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Absorption, emission, and fluorescence excitation spectra of pure solutions of chlorophyll a (Chl a) and chlorophyll b (Chl b) in diethyl ether and of equimolecular mixed solutions of the two pigments, were determined at room temperature as functions of concentration (in the range from 5 × 10-6 M to 4 × 10-3 M) and of wavelength of the exciting light (in the regions 380-465 and 550-650 nm). The efficiency of energy transfer from Chl b to Chl a, derived from these data, was found to depend on the wavelength of exciting light. Furthermore, the transfer efficiency calculated from sensitization of Chl a fluorescence by Chl b was substantially smaller than that calculated from quenching of Chl b fluorescence by Chl a. Both these effects are tentatively explained as evidence of superposition of a “fast” energy transfer (taking place before the Boltzmann distribution of vibrational energy had been reached) upon the “delayed” transfer, which takes place after vibrational equilibration. The first-named mechanism is made possible by overlapping of the absorption bands of the two pigments; the second, by overlapping of the emission band of Chl b and the absorption band of Chl a. The first mechanism can lead to repeated transfer of excitation energy between pigment molecules, the second only to a one-time transfer from the donor to the acceptor. Both mechanisms could be of the same, second-order type, with the transfer rate proportional to r-6. An alternative is for the fast mechanism to be of the first order, with the transfer rate proportional to r-3, but spectroscopic evidence seems to make this alternative less probable.  相似文献   
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Summary Bud scars were prepared from the cell walls of Saccharomyces cerevisiae by means of an exo--d-(13)-glucanase. On acid hydrolysis, these structures were shown to consist of mannose (85%), glucose (4%) and glucosamine (2.7%). In addition the isolated bud scars were incubated either with mercurylabelled Concanavalin A or with Concanavalin A coated colloidal gold. They were then examined by electron microscopy and were found to be heavily marked, indicating the presence of mannan. It was thus shown that mannan is a true component of bud scars, which until now had been thought to consist solely of chitin and glucan.  相似文献   
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Antigenic mannans isolated from the cells ofSaccharomyces fermentati, Saccharomyces rosei,Saccharomyces delbrueckii, Torulopsis colliculosa, Candida albicans andSaccharomyces cerevisiae were examined for their reactivity withSaccharomyces fermentati andCandida albicans antisera. Mannans ofTorulaspora as well asCandida albicans showed high cross-reactivity with the investigated antisera, which could be due to the presence of long side chains established by the partial acetolysis method. The low specific rotations ofSaccharomyces fermentati, Saccharomyces rosei andTorulopsis colliculosa mannans indicate a predominance of β-glycosidio linkages, whereasSaccharomyces delbrueckii andCandida albicans mannans possess predominantly α-linkages.Saccharomyces cerevisiae mannan showed different structural and immunological properties.  相似文献   
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This is the first in a series of papers dealing with the structure of cell walls isolated from suspension-cultured sycamore cells (Acer pseudoplatanus). These studies have been made possible by the availability of purified hydrolytic enzymes and by recent improvements in the techniques of methylation analysis. These techniques have permitted us to identify and quantitate the macromolecular components of sycamore cell walls. These walls are composed of 10% arabinan, 2% 3,6-linked arabinogalactan, 23% cellulose, 9% oligo-arabinosides (attached to hydroxyproline), 8% 4-linked galactan, 10% hydroxyproline-rich protein, 16% rhamnogalacturonan, and 21% xyloglucan.  相似文献   
947.
Résumé Dans l'hypophyse du rat, la microscopie électronique permet de mettre en évidence à l'intérieur de tous les cordons épithéliaux de la pars distalis un réseau de cellules agranulaires: les cellules stellaires et folliculo-stellaires, satellites des cellules granuleuses hormonogènes. Les cellules de ce réseau se caractérisent à la fois par la multiplicité de leurs prolongements et par leur organisation autour de cavités pour la plupart submicroscopiques, «les follicules». Les cellules folliculo-stellaires correspondent à une partie des cellules chromophobes de la microscopie photonique.La fente hypophysaire, par de nombreux caractères, semble faire partie de ce système folliculo-stellaire, dont elle pourrait représenter une région privilégiée par sa situation, ses dimensions et son contenu.L'existence des cellules folliculo-stellaires dans un grand nombre d'espèces, leurs caractères cytologiques hautement différenciés, leurs relations étroites avec le milieu intérieur interstitiel et leurs modifications en fonction de l'âge et des conditions expérimentales permettent de penser qu'elles sont étroitement attachées à la fonction glandulaire.
The network of the folliculo-stellate cells and the follicles of the adenohypophysis in the rat (pars distalis)
Summary Electron microscopic investigation of the rat anterior pituitary reveals, throughout the whole pars distalis, a cellular network composed of agranular cells. These cells, the stellate and folliculo-stellate cells, are satellites of the granulated secretory cells.The cells of the network are characterized both by their multiple cytoplasmic processes and by their organization around cavities, most of them submicroscopic, the follicles. Those cells probably represent a large part of the chromophobe cells previously observed by light microscopy.On account of several characters, the pituitary cleft seems to be related to the réseau folliculo-stellaire and could be a peculiar part of this system because of its localization, size and contents.The réseau folliculo-stellaire is present in numerous species, showing a typical and differentiated cytology, and close relationships with the interstitial medium. Owing to its morphology and to modifications according to age and experimental conditions, this network seems to be a system intimately involved in the glandular function.
Je remercie Mr. le Professeur J. Racadot et toute l'équipe du Laboratoire pour l'aide apportée: Mme O. Racadot (clichés), Mme G. Porcile (tirages, manuscrit), Mlle B. Marie (technique), Mme A. Combrier (manuscrit). Ce travail a été effectué sous la direction de Mr. le Professeur L. Olivier que je remercie vivement pour ses conseils et pour son aide lors de la rédaction du manuscrit.  相似文献   
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