全文获取类型
收费全文 | 33706篇 |
免费 | 3926篇 |
国内免费 | 1308篇 |
专业分类
38940篇 |
出版年
2024年 | 36篇 |
2023年 | 217篇 |
2022年 | 563篇 |
2021年 | 1023篇 |
2020年 | 659篇 |
2019年 | 798篇 |
2018年 | 927篇 |
2017年 | 803篇 |
2016年 | 1027篇 |
2015年 | 1384篇 |
2014年 | 1661篇 |
2013年 | 1887篇 |
2012年 | 2162篇 |
2011年 | 2140篇 |
2010年 | 1291篇 |
2009年 | 1201篇 |
2008年 | 1394篇 |
2007年 | 1253篇 |
2006年 | 1224篇 |
2005年 | 1027篇 |
2004年 | 924篇 |
2003年 | 822篇 |
2002年 | 808篇 |
2001年 | 2547篇 |
2000年 | 2324篇 |
1999年 | 1707篇 |
1998年 | 582篇 |
1997年 | 572篇 |
1996年 | 508篇 |
1995年 | 466篇 |
1994年 | 393篇 |
1993年 | 310篇 |
1992年 | 805篇 |
1991年 | 648篇 |
1990年 | 555篇 |
1989年 | 443篇 |
1988年 | 355篇 |
1987年 | 269篇 |
1986年 | 210篇 |
1985年 | 155篇 |
1984年 | 104篇 |
1983年 | 76篇 |
1982年 | 52篇 |
1981年 | 43篇 |
1980年 | 29篇 |
1979年 | 31篇 |
1978年 | 27篇 |
1976年 | 31篇 |
1973年 | 30篇 |
1970年 | 24篇 |
排序方式: 共有10000条查询结果,搜索用时 0 毫秒
31.
32.
An insect larval toxin designated CryII is produced by several subspecies of Bacillus thuringiensis and differs from the other major delta-endotoxins in these bacteria in its size, toxicity profile and presence as part of an operon with three open reading frames (ORF). Such an operon from a novel B. thuringiensis isolate has been cloned and differs from one previously characterized in the following ways: (a) the size and number of amino acid repeats in one of the ORFs; (b) the smaller size of the CryII protoxin and the presence of a unique 110-kDa CryII-related antigen; and (c) high larvicidal activity for a particular Lepidopteran but low activity for a Dipteran. Various subclones of this operon were introduced into a plasmid-free B. thuringiensis strain and only the cryII gene was found to be necessary for protoxin accumulation. 相似文献
33.
A frameshift mutation (2869insG) in the second transmembrane domain of the CFTR gene: identification, regional distribution, and clinical presentation. 下载免费PDF全文
34.
A. Doisy S. Paillasson P. Tracqui F. Germain F. Leitner M. Robert-Nicoud X. Ronot 《Cell biology and toxicology》1996,12(4-6):363-366
The organization of eukaryotic chromatin is not static but changes as a function of cell status during processes such as proliferation, differentiation, and migration. DNA quantification has not been used extensively to investigate chromatin dynamics in combination with cellular migration. In this context, an optimized DNA-specific, nonperturbant method has been developed for studying chromatin organization, using the fluorescent vital bisbenzimidazole probe Hoechst 33342: this property has been described by Hamori et al. (1980). Computer-assisted image analysis was used to follow migratory activity and chromatin organization of L929 fibroblasts during in vitro wound healing. Cell movements were analyzed using an optical flow technique, which consists in the calculation of the velocity field of cells and nuclear movements in the frame. This system allows the correlation of cell migration and position in the cell cycle. It makes it possible to study chromatin dynamics using a quantitative analysis of nuclear differentiation reorganization (nuclear texture) and to correlate this with migration characteristics. The present system would be of interest for studying cell-extracellular matrix interactions using differing substrates, and also the migratory response to chemotactic factors. Such a model is a prerequisite for gaining better understanding of drug action. 相似文献
35.
36.
