全文获取类型
收费全文 | 6504篇 |
免费 | 331篇 |
国内免费 | 234篇 |
专业分类
7069篇 |
出版年
2024年 | 8篇 |
2023年 | 110篇 |
2022年 | 148篇 |
2021年 | 160篇 |
2020年 | 153篇 |
2019年 | 168篇 |
2018年 | 139篇 |
2017年 | 128篇 |
2016年 | 132篇 |
2015年 | 203篇 |
2014年 | 340篇 |
2013年 | 424篇 |
2012年 | 274篇 |
2011年 | 273篇 |
2010年 | 237篇 |
2009年 | 262篇 |
2008年 | 330篇 |
2007年 | 274篇 |
2006年 | 248篇 |
2005年 | 238篇 |
2004年 | 242篇 |
2003年 | 215篇 |
2002年 | 221篇 |
2001年 | 155篇 |
2000年 | 133篇 |
1999年 | 138篇 |
1998年 | 146篇 |
1997年 | 126篇 |
1996年 | 129篇 |
1995年 | 158篇 |
1994年 | 143篇 |
1993年 | 127篇 |
1992年 | 99篇 |
1991年 | 108篇 |
1990年 | 101篇 |
1989年 | 76篇 |
1988年 | 78篇 |
1987年 | 59篇 |
1986年 | 47篇 |
1985年 | 68篇 |
1984年 | 69篇 |
1983年 | 39篇 |
1982年 | 50篇 |
1981年 | 23篇 |
1980年 | 25篇 |
1979年 | 19篇 |
1978年 | 6篇 |
1977年 | 8篇 |
1976年 | 6篇 |
1973年 | 2篇 |
排序方式: 共有7069条查询结果,搜索用时 0 毫秒
51.
Franz Uiblein 《Environmental Biology of Fishes》1992,33(3):311-316
Synopsis Experimental data on snapping behavior of laboratory reared zährte, Vimba elongata, indicate that this species chooses between different food searching methods. If visibility is good, mainly directed snaps are employed for immediate food location. However, under conditions of reduced visibility undirected snapping and sampling methods are adopted. In the field, zährte may use sampling to acquire foraging benefits from stochastically distributed, hidden resources, like sediment dwelling prey. In the experiments this species continued to sample the bottom even in situations without any chance of prey detection. It is therefore concluded that zährte's searching decisions, apart from incorporating external information on prey occurrence, are controlled by internal expectations of long term benefits derived from sampling. 相似文献
52.
53.
Pea lectin is correctly processed,stable and active in leaves of transgenic potato plants 总被引:5,自引:0,他引:5
Glyn A. Edwards Andrew Hepher Stephen P. Clerk Donald Boulter 《Plant molecular biology》1991,17(1):89-100
A gene encoding the preproprotein of the pea (Pisum sativum) lectin was expressed in transgenic potato plants using a cauliflower mosaic virus (CaMV) 35S promoter or a tobacco ribulose bisphosphate carboxylase small subunit (ssRubisco) promoter. Presence of the pea lectin to levels greater than 1% of total soluble leaf protein was detected by radioimmunoassay (RIA). The pattern of expression derived from the two promoters was established using both RIA and a squash-blot immunolocalisation technique. Western blotting demonstrated that the preproprotein was correctly processed, generating and subunits that assembled to give an isolectin form observed in pea seeds and roots. It was also found that the haemagglutination activity and specificity of pea lectin synthesised in transgenic potato leaves was comparable to purified lectin from pea cotyledons. 相似文献
54.
