全文获取类型
收费全文 | 1982篇 |
免费 | 111篇 |
国内免费 | 36篇 |
出版年
2023年 | 34篇 |
2022年 | 36篇 |
2021年 | 55篇 |
2020年 | 42篇 |
2019年 | 42篇 |
2018年 | 48篇 |
2017年 | 50篇 |
2016年 | 36篇 |
2015年 | 42篇 |
2014年 | 107篇 |
2013年 | 93篇 |
2012年 | 46篇 |
2011年 | 67篇 |
2010年 | 84篇 |
2009年 | 100篇 |
2008年 | 80篇 |
2007年 | 112篇 |
2006年 | 88篇 |
2005年 | 74篇 |
2004年 | 63篇 |
2003年 | 54篇 |
2002年 | 51篇 |
2001年 | 41篇 |
2000年 | 37篇 |
1999年 | 23篇 |
1998年 | 31篇 |
1997年 | 30篇 |
1996年 | 9篇 |
1995年 | 23篇 |
1994年 | 22篇 |
1993年 | 19篇 |
1992年 | 23篇 |
1991年 | 27篇 |
1990年 | 21篇 |
1989年 | 25篇 |
1988年 | 33篇 |
1987年 | 21篇 |
1986年 | 11篇 |
1985年 | 19篇 |
1984年 | 46篇 |
1983年 | 55篇 |
1982年 | 47篇 |
1981年 | 53篇 |
1980年 | 34篇 |
1979年 | 31篇 |
1978年 | 8篇 |
1977年 | 6篇 |
1975年 | 4篇 |
1974年 | 4篇 |
1972年 | 5篇 |
排序方式: 共有2129条查询结果,搜索用时 241 毫秒
31.
ABSTRACT. A procedure was developed to purify a coated vesicle fraction from the protozoan parasite Trypanosoma brucei. Electron microscopy revealed a difference between T. brucei coated vesicles and clathrin-coated vesicles from other eukaryotes: trypanosome vesicles were larger (100 to ISO nm in diameter) and contained an inner coat of electron-dense material in addition to the external coat. Evidence suggests that the internal coat is the parasite's variant surface glycoprotein (VSG) coat. The SDS-PAGE analysis shows the major protein of T. brucei coated vesicles has a molecular mass of 61 kD, similar to VSG; this protein was recognized in an immunoblot by anti-VSG serum. Trypanosome coated vesicles also contain a protein which comigrates with the major protein (clathrin) of coated vesicles purified from rat brains. However, this protein is a minor component and it is not serologically cross-reactive with mammalian clathrin. Immunoblot analysis demonstrated that the parasite vesicles contained host IgG, IgM, and serum albumin. 相似文献
32.
Andreas Schmid Gerhard Burckhardt Heinz Gögelein 《The Journal of membrane biology》1989,111(3):265-275
Summary Endocytotic vesicles from rat kidney cortex, isolated by differential centrifugation and enriched on a Percoll gradient, contain both an electrogenic H+ translocation system and a conductive chloride pathway. Using the dehydration/rehydration method, we fused vesicles of enriched endosomal vesicle preparations and thereby made them accessible to the patch-clamp technique. In the fused vesicles, we observed Cl– channels with a single-channel conductance of 73±2 pS in symmetrical 140mm KCl solution (n=25). The current-voltage relationship was linear in the range of –60 to +80 mV, but channel kinetic properties dependended on the clamp potential. At positive potentials, two sublevels of conductance were discernible and the mean open time of the channel was 10–15 msec. At negative voltages, only one substate could be resolved and the mean open time decreased to 2–6 msec. Clamp voltages more negative than –50 mV caused reversible channel inactivation. The channel was selective for anions over cations. Ion substitution experiments revealed an anion permeability sequence of Cl–=Br–=I–>SO
4
2–
F–. Gluconate, methanesulfonate and cyclamate were impermeable. The anion channel blockers 4,4-diisothiocyanatostilbene-2,2-disulfonic acid (DIDS, 1.0mm) and 5-nitro-2-(3-phenylpropylamino)-benzoic acid (NPPB, 0.1mm) totally inhibited channel activity. Comparisons with data obtained from radiolabeled Cl–-flux measurements and studies on the H+ pump activity in endocytotic vesicle suspensions suggest that the channel described here is involved in maintenance of electroneutrality during ATP-driven H+ uptake into the endosomes. 相似文献
33.
