全文获取类型
收费全文 | 32967篇 |
免费 | 2959篇 |
国内免费 | 22篇 |
出版年
2023年 | 148篇 |
2022年 | 341篇 |
2021年 | 792篇 |
2020年 | 426篇 |
2019年 | 557篇 |
2018年 | 666篇 |
2017年 | 556篇 |
2016年 | 996篇 |
2015年 | 1677篇 |
2014年 | 1757篇 |
2013年 | 2063篇 |
2012年 | 2735篇 |
2011年 | 2764篇 |
2010年 | 1691篇 |
2009年 | 1396篇 |
2008年 | 2076篇 |
2007年 | 2048篇 |
2006年 | 1987篇 |
2005年 | 1710篇 |
2004年 | 1733篇 |
2003年 | 1542篇 |
2002年 | 1489篇 |
2001年 | 327篇 |
2000年 | 253篇 |
1999年 | 306篇 |
1998年 | 323篇 |
1997年 | 236篇 |
1996年 | 224篇 |
1995年 | 182篇 |
1994年 | 167篇 |
1993年 | 160篇 |
1992年 | 157篇 |
1991年 | 183篇 |
1990年 | 145篇 |
1989年 | 132篇 |
1988年 | 120篇 |
1987年 | 106篇 |
1986年 | 115篇 |
1985年 | 122篇 |
1984年 | 118篇 |
1983年 | 116篇 |
1982年 | 125篇 |
1981年 | 123篇 |
1980年 | 105篇 |
1979年 | 83篇 |
1978年 | 62篇 |
1976年 | 59篇 |
1975年 | 68篇 |
1974年 | 56篇 |
1973年 | 56篇 |
排序方式: 共有10000条查询结果,搜索用时 31 毫秒
81.
Carole L. Harker Philip M. Mullineaux John A. Bryant Andrew J. Maule 《Plant molecular biology》1987,8(3):275-287
Specific antisera were prepared to the inclusion body protein (gene VI product) and the gene I product of cauliflower mosaic virus (CaMV). Translational fusions between the lacZ gene and gene VI or gene I were constructed by cloning the relevant DNA fragments into the expression vectors pUR290, pUR291 or pUR292. Large amounts of fusion protein were synthesized when the inserted DNA fragment was in frame with the lacZ gene of the expression vector. These fusion proteins were used to raise specific antisera to gene VI and gene I proteins of CaMV. Antiserum to the gene VI product detected a range of proteins in crude extracts and in a subcellular fraction enriched for virus inclusion bodies. This range of proteins was further shown to be related to gene VI by Staphylococcus aureus V8 partial proteolysis. Antiserum to the gene I product detected viral specific proteins of 46, 42 and 38 K in preparations of CaMV replication complexes from infected plants but not in any other subcellular fraction. 相似文献
82.
A stable carbon isotope study of dissolved inorganic carbon cycling in a softwater lake 总被引:3,自引:0,他引:3
Andrew L. Herczeg 《Biogeochemistry》1987,4(3):231-263
The dissolved inorganic carbon (DIC) cycle in a softwater lake was studied using natural variations of the stable isotopes of carbon,12C and13C. During summer stratification there was a progressive decrease in epilimnion DIC concentration with a concomitant increase in 13CDIC), due to preferential uptake of12C by phytoplankton and a change in the dominant CO2 source from inflow andin situ oxidation to invasion from the atmosphere. There was an increase in hypolimnion DIC concentration throughout summer with a concomitant general decrease in 13CDIC from oxidation of the isotopically light particulate organic carbon that sank down through the thermocline from the epilimnion.Mass balance calculations of DI12C and DI13C in the epilimnion for the summer (June 23–September 25) yield a mean rate of net conversion of DIC to organic carbon (Corg) of 430 ± 150 moles d-1 (6.5 ± 1.8 m moles m-2 d-1. Net CO2 invasion from the atmosphere was 420 ± 120 moles d-1 (6.2 ± 1.8 m moles m-2 d-1) with an exchange coefficient of 0.6 ± 0.3m d-1. These results imply that at least for the summer months the phytoplankton obtained about 90% of their carbon from atmosphere CO2. About 50% of CO2 invasion and conversion to Corg for the summer occurred during a two week interval in mid-summer.DIC concentration increased in the hypolimnion at a rate of 350 ± 70 moles DIC d-1 during summer stratification. The amount of DIC added to the hypolimnion was equivalent to 75 ± 20% of net conversion of DIC to Corg in the euphotic zone over spring and summer implying rapid degradation of POC in the hypolimnion. The 13C of DIC added to the deep water (-22.) was too heavy to have been derived from oxidation of particulate organic carbon alone. About 20% of the added DIC must have diffused from hypolimnetic sediments where relatively heavy CO2 (-7) was produced by a combination of POC oxidation and as a by-product of methanogenesis. 相似文献
83.
