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981.
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The structure of the c-myc oncogene in 17 cervical tumors and patient-matched nontumor tissues from Chinese patients residing in Taiwan was analysed. In contrast to recent reports on Mexican patients, none of the samples showed rearrangements and sequence amplification in the c-myc gene. The discrepancy may be explained by different carcinogenesis mechanisms being in operation in different geographic regions. Although no structural alterations in the c-myc gene were found in seven cervical carcinoma cell lines analysed, Northern blot analysis indicated different levels of c-myc gene expression which may be related to the presence of human papillomavirus (HPV) sequence in the cell and suggests a possible c-myc-hpv interaction in some stages of the transformation process.  相似文献   
985.
Effect of selenium on the growth of three human colon cancer cell lines   总被引:2,自引:0,他引:2  
The effects of selenium were investigated on three human colon cancer cell lines: Caco 2, HRT 18, and HT 29. At low concentrations (10-100 nM), selenium stimulated cell growth in serum-free medium. Thus, selenium is an essential trace element for cell proliferation. At higher concentrations, selenium inhibited cell growth. The rate of 75Se uptake was the same in all of the cell lines studied, but the quantity incorporated differed. GSH-Px activity was dependent on the selenium content of the medium. DNA and protein synthesis paralleled the growth curve. Comparison with the curve of viability revealed that selenium inhibited cell growth in two ways: by inhibiting DNA synthesis, without affecting cell viability, and, at higher doses, by cytotoxicity.  相似文献   
986.
In 12 anaesthetized dogs acute effects of serotonin on the atrioventricular conduction system were studied by obtaining intracardiac electrograms. The significant increase in the heart rate and decrease in aortic pressure elicited by an intravenous infusion of 50 mg/kg.min serotonin for 30 minutes were comparable to those observed in previous investigations. Our data indicate a serotonin induced acceleration of the sinus node pacemaker and atrioventricular conduction by direct and indirect mechanisms.  相似文献   
987.
988.
The action of T-activin on peritoneal macrophages of CBA mice after its introduction into the animals has been studied. In intact mice the phagocytic activity of macrophages and their resistance to the cytopathogenic action of Salmonella typhimurium live cells remains unchanged. The injection of corpuscular pertussis vaccine into mice leads to a decrease in the resistance of macrophages to the action of salmonellae. The simultaneous injection of T-activin into mice in doses of 0.1 and 1.0 microgram per animal abolishes the damaging action of the vaccine. The analysis of the in vitro action of T-activin on macrophages of intact mice revealed that the preliminary incubation of cells with the preparation sharply increases their resistance to the action of salmonellae, while its introduction simultaneously with bacteria or after them rapidly leads to the death of macrophages. The action of T-activin is supposed to be linked with triggering the biosynthetic processes mediating the resistance of macrophages to the cytopathogenic action of salmonellae.  相似文献   
989.
The investigational drug flavone-8-acetic acid (FAA) potently augments NK activity in the spleen, liver, lungs, and peritoneum in a dose-dependent manner after i.v. or i.p. administration. Augmented NK activity peaks by 24 h after FAA injection and returns to normal after 6 days. Combined treatment of established murine renal cancer with FAA and rIL-2 results in up to 80% long term survival whereas FAA or rIL-2 alone were unable to induce any long term survivors. The optimal dose of rIL-2 required for use with FAA was in the range of 10,000 to 30,000 U/day. Further studies demonstrated that the regimen of FAA plus rIL-2 administration that was effective in treating established murine renal cancer also induced a more potent augmentation of NK activity than did either FAA or rIL-2 alone. Subsequent studies revealed that the therapeutic effectiveness of FAA plus rIL-2 was significantly reduced when tumor-bearing mice were treated with anti-asialo GM1 serum. These results are consistent with a role for augmented NK activity in the therapeutic effects of FAA plus rIL-2 murine renal cancer. In addition, these studies demonstrate that FAA and rIL-2 is a useful approach for cancer treatment in that subtoxic doses of rIL-2 can be used and significant anti-tumor efficacy occurs even without accompanying adoptive immunotherapy.  相似文献   
990.
