全文获取类型
收费全文 | 9215篇 |
免费 | 670篇 |
国内免费 | 2篇 |
出版年
2024年 | 4篇 |
2023年 | 51篇 |
2022年 | 126篇 |
2021年 | 220篇 |
2020年 | 132篇 |
2019年 | 172篇 |
2018年 | 226篇 |
2017年 | 188篇 |
2016年 | 312篇 |
2015年 | 500篇 |
2014年 | 582篇 |
2013年 | 682篇 |
2012年 | 819篇 |
2011年 | 841篇 |
2010年 | 550篇 |
2009年 | 425篇 |
2008年 | 555篇 |
2007年 | 559篇 |
2006年 | 484篇 |
2005年 | 499篇 |
2004年 | 421篇 |
2003年 | 399篇 |
2002年 | 346篇 |
2001年 | 80篇 |
2000年 | 56篇 |
1999年 | 81篇 |
1998年 | 90篇 |
1997年 | 64篇 |
1996年 | 54篇 |
1995年 | 56篇 |
1994年 | 45篇 |
1993年 | 41篇 |
1992年 | 24篇 |
1991年 | 26篇 |
1990年 | 27篇 |
1989年 | 17篇 |
1988年 | 13篇 |
1987年 | 11篇 |
1986年 | 13篇 |
1985年 | 9篇 |
1984年 | 11篇 |
1983年 | 13篇 |
1982年 | 15篇 |
1981年 | 11篇 |
1980年 | 5篇 |
1979年 | 5篇 |
1978年 | 7篇 |
1977年 | 5篇 |
1976年 | 5篇 |
1975年 | 3篇 |
排序方式: 共有9887条查询结果,搜索用时 31 毫秒
61.
Claudia Crestini Alessandro D'Annibale Giovanni Giovannozzi-Sermanni 《Biotechnology Techniques》1996,10(4):243-248
Summary Total and specific activities of extra-cellular laccases from Lentinus edodes were enhanced by adding corn straw and chestnut juice to the liquid growth medium. The aqueous extracts were chemically characterized and revealed the presence of several phenolic and non-phenolic compounds. Extensive extraction of these components from the tested extracts completely annulled their stimulating properties on laccase production, suggesting that these compounds can act at micromole levels. 相似文献
62.
This article presents for the first time a modified protocol for RNase protection analysis that allows the substitution of32P with33P without loss of the high sensitivity of this method achieved with32P. With this protocol, we were able to detect at least 1 pg of specific mRNA. In the RNase protection analysis33P labeled riboprobes are more advantageous with regard to an easier handling and better resolution. 相似文献
63.
Rapeseed (Brassica napus) is a crop relatively tolerant to salt and sodium. Our objective was to study the interactions between Na, K and Ca and their relationship with its yield under the isolated effects of soil salinity or sodicity.Two experiments were carried out using pots filled with the Ah horizon of a Typic Natraquoll. There were three salinity levels (2.3 dS m-1; 6.0 dS m-1 and 10.0 dS m-1) and three sodicity levels, expressed as sodium adsorption ratios (SAR: 12; 27 and 44). The soil was kept near field capacity.As soil salinity increased, the K/Na and Ca/Na ratios in the tissues decreased markedly but yields and aerial biomass production were not affected. As soil SAR value increased, the K/Na and Ca/Na ratios in plants and K-Na and Ca-Na selectivities decreased. Plants could not maintain their Ca concentration in soil with a high SAR. The grain yield and biomass production diminished significantly in the highest SAR treatment. Our results are consistent with those showing detrimental osmotic effects of salts in Brassica napus. Conversely, under sodicity, the K/Na and Ca/Na ratios in plant tissues decreased considerably, in accordance with grain and biomass production. These results show that the effects of sodicity are different from those of salinity. 相似文献
64.
65.
Henri Wintz Hsu-Ching Chen Claudia A. Sutton Catharine A. Conley Angela Cobb David Ruth Maureen R. Hanson 《Plant molecular biology》1995,28(1):83-92
The expression of a 25 kDa protein, encoded by the fused mitochondrial pcf gene, is associated with cytoplasmic male sterility (CMS) in petunia. To investigate the role of the 25 kDa protein in CMS we have transformed petunia and tobacco plants with constructs expressing a portion of the urfS sequence of the pcf cDNA which encodes the 25 kDa protein. The urfS sequence was fused with two different mitochondrial targeting sequences. The chimeric gene coding region was placed under the control of the CaMV 35S promoter or a tapetum-specific promoter. Expression of the PCF protein was obtained in mitochondria of transgenic petunia and tobacco plants, yet fertility of the plants was not affected. Analysis of the location of the urfS-encoded protein revealed that it fractionates primarily into the soluble fraction in the transgenic plants whereas the genuine 25 kDa protein is found primarily in the soluble fraction but also in the membrane portion of immature buds from CMS petunia plants. Fertile transgenic plants were obtained which expressed the 25 kDa protein in the tapetal layer of post-meiotic anthers, while CMS plants express the endogenous 25 kDa protein in both the tapetal layer and sporogenous tissue of pre-meiotic anthers. 相似文献
66.
