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991.
Cell wall is a key structure of the plant organism engaged in numerous functions, and plants spend enormous resources on cell wall formation. Cell wall components are the most widespread organic substances on the Earth. However important is assembling plant cell wall polysaccharides, this process has been insufficiently studied by the methods of molecular genetics; in particular, too little is known of the genes that code for the relevant enzymes (glycosyltransferases, GT). The review addresses the current situation by expounding on GT classification, describing the characteristics of enzymes that synthesize cell wall polysaccharides, and summing up the existing knowledge of already identified and putative cellulose and callose synthases and GT localized in the Golgi apparatus. The methodology for searching and characterizing new genes that participate in cell wall formation is under discussion.__________Translated from Fiziologiya Rastenii, Vol. 52, No. 3, 2005, pp. 443–462.Original Russian Text Copyright © 2005 by Gorshkova, Nikolovski, Finaev. 相似文献
992.
Gene expression of the biosynthetic enzymes and biosynthesis of starch during Rice Grain development 总被引:1,自引:0,他引:1
Amylose and amylopectin are determinants of the physicochemical properties for starch and grain quality in rice. Their biosynthesis
is catalyzed by the interplay of ADP-glucose pyrophosphorylase (AGPase), granule-bound starch synthase (GBSS), soluble starch
synthase (SSS), a starch branching enzyme (SBE), and a starch debranching enzyme (SDE). In this study, the genes for these
enzymes were highly expressed 7 to 28 days after flowering during grain development, and their expression closely matched
increases in both starch content and grain weight Among all the tested cultivars, amylose contents in the rice grains remained
essentially constant throughout their development The AGPase gene was highly expressed in the high-yield cultivars of both
glutinous and non-glutinous rice. The SSS gene was actively expressed when mature GBSS mRNA decreased. Genes responsible for
amylopectin biosynthesis were simultaneously expressed in the late stage of grain development. We have now demonstrated that
the expression patterns of starch biosynthetic genes differ between glutinous and non-glutinous rice, and between Tongil (a
Japonica/ Indica hybrid) and Japonica types. 相似文献
993.
Pérez-Vich Begoña Knapp Steven J. Leon Alberto J. Fernández-Martínez José M. Berry Simon T. 《Molecular breeding : new strategies in plant improvement》2004,13(4):313-322
Increased stearic acid (C18:0) content in the seed oil of sunflower would improve the oil quality for some edible uses. The sunflower line CAS-20 (C18:0 genotype Es1Es1es2es2), developed from the high C18:0 mutant line CAS-3 (C18:0 genotype es1es1es2es2; 25% C18:0), shows increased C18:0 levels in its seed oil (8.6%). The objective of this research was to map quantitative trait loci (QTL) conferring increased C18:0 content in CAS-20 in an F2 mapping population developed from crosses between HA-89 (wild type Es1Es1Es2Es2; low C18:0) and CAS-20, which segregates independently of the macromutation Es1 controlling high C18:0 content in CAS-3. Seed oil fatty acid composition was measured in the F2 population by gas-liquid chromatography. A genetic linkage map of 17 linkage groups (LGs) comprising 80 RFLP and 19 SSR marker loci from this population was used to identify QTL controlling fatty acid composition. Three QTL affecting C18:0 content were identified on LG3, LG11, and LG13, with all alleles for increased C18:0 content inherited from CAS-20. In total, these QTL explained 43.6% of the C18:0 phenotypic variation. Additionally, four candidate genes (two stearate desaturase genes, SAD6 and SAD17, and a FatA and a FatB thioesterase gene) were placed on the QTL map. On the basis of positional information, QTL on LG11 was suggested to be a SAD6 locus. The results presented show that increased C18:0 content in sunflower seed oil is not a simple trait, and the markers flanking these QTL constitute a powerful tool for plant breeding programs. 相似文献
994.
黑色素皮质素受体激动剂的高通量筛选模型研究 总被引:1,自引:0,他引:1
为了建立黑色素皮质素受体(MC4R)激动剂的高通量筛选方法,将人的MC4R基因质粒(hMC4R/pCDNA3.1)与报告基因质粒(3×CRE/3×MRE/SRE-LUC)按1∶5的比例共转染到HEK293细胞,通过G418筛选,建立了稳定的MC4R激动剂筛选细胞株.利用MC4R内源激动剂α-MSH探索和优化了每孔接种细胞数目、激动剂孵育时间、溶剂DMSO终浓度、荧光素酶底物浓度等筛选条件,建立了可靠的筛选方法.实验表明:当细胞数目为4×104个/孔,激动剂孵育时间为8 h,每孔DMSO终浓度小于1%和α-MSH终浓度为1 μmol/L时,系统Z'-因子接近0.7,能够用于MC4R激动剂的高通量筛选. 相似文献
995.