Vidadi M. Yusibov Pak Chun II Viacheslav M. Andrianov Eleonora S. Piruzian 《Plant molecular biology》1991,17(4):825-836
The tumour-inducing T-DNA gene 4 (T-cyt gene) of the nopaline Ti plasmid pTiC58 was cloned and introduced into tobacco cells by leaf disc transformation using Agrobacterium plasmid vectors. Tobacco shoots exposed to elevated cytokinin levels were unable to develop roots and lacked apical dominance. Using exogenously applied phytohormone manipulations we were able to regenerate morphologically normal transgenic tobacco plants which differed in endogenous cytokinin levels from normal untransformed plants. Although T-cyt gene mRNA levels, as revealed by dot-blot hybridization data, in these rooting plants were only about half those in primary transformed shoots the total amount of cytokinins was much lower than in crown gall tissue or cytokinin-type transformed shoots as reported by others. Nevertheless the cytokinin content in T-cyt plants was about 3 times greater than in control tobacco plants.Elevated cytokinin levels have been shown to change the expression of several plant genes, including some nuclear genes encoding chloroplast proteins. Our results show that the mRNA levels of chloroplast rbcL gene increase in cytokinin-type transgenic tobacco plants as compared with untransformed plants. Data obtained suggest that T-cyt transgenic plants are a good model for studying plant gene activity in different parts of the plant under endogenous cytokinin stress. 相似文献
55.
High-level expression of a tobacco chitinase gene in Nicotiana sylvestris. Susceptibility of transgenic plants to Cercospora nicotianae infection 总被引:12,自引:0,他引:12
Jean-Marc Neuhaus Patricia Ahl-Goy Ursula Hinz Susan Flores Frederick Meins Jr. 《Plant molecular biology》1991,16(1):141-151
Endochitinases (E.C. 3.2.14, chitinase) are believed to be important in the biochemical defense of plants against chitin-containing fungal pathogens. We introduced a gene for class I (basic) tobacco chitinase regulated by Cauliflower Mosaic Virus 35S-RNA expression signals into Nicotiana sylvestris. The gene was expressed to give mature, enzymatically active chitinase targeted to the intracellular compartment of leaves. Most transformants accumulated extremely high levels of chitinase-up to 120-fold that of non-transformed plants in comparable tissues. Unexpectedly, some transformants exhibited chitinase levels lower than in non-transformed plants suggesting that the transgene inhibited expression of the homologous host gene. Progeny tests indicate this effect is not permanent. High levels of chitinase in transformants did not substantially increase resistance to the chitin-containing fungus Cercospora nicotiana, which causes Frog Eye disease. Therefore class I chitinase does not appear to be the limiting factor in the defense reaction to this pathogen. 相似文献
56.
P-glycoprotein as multidrug transporter: a critical review of current multidrug resistant cell lines
MDR has been studied extensively in mammalian cell lines. According to usual practice, the MDR phenotype is characterized by the following features: cross resistance to multiple chemotherapeutic agents (lipophilic cations), defective intracellular drug accumulation and retention, overexpression of P-gp (often accompanied by gene amplification), and reversal of the phenotype by addition of calcium channel blockers. An hypothesis for the function of P-gp has been proposed in which P-gp acts as a carrier protein that actively extrudes MDR compounds out of the cells. However, basic questions, such as what defines the specificity of the pump and how is energy for active efflux transduced, remain to be answered. Furthermore, assuming that P-gp acts as a drug transporter, one will expect a relationship between P-gp expression and accumulation defects in MDR cell lines. A review of papers reporting 97 cell lines selected for resistance to the classical MDR compounds has revealed that a connection exists in most of the reported cell lines. However, several exceptions can be pointed out. Furthermore, only a limited number of well characterized series of sublines with different degrees of resistance to a single agent have been reported. In many of these, a correlation between P-gp expresson and transport properties can not be established. Co-amplification of genes adjacent to the mdr1 gene, mutations [122], splicing of mdr1 RNA [123], modulation of P-gp by phosphorylation [124] or glycosylation [127], or experimental conditions [26,78] could account for some of the complexity of the phenotype and the absence of correlation in some of the cell lines. However, both cell lines with overexpression of P-gp without increased efflux [i.e., 67,75] and cell lines without P-gp expression and accumulation defects/increased efflux [i.e., 25,107] have been reported. Thus, current results from MDR cell lines contradict - but do not exclude - that P-gp acts as multidrug transporter. Other models for the mechanism of resistance have been proposed: (1) An energy-dependent permeability barrier working with greater efficacy in resistant cells. This hypothesis is supported by studies of influx which, although few, all except one demonstrate decreased influx in resistant cells; (2) Resistant cells have a greater endosomal volume, and a greater exocytotic activity accounts for the efflux. Furthermore, large amounts of P-gp in the plasma membrane altering the ultrastructure and generalized changes, such as increases or decreases in membrane fluidity, alterations in lipid composition, changes in transmembrane pH gradient and membrane potential have been described in MDR cell lines and could account for some of the findings. 相似文献
57.
