全文获取类型
收费全文 | 1827篇 |
免费 | 160篇 |
国内免费 | 2篇 |
专业分类
1989篇 |
出版年
2021年 | 18篇 |
2020年 | 9篇 |
2019年 | 19篇 |
2018年 | 27篇 |
2017年 | 17篇 |
2016年 | 31篇 |
2015年 | 60篇 |
2014年 | 65篇 |
2013年 | 83篇 |
2012年 | 94篇 |
2011年 | 84篇 |
2010年 | 61篇 |
2009年 | 54篇 |
2008年 | 93篇 |
2007年 | 90篇 |
2006年 | 92篇 |
2005年 | 102篇 |
2004年 | 116篇 |
2003年 | 107篇 |
2002年 | 96篇 |
2001年 | 35篇 |
2000年 | 21篇 |
1999年 | 18篇 |
1998年 | 34篇 |
1997年 | 23篇 |
1996年 | 32篇 |
1995年 | 19篇 |
1994年 | 17篇 |
1993年 | 26篇 |
1992年 | 23篇 |
1991年 | 14篇 |
1990年 | 20篇 |
1989年 | 14篇 |
1988年 | 17篇 |
1987年 | 16篇 |
1986年 | 9篇 |
1985年 | 9篇 |
1984年 | 18篇 |
1983年 | 16篇 |
1982年 | 24篇 |
1981年 | 20篇 |
1980年 | 22篇 |
1979年 | 9篇 |
1978年 | 16篇 |
1977年 | 12篇 |
1975年 | 11篇 |
1974年 | 17篇 |
1973年 | 21篇 |
1970年 | 9篇 |
1960年 | 9篇 |
排序方式: 共有1989条查询结果,搜索用时 13 毫秒
51.
Józef Kładny Janina Suchy Ewa Kłujszo-Grabowska Tomasz Kacperski Rodney J. Scott Grzegorz Kurzawski Jan Lubiński 《Cancer epidemiology》2009,33(2):161-163
Background: Genetic predispositions to disease have focused on highly penetrant causative changes in tumor suppressor genes or genes associated with DNA mismatch repair. New investigations are revealing new genetic associations with disease that are more subtle in their association with disease and require characterization. Methods: In this report we have examined the tumor characteristics in a group of patients who have been shown to harbor two polymorphisms in two genes that are associated with the immune system NOD2 and TNFα. Results: Colorectal cancers from patients with NOD2 3020insC and TNFα-1031T/T constitutional changes are mostly right-sided disease (OR = 2.21, p = 0.03) with a tendency to higher stages (OR = 2.41, p = 0.06), increased number of associated polyps (OR = 1.77, p = 0.16) and later age of average age of disease onset (p = 0.039). Conclusion: The results reveal that there appear to be specific characteristics associated with the tumors that may aid in determining management strategies to reduce the risk of disease. 相似文献
52.
Exposure of bovine aortic endothelial cells in vitro to oxidative stress causes a cascade of changes in cell function, culminating in cell death if the stress is sufficiently severe. Oxidative modification of proteins, as measured by the reaction of 2,4-dinitrophenylhydrazine with carbonyl groups of oxidized proteins, increased three- to fourfold in endothelial cells exposed to hydrogen peroxide or to a xanthine/xanthine oxidase system. The increase in oxidative modification of protein occurred rapidly, preceding loss of cellular ATP and eventual cell death. Oxidative modification of protein was paralleled by loss of activity of the key metabolic enzymes, glucose-6-phosphate dehydrogenase and glyceraldehyde-3-phosphate dehydrogenase. The finding that oxidative modification of protein is an early event following oxidative stress suggests that oxidative modification of protein is not only a marker for oxidative damage but also a causal factor in oxidative injury. Published by Elsevier Science Inc. 相似文献
53.
