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971.
972.
973.
Length-weight relationships (LWRs) were assessed from four fish species in Hei River in northwest China. All specimens were collected using (fishing1 km along the river and 3 meters along the river bank) and netting (gill nets, nets: 30 × 1.2 m; mesh size: 3 × 3 cm) and shrimp cages (nets: 20.0 × 0.5 × 0.4m; mesh size: 0.5 cm) seasonally from April 2019 to October 2020. The gill nets and shrimp cages were soaked in water in the afternoon and pulled in around 10 a.m. the next day after an overnight stay. These specimens were measured for total length (L, 0.1 cm) and body weight (W, 0.1 g) while the specimens were fresh. The parameters for the LWRs were estimated with the basic statistical analyses. The study provided the new maximum total length for Gymnocypris chilianensis (21.0 cm) and Triplophysa tenuis (17.0 cm).  相似文献   
974.
C L Tai  W K Chi  D S Chen    L H Hwang 《Journal of virology》1996,70(12):8477-8484
To assess the RNA helicase activity of hepatitis C virus (HCV) nonstructural protein 3 (NS3), a polypeptide encompassing amino acids 1175 to 1657, which cover only the putative helicase domain, was expressed in Escherichia coli by a pET expression vector. The protein was purified to near homogeneity and assayed for RNA helicase activity in vitro with double-stranded RNA substrates prepared from a multiple cloning sequence and an HCV 5' nontranslated region (5'-NTR) or 3'-NTR. The enzyme acted successfully on substrates containing both 5' and 3' single-stranded regions (standard) or on substrates containing only the 3' single-stranded regions (3'/3') but failed to act on substrates containing only the 5' single-stranded regions (5'/5') or on substrates lacking the single-stranded regions (blunt). These results thus suggest 3' to 5' directionality for HCV RNA helicase activity. However, a 5'/5' substrate derived from the HCV 5'-NTR was also partially unwound by the enzyme, possibly because of unique properties inherent in the 5' single-stranded regions. Gel mobility shift analyses demonstrated that the HCV NS3 helicase could bind to either 5'- or 3'-tailed substrates but not to substrates lacking a single-stranded region, indicating that the polarity of the RNA strand to which the helicase bound was a more important enzymatic activity determinant. In addition to double-stranded RNA substrates, HCV NS3 helicase activity could displace both RNA and DNA oligonucleotides on a DNA template, suggesting that HCV NS3 too was disposed to DNA helicase activity. This study also demonstrated that RNA helicase activity was dramatically inhibited by the single-stranded polynucleotides. Taken altogether, our results indicate that the HCV NS3 helicase is unique among the RNA helicases characterized so far.  相似文献   
975.
蕤核叶片化学成分的研究   总被引:1,自引:0,他引:1  
通过对蕤核叶片化学成分进行定性检测,测出其含有蛋白质、氨基酸、多肽类、生物碱、糖类、黄酮类、有机酸、蒽醌类、酚类和鞣质、挥发油和皂甙这些物质。对不同叶位生物碱和黄酮类物质分布规律进行研究,发现随着叶位降低,两类物质含量呈现先增加后减小的规律,高含量部位分布于第三、四叶位。同时,随着叶位降低,不同叶位叶面积逐渐增加,变化差异显著。  相似文献   
976.
In neuronal development, dynamic rearrangement of actin promotes axonal growth cone extension, and spatiotemporal translation of local mRNAs in response to guidance cues directs axonal growth cone steering, where cofilin plays a critical role. While regulation of cofilin activity is well studied, regulatory mechanism for cofilin mRNA translation in neurons is unknown. In eukaryotic cells, proteins can be synthesized by cap‐dependent or cap‐independent mechanism via internal ribosome entry site (IRES)‐mediated translation. IRES‐mediated translation has been reported in various pathophysiological conditions, but its role in normal physiological environment is poorly understood. Here, we report that 5′UTR of cofilin mRNA contains an IRES element, and cofilin is predominantly translated by IRES‐mediated mechanism in neurons. Furthermore, we show that IRES‐mediated translation of cofilin is required for both axon extension and axonal growth cone steering. Our results provide new insights into the function of IRES‐mediated translation in neuronal development.  相似文献   
977.
The translation products of chromosomal DNAs of Pseudomonas aeruginosa encoding phospholipase C (heat-labile hemolysin) have been examined in T7 promoter plasmid vectors and expressed in Escherichia coli cells. A plasmid carrying a 4.7-kilobase (kb) DNA fragment was found to encode the 80-kilodalton (kDa) phospholipase C as well as two more proteins with an apparent molecular mass of 26 and 19 kDa. Expression directed by this DNA fragment with various deletions suggested that the coding region for the two smaller proteins was contained in a 1-kb DNA region. Moreover, the size of both proteins was reduced by the same amount by an internal BglII-BglII DNA deletion, suggesting that they were translated from overlapping genes. Similar results were obtained with another independently cloned 6.1-kb Pseudomonas DNA, which in addition coded for a 31-kDa protein of opposite orientation. The nucleotide sequence of the 1-kb region above revealed an open reading frame with a signal sequence typical of secretory proteins and a potential in-phase internal translation initiation site. Pulse-chase and localization studies in E. coli showed that the 26-kDa protein was a precursor of a secreted periplasmic 23-kDa protein (PlcR1) while the 19-kDa protein (PlcR2) was mostly cytoplasmic. These results indicate the expression of Pseudomonas in-phase overlapping genes in E. coli.  相似文献   
978.
Abstract

The concentrations of glucose-6-phosphate dehydrogenase, adenosine triphosphate and 2,3-diphosphoglycerate were measured in various fractions of normal human erythrocytes separated by velocity sedimentation in isotonic saline and sucrose buffer based on their tendency to aggregate. The levels of 2,3-diphosphoglycerate varied most drastically in fresh erythrocytes, being lowest in fast sedimenting cells and highest in slowly sedimenting cells. This result implies that the 2,3-diphosphoglycerate concentrations is not constant in all normal human erythrocytes and that 2,3-diphosphoglycerate may be involved in the mechanism of red cell clumping in vitro.  相似文献   
979.
凹叶厚朴大、小孢子发生和雌、雄配子体发育的研究   总被引:7,自引:0,他引:7  
凹叶厚朴花药四囊型,腺质绒毡层有1-2层细胞,小孢子形成时胞质分裂方式为修饰性同时型,小孢子四分体排列方式为左右对称型.成熟花粉粒为二细胞型。四分体和小孢子在发生时有不规则变形。子房单心皮,心皮腹面壁上着生2个胚珠,胚珠倒生型,厚珠心,双珠被;孢原细胞一个,并且自表皮下第2层细胞处分化。胚囊发育为单孢蓼型。凹叶厚朴的胚胎学特征与木兰科其它植物的胚胎学特征基本相同,属于较原始的被子植物胚胎类型。在凹叶厚朴大、小孢子发生和雌、雄配子体发育过程中存在部分败育现象。本文初步探讨了凹叶厚朴濒危的生殖生物学原因。  相似文献   
980.
This study compared heat strain during walking while wearing impermeable protective suits between fan-precooling and nonprecooling conditions. Six males engaged in 60 min of walking at a moderate speed (~2.5 km/h) in a hot environment (37 °C, 40 % relative humidity). Fanning using a fan (4.5 m/s) and spraying water over the body before wearing the suits produced significantly lower rectal temperature before the walking (37.3?±?0.1 °C vs. 37.0?±?0.1 °C, P?P?相似文献   
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