全文获取类型
收费全文 | 3743篇 |
免费 | 335篇 |
国内免费 | 2篇 |
出版年
2023年 | 7篇 |
2022年 | 7篇 |
2021年 | 52篇 |
2020年 | 54篇 |
2019年 | 52篇 |
2018年 | 44篇 |
2017年 | 53篇 |
2016年 | 99篇 |
2015年 | 154篇 |
2014年 | 177篇 |
2013年 | 227篇 |
2012年 | 297篇 |
2011年 | 292篇 |
2010年 | 181篇 |
2009年 | 166篇 |
2008年 | 221篇 |
2007年 | 237篇 |
2006年 | 223篇 |
2005年 | 231篇 |
2004年 | 235篇 |
2003年 | 197篇 |
2002年 | 204篇 |
2001年 | 33篇 |
2000年 | 21篇 |
1999年 | 44篇 |
1998年 | 51篇 |
1997年 | 45篇 |
1996年 | 28篇 |
1995年 | 27篇 |
1994年 | 23篇 |
1993年 | 41篇 |
1992年 | 26篇 |
1991年 | 21篇 |
1990年 | 24篇 |
1989年 | 28篇 |
1988年 | 20篇 |
1987年 | 17篇 |
1986年 | 20篇 |
1985年 | 15篇 |
1984年 | 20篇 |
1983年 | 17篇 |
1982年 | 17篇 |
1981年 | 16篇 |
1980年 | 9篇 |
1979年 | 15篇 |
1978年 | 12篇 |
1977年 | 12篇 |
1976年 | 10篇 |
1974年 | 10篇 |
1968年 | 6篇 |
排序方式: 共有4080条查询结果,搜索用时 15 毫秒
41.
42.
Purified thermostable alcohol dehydrogenase allozymes ADH-71k and ADH-FCh.D. ofDrosophila melanogaster have been compared with the two common enzyme forms ADH-F and ADH-S. Enzyme kinetic parameters for various primary and secondary alcohols were determined under standard conditions used previously. Both ADH-71k and ADH-FCh.D. show ADH-S-like reaction kinetics andK
m values, due to retrograde evolution at site 214, Pro Ser. Inhibition studies with alcohol dehydrogenase inhibitors pyrazole, 4-methylpyrazole, and cibacron blue 3GA were also performed. Activity measurements on crude extracts of larvae and flies from isogenic lines of ADH-FCh.D. revealed a consistently higher activity than in ADH-71k-containing strains, in contrast to the original strains.K.Th.E is indebted to the Royal Norwegian Council for Technological and Scientific Research for their postdoctoral fellowship. Prof. J. S. McKinley-McKee gave me the opportunity to work in his laboratory. I thank Dr. Knut Sletten of the Biochemical Institute for the kind gift of 2-methoxyethanol and amino acid analysis of some samples. The Biological Institute, Oslo, Section of General Genetics, is gratefully acknowledged for enabling me to use their fly-breeding facilities. Dr. John B. Gibson provided us with a sample of FCh.D. flies for the construction of isogenic lines in which Dr. Johan Hageman participated, owing to Postdoctoral Grant 436-931-P from the Foundation of Biological Research (BION), which is subsidized by the Netherlands Organization for Scientific Research (NWO). J. H. and Paula Truyens were involved in the measurements on the crude extracts. Work at Victoria University was supported by the VUW Internal Grant Committee. 相似文献
43.
