全文获取类型
收费全文 | 79284篇 |
免费 | 6134篇 |
国内免费 | 5956篇 |
出版年
2024年 | 177篇 |
2023年 | 1122篇 |
2022年 | 1774篇 |
2021年 | 2079篇 |
2020年 | 2011篇 |
2019年 | 2522篇 |
2018年 | 2438篇 |
2017年 | 1973篇 |
2016年 | 2134篇 |
2015年 | 2755篇 |
2014年 | 3824篇 |
2013年 | 5261篇 |
2012年 | 2940篇 |
2011年 | 4033篇 |
2010年 | 3316篇 |
2009年 | 4342篇 |
2008年 | 4479篇 |
2007年 | 4589篇 |
2006年 | 4265篇 |
2005年 | 4194篇 |
2004年 | 3650篇 |
2003年 | 3260篇 |
2002年 | 2960篇 |
2001年 | 1982篇 |
2000年 | 1752篇 |
1999年 | 1835篇 |
1998年 | 1804篇 |
1997年 | 1500篇 |
1996年 | 1259篇 |
1995年 | 1344篇 |
1994年 | 1201篇 |
1993年 | 1051篇 |
1992年 | 941篇 |
1991年 | 708篇 |
1990年 | 607篇 |
1989年 | 563篇 |
1988年 | 546篇 |
1987年 | 492篇 |
1986年 | 394篇 |
1985年 | 492篇 |
1984年 | 623篇 |
1983年 | 426篇 |
1982年 | 447篇 |
1981年 | 270篇 |
1980年 | 275篇 |
1979年 | 209篇 |
1978年 | 137篇 |
1977年 | 90篇 |
1976年 | 85篇 |
1973年 | 67篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
991.
Selenite has been shown to undergo intracellular metabolism that results in its conversion to other low molecular weight Secontaining
species and also to its incorporation into a selenocysteine residue in selenoprotein. In order to investigate whether the
incorporation into protein is required for the cytotoxic effects of selenite, we have examined whether inhibition of protein
synthesis prevents the inhibitory effect of selenite on the ability of cells to form colonies or to synthesize RNA. We have
found that treatment of HeLa cells with cycloheximide inhibited protein synthesis by >90% but had no effect on the inhibitory
effect of selenite on cell colony formation or RNA synthesis. Since protein synthesis is not necessary for these cytotoxic
effects of selenite they are unlikely to result from an increase in the synthesis of selenoproteins. 相似文献
992.
We propose yet another function for the unique appressed thylakoids of grana stacks of higher plants, namely that during prolonged high light, the non-functional, photoinhibited PS II centres accumulate as D1 protein degradation is prevented and may act as dissipative conduits to protect other functional PS II centres. The need for this photoprotective mechanism to prevent high D1 protein turnover under excess photons in higher plants, especially those grown in shade, is due to conflicting demands between efficient use of low irradiance and protection from periodic exposure to excessive irradiance. 相似文献
993.
Jeffrey P. Woessner Arthur J. Molendijk Piet van Egmond Frans M. Klis Ursula W. Goodenough Michel A. Haring 《Plant molecular biology》1994,26(3):947-960
Based on our previous work demonstrating that (SerPro)x epitopes are common to extensin-like cell wall proteins in Chlamydomonas reinhardtii, we looked for similar proteins in the distantly related species C. eugametos. Using a polyclonal antiserum against a (SerPro)10 oligopeptide, we found distinct sets of stage-specific polypeptides immunoprecipitated from in vitro translations of C. eugametos RNA. Screening of a C. eugametos cDNA expression library with the antiserum led to the isolation of a cDNA (WP6) encoding a (SerPro)x-rich multidomain wall protein. Analysis of a similarly selected cDNA (VSP-3) from a C. reinhardtii cDNA expression library revealed that it also coded for a (SerPro)x-rich multidomain wall protein. The C-terminal rod domains of VSP-3 and WP6 are highly homologous, while the N-terminal domains are dissimilar; however, the N-terminal domain of VSP-3 is homologous to the globular domain of a cell wall protein from Volvox carteri. Exon shuffling might be responsible for this example of domain conservation over 350 million years of volvocalean cell wall protein evolution. 相似文献
994.
Insect resistance of transgenic plants that express modified Bacillus thuringiensis cryIA(b) and cryIC genes: a resistance management strategy 总被引:7,自引:0,他引:7
995.
996.
Adaptation of Escherichia coli to high osmolarity environments: Osmoregulation of the high-affinity glycine betaine transport system ProU 总被引:10,自引:0,他引:10
Abstract: A sudden increase in the osmolarity of the environment is highly detrimental to the growth and survival of Fscherichia coli and Salmonella typhimurium since it triggers a rapid efflux of water from the cell, resulting in a decreased turgor. Changes in the external osmolarity must therefore be sensed by the microorganisms and this information must be converted into an adaptation process that aims at the restoration of turgor. The physiological reaction of the cell to the changing environmental condition is a highly coordinated process. Loss of turgor triggers a rapid influx of K+ ions into the cell via specific transporters and the concomitant synthesis of counterions, such as glutamate. The increased intracellular concentration of K+ -glutamate allows the adaptation of the cell to environments of moderately high osmolarities. At high osmolarity, K+ -glutamate is insufficient to ensure cell growth, and the bacteria therefore replace the accumulated K+ ions with compounds that are less d eleterious for the cell's physiology. These compatible solutes include polyoles such as trehalose, amino acids such as proline, and methyl-amines such as glycine betaine. One of the most important compatible solutes for bacteria is glycine betaine. This potent osmoprotectant is widespread in nature, and its intracellular accumulation is achieved through uptake from the environment or synthesis from its precursor choline. In this overview, we discuss the properties of the high-affinity glycine betaine transport system ProU and the osmotic regulation of its structural genes. 相似文献
997.
