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   57869篇
  免费   4601篇
  国内免费   4479篇
  66949篇
  2024年   142篇
  2023年   789篇
  2022年   1852篇
  2021年   3044篇
  2020年   2081篇
  2019年   2501篇
  2018年   2344篇
  2017年   1806篇
  2016年   2544篇
  2015年   3627篇
  2014年   4380篇
  2013年   4436篇
  2012年   5286篇
  2011年   4762篇
  2010年   2882篇
  2009年   2598篇
  2008年   2937篇
  2007年   2634篇
  2006年   2261篇
  2005年   1886篇
  2004年   1509篇
  2003年   1420篇
  2002年   1072篇
  2001年   909篇
  2000年   889篇
  1999年   810篇
  1998年   499篇
  1997年   454篇
  1996年   477篇
  1995年   422篇
  1994年   413篇
  1993年   325篇
  1992年   446篇
  1991年   324篇
  1990年   284篇
  1989年   260篇
  1988年   210篇
  1987年   194篇
  1986年   176篇
  1985年   155篇
  1984年   115篇
  1983年   122篇
  1982年   81篇
  1981年   45篇
  1980年   51篇
  1979年   63篇
  1976年   46篇
  1974年   54篇
  1973年   45篇
  1972年   53篇
排序方式: 共有10000条查询结果,搜索用时 0 毫秒
951.
目的: 研究一氧化氮(NO)和内皮素-1(ET-1)在大鼠肢体缺血/再灌注(LI/R)后脑损伤中的作用,探讨NO/ET-1平衡关系的变化对脑损伤的影响.方法: 在大鼠LI/R损伤模型上,应用NO合成前体物质L-精氨酸(L-Arg)、一氧化氮合酶(NOS)抑制剂氨基胍(AG)、ETA受体阻断剂BQl23进行干预,观察血浆 NO、ET-1、MDA、XOD、SOD、LDH及脑组织tNOS、iNOS、cNOS、NO、ET-1、MDA、XOD、MPO、 SOD的变化.结果: 与对照组比较,I/R组血浆MDA、XOD、LDH及脑组织MDA、XOD、MPO升高,SOD活性降低(P<0.01),脑组织tNOS和iNOS明显升高,而cNOS明显降低(P<0.01),I/R组血浆及脑组织NO、ET-1增加,NO/ET-1比值降低,脑损伤加重.应用L-Arg及BQ123后,血浆及脑组织NO/ET-1比值较I/R组升高,脑损伤减轻,应用AG后,NO/ET-1比值降低,脑损伤进一步加重.结论: 肢体缺血/再灌注后,一氧化氮与内皮素-l的比值降低时脑损伤加重.  相似文献   
952.
Eimeria acervulina 3-1E antigen gene and mature chicken interleukin 15 (mChIL-15) gene were cloned into expression vector pcDNA3.1(+) in different forms, produced DNA vaccine pcDNA3.1-3-1E, and pcDNA3.1-3-1E-linker-mChIL-15 co-expressing E. acervulina 3-1E gene and mChIL-15 gene, respectively. The expression of objective gene in vitro was detected by indirect fluorescent antibody technique and immunohistochemistry. The two DNA vaccines were administered by intramuscular leg injection. An animal challenge experiment was carried out to evaluate the immune protective efficacy of the vaccines. The results indicated that DNA vaccines were successfully constructed and the expression of objective gene could be detected in vitro. The animal experimental results showed that both DNA vaccines could provide partial protection against homologous challenge in chickens. The chimeric DNA vaccine, pcDNA3.1-3-1E-linker-mChIL-15, could significantly increase oocyst decrease ratio, reduce the average lesion score in the duodenum, improve body weight gain, and increase anti-coccidial index (ACI) compared to the DNA vaccine pcDNA3.1-3-1E. Taken together, these results demonstrate ChIL-15 enhance the immunogenicity of 3-1E DNA vaccine, and co-expression of cytokine and optimized surface antigen of Eimeria may be a promising method to enhance immunogenicity of DNA vaccines in poultry.  相似文献   
953.
