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101.
Uptake of Exogenous Glutamate and Aspartate by Circumventricular Organs but Not Other Regions of Brain 总被引:1,自引:1,他引:0
Madelon T. Price John W. Olney Oliver H. Lowry Susan Buchsbaum 《Journal of neurochemistry》1981,36(5):1774-1780
Abstract: Glutamate (Glu) and aspartate (Asp) concentrations in blood and selected regions of brain were measured at sequential intervals over a 3-h period following subcutaneous administration of Glu, Asp, or Glu plus Asp (2 mg/g body wt) to 4-day-old mouse or rat pups. Marked serum elevations of the administered amino acids (peak values exceeding 200 times control levels) were detected within 1 h. In circumventricular organ (CVO) regions of brain, which are thought to have no blood-brain barriers, a sharp and steady increase in tissue concentrations of the administered amino acids (peak values 4–10 times higher than control levels) occurred during a 15–120 min interval, whereas no appreciable increases were detected in other brain regions. When 2 mg/g Glu plus 2 mg/g Asp were administered, CVO tissue concentrations of each amino acid rose to approximately the same level obtained when the individual amino acids were given. It is concluded that blood-brain barriers preventing net entry of Glu or Asp into brain proper are relatively well established by the 4th postnatal day in rodents, but that CVO brain regions lack such barriers; selective access of blood-borne Glu or Asp to CVO neurons explains why these neurons are selectively destroyed by systemic administration of these neurotoxic amino acids. 相似文献
102.
Complete accounts of the natural products chemistry of Bonnemaisonia nootkana, B. asparagoides, B. hamifera and Trailliella intricata are described. In contrast to the chemistry of the closely related alga Asparagopsis, Bonnemaisonia spp. do not produce halomethanes, but instead an array of C7-C9 halogen-containing ketones, alcohols and carboxylic acids. Biomimetic syntheses of these compounds suggest they are precursors and products of in vivo Favorsky rearrangements. 相似文献
103.
Cytogenetic and electrophoretic analyses on 2n = 28 strains ofAsphodelus cerasiferus strongly suggest that the basic number x = 14 of the genusAsphodelus is of secondary polyploid origin from x = 7. 相似文献
104.
Constance Oliver 《In vitro cellular & developmental biology. Plant》1980,16(4):297-305
Summary Methods have been developed for isolating and maintaining differentiated rat exorbital lacrimal, parotid, and pancreatic acinar
cells for up to 1 month in culture. The dissociated cells retained their differentiated morphology when cultured as suspension
cultures at 35°C with the appropriate secretagogue (exorbital lacrimal, 10−6
M carbamyl choline; pancreas 10−5
M carbamyl choline; parotid, 10−6
M isoproterenol). Under these conditions the cells remained viable and differentiated for up to 4 weeks in culture and continued
to incorporate3H-leucine at rates similar to those of freshly isolated cells. If secretagogue was omitted from the medium, the cells rapidly
degenerated. These results indicate that differentiated from the medium, the cells rapidly degenerated. These results indicate
that differentiated exocrine gland acinar cells may be maintained in vitro and utilized as a model system for the study of
secretory processes. 相似文献
105.
Insulin antagonism of glucocorticoid induction of tyrosine aminotransferase in cultured foetal hepatocytes 总被引:7,自引:0,他引:7
Polyadenylated RNA from developing Artemia salina cysts was fractionated by centrifugation through a sucrose gradient containing methylmercuric hydroxide (CH3HgOH). Aliquots of each fraction were directly added to a rabbit reticulocyte lysate to program protein synthesis in vitro. The translation products were assayed for eukaryotic elongation factor Tu (eEF-Tu) by immunoprecipitation with an antibody raised in rabbits and purified by affinity chromatography. The immunoprecipitated radioactivity was analyzed by polyacrylamide gel electrophoresis in the presence of sodium dodecylsulphate. Sequences coding for eEF-Tu sediment in the 20-S region of the gradient and form a major component of the poly(A)-containing RNA. The mRNA of the 20-S region, comprising about 10% of the poly(a)-containing RNA fractionated on the gradient, has been translated in vitro and 30% of the translation products represent immunoprecipitable eEF-Tu protein chains with an Mr of 50000. 相似文献
106.
The marine opisthobranch molluscAplysia punctata was cultured at the Laboratoire de Biologie Marine in Concarneau, France.A. punctata veligers settled and underwent metamorphosis on the algaLomentaria articulata, but not onUlva spp., Palmaria marina, Laminaria spp. andFucus spp.Research supported by grants from The Arts Foundation and the Lerner Fund for Marine Research of the American Museum of Natural History. We wish to thank Director Yves Legal, College de France for his support and cooperation. 相似文献
107.