Electron microscopy of single-stranded structures in the DNA of competent Haemophilus influenzae cells. 总被引:4,自引:3,他引:1 下载免费PDF全文
Chromosomal DNAs from exponential-phase and competent cells of Haemophilus influenzae were examined by electron microscopy to determine whether the chromosome undergoes structural changes during competence development. Single-stranded gaps and single-stranded tails formed in chromosomal DNA during competence development. The generation of gaps was dependent on the rec-2 function. Since the rec-2 mutant is defective in the translocation of donor DNA, it was inferred that the gaps were involved in the translocation step of transformation. The generation of single-stranded tails was independent of the rec-1 and rec-2 genes. Therefore, these structures were assumed to play no direct role in the interaction of donor and recipient DNAs during transformation. Gaps were preferentially associated with a readily denaturable, possibly A + T-rich fraction of the genome. This finding raised the possibility that hot spots for transformation might be associated with A + T-rich DNA. 相似文献
84.
85.
H Golding T Mizuochi S A McCarthy C A Cleveland A Singer 《Journal of immunology (Baltimore, Md. : 1950)》1987,138(1):10-17
The goal of the present study was to evaluate the relationship among function, Lyt phenotype, and MHC recognition specificity in primary allospecific T cell populations. By using Lyt-2+ and L3T4+ T cells obtained from the same responder populations, we assessed the ability of T cells of each phenotype to generate cytotoxic effector cells (CTL) and IL 2-secreting helper T cells in response to either class I or class II MHC allodeterminants. It was found that a discordance between Lyt phenotype and MHC recognition specificity does exist in primary allospecific T cells, but only in one T cell subpopulation with limited functional potential: namely, Lyt-2+ T cells with cytotoxic, but not helper, function that recognize class II MHC alloantigens. Target cell lysis by these Lyt-2+ class II-allospecific CTL was inhibited by anti-Ia monoclonal antibodies (mAb), but not anti-Lyt-2 mAb, indicating that they recognized class II MHC determinants as their "restriction" specificity and not as their "nominal" specificity even though they were Lyt-2+. A second allospecific T cell subset with limited functional potential was also identified but whose Lyt phenotype and MHC restriction specificity were not discordant: namely, an L3T4+ T cell subset with helper, but not cytotoxic, function specific for class I MHC allodeterminants presented in the context of self-Ia. Thus, the present study demonstrates that primary allospecific T cell populations contain phenotypically identical subpopulations of helper and effector cells that express fundamentally different MHC recognition specificities. Because the recognition specificities expressed by mature T cells reflect the selection pressures they encountered during their differentiation into functional competence, these findings suggest that functionally distinct but phenotypically identical T cell subsets may be selected independently of one another during ontogeny. Thus, the existence of Lyt-2+ CTL specific for class II allodeterminants can be explained by the hypothesis that the association of Lyt phenotype with MHC recognition specificity results from the process of thymic selection that these Lyt-2+ effector cells avoid. 相似文献
86.
87.
88.
Andrew G. Clark 《Genetics》1987,115(3):569-577
Several population genetic models allowing natural selection to act on Y-linked polymorphism are examined. The first incorporates pleiotropic effects of a Y-linked locus, such that viability, segregation distortion, fecundity and sexual selection can all be determined by one locus. It is shown that no set of selection parameters can maintain a stable Y-linked polymorphism. Interaction with the X chromosome is allowed in the next model, with viabilities determined by both X- and Y-linked factors. This model allows four fixation equilibria, two equilibria with X polymorphism and a unique point with both X- and Y-linked polymorphism. Stability analysis shows that the complete polymorphism is never stable. When X- and Y-linked loci influence meiotic drive, it is possible to have all fixation equilibria simultaneously unstable, and yet there is no stable interior equilibrium. Only when viability and meiotic drive are jointly affected by both X- and Y-linked genes can a Y-linked polymorphism be maintained. Unusual dynamics, including stable limit cycles, are generated by this model. Numerical simulations show that only a very small portion of the parameter space admits Y polymorphism, a result that is relevant to the interpretation of levels of Y-DNA sequence variation in natural populations. 相似文献
89.
Andrew P. Vayda 《Human ecology: an interdisciplinary journal》1987,15(4):519-521
90.
Molecular cloning of cDNA for human prostatic acid phosphatase 总被引:1,自引:0,他引:1
A human liver cDNA library in λgt11 was screened with polyclonal antiserum to human acid phosphatase isoenzyme 2a/4. About eleven positive clones have been obtained. Two clones, λ Hap21 and λ Hap22 were further characterized: clone λHap21 contained a 0.8-kb cDNA insert and clone λHap22 a 1.8–2.0-kb insert. XbaI digestion of λHap22 generated two fragments of 1.0 and 0.9 kb. BglII digestion resulted in a 1.2-kb fragment and several smaller fragments of undetermined size. Clone 1 Hap22 contained all the genes carried by λ gt11(lac 5cI857nin 5Sam 100) and the 2-kb insert. An Escherichia coli(λHap22) lysogen was generated, and its acid phosphatase activity was approximately ten-fold higher than that in the control nonlysogenic lysate. Western-blot analysis of total proteins present in this E. coli(λHap22) lysate revealed that the non-induced λHap22 prophage directed the synthesis of an approx. 175-kDa protein. This protein was recognized by antibody to the human acid phosphatase isoenzyme 2a/4 and anti-β-galactosidase and was produced only upon induction with IPTG. These results indicated that AHap22 carried a major portion of the gene coding for the human acid phosphatase isoenzyme 2a and/or 4 and this protein fragment of acid phosphatase was sufficient to manifest enzymatic activity. 相似文献