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11.
Short-term aluminium uptake by tobacco cells: Growth dependence and evidence for internalization in a discrete peripheral region 总被引:1,自引:0,他引:1
Short-term uptake and initial localization of aluminium (Al) were investigated in cultured cells of Nicotiana tabacum L. cv. BY-2. Graphite furnace atomic absorption spectrometry and an in vivo Al-sensitive fluorometric assay, employing morin, yielded similar results in all experiments. Aluminium uptake was critically dependent on cell growth. As opposed to negligible uptake in stationary-phase cells, Al uptake (20 μ M AlCl3 , pH 4.5, 23°C) by actively growing cells was detectable within 5 min, with an initial rate of 16 nmol Al (106 cells)−1 h−1 . Increased CaCl2 levels (up to 20 m M ), low temperature (4°C), and pre-chelation of Al to citrate greatly reduced Al uptake (by 75–90%). A pH-associated permeabilization of cells at pH 4.5, as monitored by trypan blue, was observed in some growing cells. Although permeability to trypan blue was not a requirement for Al uptake, enhanced membrane permeability at pH 4.5, relative to pH 5.6, may contribute to Al uptake. Aluminium was observed to localize mainly in a pronounced and discrete fluorescent zone at the cell periphery (2–30 μm wide), presumably in the cortical cytosol and/or the adjoining plasma membrane section, although the possibility cannot be excluded that some Al resided in the cell wall apposing this discrete region. However, as judged by the Al-morin assay, there were no detectable Al levels in the remaining, larger portion of the cell wall. The potential of the Al-morin method in Al toxicity studies is illustrated. 相似文献
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Summary In a preceding paper the following facts have been shown (Mohr undNoblé 1960): Dark grown seedlings ofLactuca sativa L. var.Grand Rapids (tip burn resistant strain) do not form an appreciable plumular hook. But a normal plumular hook, as is formed for instance byPhaseolus vulgaris in complete darkness, can be induced by red light. This formation of the plumular hook is controlled by the phytochrome system. — The hook which has been closed by red radiation can be reopened by light. In this respect only the high energy reaction of photomorphogenesis is effective. This reaction system shows peaks of action in the blue and in the far-red part of the visible spectrum (cf.Mohr 1962).The present paper deals with the investigation of the anatomical and cellular changes which lead to hook formation and reopening. The movements of the hook always take place in the cotyledonary plane. Bending of the hook accurs because the cells on the potentially outer side of the future hook increase their rate of elongation, unbending of the hook is due to a rapid increase in rate of elongation of the cells on the inner side of the closed hook. Cell dividions are apparently not involved either in the bending or in the unbending of the hook. It is concluded, that the apical part of the hypocotyl is a highly complex organ the potentialities of which can be described only with the help of physiological experimentation. The conventional anatomical or cytological approaches are not adequate to describe in detail the pattern of differentiation which must be present in the apical part of the hypocotyl according to the reactions which can be induced by light.
Mit 13 Textabbildungen
Als Plumulahaken (=plumular hook) bezeichnen wir die auffällige Einkrümmungszone im Apikalbereich einer Keimpflanze. Ein knapper und klarer Begriff hat sich offenbar in der deutschen Literatur nicht durchgesetzt. AuchTroll (1959) spricht nur allgemein von einer apikalen Krümmung des Keimsprosses. Bei dem Plumulahaken derLactuca-Keimlinge handelt es sich um eine Einkrümmung des apikalen Hypokotylbereichs. 相似文献
Mit 13 Textabbildungen
Als Plumulahaken (=plumular hook) bezeichnen wir die auffällige Einkrümmungszone im Apikalbereich einer Keimpflanze. Ein knapper und klarer Begriff hat sich offenbar in der deutschen Literatur nicht durchgesetzt. AuchTroll (1959) spricht nur allgemein von einer apikalen Krümmung des Keimsprosses. Bei dem Plumulahaken derLactuca-Keimlinge handelt es sich um eine Einkrümmung des apikalen Hypokotylbereichs. 相似文献
15.
Membrane potential of Thermoplasma acidophila. 总被引:5,自引:0,他引:5
16.
The obligate, thermophilic, acidophilic mycoplasma, Thermoplasma acidophilum, grows optimally at 56° C and pH 2.0. Its plasma membrane possessed 21–22 protein bands that were resolved by polyacrylamide gel electrophoresis. One major membrane protein, molecular weight 152 000, which stained for carbohydrate with periodic acid-Schiff reagent, accounted for 32% (w/w) of the total membrane proteins. It was isolated and further purified by concanavalin A affinity chromatography. The carbohydrate content amounted to less than 10% (w/w) compared to that of the entire glycoprotein. The carbohydrate moiety consisted mainly of mannose residues with branched α 1 → 2 linkages at the non-reducing ends of the glycopeptide as determined by permethylation followed by gas chromatography-mass spectrometry analysis. The reducing end was an N-glycosidic linkage between asparagine and N-acetylglucosamine. The amino acid composition of this glycoprotein showed 62 mol% hydrophobic residues, while the acidic amino acid content contributed 9 mol% more than that of the basic amino acids. The existence of membrane glycoproteins in the procaryotic, wall-less T. acidophilum may provide a protective coat for the plasma membrane. The stereochemistry and the conformation of the carbohydrate chains, in conjunction with water turgor, may contribute to the rigidity of the membrane and the cation binding. 相似文献
17.
