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   20950篇
  免费   1957篇
  国内免费   2967篇
  2024年   51篇
  2023年   327篇
  2022年   677篇
  2021年   1097篇
  2020年   792篇
  2019年   1048篇
  2018年   955篇
  2017年   782篇
  2016年   1012篇
  2015年   1399篇
  2014年   1657篇
  2013年   1741篇
  2012年   2102篇
  2011年   1859篇
  2010年   1164篇
  2009年   1088篇
  2008年   1218篇
  2007年   1065篇
  2006年   949篇
  2005年   806篇
  2004年   692篇
  2003年   585篇
  2002年   519篇
  2001年   379篇
  2000年   302篇
  1999年   261篇
  1998年   187篇
  1997年   167篇
  1996年   143篇
  1995年   98篇
  1994年   101篇
  1993年   64篇
  1992年   89篇
  1991年   63篇
  1990年   77篇
  1989年   52篇
  1988年   35篇
  1987年   34篇
  1986年   41篇
  1985年   34篇
  1984年   26篇
  1983年   26篇
  1982年   17篇
  1981年   16篇
  1980年   9篇
  1979年   18篇
  1978年   6篇
  1977年   9篇
  1976年   9篇
  1975年   7篇
排序方式: 共有10000条查询结果,搜索用时 0 毫秒
61.
利用PCR方法对单纯疱疹病毒Ⅱ型糖蛋白D(HSV-2gD)基因进行了修饰,在其5'端删去约500bp的非编码区,仅保留ATG上游7个bp。将修饰后的HSV-2gD基因插入到带有痘苗病毒天坛株TK基因区段的痘苗表达质粒pJSA1175,置于痘苗病毒P7.5k早/晚期启动子控制下。将此重组质粒用脂质体Lipofectin方法转染已受野型TK ̄+痘苗病毒天坛株感染的TK ̄-143细胞,通过同源重组机制和标志基因LacZ产物的蓝斑显色作用,以及BudR试剂对TK表型的选择压力,筛选出整合有HSV-2gD基因的重组痘苗病毒。Southem杂交表明,HSV-2gD基因已正确地插入痘苗病毒TK基因区内;间接免疫荧光检测显示,HSV-2gD蛋白已得到有效表达,且主要分布于细胞膜。重组病毒免疫家兔可产生明显的抗HSV-2gD中和抗体。用重组病毒免疫小鼠,3周后可使94%(17/18)的小鼠对抗HSV-2的致死量攻击,表明重组病毒具有明显的免疫保护作用。  相似文献   
62.
为用转基因方法治疗巴金森氏病大鼠模型,本研究采用分子克隆技术,将合成多巴胺的关键酶-酪氨酸羟化酶(TH)的基因,克隆进入以巨细胞病毒CMV为启动子的载体质粒内,经限制性内切酶定位分析证实该重组的DNA质粒的可靠性。携带TH基因的PCMVTH质粒以LIPO-FECTIN介导,在培养的原代骨骼肌细胞中高效表达。本研究为进一步用转基因的细胞植入脑内以治疗巴金森氏病打下一定基础。  相似文献   
63.
 Bi(Ⅲ)与金属硫蛋白作用性质研究张保林,黄辉,朱凌燕,岳晟,唐雯霞(南京大学配位化学研究所,配位化学国家重点实验室,南京210093)如何降低顺铂或其它抗癌铂的毒性,一直是癌症化疗中的重要课题之一,最近研究发现预先给大鼠或肺癌病人服用铋盐,可以极大...  相似文献   
64.
小麦条锈菌毒性小种及其无毒性突变型侵染初期,是不亲和反应的小麦叶片内可翻译mRNA水平迅速增加,而呈亲和反应叶片的增加幅度小且滞后。同时前者的Poly(A+)-RNA水平高于未接种对照,后者低于对照。32P标记实验证实不亲和反应叶片Poly(A+)-RNA的合成增加早于亲和反应叶片。Poly(A+)-RNA体外翻译产物经SDS-PAGE分离后,放射自显影图谱显示一些多肽条带的35S-Met相对掺入量有定量差异。  相似文献   
65.
Studies of cell pellets: I. Electrical properties and porosity.   总被引:2,自引:1,他引:1  
I G Abidor  L H Li    S W Hui 《Biophysical journal》1994,67(1):418-426
Cell pellets formed by centrifugation provided a good system to study the osmotic behavior, electroporation, and interaction between cells. Rabbit erythrocyte pellets were used in this study because they were simpler than nucleated cells to model analytically. Structurally, cell pellets possessed properties of porous solid bodies and gels. Electrically, cell pellets were shown to behave as a parallel set of resistance, Rp, and capacitance, Cp. Information on pellet structures was obtained from electric measurements. The pellet resistance reflected the intercellular conductivity (porosity and gap conductivity), whereas the pellet capacitance depended mostly on membrane capacitance. The pellet resistance was more sensitive to experimental conditions. The intercellular gap distance can be derived from pellet porosity measurements, providing the cell volume and surface area were known. Rp increased and relaxed exponentially with time when centrifugation started and stopped; the cycles were reversible. When supernatants were exchanged with solutions containing hypotonic electrolytes or macromolecules (such as PEG) after the pellets were formed, complicated responses to different colloidal osmotic effects were observed. A transient decrease followed by a large increase of Rp was observed after the application of a porating electric pulse, as expected from a momentary membrane breakdown, followed by a limited colloidal-osmotic swelling of pelleted cells. The equilibrium values of Rp, Cp, pellet porosity, and intercellular distances were measured and calculated as functions of cell number, centrifugation force, and ionic strength of the exchanged supernatant. Thus, the structure and properties of cell pellets can be completely characterized by electrical measurements.  相似文献   
66.