Salman Gailani William F. McLimans Annie Nussbaum Frances Robinson Oliver Roholt 《In vitro cellular & developmental biology. Plant》1976,12(5):363-372
Summary Two thin film culture systems, the controlled environment steady state system (SS) and the rocker tube configuration of that
system (RT), were used to identify some of the conditions that appear to maintain morphologic and functional characteristics
of cells of human bone marrow explants in vitro. The systems configuration assured continual gassing, control and easy monitoring
of the cultures. Cytocentrifuge preparations of media of specimens cultured in RT disclosed, though in decreasing numbers,
various hematopoietic cells for periods exceeding one month. Hematopoietic cells shed from specimens cultured in the SS system
were retained in the culture tubes; cells of the myelocytic series predominated for the first 2 weeks while an increasing
number of monocytes and macrophages appeared in the media of older cultures. Histologic examination of cultured explants disclosed
preservation of the marrow architecture and the persistence of hematopoietic cells. Specimens cultured in RT tubes tended
to be less cellular than similar cultures placed in dialysis bags or as cultured in the SS system. Immunoglobulins (Ig) were
released into the culture media at a constant rate throughout the period of culture. Specimens that were cultured at a controlled
pH of 7.4 released 2 to more than 4 times as much Ig as similar specimens maintained at a pH level of 7.1. There were no definitive
differences in Ig levels in the cultures maintained at comparable pH levels and overlaid with various CO2 concentrations, i.e. 2%, 5%, 10%; similarly, no differences in Ig levels were found in specimens cultured in media containing
fetal bovine sera as opposed to horse sera.
Supported by U.S.P.H.S. Grant CA-5834 from the National Cancer Institute.
Department of Medicine A.
Department of Cell Physiology
Department of Immunology and Immunochemistry. 相似文献
108.
Chicken liver Cd, Zn-thionein (metallothionein) was isolated from Cd-pretreated chickens weighing 1 500 g. The native Cd, Zn-thionein contained 9 g-atoms of metals per 12 000 g of protein. Upon the addition of Cu(CH3CN)4ClO4, all Cd2 and Zn2 were successfully replaced. 15 g-atoms of Cu from the acetonitrile perchlorate complex were bound to the protein. Due to the absence of aromatic amino acid residues, thionein has unique ultraviolet and circular dichroism properties. The shoulder of the ultraviolet spectrum at 250 nm (A250 X A280(-1) = 23.9) was shifted to 275 nm (A250 X A280(-1) = 1.6). No significant absorption was detected in the visible region. Th conformational changes of the protein moiety were much more visible in the circular dichroism spectra. The titration with Cu(CH3CH)2 caused the appearence of three new Cotton effects: 257.5 nm (+), 350 nm (+) and 301 nm (-). The negative Cotton effect at 239 nm of the original metallothionein was completely levelled off. The binding strength of copper with thionein is extraordinarily high: it survives proton treatment up to pH 1.9. Displacement of the Cd2 by Cu employing Cd-thionein which was formed at pH 2.2 resulted in the same circular dichroism properties as observed for Cu-thionein. D-Penicillamine proved a suitable model for the metal-free thionein, since redox reactions and polymerization of the sterically hindered thiol residue are known to be slow. The correlation of the circular dichroism properties of either copper complex using thionein or D-penicillamine was surprisingly high. Circular dichroism measurements of Cu(I)-D-penicillamine revealed Cotton effects at 255 nm (+), 280 nm (+) and 355 nm (-). Upon examining the red-violet mixed Cu(-i)-cu(II)-D-penicillamine complex, Cotton bands in the visible region at 425 nm (-) and 495 nm (+) were seen. In many blue copper enzymes, the copper is assumed to be in the neighborhood of both cysteine and aromatic amino acid residues, which are known to play an important role in the electron transfer. This is not the case in the Cu-thionein, which would explain many different properties of this copper protein. It is very attractive to conclude that the sterically hindered SH-group of D-penicillamine reacts with excess copper in a specific way, similar to the Cu-thionein. This phenomenon could explain the considerable success of D-penicillamine in the treatment of Wilson's disease. 相似文献
109.
110.
Synthesis and turnover of the regularly arranged surface protein of Acinetobacter sp. relative to the other components of the cell envelope. 总被引:6,自引:5,他引:1 下载免费PDF全文
The formation of the components of the cell envelope of Acinetobacter sp. 199A was investigated by measuring the incorporation of [3H]leucine into protein, [14C]galactose into lipopolysaccharide, 32P into phospholipid, and [3H]diaminopimelic acid into peptidoglycan. Whereas the lipopolysaccharide and intrinsic protein of the outer membrane were stable, some of the regularly arranged surface protein, the alpha-protein, was lost into the growth medium. Only newly synthesized alpha-protein was lost. The peptidoglycan of the murein layer was also labile. Selective inhibition of the formation of individual components of the cell envelope with penicillin, chloramphenicol, and bacitracin showed that incorporation of protein into the outer membrane required the simultaneous formation of complete lipopolysaccharide. The converse was not true: protein synthesis was not required for lipopolysaccharide incorporation. Formation of the outer membrane and the murein layer proceeded independently. 相似文献