damage response (DDR) to suppress ribosomal RNA (rRNA) synthesis. Whether other viruses utilise this mechanism has not been examined. We report that sub-nucleolar Treacle targeting and modulation is conserved between M proteins of multiple Henipaviruses, including Nipah virus and other potentially zoonotic viruses. Furthermore, this function is also evident for P3 protein of rabies virus, the prototype virus of a different RNA virus family (Rhabdoviridae), with Treacle depletion in cells also found to impact virus production. These data indicate that unrelated proteins of viruses from different families have independently developed nucleolar/Treacle targeting function, but that modulation of Treacle has distinct effects on infection. Thus, subversion of Treacle may be an important process in infection by diverse NSVs, and so could provide novel targets for antiviral approaches with broad specificity. 相似文献