全文获取类型
收费全文 | 11151篇 |
免费 | 634篇 |
国内免费 | 1039篇 |
专业分类
12824篇 |
出版年
2023年 | 121篇 |
2022年 | 194篇 |
2021年 | 213篇 |
2020年 | 238篇 |
2019年 | 316篇 |
2018年 | 305篇 |
2017年 | 279篇 |
2016年 | 303篇 |
2015年 | 272篇 |
2014年 | 524篇 |
2013年 | 703篇 |
2012年 | 436篇 |
2011年 | 543篇 |
2010年 | 492篇 |
2009年 | 597篇 |
2008年 | 713篇 |
2007年 | 674篇 |
2006年 | 597篇 |
2005年 | 519篇 |
2004年 | 502篇 |
2003年 | 431篇 |
2002年 | 375篇 |
2001年 | 292篇 |
2000年 | 282篇 |
1999年 | 229篇 |
1998年 | 189篇 |
1997年 | 187篇 |
1996年 | 140篇 |
1995年 | 148篇 |
1994年 | 137篇 |
1993年 | 116篇 |
1992年 | 117篇 |
1991年 | 79篇 |
1990年 | 87篇 |
1989年 | 65篇 |
1988年 | 61篇 |
1987年 | 53篇 |
1986年 | 54篇 |
1985年 | 130篇 |
1984年 | 186篇 |
1983年 | 118篇 |
1982年 | 125篇 |
1981年 | 102篇 |
1980年 | 105篇 |
1979年 | 96篇 |
1978年 | 78篇 |
1977年 | 72篇 |
1976年 | 67篇 |
1975年 | 50篇 |
1974年 | 57篇 |
排序方式: 共有10000条查询结果,搜索用时 0 毫秒
51.
James W. Cosgrove John J. Heikkila Alexander Marks Ian R. Brown 《Journal of neurochemistry》1983,40(3):806-813
Abstract: Free and membrane-bound polysomes were isolated from the cerebral hemispheres and cerebellum of the young adult rabbit. The two polysomal populations were translated in an mRNA-dependent cell-free system derived from rabbit reticulocytes. Analysis of the [35 S]methionine-labeled translation products on two-dimensional polyacrylamide gels indicated an efficient separation of the two classes of brain polysomes. The relative synthesis of S100 protein by free and membrane- bound polysomes was determined by direct immuno-precipitation of the cell-free translation products in the presence of detergents to reduce nonspecific trapping. Synthesis of S100 protein was found to be twofold greater on membrane-bound polysomes compared with free polysomes isolated from either the cerebral hemispheres or the cerebellum. In addition, the proportion of poly- (A+)mRNA coding for SlOO protein was also twofold greater in membrane-bound polysomes compared with free polysomes isolated from the cerebral hemispheres. These results indicate that the cytoplasmic S100 protein is synthesized predominantly on membrane-bound polysomes in the rabbit brain. We suggest that the nascent S100 polypeptide chain translation complex is attached to the rough endoplasmic reticulum by an ionic interaction involving a sequence of 13 basic amino acids in S100 protein. 相似文献
52.
Perry Barrett Peter-M. Kloetzel John Sommerville 《Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression》1983,740(4)
During early oogenesis in amphibia, most of the 5 S RNA and tRNA is stored in a ribonucleoprotein particle that sediments at 42 S. In Xenopus laevis the 42 S particle contains two major proteins: of Mr 48 000 (P48) and 43 000 (P43). It is shown that heterogeneity in composition of the 42 S particle reflects a changing situation whereby initially, both 5 S RNA and tRNA are complexed with P48 (1 molecule 5 S RNA: 1 molecule P48; 2 or 3 molecules tRNA: 1 molecule P48), but later, tRNA becomes increasingly associated with P43 (in a 1:1 ratio) although 5 S RNA remains complexed with a cleavage product of P48. These changes relate to the eventual utilization of the excess 5 S RNA and tRNA in ribosome assembly and protein synthesis. 相似文献
53.
Michael Ready Sandra Bird Gail Rothe J.D. Robertus 《Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression》1983,740(1):19-28
It has been known for some time that pokeweed antiviral protein acts by enzymatically inhibiting protein synthesis on eucaryotic ribosome systems. The site of this action is known to be the ribosome itself. In this paper we show that the pokeweed antiviral protein reaction against ribosomes is a strong function of salt concentrations, where 160 mM K+ and 3 mM Mg2+ retards the reaction, while 20 mM K+ and 2 mM Mg2+ allows maximum reaction rate. It is also shown, however, that an unidentified protein in the postribosomal supernatant solution, together with ATP, allows the ribosome to be attacked even in the presence of high salt. Kinetic analysis of the antiviral protein reaction has been carried out under both sets of conditions, and reveals that the turnover number for the enzyme is about 300–400 mol/mol per min. in each case. The Km for ribosomes is 1 μM in the presence of low salt and 0.2 μM at higher salt in the presence of postribosomal supernatant factors plus ATP. The antiviral protein reaction is also shown to be pH dependent and is controlled by a residue with pKa value of approx. 7.0, apparently a histidine. Stoichiometric reaction of the enzyme with iodoacetamide results in a significant loss of antiribosomal activity. 相似文献
54.