殷红  高杨 《菌物研究》2010,8(1):44-47
S-NU-3-2菌株是对源自药用植物黄檗的内生真菌S6进行诱变获得的小檗碱产量比出发菌株有明显提高的突变株,本研究对其培养条件进行了优化,以期进一步提高其产量,为开发利用真菌发酵生产植物活性成分的新途径奠定基础。以菌丝生长和小檗碱产量为指标,筛选出了适宜该菌株发酵的基本培养基、碳源、氮源、光照和培养温度,并经进一步的正交试验优化,得出该高产菌株的最佳培养条件为豆芽汁基本培养基含蔗糖3%,酵母膏0.2%,pH7.0,温度26℃,全光照培养。与初始培养条件相比,在优化后的条件下,该菌株的小檗碱得率提高了47.2%,菌体生物量提高了24%。  相似文献   
954.
蛋白质组学是后基因组时代的新兴研究领域,详细介绍了蛋白质组学的原理和方法在农业生物科学研究中的最新应用进展,提出了蛋白质组学技术目前所面临的问题,并展望了今后的发展前景.  相似文献   
955.
从解淀粉芽孢杆菌Baillus amyloliquefaciens CICIM B2125中克隆了BamHI甲基转移酶基因(bamHIM),并在大肠杆菌JM109中得到了成功表达.该基因含有1 271 bp的开放阅读框(ORF),编码423个氨基酸,成熟蛋白分子量为49 kD.该基因在自身启动子引导下,表达了具有活性的BamHI甲基转移酶(M.BamHI).该酶可以将BamHI位点的碱基甲基化.氨基酸序列分析表明该酶存在有NADB_Rossmann结构域.  相似文献   
956.
ATP binding cassette transporter A1 (ABCA1) is a widely expressed lipid transporter essential for the generation of HDL. ABCA1 is particularly abundant in the liver, suggesting that the liver may play a major role in HDL homeostasis. To determine how hepatic ABCA1 affects plasma HDL cholesterol levels, we treated mice with an adenovirus (Ad)-expressing human ABCA1 under the control of the cytomegalovirus promoter. Treated mice showed a dose-dependent increase in hepatic ABCA1 protein, ranging from 1.2-fold to 8.3-fold using doses from 5 x 108 to 1.5 x 109 pfu, with maximal expression observed on Day 3 posttreatment. A selective increase in HDL cholesterol occurred at Day 3 in mice treated with 5 x 108 pfu Ad-ABCA1, but higher doses did not further elevate HDL cholesterol levels. In contrast, total cholesterol, triglycerides, phospholipids, non-HDL cholesterol, and apolipoprotein B levels all increased in a dose-dependent manner, suggesting that excessive overexpression of hepatic ABCA1 in the absence of its normal regulatory sequences altered total lipid homeostasis. At comparable expression levels, bacterial artificial chromosome transgenic mice, which express ABCA1 under the control of its endogenous regulatory sequences, showed a greater and more specific increase in HDL cholesterol than Ad-ABCA1-treated mice. Our results suggest that appropriate regulation of ABCA1 is critical for a selective increase in HDL cholesterol levels.  相似文献   
957.
Neurogenesis in the adult mammalian hippocampus may contribute to repairing the brain after injury. The signals that regulate neurogenesis in the dentate gyrus following ischemic stroke insult are not well known. We have previously reported that inducible nitric oxide synthase (iNOS) expression is necessary for ischemia-stimulated neurogenesis in the adult dentate gyrus. Here, we show that mice subjected to 90 min of middle cerebral artery occlusion (MCAO) significantly increased the number of new neurons and up-regulated iNOS expression in the dentate gyrus. Blockade of the L-type voltage-gated Ca(2+) channel (L-VGCC) prevented neurogenesis in the dentate gyrus and subventricular zone (SVZ), and down-regulated iNOS expression in the dentate gyrus after cerebral ischemia. This study suggests that Ca(2+) influx through L-VGCC is involved in ischemia-induced neurogenesis by up-regulating iNOS expression.  相似文献   
958.