Summary In tip-growingChara rhizoids, the in-vivo saltatory movements of Golgi vesicles were recorded. The movements in radial direction back and forth between the ER aggregate and the plasma membrane occurred three times more often than movements passing the ER aggregate tangentially. The mean velocity of the class of Golgi vesicles observed (0.4–1 m in diameter) was approx. 0.3 m/s. Higher speed of 1–1.5 m/s occurred only in radial directions. Possibly, the ER aggregate is involved in guidance of the Golgi vesicles.Abbreviations DIC
differential interference contrast
- ER
endoplasmic reticulum
- OsFeCN
osmium tetroxide-potassium ferricyanide
Dedicated to the memory of Professor O. Kiermayer 相似文献
34.
Recent years have seen the convergence of both genetic and biochemical approaches in the study of protein translocation inE. coli. The powerful combination of these approaches is exemplified in the use of anin vitro protein synthesis-protein translocaltion system to analyze the role of genetically defined components of the protein translocation machinery. We describe in this review recent results focusing on the function of thesecA, secB, andsecY gene products and the demonstration of their requirement forin vitro protein translocation. The SecA protein was recently shown to possess ATPase activity and was proposed to be a component of the translocation ATPase. We present a speculative working model whereby the translocator complex is composed of the integral membrane proteins SecY, SecD, SecE, and SecF, forming an aqueous channel in the cytoplasmic membrane, and the tightly associated peripheral membrane protein SecA functioning as the catalytic subunit of the translocator or protein-ATPase. 相似文献
35.
Callus was induced from juice vesicles of satsuma mandarin on Murashige & Skoog medium supplemented with -naphthaleneacetic acid (NAA), kinetin (K) and gibberellin (GA). Adventitious embryoids arose from the callus tissue on the medium containing 1 mgl–1 NAA alone. The embryoids grew into embryos which resulted in a plantlet on medium containing 1 mgl–1 GA.Abbreviations GA
gibberellin
- K
kinetin
- NAA
-naphthaleneacetic acid 相似文献
36.
Sandra Afione Luciano Debeljuk Adriana Seilicovich Daniel Pisera Mercedes Lasaga María del Carmen Díaz Beatriz Duvilanski 《Peptides》1990,11(6):1065-1068
In the present work we examined the effect of the neutralization of endogenous substance P by the administration of an anti-substance P serum (ASPS) on GABA concentration in the anterior pituitary in hyperprolactinemic conditions induced by 5-hydroxytryptophan or by grafting anterior pituitaries. ASPS reduced the increase in the anterior pituitary GABA concentration induced by hyperprolactinemia. In vitro experiments showed that substance P inhibited K+-evoked GABA efflux from hypothalamic fragments and decreased GABA concentration in the anterior pituitary but ASPS increased it. Our results demonstrate that substance P modifies hypothalamic GABA release and anterior pituitary GABA concentration and suggest that an interaction exists between substance P and GABA. 相似文献
37.
38.
