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121.
Lipid composition of brain myelin from normal and hyperphenylalaninemic chick embryos 总被引:1,自引:0,他引:1
M J Alejandre C Marco H Ramirez J L Segovia E Garcia-Peregrin 《Comparative biochemistry and physiology. B, Comparative biochemistry》1984,77(2):329-332
The influence of hyperphenylalaninemia on the lipid composition of brain myelin has been investigated in 19-day-old chick embryos. CNP-ase activity was used as myelin marker enzyme for myelin isolation. CNP-ase activity was significantly lower in hyperphenylalaninemic myelin when compared with control. No significant differences were observed after experimental treatment in the total lipid content of myelin as well as in the proportion of cholesterol:phospholipid:galactolipid. Nevertheless, a clear increase in the percentage of esterified cholesterol was found. No appreciable alterations were observed in the phospholipid composition of brain myelin from both control and hyperphenylalaninemic chick embryos. However, the ratio of unsaturated to saturated fatty acids in serine plasmalogen and sphingomyelin was considerably increased by this treatment. This ratio in choline and ethanolamine phosphatides from treated embryos did not differ from that of controls. 相似文献
122.
123.
The rise in ethylene production accompanying the respiration climacteric and senescence of cut carnation flowers (Dianthus caryophyllus L. cv. White Sim) was associated with a 30-fold increase in the concentration of 1-aminocyclopropane-1-carboxylic acid (ACC) in the petals (initial content 0.3 nmol/g fresh weight). Pretreatment of the flowers with silver thiosulfate (STS) retarded flower senescence and prevented the increase in ACC concentration in the petals. An increase in ACC in the remaining flower parts, which appeared to precede the increase in the petals, was only partially prevented by the STS pretreatment. Addition of aminoxyacetic acid (2 mM) to the solution in which the flowers were kept completely inhibited accumulation of ACC in all flower parts.Abbreviations ACC
1-aminocyclopropane-1-carboxylic acid
- AOA
-aminoxyacetic acid
- STS
silver thiosulfate complex 相似文献
124.
Tannic acid impregnation has revealed the existence of a T-system in the helical fibers of Branchiobdella pentodonta (Annelida, Clitellata). T-tubules are L-shaped inside the fiber, within the plane of the I-band: after a short horizontal tract they run longitudinally for a long tract keeping contact with many sarcoplasmic reticulum cisternae and forming dyads. The presence of a T-system in this annelid, the only one demonstrated up to now in annelids, is to be ascribed to the thickness of the contractile layer of those fibers. 相似文献
125.
Antonio De Marco Harald Tschesche Gerhard Wagner Kurt Wüthrich 《European biophysics journal : EBJ》1977,3(3-4):303-315
In the 1H NMR spectra obtained at 360 MHz after digital resolution enhancement, the multiplet resonances of the methyl groups in the basic pancreatic trypsin inhibitor (BPTI) were resolved. With suitable double irradiation techniques the individual methyl resonances were assigned to the different types of aliphatic amino acid residues. Furthermore, from pH titration and comparison of the native protein with chemically modified BPTI, the resonance lines of Ala 16 in the active site and Ala 58 at the C-terminus were identified. Potential applications of the resolved methyl resonances as natural NMR probes for studies of the molecular conformations are discussed. 相似文献
126.
Enkephalin-binding systems in human plasma 总被引:1,自引:0,他引:1
Roberta Possenti Valeria De Marco Ornella Cherubini L. Giorgio Roda 《Neurochemical research》1983,8(4):423-432
Three amino acid-containing fractions present in human plasma are shown to bind both leu and met-enkephalin: serum albumin and two species of a much lower molecular weight, in all likelihood polypeptides. The amount of enkephalin associated with serum albumin seems comparatively smaller than that associated with the two low molecular weight systems. These systems jointly are apparently capable of binding a significant part of the circulating enkephalins. The possibility is suggested that the interactions described may play a role in maintaining the integrity of circulating enkephalins. 相似文献
127.
Joyce M. Fisher Marco Rabinovitz 《Biochemical and biophysical research communications》1982,104(2):851-853
A specific copper chelator, 2,9-dimethyl-4,7-diphenyl-1,10-phenanthrolinedisulfonic acid substituted for mercaptoethanol to support growth of a L1210 lymphoma in primary culture. Added Cu++, but not Zn++ or Fe++ interfered with growth promotion by the chelator. It also can protect an established L1210 culture, which does not require mercaptoethanol, from cytotoxicity of two bis-thiosemicarbazones. Since these are known to require copper for cytotoxicity, the results indicate that 2,9-dimethyl-4,7-diphenyl-1,10-phenanthrolinedisulfonic acid acts by removing a source of endogenous copper in the tissue culture medium which prevents growth of the primary culture. 相似文献
128.