Internalisation of cell-penetrating peptides into tobacco protoplasts   总被引:1,自引:0,他引:1  
Cells are protected from the surrounding environment by plasma membrane which is impenetrable for most hydrophilic molecules. In the last 10 years cell-penetrating peptides (CPPs) have been discovered and developed. CPPs enter mammalian cells and carry cargo molecules over the plasma membrane with a molecular weight several times their own. Known transformation methods for plant cells have relatively low efficiency and require improvement. The possibility to use CPPs as potential delivery vectors for internalisation in plant cells has been studied in the present work. We analyse and compare the uptake of the fluorescein-labeled CPPs, transportan, TP10, penetratin and pVEC in Bowes human melanoma cells and Nicotiana tabacum cultivar (cv.) SR-1 protoplasts (plant cells without cell wall). We study the internalisation efficiency of CPPs with fluorescence microscopy, spectrofluorometry and fluorescence-activated cell sorter (FACS). All methods indicate, for the first time, that these CPPs can internalise into N. tabacum cv. SR-1 protoplasts. Transportan has the highest uptake efficacy among the studied peptides, both in mammalian cells and plant protoplast. The internalisation of CPPs by plant protoplasts may open up a new effective method for transfection in plants.  相似文献   
959.
米槠与杉木细根凋落物是否在自身群落中分解得更快?   总被引:1,自引:0,他引:1  
本研究应用网袋法对福建省万木林自然保护区米槠(Castanopsis carlesii)、杉木(Cunninghamia lanceolata)细根在米槠林群落和杉木林群落交叉分解进行了为期2年的研究。结果表明,0-1mm、1-2mm米槠细根在米槠群落比在杉木群落分解速率快,而相同径级杉木细根在两群落分解差异较大。0—1mm杉木细根在杉木群落的分解速率高于米槠群落,而1—2mm杉木细根在杉木群落的分解速率只及米槠群落的48%。米槠、杉木细根在两群落分解的差异表明,群落立地条件对细根分解存在较大的影响。  相似文献   
960.
目的:研究一株自制的c-erbB-2单克隆抗体A18在乳腺癌中表达的特性。方法:应用免疫组织化学SP法、蛋白质印迹分析法和荧光激活的流式细胞分选检测技术检测A18在635例乳腺癌组织、100例癌旁乳腺组织、不表达c-erbB-2的NIH/3T3(鼠成纤维细胞)和NE91(转表皮生长因子受体基因的NR6鼠成纤维面积)细胞株及高表达c-erbB-2的T6-17(转c-erbB-2-基因的NIH/3T3细胞)和SKBR3(人乳腺癌细胞)细胞株中的表达状况,并与市售进口c-erbB-2抗体(MaximBiotech产品)进行了平行对照研究。A18系采用细胞表面区域表位包埋法免疫小鼠制备而成,,结果:A18阳性染色定位于细胞膜,部分伴微弱的细胞浆着色,无明显非特异性染色,A18和进口抗体对NIH/3T3、NE91细胞均呈阴性,T6-17、SKBR3细胞均呈阳性,在乳腺癌组织中,A18的阳性率为60.3%,明显高于癌旁乳腺组织的5.0%,A18与进口同类单抗的阴性、阳性及总符合率分别为84.0%、82.8%及83.2%,与进口同类多抗的阴性,阳性及总符合率分别为88.0%、90.2%和89.5%。A1和进口同类单抗与乳腺癌临床病理特征的关系一致。经反复冻融7次或4℃保存10个月A18效价仍保持在3μg/ml。结论:A18特异性强,定位准确,效价高而稳定、可用于临床乳腺癌的检测。  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