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991.
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Yin Shouliang Li Zilong Wang Xuefeng Wang Huizhuan Jia Xiaole Ai Guomin Bai Zishang Shi Mingxin Yuan Fang Liu Tiejun Wang Weishan Yang Keqian 《Applied microbiology and biotechnology》2016,100(24):10563-10572
Applied Microbiology and Biotechnology - Heterologous expression is an important strategy to activate biosynthetic gene clusters of secondary metabolites. Here, it is employed to activate and... 相似文献
994.
995.
昆虫病原线虫共生菌的分类 总被引:2,自引:1,他引:2
昆虫病原线虫共生菌是存在于昆虫病原线虫肠道内的一类细菌 ,属肠杆菌科 (Enterobacteriaceae) ,兼性厌氧 ,包括致病杆菌属 (Xenorhabdus) [1] 和光杆状菌属 (Photorhabdus) [2 ] ,它们分别与斯氏线虫属 (Stein ernema)和异小杆线虫属 (Heterorhabditis)的线虫共生[3] 。在自然界 ,共生菌存在于 3龄侵染期线虫的肠道中[4 ] ,不能从土壤中分离获得 ,是昆虫病原线虫的主要致病因子。昆虫病原线虫共生菌直到 2 0世纪 5 0年代末期才被发现 ,其分类地位也经常发生变动 ,鉴定工作尽管几十年来陆陆续续时有报道 ,但并不十分深入和系统。近年来 ,… 相似文献
996.
Tsang EW Yang J Chang Q Nowak G Kolenovsky A McGregor DI Keller WA 《Plant molecular biology》2003,51(2):191-201
Chlorophyll reduction in the seed of Brassica can be achieved by downregulating its synthesis. To reduce chlorophyll synthesis, we have used a cDNA clone of Brassica napus encoding glutamate 1-semialdehyde aminotransferase (GSA-AT) to make an antisense construct for gene manipulation. Antisense glutamate 1-semialdehyde aminotransferase gene (Gsa) expression, directed by a Brassica napin promoter, was targeted specifically to the embryo of the developing seed. Transformants expressing antisense Gsa showed varying degrees of inhibition resulting in a range of chlorophyll reduction in the seeds. Seed growth and development were not affected by reduction of chlorophyll. Seeds from selfed transgenic plants germinated with high efficiency and growth of seedlings was vigorous. Seedlings from T2 transgenic lines segregated into three distinctive phenotypes: dark green, light green and yellow, indicating the dominant inheritance of Gsa antisense gene. These transgenic lines have provided useful materials for the development of a low chlorophyll seed variety of B. napus. 相似文献
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998.
Lacquer polysaccharide (LP) was isolated from the sap of lac tree (Rhus vernicifera). Its derivatives, carboxymethyl LP, sulfated LP and debranching LP were prepared. Their structure was analyzed by GPC, FT-IR and NMR spectroscopy. The sugar components of carboxymethyl and sulfated LPs hardly changed, but the molecular weight of the former decreased. The side chains of LPs were partially removed using sodium periodate in mild conditions and the pyranose ring β-configuration of products obtained was not changed. Bioactivity of natural and modified LPs against leukopenia induced by cyclophosphamide (CP) was investigated in mice. LP exhibited a significant bioactivity (P<0.05) compared to positive control group (CP). The bioactivity could increase slightly with the increasing of the contents of carboxymethyl groups. However, with the removal of the side chains and the incorporation of sulfate groups, the bioactivity gradually decreased. These showed that the bioactivity of lacquer polysaccharides against leukopenia induced by CP was strongly dependent on the types of ionic groups of the polysaccharides and concerned with the side chains with 4-O-methyl-β-glucuronic acid in the terminal. 相似文献
999.
Engineering Streptomyces clavuligerus deacetoxycephalosporin C synthase for optimal ring expansion activity toward penicillin G 总被引:1,自引:0,他引:1
Wei CL Yang YB Wang WC Liu WC Hsu JS Tsai YC 《Applied and environmental microbiology》2003,69(4):2306-2312
The deacetoxycephalosporin C synthase (DAOCS) from Streptomyces clavuligerus was engineered with the aim of enhancing the conversion of penicillin G into phenylacetyl-7-aminodeacetoxycephalosporanic acid, a precursor of 7-aminodeacetoxycephalosporanic acid, for industrial application. A single round of random mutagenesis followed by the screening of 5,500 clones identified three mutants, G79E, V275I, and C281Y, that showed a two- to sixfold increase in the k(cat)/K(m) ratio compared to the wild-type enzyme. Site-directed mutagenesis to modify residues surrounding the substrate resulted in three mutants, N304K, I305L, and I305M, with 6- to 14-fold-increased k(cat)/K(m) values. When mutants containing all possible combinations of these six sites were generated to optimize the ring expansion activity for penicillin G, the double mutant, YS67 (V275I, I305M), showed a significant 32-fold increase in the k(cat)/K(m) ratio and a 5-fold increase in relative activity for penicillin G, while the triple mutant, YS81 (V275I, C281Y, I305M), showed an even greater 13-fold increase in relative activity toward penicillin G. Our results demonstrate that this is a robust approach to the modification of DAOCS for an optimized DAOCS-penicillin G reaction. 相似文献
1000.
Rab39, a novel Golgi-associated Rab GTPase from human dendritic cells involved in cellular endocytosis 总被引:5,自引:0,他引:5
Chen T Han Y Yang M Zhang W Li N Wan T Guo J Cao X 《Biochemical and biophysical research communications》2003,303(4):1114-1120
Rab GTPases are Ras-like small molecular weight GTP binding proteins that are involved in various steps along the exocytic and endocytic pathways. Here we report that Rab39, a novel Rab protein, is a Golgi-associated protein involved in endocytosis of HeLa cells. Full-length cDNA of Rab39 contains 1251bp with an open reading frame (ORF) of 636bp, which is predicted to encode a 211 aa protein. By blast analysis of Rab39 cDNA and protein sequence with homologues, we find that Rab39 may be a short variant of Rab34. Rab39 contains conserved motifs involved in phosphate/guanosine binding and a microbody C-terminal targeting signal. RT-PCR analysis indicates that Rab39 is mainly detected in epithelial cell lines, and Northern blot analysis shows that Rab39 is expressed ubiquitously in human tissues. By using FITC-BSA as an endocytic tracer, we show that Rab39 can facilitate endocytosis in HeLa cells when expressed either transiently or stably. Confocal microscopy examination of Rab39 subcellular localization suggests that Rab39 is associated with Golgi-associated organelles. Our findings demonstrate that Rab39 is a novel Rab GTPase involved in cellular endocytosis. 相似文献