Twila Jackson Michael F. Allard Catherine M. Sreenan Lisa K. Doss Sanford P. Bishop Judith L. Swain 《Molecular and cellular biochemistry》1991,104(1-2):15-19
Transgenic animals provide a model system to elucidate the role of specific proteins in development. This model is now being used increasingly in the cardiovascular system to study cardiac growth and differentiation. During cardiac myocyte development a transition occurs from hyperplastic to hypertrophic growth. In the heart the switch from myocyte proliferation to terminal differentiation is synchronous with a decrease in c-myc mRNA abundance. To determine whether c-myc functions to regulate myocyte proliferation and/or differentiation, we examined the in vivo effect of increasing c-myc expression during fetal development and of preventing the decrease in c-myc mRNA expression that normally occurs during myocyte development. The model system used was a strain of transgenic mice exhibiting constitutive expression of c-myc mRNA in cardiac myocytes throughout development. Increased c-myc mRNA expression is associated with both atrial and ventricular enlargement in the transgenic mice. This increase in cardiac mass is secondary to myocyte hyperplasia, with the transgenic hearts containing greater than twice as many myocytes as nontransgenic hearts. The results of this study indicate that constitutive expression of c-myc mRNA in the heart during development results in enhanced hyperplastic growth, and suggest a regulatory role for the c-myc protooncogene in cardiac myogenesis. 相似文献
58.
Jorge E. Moreira Arthur R. Hand L. A. Håkan Borg Stellan Sandler Michael Welsh Nils Welsh Décio L. Eizirik 《Virchows Archiv. B, Cell pathology including molecular pathology》1991,60(1):337-344
We have previously described a preferential reduction in the secretory response to nutrient secretagogues in pancreatic mouse
islets maintained in culture after in vitro exposure to streptozotocin (SZ). This reduction was associated with an impaired
substrate metabolism at the mitochondrial level. To further clarify this issue, mouse pancreatic islets were exposed in vitro
to 2.2 mM SZ for 30 min. At 4 h after SZ treatment ultrastructural changes were apparent in the endoplasmic reticulum and
Golgi areas of the B-cells. However, 2 and 6 days following SZ exposure the B-cells appeared well preserved, except for a
marked decrease in the number of insulin-containing secretory granules. A morphometric analysis of the B-cells 6 days after
SZ exposure showed a normal B-cell size and a normal volume fraction of B-cell mitochondria. However, there was a decrease
in total islet size and a 13% decrease in the volume fraction of B-cells in the islets. These mouse islets exhibited a decreased
content of the mitochondrial DNA-encoded cytochrome b mRNA, as evaluated by dot-blot analysis. As a whole, the data obtained
indicate that SZ treatment does not induce a decrease in the number of mitochondria or long-lasting ultrastructural damage
to this organelle. However, there is a clear decrease in the cytochrome b mRNA, suggesting that SZ can induce damage to the
mitochondrial DNA. 相似文献
59.
60.
Flora Sánchez Angeles Touriño Susana Traseira Agustín Pérez-Aranda Víctor Rubio Miguel A. Peñalva 《Molecular & general genetics : MGG》1986,205(2):248-252
Summary We cloned the Penicillium chrysogenum trpC gene from a genomic library by complementation of an Escherichia coli trpC mutant lacking phosphoribosylanthranilate isomerase activity. The gene ecodes a 2.7 kb poly(A)+ RNA. We localized the gene by sequence analysis in a 2.9 kb DNA insert found in the smallest plasmid selected from the library. Sequence data strongly suggest that the organization of the gene is similar to that described in other Ascomycetes. We found that a DNA fragment which codes only for the carboxy-terminal protion of the polypeptide is sufficient for complementation of the E. coli trpC9830 mutation. 相似文献