Perras Michel R.; Abrams Suzanne R.; Balsevich John J. 《Journal of experimental botany》1994,45(11):1565-1573
The uptake of [3H]-abscisic acid in barley (Hordeum vulgareL. cv. Heartland) cell cultures was found to be mediated throughboth non-saturable and saturable components. The kinetic parametersof the saturable component, determined at pH 4.5 and 21 °C,showed a Km for natural or (+ )-ABA of 1.3±0.7µMand an apparent Vmex of 7.0 ± 2.8 nmol g1 cellsh1. The carrier showed a strong preference for the naturalenantiomer of ABA as compared to the unnatural one. Other substancestested, e.g. amino acids, organic acids, and other growth regulators,did not appear to interfere with the carrier-mediated uptakeof ABA. At low external concentrations of ABA (below 2.0 µM),the saturable component was greater than the diffusion component.Similarly, between pH 4.0 and 6.0, the saturable uptake wasresponsible for more than 50% of the total uptake. The carriermay be important in vivo for mediating uptake when endogenouslevels of ABA are low (c. 1 µM). The carrier specificity was evident in inhibition experimentsdone with ABA analogues. Our data showed that the carrier couldaccommodate small modifications in the ABA structure. Four analogueswere able to compete efficiently with ( + )-ABA for the bindingsite of the carrier. Three of these competitors were of the(+)-series. Only one ( )-analogue, ()-ABA, wasable to inhibit markedly the saturable uptake of ( + )-ABA.The induction of the ABA-respons-ive gene WCS120 (Houde et al.,1992) presented stricter requirements for the ABA molecule thanthe carrier, although with a similar preference for the ( +)-analogues. Besides ( + )-ABA itself, only two of the analoguestested, both ( + )-series, were able to induce the WCS120 geneafter a 24 h incubation period. The absence of correlation betweenthe activity of the analogues as ABA inhibitors in the carriersystem, and their capacity to induce the WCS120 gene tend tosuggest that the carrier is not directly involved in the signaltransduction pathway leading to the induction of this specificgene. Key words: Abscisic acid, barley, gene induction, Hordeum vulgare, uptake carrier 相似文献
44.
Eric Glasgow †Robert K. Druger †Chana Fuchs †Edward M. Levine †Suzanne Giordano † Nisson Schechter 《Journal of neurochemistry》1994,63(2):470-481
Abstract: In efforts to determine the primary structure of intermediate filament proteins in the goldfish visual pathway, we isolated clones from a retinal λgt11 cDNA expression library that represent goldfish vimentin. We show that there are at least two forms of goldfish vimentin, designated as vimentin α and vimentin β. RNase protection assays indicate that vimentin α mRNA is expressed in low amounts in retina, optic nerve, and brain and in higher amounts in spinal cord. In contrast, vimentin β mRNA is expressed in low amounts in retina, optic nerve, brain, and spinal cord and in very high amounts in eye lens. Immunohistochemical studies show that in the optic nerve, vimentin α is mainly restricted to blood vessels, meninges, and septa. Light staining is observed with this antibody in an astrocytic glial pattern throughout the optic nerve. Two-dimensional gel analysis shows that all of these goldfish vimentins are low abundant components of optic nerve cytoskeletal preparations. 相似文献
45.
Suzanne A. Adjoa Claude Bouchard Pieter Coetzer Tim D. Noakes France T. Dionne 《Human genetics》1994,93(3):347-348
A DNA polymorphism of the nuclear-encoded subunit Va of the human cytochrome c oxidase (COX), a mitochondrial respiratory enzyme, is reported. No polymorphism was detected in genes for the subunits IV and Vb of the same enzyme. 相似文献
46.
Russell B. Lingham Keith C. Silverman Gerald F. Bills Carmen Cascales Manual Sanchez Rosalind G. Jenkins Suzanne E. Gartner Isabel Martin Maria T. Diez Fernando Peláez Sagrario Mochales Yu-Lin Kong Richard W. Burg Maria S. Meinz Leeyuan Huang Mary Nallin-Omstead Scott D. Mosser Michael D. Schaber Charles A. Omer David L. Pompliano Jackson B. Gibbs Sheo B. Singh 《Applied microbiology and biotechnology》1993,40(2-3):370-374
Chaetomellic acids A and B, isolated from Chaetomella acutiseta, are specific inhibitors of farnesyl-protein transferase that do not inhibit geranylgeranyl transferase type 1 or squalene synthase. Chaetomellic acids A and B are reversible inhibitors, resemble farnesyl diphosphate and probably inhibit FPTase by substituting for farnesyl diphosphate. Chaetomellic acid production appears to be widespread within the genus Chaetomella.
Correspondence to: R. B. Lingham 相似文献
47.
