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991.
Anticodon nuclease is a bacterial restriction enzyme directed against tRNA(Lys). We report that anticodon nuclease also cleaves mammalian tRNA(Lys) molecules, with preference and site specificity shown towards the natural substrate. Expression of the anticodon nuclease core polypeptide PrrC in HeLa cells from a recombinant vaccinia virus elicited cleavage of intracellular tRNA(Lys),3. The data justify an inquiry into the possible application of anticodon nuclease as an inhibitor of tRNA(Lys),3-primed HIV replication. They also indicate that the anticodon region of tRNA(Lys) is a substrate recognition site and suggest that PrrC harbors the enzymatic activity.  相似文献   
992.
The use of short tandem repeat polymorphisms (STRPs) as marker loci for linkage analysis is becoming increasingly important due to their large numbers in the human genome and their high degree of polymorphism. Fluorescence-based detection of the STRP pattern with an automated DNA sequencer has improved the efficiency of this technique by eliminating the need for radioactivity and producing a digitized autoradiogram-like image that can be used for computer analysis. In an effort to simplify the procedure and to reduce the cost of fluorescence STRP analysis, we have developed a technique known as multiplexing STRPs with tailed primers (MSTP) using primers that have a 19-bp extension, identical to the sequence of an M13 sequencing primer, on the 5′ end of the forward primer in conjunction with multiplexing several primer pairs in a single polymerase chain reaction (PCR) amplification. The banding pattern is detected with the addition of the M13 primer-dye conjugate as the sole primer conjugated to the fluorescent dye, eliminating the need for direct conjugation of the infrared fluorescent dye tn the STRP primers. The use of MSTP for linkage analysis greatly reduces the number of PCR reactions. Up to five primer pairs can be multiplexed together in the same reaction. At present, a set of 148 STRP markers spaced at an average genetic distance of 28 cM throughout the autosomal genome can be analyzed in 37 sets of multiplexed amplification reactions. We have automated the analysis of these patterns for linkage using software that both detects the STRP banding pattern and determines their sizes. This information can then be exported in a user-defined format from a database manager for linkage analysis.  相似文献   
993.
994.
Roe deer ( Capreolus capreolus ) spacing behaviour, during the period between mother-fawn separation and home range establishment, was studied in southern Sweden during 1987–1992. Data were collected, using telemetry, in two non-hunted populations. Females dispersed either as yearlings, or as 2- or 3-year-olds after having migrated between non-overlapping summer and winter ranges for one and two seasons, respectively. Seasonal migration usually ended with permanent settlement in the new summer area. Males dispersed as one- or two-year-olds, or remained philopatric. Median distance moved was c. 2 km with no significant sex-bias. Both populations underwent one increase, and one stable phase. During the increase phase, the frequency of yearling dispersal was 70% in one of the populations, but dropped to 20% at high density. This drop paralleled a 14% decrease in yearling winter weights. In the other population, yearling dispersal frequency was 56% during the increase phase. This population stopped increasing at an intermediate density and dispersal frequency was kept at 75%. Weights remained high in this population. In neither of the populations, at intermediate and high densities, was a sex-bias in dispersal among yearlings evident. Dispersers were on average heavier than philopatrics. High juvenile winter weight did not predestinate yearlings to dispersal, whereas low weight seemed to prevent dispersal. On the basis of these relationships, we propose a hypothesis relating dispersal to body condition, in order to explain dispersal tendency at different population densities. Further, we suggest the reason for female migration is the advantage of residing in a group during winters when predation risk is high. Since it is difficult for females (but not for males) to join non-relatives, dispersers must go back to the natal area as long as they have too few offspring to form their own matriarchal group.  相似文献   
995.
Two strains ofAspergillus niger were cultured in solid-state fermentation system on carob pods ground from 1.25 to 8 mm diam. A particle size of 2.5 mm gave the highest protein content of the final product (20%, w/w) and 52% of the total soluble carbohydrates were utilized. The total tannin concentration of the carob pods decreased by 83% in 4 days of fermentation.T. Smail and O. Salhi are with the Laboratory of Microbiology, U.R.B.A.F., Institute of Biology, Tizi-Ouzou University, Algeria. J.S. Knapp is with the Department of Microbiology, The University of Leeds, Leeds LS2 9JT, UK;  相似文献   
996.
997.
Adult healthy subjects did not manifest any difference in latency and amplitude of the wave P300 elicited by a positive ("good") and negative ("error") reinforcing stimuli. After the negative reinforcement, the P300 wave amplitude decreases in response to the standard stimulus (light bars) and increases to a lesser degree in response to test stimuli (the same bars but presented with different pauses). In the processes of learning to assess time microintervals in comparison with the standard, the latency of wave P300 to the test stimuli shortens. It is suggested that formation and consolidation of feedback connection elaborated with the participation of a reinforcing verbal stimulus constitute the physiological basis for learning of comparative assessment of time microintervals.  相似文献   
998.
Cells were subjected to a range of 45Ca2+ influx loads with A23187. We measured cell 45Ca2+ with time and A23187 dose, and the apparent 45Ca2+ influxes (≡“J(in,app)”) at Ca2+ steady state. We also measured endogeneous exchangeable and total cell Ca2+, which were 50 and 17–220 μM respectively. The effects of A23187 and Ca2+ on cell ATP, swelling, net Cl permeability, and cell morphology were measured. These were modest and do not affect our conclusions.J(in,app) 3 × 10−4 [A23187]2.9·[Ca2+(o)]μmoles/l·min with 92–552 μM [Ca2+(o)] (≡ external Ca2+ concentration) and 0–7 μM A23187. J(in,app) was increased an order of magnitude by vanadate and is probably much less than the true influx. The least unlikely explanation found for the high [A23187] exponent, 2.9, was that most of the Ca2+ crossing the membrane is expelled by the pump before it can move deeper into the cell.Calcium pumping increased rapidly in response to increased influx, but the steady state cell 45Ca2+ was approximately proportional to J(in,app) rather than approximately constant between 10 and 120 μmoles/l·min with 184 μM [Ca2+(o)]. This is not the result expected from a simple feedback mechanism.At high A23187 doses the pump appears fully activated resulting in a linear relation between cell/medium 45Ca2+ and [A23187]−2. From the plot we calculated α≡free/total exchangeable Ca2+ = 0.38 ± 0.08 (n = 3) and a maximum pump rate, “Pmax” = 78 μmole/l·min. Pmax is underestimated insofar as J(in,app) is less than the true influx.  相似文献   
999.
When isolated liver nuclei from methylchol-anthrene-treated rats are incubated with benzopyrene, covalent adducts are formed between DNA and the ultimate carcinogen, benzopyrene diol epoxide. Brief digestion with DNaseI, or micrococcal nuclease has been used to demonstrate that benzopyrene metabolites bind more readily to DNA in chromatin regions with a more open, active conformation than to inactive chromatin.  相似文献   
1000.
Carbostimulin is studied for the effect it exerts on indices of the acid-base equilibrium of blood, content of certain tricarboxylic-cycle metabolites and free amino acids and formation of antibodies in rats. It is established that carbostimulin feeding increases the total carbon dioxide, pyruvate and lactate concentration in blood, the content of ammonium, glutamine and certain free amino acids being decreased. Oxidation processes in the liver mitochondria and biosynthesis of antibodies in experimental animals are shown to be more intensive than in the control ones.  相似文献   
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