The infectivities of Steinernema carpocapsae, S. glaseri, S. scapterisci, and Heterorhabditis bacteriophora to Japanese beetle larvae, Popillia japonica, and house cricket adults, Acheta domesticus, were compared using external exposure and hemocoelic injection. Only H. bacteriophora and S. glaseri caused high P. japonica mortality after external exposure. When nematodes were injected, P. japonica had a strong encapsulation and melanization response to all species except S. glaseri. Heterorhabditis bacteriophora and S. carpocapsae were able to overcome the immune response, but S. scapterisci was not. All species except S. scapterisci were able to kill and reproduce within the host. Only S. scapterisci and S. carpocapsae caused A. domesticus mortality after external exposure. When nematodes were injected, A. domesticus had a strong immune response to all species except S. scapterisci. Steinernema carpocapsae effectively overcame the strong immune response and caused high host mortality, but S. glaseri and H. bacteriophora did not. Steinernema scapterisci caused high host mortality and reproduced, S. glaseri and H. bacteriophora caused low host mortality but only S. glaseri reproduced, and S. carpocapsae was able to kill the host but reproduced poorly. Most (ca. 90%) of the S. carpocapsae in the hemocoel of P. japonica became encapsulated and melanized within 8 hours postinjection. The symbiotic bacterium, Xenorhabduf nematophilus, was often released before this encapsulation and melanization.  相似文献   
67.
Chinese Hamster Ovary (CHO) cells were fused by subjecting cell suspensions to an exponentially decaying electric pulse in the presence of polyethylene glycol (PEG), Dextran or Ficoll. PEG (MW 1,000, 3,350, 8,000, 10,000 and 18,500), Dextran (MW 71,200) and Ficoll (MW 400,000) were added to the pulsing medium. A single exponential electric pulse with peak field strength of 4 kV/cm, and a half-time of 0.72 msec was used. The combination of two techniques, PEG-induced fusion and electrofusion, resulted in highly efficient fusion of CHO cells. Fusion yields (FY) at different concentrations of these polymers were measured using phase-contrast microscopy. FY was highly dependent on the concentration of PEG in media, while the presence of Dextran and Ficoll had no influence on fusion yield. PEG with MW 8,000 was found to be the most effective in causing cell aggregation, and to give the highest FY (40%). An optimal concentration for fusion was found for PEG of each molecular weight. Diluting cells suspended in higher concentrations of PEG to these optimal concentrations after the pulse application regained the optimal FY. It was concluded that PEG-induced prepulse aggregation and moderate cell swelling immediately after the pulse were important factors in achieving high fusion yields.This work is supported by a grant GM-30969 from the National Institutes of Health. Traveling fellowship to N.G.S. was supported from Foundation Cyrill and Methodius and grant N-189 from MCES of Bulgaria.  相似文献   
68.
Summary Heavy metals in electroplating effluent inhibited specific methanogenic activity (SMA) of anaerobic starch-degrading granules. The SMA of granules on the degradation of starch were reduced by 50% when each gram of biomass was in contact individually with 105 mg of zinc, 120 mg of nickel, 180 mg of copper, 310 mg of chromium, or >400 mg of cadmium. Granules had higher toxicity-resistance than flocculent sludge, due to their layered structure.  相似文献   
69.
旋毛虫肌幼虫ES抗原的基因克隆及高效表达   总被引:7,自引:0,他引:7  
作者对编码旋毛虫肌幼虫ES抗原的部分结构基因进行了克隆、鉴定和表达。用RNA PCR技术直接从旋毛虫肌幼虫总RNA中反转录并扩增出0.7kh的靶DNA,酶切分析后将其克隆到融合表达载体pEx3lC中。SDS—PAGE电泳表明,含重组子的大肠杆菌能够表达出一分子量为37kDa的融合蛋白(P37),后者占菌体总蛋白的22%以上,并以包含体形式存在于菌体中。经对纯化后表达蛋白的ELlSA检测,证明它能被猪旋毛虫病阳性血清和抗旋毛虫单克隆抗体识别。研究结果揭示,重组蛋白P37对于研制旋毛虫病诊断抗原和免疫抗原具有潜在的应用价值。  相似文献   
70.
小麦体细胞胚发生的超微结构研究   总被引:24,自引:0,他引:24  
对小麦(Triticum aestivum L.)幼胚培养中体细胞胚发生过程的超微结构变化进行了研究,结果如下:(1)原体细胞中大液泡消失,存在大量小液泡,细胞质的电子密度加强,核大,核仁明显,出现多核仁;(2)细胞器数量和种类,如质体、核糖体和线粒体增加;(3)细胞壁加厚,胞间连丝逐渐消失,细胞器数量丰富,胚性细胞中积累淀粉;(4)细胞壁加厚的胚性细胞中存在核仁液泡、自体吞噬泡和分泌泡;(5)多细胞原胚、球形胚和梨形胚被一层外壁包围,但胚体内细胞间广泛存在胞间连丝;(6)成熟胚生长点部位的细胞内质体中出现膜系结构,已向叶绿体转变,类囊体已形成  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