Summary The influence of mercury on microbial populations and activity of two soils from Tanzania was studied. Aretan (2-methoxyethylmercury chloride) slightly affected the microbial population of the Morogoro (Oxisol) soil, which was 107 c.f.u./g in control soil and 106 c.f.u./g in the presence of 2000 mg Hg/kg soil. Mercuric chloride at >8 mg Hg/kg soil increased the population slightly, with a sharp decrease at >100 mg Hg/kg soil, dropping ultimately to 103 c.f.u./g at 2000 mg Hg/kg soil. In the Arusha (Andept) soil, the microbial response to the two mercury compounds was the opposite of that for the Morogoro soil. Aretan sharply reduced the nitrogenase activity of aerobically incubated Morogoro soils at Hg levels >24 mg/kg, resulting in very low activity at >50 mg Hg/kg soil. Mercuric chloride increased the activity, which showed a peak at 24 mg Hg/kg soils, followed by a sharp drop at 30 mg Hg/kg and remained low thereafter. In the Arusha soil, the activity was reduced gradually by both Aretan and HgCl2. The response of the activity under anaerobic incubation in the Morogoro soil was the opposite of that under aerobic incubation, in that it was Aretan which at first increased the activity. In the Arusha soil the activity under anaerobic incubation decreased gradually over the entire range of added Hg. Nitrification was decreased by HgCl2 atlevels of <2 and <10 mg Hg/kg soil in the Arusha and Morogoro soils, respectively. The tolerance to Hg by microorganisms in this study was in the order: total population > nitrogen fixers > nitrifiers. This may be explained in terms of species diversity of the microorganisms, which may be expected to follow the same sequence.
Population et activités microbiennes dans deux sols de Tanzanie sous l'influence du mercure
Résumé On étudie l'influence du mercure sur les populations et les activités microbiennes de deux sols en provenance de Tanzanie. L'Aretan (chlorure de 2-méthoxyéthylmercure) n'affecte que faiblement la population microbienne du sol de Morogoro (oxisol), qui compte 107 individus par g dans le sol témoin et 106 individus en présence de 2000 mg de mercure par kg de sol. Le chlorure mercurique, à une dose supérieure à 8 mg de mercure par kg de sol, augmente quelque peu la population. Celle-ci décroît brutalement au delà de 100 mg de mercure par kg de sol, pour tomber finalement à 103 individus par g à 2000 mg de mercure par kg de sol. Dans le sol d'Arusha (Andept), la réponse microbienne aux deux composés mercuriels est l'inverse de celle obtenue avec le sol de Morogoro. L'Aretan réduit fortement l'activité de la nitrogénase de sols de Morogoro incubés en aérobiose à des teneurs en mercure au delà de 24 mg par kg. L'activité devient très faible au delà de 50 mg de mercure par kg de sol. Le chlorure mercurique augmente cette activité, avec un pic de 24 mg de mercure par kg de sol, suivi d'une chute sévère à 30 mg de mercure par kg. L'activité demeure faible aux doses plus fortes. Dans le sol d'Arusha, l'activité est réduite progressivement tant par l'Aretan que par HgCl2. La réponse de l'activité en incubation anaérobie dans le sol de Morogoro est l'inverse de celle en incubation aérobie en ceci que c'est l'Aretan, cette fois-ci, qui augmente d'abord l'activité. Dans le sol d'Arusha, l'activité en incubation anaérobie décroît progressivement sur l'échelle entière des concentrations d'ajout de mercure. La nitrification est réduite par HgCl2 à des seuils au dessous de 2 et 10 mg de mercure par kg de sol, respectivement pour les sols d'Arusha et de Morogoro. La tolérance des microorganismes au mercure dans cette étude est dans l'ordre: population totale > fixateurs d'azote > nitrificateurs. Ceci peut être expliqué en termes de diversité des espèces de microorganismes qui suit vraisemblablement la même séquence.
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