José Antonio Jarillo Juan Capel Antonio Leyva José Miguel Martínez-Zapater Julio Salinas 《Plant molecular biology》1994,25(4):693-704
We have isolated two Rare Cold-Inducible (RCI1 and RCI2) cDNAs by screening a cDNA library prepared from cold-acclimated etiolated seedlings of Arabidopsis thaliana with a subtracted probe. RNA-blot hybridizations revealed that the expression of both RCI1 and RCI2 genes is induced by low temperature independently of the plant organ or the developmental stage considered. However, RCI1 mRNA accumulates faster and at higher levels than the RCI2 one indicating that these genes have differential responsiveness to cold stress. Additionally, when plants are returned to room temperature, RCI1 mRNA decreases faster than RCI2. In contrast to most of the cold-inducible plant genes characterized, the expression of RCI1 and RCI2 is not induced by ABA or water stress. The nucleotide sequences of RCI1 and RCI2 cDNAs predict two acidic polypeptides of 255 and 251 amino acids with molecular weights of 29 and 28 kDa respectively. The alignment of these polypeptides indicates that they have 181 identical amino acids suggesting that the corresponding genes have a common origin. Sequence comparisons reveal no similarities between the RCI proteins and any other cold-regulated plant protein so far described. Instead, they demonstrate that the RCI proteins are highly homologous to a family of proteins, known as 14-3-3 proteins, which are thought to be involved in the regulation of multifunctional protein kinases. 相似文献
998.
999.
A. J. Soitamo G. Zhou A. K. Clarke G. Öquist E-M. Aro P. Gustafsson 《Plant molecular biology》1994,26(2):709-721
The unicellular cyanobacterium Synechococcus sp. PCC 7942 has three psbA genes encoding two different forms of the photosystem II reaction centre protein D1 (D1:1 and D1:2). The level of expression of these psbA genes and the synthesis of D1:1 and D1:2 are strongly regulated under varying light conditions. In order to better understand the regulatory mechanisms underlying these processes, we have constructed a strain of Synechococcus sp. PCC 7942 capable of over-producing psbA mRNA and D1 protein. In this study, we describe the over-expression of D1:1 using a tac-hybrid promoter in front of the psbAI gene in combination with lacI
Q
repressor system. Over-production of D1:1 was induced by growing cells for 12 h at 50 mol photons m-2 s-1 in the presence of 40 or 80 g/ml IPTG. The amount of psbAI mRNA and that of D1:1 protein in cells grown with IPTG was three times and two times higher, respectively. A higher concentration of IPTG (i.e., 150 g/ml) did not further increase the production of the psbAI message or D1:1. The over-production of D1:1 caused a decrease in the level of D1:2 synthesised, resulting in most PSII reaction centres containing D1:1. However, the over-production of D1:1 had no effect on the pigment composition (chlorophyll a or phycocyanin/number of cells) or the light-saturated rate of photosynthesis. This and the fact that the total amounts of D1 and D2 proteins were not affected by IPTG suggest that the number of PSII centres within the membranes remained unchanged. From these results, we conclude that expression of psbAI can be regulated by using the tac promoter and lacI
Q
system. However, the accumulation of D1:1 protein into the membrane is regulated by the number of PSII centres. 相似文献
1000.
Hermann Schmidt Thomas Dresselhaus Friedrich Buck Ernst Heinz 《Plant molecular biology》1994,26(2):631-642
A plastidial membrane-bound n-6 desaturase from spinach (Spinacia oleracea) was purified from chloroplast envelope membranes by anion exchange, cation exchange and ferredoxin-affinity chromatography. The molecular mass of the protein was estimated by SDS-PAGE to be 40 kDa. The highest specific activity of the desaturase in the final preparation was 196 nmol/min per mg protein with free oleic acid as the substrate. The N-terminal amino acid sequence of the blotted protein was determined and used for the construction of a degenerated and inosine-containing oligonucleotide primer for PCR experiments with cDNA transcribed from leaf mRNA. A 3-RACE experiment with this primer amplified a single band of 1500 bp that after sequencing showed an open reading frame of 382 amino acids corresponding to a protein of 43 kDa. The 5 end of the cDNA was amplified by a 5-RACE experiment and isolated as a 500 bp fragment. Sequencing of this DNA revealed an additional 65 amino acids at the N-terminus of the native protein that are attributed to a plastidial leader peptide. With appropriate primers derived from these sequences a full-length clone was amplified by PCR and sequenced. Comparison of the plastidial oleate desaturase with the homologous enzyme from cyanobacteria showed about 50% amino acid homology. Comparison with other desaturases revealed three histidine boxes with the general sequence HXXXH that are highly conserved in all membrane-bound desaturases. These boxes might be involved in metal ion complexation required for reduction of oxygen. 相似文献