Ras interaction with the GTPase-activating protein (GAP) 总被引:18,自引:0,他引:18
M D Schaber V M Garsky D Boylan W S Hill E M Scolnick M S Marshall I S Sigal J B Gibbs 《Proteins》1989,6(3):306-315
Biologically active forms of Ras complexed to GTP can bind to the GTPase-activating protein (GAP), which has been implicated as possible target of Ras in mammalian cells. In order to study the structural features of Ras required for this interaction, we have evaluated a series of mutant ras proteins for the ability to bind GAP and a series of Ras peptides for the ability to interfere with this interaction. Point mutations in the putative effector region of Ras (residues 32-40) that inhibit biological activity also impair Ras binding to GAP. An apparent exception is the Thr to Ser substitution at residue 35; [Ser-35]Ras binds to GAP as effectively as wild-type Ras even though this mutant is biologically weak in both mammalian and S. cerevisiae cells. In vitro, [Ser-35]Ras can also efficiently stimulate the S. cerevisiae target of Ras, adenylyl cyclase, indicating that other factors may influence Ras/protein interactions in vivo. Peptides having Ras residues 17-44 and 17-32 competed with the binding of Ras to E. coli-expressed GAP with IC50 values of 2.4 and 0.9 microM, respectively, whereas Ras peptide 17-26 was without effect up to 400 microM. A related peptide from the yeast GTP-binding protein YPT1 analogous to Ras peptide 17-32 competed with an IC50 value of 19 microM even though the YPT1 protein itself is unable to bind to GAP. These results suggest that determinants within Ras peptide 17-32 may be important for Ras binding to GAP. 相似文献
55.
Gillian Henderson 《Biometals》1989,2(2):83-88
Summary Growth ofSaccharomyces cerevisiae on non-fermentable medium was more sensitive to inhibition by chromate than growth on fermentable medium. Chromate was selectively toxic against oxygen uptake in cells grown in non-fermentable medium and also inducedpetite mutations. CdO demonstrated similar but lesser effects on growth and respiration. However, molybdate had little toxicity to yeast non-fermentable growth and stimulated oxygen uptake in cells grown in fermentable and non-fermentable media. These results suggest that chromate, a carcinogen, may act more directly against the mitochondria ofS. cerevisiae than related chemical species, CdO and molybdate. 相似文献
56.
Robert L. Uffen Annette Colbeau Pierre Richaud Paulette M. Vignais 《Molecular & general genetics : MGG》1990,221(1):49-58
Summary
Rhodocyclus gelatinosus grew photosynthetically in the light and consumed H2 at a rate of about 665 nmol/min per mg protein. The uptake-hydrogenase (H2ase) was found to be membrane bound and insensitive to inhibition by CO. The structural genes of R. gelatinosus uptake-H2ase were isolated from a 40 kb cosmid gene library of R. gelatinosus DNA by hybridization with the structural genes of uptake-H2ase of Bradyrhizobium japonicum and Rhodobacter capsulatus. The R. gelatinosus genes were localized on two overlapping DNA restriction fragments subcloned into pUC18. Two open reading frames (ORF1 and ORF2) were observed. ORF1 contained 1080 nucleotides and encoded a 39.4 kDa protein. ORF2 had 1854 nucleotides and encoded a 68.5 kDa protein. Amino acid sequence analysis suggested that ORF1 and ORF2 corresponded to the small (HupS) and large (HupL) subunits, respectively, of R. gelatinosus uptake-H2ase. ORF1 was approximately 80% homologous with the small, and ORF2 was maximally 68% homologous with the large subunit of typical membrane-bound uptake-H2ases. 相似文献
57.
Determination of the entire nucleotide sequence of the aphid 28S ribosomal RNA gene (28S rDNA) revealed that it is 4,147 by
in length with a G + C content of 60.3%. Based on the nucleotide sequence, we constructed a presumed secondary-structure model
of the aphid 28S rRNA which indicated that the aphid 28S rRNA is characterized by the length and high G + C content of its
variable regions. The G + C content of the aphid's variable regions was much higher than that of the entire sequence of the
28S rRNA, which formed a striking contrast to those ofDrosophila with the G + C content much lower than the entire 28S molecule. In this respect, the aphid 28S rRNA somewhat resembled those
of vertebrates. This is the third report of a complete large-subunit rRNA sequence from an arthropod, and the first 28S rRNA
sequence for a nondipterous insect.
Correspondence to: H. Ishikawa 相似文献
58.
A note on optimality in lattice square designs 总被引:1,自引:0,他引:1
59.
60.
Bodvin Torjan Indergaard Mentz Norgaard Erik Jensen Arne Skaar Arne 《Hydrobiologia》1996,335(1):83-86
A method has been developed for the determination of H2S and FeS in sediments. FeS is converted into H2S which is flushed from the samples directly into an excess of chlorine bleach, NaC1O or KClO with some Zn2+ added. Either the excess can be titrated back potentiometrically with As2O3, or the sulphate formed can be measured colorimetrically. The precision is primarily controlled by the homogeneity of the
sediment suspensions and can be better than 99%. 相似文献