Summary A polyclonal antibody against -1,3-glucan, callose, extracted from the pollen tube wall ofCamellia japonica was raised in mice and, using it as a probe, the localization of callose in the germinated pollen was studied. By confocal laser scanning microscopy, callose was found in the tip region of the pollen tube and the tube wall; the immuno-fluorescence in the tube wall was less toward the base of the tube. In contrast, the tip region did not fluoresce although the whole of the tube wall did strongly with aniline blue, the specific dye for callose. Immuno-electron microscopy showed that callose was also found in Golgi vesicles which concentrated in the tip region of the pollen tube, the inner layer of the tube wall, callose plugs, and Golgi vesicles in the pollen grain. Immuno-gold labeling was often detected on the fibrous structures in Golgi vesicles and callose plugs. Based on these results, the participation of Golgi vesicles in the formation of the tube wall and callose plugs was discussed.Abbreviation TBS
Tris-buffered saline
- Tris
Tris(hydroxy-methyl)-aminomethane
- PBS
phosphate-buffered saline
- BSA
bovine serum albumin
- ELISA
enzyme-linked immunosorbent assay
- CLSM
confocal laser scanning microscopy
- DP
degree of polymerization 相似文献
39.
Abstract A dense population of the purple sulfur bacterium Amoebobacter purpureus in the chemocline of meromictic Mahoney Lake (British Columbia, Canada) underwent consistent changes in biomass over a two year study period. The integrated amount of bacteriochlorophyll reached maxima in August and declined markedly during early fall. Bacteriochlorophyll was only weakly correlated with the light intensity and water temperature in the chemocline. In the summer, bacterial photosynthesis was limited by sulfide availability. During this period the intracellular sulfur concentration of A. purpureus cells decreased. A minimum concentration was measured at the top of the bacterial layer in August, when specific photosynthetic rates of A. purpureus indicated that only 14% of the cells were photosynthetically active. With the exception of a time period between August and September, the specific growth rates calculated from CO2 fixation rates of A. purpureus were similar to growth rates calculated from actual biomass changes in the bacterial layer. Between August and September 86% of the A. purpureus biomass disappeared from the chemocline and were deposited on the littoral sediment of Mahoney Lake or degraded within the mixolimnion. This rise of cells to the lake surface was not mediated by an increase in the specific gas vesicle content which remained constant between April and November. The upwelling phenomenon was related to the low sulfur content of A. purpureus cells and a low resistance of surface water layers against vertical mixing by wind. 相似文献
40.
Jeremy E. Schonhorn Marianne Wessling-Resnick 《Molecular and cellular biochemistry》1994,135(2):159-169
The fungal metabolite brefeldin A (BFA) induces profound alterations in the morphology of intracellular organelles. Although BFA promotes the formation of extensive tubular endosomal domains, our understanding of the effects of the antibiotic on vesicle traffic events associated with endocytosis is limited. Thus, alterations in the transferrin (Tf) receptor's endocytic/recycling pathway upon treatment of human erythroleukemia K562 cells with BFA were studied as a pharmacological response. Treatment of K562 cells with BFA caused a down-regulation in the number of cell surface Tf receptors. This effect is highly reminiscent of the well-known action of phorbol 12-myristate 13-acetate (PMA) on Tf receptor traffic in K562 cells. However, our results demonstrate that these two agents down-regulate the Tf receptor via different mechanisms. The effects of BFA and PMA were additive when K562 cells were incubated with both together. Using the In/Sur method, the endocytic rate constant for Tf internalization was determined and PMA was found to greatly enhance ke, from 0.28 min–1 to 0.43 min–1, while BFA had little effect (Ke=0.20 min–1). In contrast, BFA-treatment alters the exocytic rate constant for return of internalized receptors to the cell surface, with the largest effect exerted on a slow-release, monensin-sensitive, compartment. The sum of the endocytic and exocytic kinetic data support a model in which BFA and PMA down-regulate the Tf receptor in K562 cells by mechanistically distinct actions, with BFA targeting exocytic monensin-sensitive intracellular compartments and PMA acting to exert a profound influence on elements of receptor internalization.Abbreviations BFA
brefeldin A
- ARF
ADP-ribosylation factor
- HRP
horseradish peroxidase
- Tf
transferrin
- PMA
phorbol 12-myristate 13-acetate
- DMSO
dimethyl sulfoxide
- PBS
phosphate-buffered saline
- HEPES
4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid
- BSA
bovine serum albumin
- FITC-Tf
fluorescein isothiocyanate-labelled transferrin 相似文献