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51.
H. Fujii S. Miwa S. Takegawa K. Takahashi A. Hirono T. Takizawa T. Morisaki H. Kanno T. Taguchi J. Okamura 《Human genetics》1984,66(2-3):276-278
Summary Two new glucose-6-phosphate dehydrogenase (G6PD) variants were discovered in Japan. The first, found in a 9-year-old male, was associated with chronic hemolysis and hemolytic crises after upper respiratory infections. The enzyme activity of the variant was 2.9% of normal. The patient's G6PD showed an increased utilization of substrate analogue, deamino-NADP, and thermal instability. The second variant occurred in a 7-year-old male with druginduced hemolysis. The main enzymatic characteristics were reduced enzyme activity, being 6.4% of normal, faster-thannormal anodal electrophoretic mobility, slightly high Michaelis constant for glucose-6-phosphate, thermal instability, and biphasic pH optima. Enzymatic properties of these variants allowed each to be distinguished from previously reported variants. The first variant was designated Gd (-) Gifu and the other, Gd (-) Fukuoka. 相似文献
52.
T. Takizawa H. Fujii S. Takegawa K. Takahashi A. Hirono T. Morisaki H. Kanno R. Oka H. Yoshioka S. Miwa 《Human genetics》1984,68(1):70-72
Summary A new glucose 6-phosphate dehydrogenase (G6PD) variant associated with chronic nonspherocytic hemolytic anemia was discovered in Japan. The patient showed hemolytic crises after upper respiratory infections. The enzyme activity was about 3.8% of the normal. The partially purified enzyme revealed slow anodal electrophoretic mobility, high Km NADP, marked thermal-instability, and increased affinity for a substrate analogue (deamino-NADP). A particular characteristic of this enzyme was a biphasic pH curve with a greatly increased activity at low pH values. From these results, this variant was clearly different from hitherto observed G6PD variants, and was designated G6PD Asahikawa. 相似文献
53.
Hana Dolezalova Matej Stepita-Klauco Jan Kucera Hideyuki Uchimura Makoto Hirano 《Journal of chromatography. B, Analytical technologies in the biomedical and life sciences》1978,146(1):67-76
Concentrations of cadaverine, monoacetylcadaverine and monopropionylcadaverine in the blood of schizophrenic and nonschizophrenic subjects were measured. Two groups, one from the U.S.A. the other from Japan, were tested. Monoacetylcadaverine and monopropionylcadaverine were found elevated in the blood of some schizophrenic patients in comparison with those in controls in each group. Their increase could be caused by a reduced monoamine oxidase activity or by an increased acylation in schizophrenic patients. 相似文献
54.
Masakiyo Iwai Hiroshi Kanno Masashi Hashino Jinichi Suzuki Takumi Yanaihara Tetsuya Nakayama 《Journal of chromatography. B, Analytical technologies in the biomedical and life sciences》1981,225(2)
A simple, rapid and highly specific method by selected ion monitoring (SIM), using 9α,11α-[2H2]estrone, [2,4-2H2]estradiol-17β and 2,4-[2H2]estriol as internal standards, was developed for the determination of serum estrogens during pregnancy. Serum samples were submitted to a simple extraction procedure and were analysed after formation of the trifluoroacetic anhydride derivative. The inter-assay coefficients of variation for estrone, estradiol-17β and estriol were 3.73%, 3.42% and 3.49%, respectively. The results obtained by SIM were compared with analysis performed using radioimmunoassay. 相似文献
55.
Plasma membranes were isolated from lactating bovine mammary gland. Two crude membrane fractions; medium/d 1.033 (light membrane) and 1.033/1.053 interfaces (heavy membrane), were obtained by Ficoll density gradient centrifugation of osmotically washed microsomal fraction. Two crude membranes were further purified separately by sucrose density gradient centrifugation. Both light and heavy membranes banded at a sucrose density of 1.14. The purified membranes appeared as heterogeneous smooth membrane vesicles on electron microscopy. The contaminating suborganelles were not detected. The yield of the purified membranes relative to the homogenate was 1.2%. The degree of purity of the membranes was shown by a great increase in the specific activity of 5′-nucleotidase over the homogenate of 20-fold for light membrane and of 16-fold for heavy membrane. The relative activities of Mg2+-ATPase, (Na+ + K+)-ATPase, γ-glutamyl transpeptidase, phosphodiesterase I, akaline phosphatase and xanthine oxidase were also high (12–18-times) and nearly 20% of these enzymes was recovered. The activity of marker enzyme for mitochondria, endoplasmic reticulum and Golgi apparatus was very low, while that of acid phosphatase for lysosome was relatively high (5-times). DNA and RNA contents were very low. The major polypeptides rich in other suborganelles were not detected profoundly in the membrane fraction and the polypeptide compositions in both light and heavy membranes were similar upon SDS-polyacrylamide gel electrophoresis. 相似文献
56.