发光酶基因lux AB标记硅酸盐细菌NBT菌株的研究 总被引:3,自引:1,他引:2
外源基因标记技术为研究土壤引入细菌的生态行为提供了有效的检测手段,通过选择不同的碳源和降低碳氮比筛选获得0.25%麦芽糖作为碳源的菌体制备培养基,对硅酸盐细菌BT菌株进行紫外诱变和抗生素抗性驯化获得—株抗利福平200μg·ml^-1的NBT-R200菌株,含发光酶基因luxAB的质粒pTR102::luxAB在辅助质粒pRK2013的帮助下转入该菌株中,从而赋予NBT菌株以发光活性和利福平、卡那霉素、四环素三种抗生素抗性.以对数生长期的菌体制备受体细胞,发现对数生长前期的细胞转移频率最高,可达6.70×10^-5,杂交比例以1:1:1适宜.标记菌株RL85的释钾能力没有丧失且有提高,发光特性稳定,连续转接20次后仍具有发光活性和3种抗生素抗性,适用于根际微生态学研究。 相似文献
996.
SHI Zhaoxing* WANG Hengliang* HU Kun FENG Erling YAO Xiao HUANG Liuyu SU Guofu HUANG Peitang & HUANG Cuifen . Beijing Institute of Biotechnology Beijing China . College of Life Science Shandong Normal University Jinan China . College of Environmental Chemical Engineering Xi’an Jiaotong University Xi’an China Correspondence should be addressed to Huang Liuyu 《中国科学:生命科学英文版》2004,47(6):494-502
~~Screening and identification of Shigella flexneri 2a virulence-related genes induced after invasion of epithelial cells1. Jin, Q., Yuan, Z., Xu, J., Wang, Y., Shen, Y., Lu, W., Wang, J., Liu, H., Yang, J., Yang, P., Zhang, X., Zhang, J., Yang, G, Wu, H., Qu, D., Dong, J., Sun, L., Xue, Y, Zhao, A., Gao, Y., Zhu, J., Kan, B., Ding, K.. Chen, S., Cheng, H., Yao, Z., He, B., Chen, R., Ma, D., Qiang, B., Wen, Y, Hou, Y., Yu, J., Genome sequence of Shigella flexneri 2… 相似文献
997.
Hernando A. del Portillo Michael Lanzer Sergio Rodriguez-Malaga Fidel Zavala Carmen Fernandez-Becerra 《International journal for parasitology》2004,34(13-14):1547
It is generally accepted that Plasmodium vivax, the most widely distributed human malaria, does not cytoadhere in the deep capillaries of inner organs and thus this malaria parasite must have evolved splenic evasion mechanism in addition to sequestration. The spleen is a uniquely adapted lymphoid organ whose central function is the selective clearance of cell and other particles from the blood, and microbes including malaria. Splenomegaly is a hallmark of malaria and no other disease seems to exacerbate this organ as this disease does. Besides this major selective clearance function however, the spleen is also an erythropoietic organ which, under stress conditions, can be responsible for close to 40% of the RBC populations. Data obtained in experimental infections of human patients with P. vivax showed that anaemia is associated with acute and chronic infections and it has been postulated that the continued parasitemia might have been sufficient to infect and destroy most circulating reticulocytes. We review here the basis of our current knowledge of variant genes in P. vivax and the structure and function of the spleen during malaria. Based on this data, we propose that P. vivax specifically adhere to barrier cells in the human spleen allowing the parasite to escape spleen-clearance while favouring the release of merozoites in an environment where reticulocytes, the predominant, if not exclusive, host cell of P. vivax, are stored before their release into circulation to compensate for the anaemia associated with vivax malaria. 相似文献
998.
999.
1000.
N. BEUVE N. RISPAIL P. LAINE J.-B. CLIQUET A. OURRY & E. LE DEUNFF 《Plant, cell & environment》2004,27(8):1035-1046
The relationship between nitrate influx, BnNrt2 nitrate transporter gene expression and amino acid composition of phloem exudate was investigated during N‐deprivation (short‐term experiment) and over a growth cycle (long‐term experiment) in Brassica napus L. The data showed a positive correlation between γ‐aminobutyric acid (GABA) in phloem exudate and nitrate uptake in the short‐ and the long‐term experiments. The hypothesis that this non‐protein amino acid could up‐regulate nitrate uptake via a long‐distance signalling pathway was tested by providing an exogenous GABA supply to the roots. The effect of GABA was compared with the effects of Gln, Glu and Asn, each known to be inhibitors of nitrate uptake. The results showed that GABA treatment induced a significant increase of BnNrt2 mRNA expression, but had less effect on nitrate influx. By contrast, Gln, Glu and Asn significantly reduced nitrate influx and BnNrt2 mRNA expression compared with the control plants. This study provides the first evidence that GABA may act as a putative long‐distance inter‐organ signal molecule in plants in conjunction with negative control exerted by Gln. The up‐regulation effect of GABA on nitrate uptake is discussed in the context of its role in N metabolism, nutritional stress and the recent discovery of a putative role of GABA as a signal molecule in plant development. 相似文献