James R. Bunzow Ge Zhang Claudia Bouvier Carmen Saez Oline K. Ronnekleiv Martin J. Kelly David K. Grandy 《Journal of neurochemistry》1995,64(1):14-24
Abstract: We have cloned and expressed a rat brain cDNA, TS11, that encodes a μ-opioid receptor based on pharmacological, physiological, and anatomical criteria. Membranes were prepared from COS-7 cells transiently expressing TS11 bound [3H]diprenorphine with high affinity (KD = 0.23 ± 0.04 nM). The rank order potency of drugs competing with [3H]diprenorphine was as follows: levorphanol (Ki = 0.6 ± 0.2 nM) ≈β-endorphin (Ki = 0.7 ± 0.5 nM) ≈ morphine (Ki = 0.8 ± 0.5 nM) ≈ [d -Ala2, N-Me-Phe4,Gly-ol5]-enkephalin (DAMGO; Ki = 1.6 ± 0.5 nM) ? U50,488 (Ki = 910 ± 0.78 nM) > [d -Pen2,5]-enkephalin (Ki = 3,170 ± 98 nM) > dextrorphan (Ki = 4,100 ± 68 nM). The rank order potencies of these ligands, the stereospecificity of levorphanol, and morphine's subnanomolar Ki are consistent with a μ-opioid binding site. Two additional experiments provided evidence that this opioid-binding site is functionally coupled to G proteins: (a) In COS-7 cells 50 µM 5′-guanylylimidodiphosphate shifted a fraction of receptors with high affinity for DAMGO (IC50 = 3.4 ± 0.5 nM) to a lower-affinity state (IC50 = 89.0 ± 19.0 nM), and (b) exposure of Chinese hamster ovary cells stably expressing the cloned μ-opioid receptor to DAMGO resulted in a dose-dependent, naloxone-sensitive inhibition of forskolin-stimulated cyclic AMP production. The distribution of mRNA corresponding to the μ-opioid receptor encoded by TS11 was determined by in situ hybridization to brain sections prepared from adult female rats. The highest levels of μ-receptor mRNA were detected in the thalamus, medial habenula, and the caudate putamen; however, significant hybridization was also observed in many other brain regions, including the hypothalamus. 相似文献
67.
Claudia M. Caillaud J. S. Pierre B. Chaubet J. P. Di Pietro 《Entomologia Experimentalis et Applicata》1995,75(1):9-18
The behaviour ofSitobion avenae (F.), was compared on resistant wheat lines ofTriticum monococcum (L.) and a susceptible variety ofTriticum aestivum (L.). Firstly, stylet penetration activities were monitored with the Electrical Penetration Graph (EPG) technique and subsequently
analysed using flow charts combined with correspondence analysis. Plant resistance was shown to be associated with repeated
penetrations without access to either the xylem or the phloem, and with numerous failures in starting a sustained sap ingestion
(as represented by pattern E2). Access to sieve elements of the phloem did not seem to be much affected on resistant plants
but it took the aphid three times as long to produce a sap ingestion pattern when maintained on the resistant lineT. monococcum no 44 (Tm44) as compared with aphids maintained on susceptible plants. As a result the total time spent in ingesting from sieve
elements was reduced by 72% on Tm44. Secondly, direct observations of freely-moving apterous adults were performed. Aphids
did not discriminate between resistant and susceptible wheat during the first 30 min of access to test leaves, but only 4
out of 25 aphids were still probing after eight hours on resistant Tm44.
The relevance of these results to possible location of the resistance factor(s) are discussed. Although detection of plant
resistance before sieve elements are reached can not be rigorously excluded, the factors involved inT. monococcum resistance toS. avenae undoubtedly occur within the phloem vessels. 相似文献
68.
Contactinhibin was found to be involved in contact-dependent inhibition of growth. The growth inhibitory activity of contactinhibin is mediated by N-linked oligosaccharides with desialylated -glycosidically linked, terminal galactose residues. Here we show that in sparse human fibroblasts contactinhibin was expressed in a biologically inactive, highly sialylated form both on the plasma membrane and intracellularily, while in confluent cells plasma membrane localized contactinhibin was present in a biologically active, low sialylated form. Plasma membranes were shown to contain a glycoprotein sialidase which is suggested to be engaged in the activation of contactinhibin in a cell contact-dependent manner. 相似文献
69.
Isolation and characterization of the mycobacterial phagosome: segregation from the endosomal/lysosomal pathway 总被引:5,自引:0,他引:5
Zahra Hasan Claudia Schlax Lotte Kuhn Ivan Lefkovits Douglas Young Jelle Thole & Jean Pieters 《Molecular microbiology》1997,24(3):545-553
Mycobacteria have the ability to persist within host phagocytes, and their success as intracellular pathogens is thought to be related to the ability to modify their intracellular environment. After entry into phagocytes, mycobacteria-containing phagosomes acquire markers for the endosomal pathway, but do not fuse with lysosomes. The molecular machinery that is involved in the entry and survival of mycobacteria in host cells is poorly characterized. Here we describe the use of organelle electrophoresis to study the uptake of Mycobacterium bovis bacille Calmette Guerin (BCG) into murine macrophages. We demonstrate that live, but not dead, mycobacteria occupy a phagosome that can be physically separated from endosomal/lysosomal compartments. Biochemical analysis of purified mycobacterial phagosomes revealed the absence of endosomal/lysosomal markers LAMP-1 and β-hexosaminidase. Combining subcellular fractionation with two-dimensional gel electrophoresis, we found that a set of host proteins was present in phagosomes that were absent from endosomal/lysosomal compartments. The residence of mycobacteria in compartments outside the endosomal/lysosomal system may explain their persistence inside host cells and their sequestration from immune recognition. Furthermore, the approach described here may contribute to an improved understanding of the molecular mechanisms that determine the intracellular fate of mycobacteria during infection. 相似文献
70.