57.
58.
Endothelin-3 stimulates production of endothelium-derived nitric oxide via phosphoinositide breakdown. 总被引:7,自引:0,他引:7
T Emori Y Hirata K Kanno K Ohta S Eguchi T Imai M Shichiri F Marumo 《Biochemical and biophysical research communications》1991,174(1):228-235
Cultured bovine endothelial cells (EC) have specific receptors for endothelin (ET)-3 functionally coupled to phosphoinositide breakdown. We studied whether ET-3 stimulates synthesis of nitric oxide (NO), an endothelium-derived relaxing factor that activates soluble guanylate cyclase in EC, and whether the ET-3-induced NO formation involves G-proteins. ET-3 dose-dependently stimulated production of intracellular cGMP in EC, of which effects were abolished by pretreatment with NG-monomethyl L-arginine, an inhibitor of NO synthesis, and methylene blue, an inhibitor of soluble guanylate cyclase. The stimulatory effects of ET-3 on cGMP production, inositol trisphosphate formation and increase in cytosolic free Ca2+ concentration were similarly blocked by pretreatment with pertussis toxin (PTX). These data suggest that ET-3 induces synthesis of NO mediated by phosphoinositide breakdown via PTX-sensitive G-protein in EC. 相似文献
59.
Annual production rates of reproductive organs inFagus crenata forests in the lower area of the species' range were studied using 10 litter traps in 1980–1986. The production rates of
dispersed pollen were estimated by multiplying the number of fallen male inflorescences per ha per year by the mean amount
of pollen per inflorescence before anthesis. Large annual fluctuations in the production rates of male and female inflorescences
were recognized, whereas their annual trends were synchronized with each other. Pollen production rates were within the range
1.0–6900 (mean: 1630)×109ha−1 yr−1, the maximum/minimum ratio attaining 7000.F. crenata was the lowest producer of pollen among seven tree species studied: the number of pollen grains equivalent to a single ovule
was in the range 6.0–14×104. Furthermore, the mean dry weight of a single pollen grain (3.77×10−5mg) was higher than for wind-pollinated species. Three factors seemed to cause the low seed fertility ofF. crenata. The dry-matter production rate in the best seed year reached 3252 kg ha−1 yr−1, of which pollen accounted for 259 kg ha−1 yr−1. Unproductive years with less than 10% of the maximum production occurred four times in a 7-yr period. In such years there
were fewer male and female inflorescences, and more fruit dropped as a result of insect damage. Lower nut dissemination would
play an important role in suppressing any increase in nut predators, and fewer flowers would be produced to avoid wastage
of photosynthates in a cool-temperate climate. 相似文献
60.
K Ohta Y Hirata T Imai K Kanno T Emori M Shichiri F Marumo 《Biochemical and biophysical research communications》1990,169(2):578-584
To elucidate the mechanism by which endothelin-1 (ET-1) is released from renal epithelial cells, we have investigated the effects of several compounds on release of ET-1-like immunoreactivity (LI) from LLCPK1 cell line. Thrombin, transforming growth factor-beta, cytokines (tumor necrotizing factor-alpha, interleukin-1 beta), and phorbol ester stimulated ET-1-LI release in a time- and dose-dependent manner. The cytokine-induced ET-1-LI release was not affected by indomethacin. Northern blot analysis using cDNA for porcine preproET-1 as a probe revealed a single major band corresponding to the size of ET-1 mRNA in LLCPK1. These data indicate that the preproET-1 gene is also expressed in renal epithelial cells and the release of ET-1 from renal cells is regulated by the similar mechanism to that from endothelial cells. 相似文献