The physical properties of the plasma membrane of the aquatic phycomycete Blastocladiella emersonii were investigated, in particular the effects of cations on membrane structure. Intact zoospores and lipid extracts were labelled with the spin-labels 5-nitroxystearate (5-NS), 12-nitroxystearate (12-NS), and 2,2,6,6-tetramethylpiperidine-1-oxyl (Tempo). Electron spin resonance spectroscopy indicated a total of three breaks in plots of the hyperfine splitting parameter, 2T|, order parameter, S, and the partition coefficient, f, vs. temperature. The first and third break points (TL and TH) were found to be independent of the external K+, Ca2+, or Mg2+ concentrations. They were similar to the break points found in aqueous dispersions of lipid extracts and correlate well with the temperature limits for zoospore viability. In contrast, the middle break point (TM) was markedly influenced by the external Ca2+ concentration. Ca2+ increased TM from 12°C (no Ca2+ added) to 22°C (10 mM Ca2+), i.e., growth temperature. K+ reversed this Ca2+ effect, downshifting TM from 22°C to 10°C. A comparison of the physico-chemical effects of these ions on the membrane, as revealed by the cation-induced shift in TM, is closely correlated with the temperature dependence and physiological effects of cations on zoospore differentiation. This suggests that cations may modify the physical state of the plasma membrane and be involved in regulating the initial changes during zoospore encystment. 相似文献
18.
Adhesion Pad Formation and the Involvement of Cutinase and Esterases in the Attachment of Uredospores to the Host Cuticle 总被引:7,自引:0,他引:7 下载免费PDF全文
We have investigated the basis of adhesion of uredospores of the obligately parasitic rust fungus Uromyces viciae-fabae to leaves of its broad bean host. Upon contact with an aqueous environment, spores form a structure that we have termed an adhesion pad. The adhesion pad is formed by both living and autoclaved spores, but only adhesion pads formed by living spores adhered to the cuticle of leaves of the host plant. Treatment of living spores with the serine-esterase inhibitor diisopropyl fluorophosphate prevented the adhesion of the pad to the leaf surface, suggesting a functional role for esterase or cutinase in the process of adhesion. A cutinase and two nonspecific serine-esterases were found to be localized on the surface of spores. These enzymes were released rapidly from the spore surface upon contact with an aqueous environment. The addition of the cutinase and the nonspecific esterases to autoclaved spores restored their ability to adhere to the host cuticle. Thus, whereas pad formation appears to be a passive response to the aqueous environment, the actual adhesion of pads to the host cuticle appears to depend on the cutinase and esterases associated with the spore surface. These results suggest a new role for cutinases and serine-esterases in the fungal infection process. 相似文献
19.
Arrhenius plots of the maximal velocities for the Ca2+ -and Mg2+ -dependent ATPase activities found in a plasma membrane-rich microsome fraction isolated from the roots of barley ( Hordeum vulgare L. cv. Conquest) were nonlinear. Arrhenius plot analyses using a relation which produced curvilinear Arrhenius plots accurately fit the data and allowed the calculation of the activation enthalpies and molar heat capacities of activation. The temperature dependence of the computed Km values for the Ca2+ - and Mg2+ -dependent ATPase activities was complex, with the highest enzyme-substrate affinities being obtained near the barley seedling growth temperature (16°C). Using electron paramagnetic resonance spectroscopy with amphiphilic cationic and anionic spin probes, it was possible to demonstrate that temperature changes and increasing Ca2+ concentrations could alter the mobility of the membrane lipid polar head groups. Inhibition of the ATPase activities by high levels of Ca2+ may result from a Ca2+-induced reduction in the lipid polar head group mobility. The possible role of lipid polar head group-protein interactions in the complex temperature dependence of the barley root ATPase kinetic constants is discussed. 相似文献
20.
An endopeptidase from the larvae of the hornet Vespa crabro has been purified to homogeneity. The enzyme has been characterized with respect to molecular weight, amino acid compositon, and amino- and carboxyl-terminal sequences. The catalytic properties of the hornet protease are similar to those of bovine chymotrypsin with respect to inactivation by phenylmethanesulfonyl fluoride and carbobenzoxyphenylalanine chloro ketone and preferential peptide bond cleavage at aromatic amino acid residues. In contrast to bovine chymotrypsin, the hornet protease is not inhibited by the basic pancreatic Kunitz inhibitor, soybean inhibitor, or chicken ovomucoid. The molecular weight, as determined by several independent methods, was found to be 14 500. The protease is a single-chain protein containing two disulfide bonds. The terminal sequences are: NH2-Ile-Val-Gly-Gly-Ile-Asp.....Gly-Lys-Tyr-Pro-Tyr-Gln-Val-Ser-Leu-Arg-COOH. 相似文献