The structure of the predicted amino acid sequence in the FX domain of Photosystem 1 was studied by molecular modeling and a working hypothesis was developed for the functional interaction of PsaC with the core heterodimer. We propose that the intervening sequences between homologous cysteines in the FX cluster form two flexible loops and participate in the binding of PsaC, and that the arginine residues in the two surface-exposed loops may promote the interaction between the P700–FX core and the subunit. The model was tested experimentally; chemical modification of arginine residues in the P700–FX core using phenylglyoxal prevented reconstitution of the core with PsaC and PsaD after insertion of FeS clusters in vitro. Treatment of the P700–FX core with trypsin also prevented reconstitution of terminal electron transfer to FAFB, although neither treatments affected the electron transfer to FX as judged by flash kinetic spectrophotometry. Electron transfer in the P700–FAFB complex was not impaired by either phenylglyoxal or trypsin treatment indicating that the small subunit(s) protect the arginine residues that become chemically modified or cleaved. The data are consistent with the working model and point to additional experiments designed to identify the specific residues involved in the interaction between the P700–FX core and PsaC.Abbreviations PG-
phenylglyoxal
- PS 1-
Photosystem 1 相似文献
48.
Two alleles of 10.1 and 8.1 kb of the human glycogen synthase gene have been revealed with the restriction enzyme EcoRI. 相似文献
49.
Jan Tumajer Krešimir Begović Vojtěch Čada Michal Jenicek Jelena Lange Jiří Mašek Ryszard J. Kaczka Miloš Rydval Miroslav Svoboda Lukáš Vlček Václav Treml 《Global Change Biology》2023,29(2):462-476
Radial tree growth is sensitive to environmental conditions, making observed growth increments an important indicator of climate change effects on forest growth. However, unprecedented climate variability could lead to non-stationarity, that is, a decoupling of tree growth responses from climate over time, potentially inducing biases in climate reconstructions and forest growth projections. Little is known about whether and to what extent environmental conditions, species, and model type and resolution affect the occurrence and magnitude of non-stationarity. To systematically assess potential drivers of non-stationarity, we compiled tree-ring width chronologies of two conifer species, Picea abies and Pinus sylvestris, distributed across cold, dry, and mixed climates. We analyzed 147 sites across the Europe including the distribution margins of these species as well as moderate sites. We calibrated four numerical models (linear vs. non-linear, daily vs. monthly resolution) to simulate growth chronologies based on temperature and soil moisture data. Climate–growth models were tested in independent verification periods to quantify their non-stationarity, which was assessed based on bootstrapped transfer function stability tests. The degree of non-stationarity varied between species, site climatic conditions, and models. Chronologies of P. sylvestris showed stronger non-stationarity compared with Picea abies stands with a high degree of stationarity. Sites with mixed climatic signals were most affected by non-stationarity compared with sites sampled at cold and dry species distribution margins. Moreover, linear models with daily resolution exhibited greater non-stationarity compared with monthly-resolved non-linear models. We conclude that non-stationarity in climate–growth responses is a multifactorial phenomenon driven by the interaction of site climatic conditions, tree species, and methodological features of the modeling approach. Given the existence of multiple drivers and the frequent occurrence of non-stationarity, we recommend that temporal non-stationarity rather than stationarity should be considered as the baseline model of climate–growth response for temperate forests. 相似文献
50.
Alberto C. Q. Pinto David H. Byrne Suzanne M. Dethier Rogers 《In vitro cellular & developmental biology. Plant》1993,29(2):55-58
Summary Ovule perforation technique and media components (plant growth regulators andl-glutamine) were tested on in vitro growth of immature (<3 mm) embryos of “Springcrest” and “Earligrande” peaches. Ovule perforation
was 2 to 4 times more effective in promoting embryo growth than leaving ovules intact.l-Glutamine (400 mg·liter−1) promoted an increase in growth but could not be used with indole-acetic acid plus kinetin because an antagonistic effect
on embryo growth occurred. The use of these exogenous plant growth regulators did not increase embryo growth over in vivo
growth. 相似文献