Sacco C. De Vries Marco C. Harmsen Martin T. R. Kuiper Hans J. M. Dons Joseph G. H. Wessels 《Plant molecular biology》1983,2(6):295-303
Summary The molecular cloning of cDNA corresponds to pea seedling mRNA sequences encoding a shoot-specific polypeptide, the small subunit of the ribulose 1,5 biphosphate carboxylase and a component of the light-harvesting chlorophyll a/b complex is described. cDNA prepared from polysomal poly(A)RNA of light-grown shoots was enriched for shoot-specific and light-induced sequences by heterologous liquid hybridization with mercurated polysomal poly(A)RNA of dark-grown roots, followed by sulfhydryl chromatography. Cloned shoot-specific sequences were identified by 2D electrophoretic analysis of hybrid release translation products. The cloned shoot-specific sequence corresponded to a mRNA of 850 nt present both in light-and dark-grown shoots, and produced anin vitro translation product of Mr27 500 and isoelectric point of 4.7. 相似文献
129.
D. Smjen Y. Weisman Z. Mor A. Harell A.M. Kaye 《The Journal of steroid biochemistry and molecular biology》1991,40(4-6):717-723
We have demonstrated previously that 17β-estradiol (E2) stimulates proliferation of skeletal tissues, both in vivo and in vitro, as measured by increased DNA synthesis and creatine kinase (CK) specific activity. The effect of E2 on bone is sex specific. E2 is active only in females and androgens only in males. By contrast, in cartilage of both sexes, dihydrotestosterone (DHT) as well as E2 stimulates CK specific activity and DNA synthesis. In bone, we find that sex steroids stimulate skeletal cell proliferation in gonadectomized as well as in immature rats. Ovariectomized (OVX) rats, between 1 and 4 weeks after surgery, show stimulation of CK by E2. The basal activity and response of CK changes with the varying endogenous levels of E2 in cycling rats, in which the highest basal activity is at proestrus and estrus and the highest response is in diestrus. In rats of all ages tested, both the basal and stimulated specific activity of CK is higher in diaphysis and epiphysis than in the uterus, or in the adipose tissue adjacent to the uterus, which has a response similar to that of the uterus itself. The effect of E2 in vivo, and in chrondroblasts and osteoblasts in vitro, is inhibited by high levels of the antiestrogen tamoxifen which, by itself, in similar high concentrations, shows stimulatory effects. In addition to the sex steroids, skeletal cells are also stimulated by secosteroid and peptide calciotrophic hormones. The interactions of the sex steroids and the other calciotrophic hormones. These results provide the first steps towards understanding the regulation of bone cell proliferation and growth by the concerted action of a variety of hormones and growth factors. 相似文献
130.
Roberta Bertelli Fabrizio Ginevri Rosanna Gusmano Gian Marco Ghiggeri 《In vitro cellular & developmental biology. Animal》1991,27(10):799-804
Summary It has been suggested that the generation of toxic radicals plays an important role in toxicity by Adriamycin (ADR) on cancer
cell lines and in vivo. We have examined the role of free radicals in determining toxicity and resistance to ADR of rat glomerular
epithelial cells in culture; this method provides a good model for analyzing the mechanisms responsible for ADR experimental
nephrosis in rats. Three points were established: a) the intra- or extracellular site of ADR toxicity; b) the role of the
superoxide anion and of the hydroxyl radical in determining intra- and-extracellular cytotoxicity; and c) the implication
of oxido-reduction cycling as a potential route for ADR semiquinone transformation. Free ADR was found to induce the same
inhibition of [3H]thymidine incorporation into DNA as ADR bound to an agarose macroporous bed which prevents the intracellular incorporation
of the drug. Specific scavenging of free radical activity by the enzymes catalase and superoxide dismutase, the hydroxyl radical
inhibitors dimethyl sulfoxide and dimethylthiourea (DMTU) and by chelation of intracellular free iron with deferoxamine produced
only a partial restoration of [3H]thymidine incorporation into DNA, which was maximal for DMTU (30% of normal incorporation). DMTU treatment was unsuccessful
in preventing the extracellular cytostatic effect of ADR. Finally, glomerular epithelial cell killing (51Cr-release method) by 5-iminodaunorubicin, an ADR analogue with a modified quinone function that prohibits oxido-reduction
cycling, was higher than unmodified ADR. These results indicate that ADR may exert its cytotoxic effects on glomerular epithelial
cells by interaction at the cell surface, whereas the intracellular compartment, principally DNA, does not seem to be the
target of ADR effects. They also suggest that the free radicals are in part responsible for ADR intracellular cytotoxicity,
but other mechanisms should also be hypothesized. Finally, the participation of the ADR semiquinone radical in oxido-reduction
cycling seems not important for the induction of the cellular damage. 相似文献