A. Benito E. Viaplana J.L. Corchero X. Carbonell A. Villaverde 《FEMS microbiology letters》1995,129(2-3):157-162
Abstract The 3D gene of foot-and-mouth disease virus encodes the viral RNA dependent RNA polymerase, also called virus infection associated (VIA) antigen, which is the most important serological marker of virus infection. This 3D gene from a serotype Cl virus has been cloned and overexpressed in Escherichia coli under the control of the strong lambda lytic promoters. The resulting 51 kDa recombinant protein has been shown to be immunoreactive with sera from infected animals. After induction of gene expression, an immediate and dramatic arrest of cell DNA synthesis occurs, similar to that produced by genotoxic doses of the drug mitomycin C. This effect does not occur during the production of either a truncated VIA antigen or other related and non-related viral proteins. The inhibition of DNA replication results in a subsequent induction of the host SOS DNA-repair response and in an increase of the mutation frequency in the surviving cells. 相似文献
37.
38.
Aurin tricarboxylic acid, the anti-AIDS compound, prevents the binding of interferon-alpha to its receptor 总被引:2,自引:0,他引:2
Y X Gan J L Weaver P S Pine K C Zoon A Aszalos 《Biochemical and biophysical research communications》1990,172(3):1298-1303
Binding of HIV to its receptor, the CD4 molecule of lymphocytes, can be prevented by chemical agents. These agents could be considered as potential anti-AIDS drugs. We have shown that aurin tricarboxylic acid (ATA, 3 microM) specifically blocks the binding of gp120, the HIV coat protein, to the CD4 molecule. We have also found that ATA prevents the binding of interferon-alpha to its receptor in a dose-dependent manner (12-50 microM range). Membrane potential shift, associated with binding of interferon-alpha to its receptor, was also blocked by ATA in a dose-dependent fashion. Our results indicate that potential anti-AIDS drugs should be screened for such undesired side effects. 相似文献
39.
Hyaluronidases are a family of enzymes that degrade hyaluronic acid (hyaluronan, HA) and widely used in many fields. A hyaluronidase producing bacteria strain was screened from the air. 16S ribosomal DNA (16S rDNA) analysis indicated that the strain belonged to the genus Bacillus, and the strain was named as Bacillus sp. A50. This is the first report of a hyaluronidase from Bacillus, which yields unsaturated oligosaccharides as product like other microbial hyaluronate lyases. Under optimized conditions, the yield of hyaluronidase from Bacillus sp. A50 could reach up to 1.5×104 U/mL, suggesting that strain A50 is a good producer of hyaluronidase. The hyaluronidase (HAase-B) was isolated and purified from the bacterial culture, with a specific activity of 1.02×106 U/mg protein and a yield of 25.38%. The optimal temperature and pH of HAase-B were 44°C and pH 6.5, respectively. It was stable at pH 5–6 and at a temperature lower than 45°C. The enzymatic activity could be enhanced by Ca2+, Mg2+, or Ni2+, and inhibited by Zn2+, Cu2+, EDTA, ethylene glycol tetraacetic acid (EGTA), deferoxamine mesylate salt (DFO), triton X-100, Tween 80, or SDS at different levels. Kinetic measurements of HAase-B towards HA gave a Michaelis constant (K
m) of 0.02 mg/mL, and a maximum velocity (V
max) of 0.27 A
232/min. HAase-B also showed activity towards chondroitin sulfate A (CSA) with the kinetic parameters, K
m and V
max, 12.30 mg/mL and 0.20 A
232/min respectively. Meanwhile, according to the sequences of genomic DNA and HAase-B’s part peptides, a 3,324-bp gene encoding HAase-B was obtained. 相似文献
40.
A method based on the infection of CaCo-2 cells and molecular hybridization with a specific cDNA probe has been developed for the detection of infectious astroviruses in environmental samples. By this procedure wild-type astroviruses have been detected in water from an area where a concurrent gastroenteritis outbreak was reported. 相似文献