Brett R. Riddle Rodney L. Honeycutt 《Evolution; international journal of organic evolution》1990,44(1):1-15
Restriction-endonuclease-site variation of mitochondrial DNA (mtDNA) was used to investigate patterns of geographic and phylogenetic divergence within the rodent genus Onychomys. Onychomys has occupied arid habitats in the western North American deserts, shrub-steppes, and grasslands since the late Tertiary. A phylogenetic analysis of the total mtDNA restriction-site variation throughout the range of Onychomys suggests that the distribution of this genus has been affected by the same Quaternary pluvial-interpluvial climatic fluctuations that have resulted in the periodic fragmentation of arid habitats in western North America. Onychomys mtDNA haplotypes define at least five discrete geographical subsets, suggesting that there are five areas of endemism for biota restricted to arid and semiarid habitats in North America. The mtDNA-haplotype phylogeny can be used to infer an hypothesis of historical relationships among the five areas of endemism as follows: ([{(Wyoming Basin + Interior Plains + Colorado Plateaus) + (Columbia Basin + Great Basin)} + Gulf Coastal Plain] + Chihuahuan) + Western Deserts. The results of this study point to the potential use of mtDNA-haplotype phylogenies to reconstruct historical biogeographic events in Quaternary time. The utility of mtDNA variation depends in part on the ecology and distribution of the species being examined. Therefore, our hypothesized area cladogram can be tested by investigating regional relationships in other western North American taxa with distributions similar to Onychomys. 相似文献
54.
Molecular Evolution of the Pathogenicity Island of Enterotoxigenic Bacteroides fragilis Strains 下载免费PDF全文
Augusto A. Franco Rodney K. Cheng Gyung-Tae Chung Shaoguang Wu Hee-Bok Oh Cynthia L. Sears 《Journal of bacteriology》1999,181(21):6623-6633
Enterotoxigenic Bacteroides fragilis (ETBF) strains, which produce a 20-kDa zinc metalloprotease toxin (BFT), have been associated with diarrheal disease in animals and young children. Studying a collection of ETBF and nontoxigenic B. fragilis (NTBF) strains, we found that bft and a second metalloprotease gene (mpII) are contained in an approximately 6-kb pathogenicity island (termed B. fragilis pathogenicity island or BfPAI) which is present exclusively in all 113 ETBF strains tested (pattern I). Of 191 NTBF strains, 100 (52%) lack both the BfPAI and at least a 12-kb region flanking BfPAI (pattern II), and 82 of 191 NTBF strains (43%) lack the BfPAI but contain the flanking region (pattern III). The nucleotide sequence flanking the left end of the BfPAI revealed a region with the same organization as the mobilization region of the 5-nitroimidazole resistance plasmid pIP417 and the clindamycin resistance plasmid pBFTM10, that is, two mobilization genes (bfmA and bfmB) organized in one operon and a putative origin of transfer (oriT) located in a small, compact region. The region flanking the right end of the BfPAI contains a gene (bfmC) whose predicted protein shares significant identity to the TraD mobilization proteins encoded by plasmids F and R100 from Escherichia coli. Nucleotide sequence analysis of one NTBF pattern III strain (strain I-1345) revealed that bfmB and bfmC are adjacent to each other and separated by a 16-bp GC-rich sequence. Comparison of this sequence with the appropriate sequence of ETBF strain 86-5443-2-2 showed that in this ETBF strain the 16-bp sequence is replaced by the BfPAI. This result defined the BfPAI as being 6,036 bp in length and its precise integration site as being between the bfmB and bfmC stop codons. The G+C content of the BfPAI (35%) and the flanking DNA (47 to 50%) differ greatly from that reported for the B. fragilis chromosome (42%), suggesting that the BfPAI and its flanking region are two distinct genetic elements originating from very different organisms. ETBF strains may have evolved by horizontal transfer of these two genetic elements into a pattern II NTBF strain. 相似文献
55.
Boyle GM Roucou X Nagley P Devenish RJ Prescott M 《Journal of bioenergetics and biomembranes》2000,32(6):595-607
We have sought to elucidate how the oligomycin sensitivity-conferring protein (OSCP) of the mitochondrial F1F0-ATP synthase (mtATPase) can influence proton channel function. Variants of OSCP, from the yeast Saccharomyces cerevisiae, having amino acid substitutions at a strictly conserved residue (Gly166) were expressed in place of normal OSCP. Cells expressing the OSCP variants were able to grow on nonfermentable substrates, albeit with some increase in generation time. Moreover, these strains exhibited increased sensitivity to oligomycin, suggestive of modification in functional interactions between the F1 and F0 sectors mediated by OSCP. Bioenergetic analysis of mitochondria from cells expressing OSCP variants indicated an increased respiratory rate under conditions of no net ATP synthesis. Using specific inhibitors of mtATPase, in conjunction with measurement of changes in mitochondrial transmembrane potential, it was revealed that this increased respiratory rate was a result of increased proton flux through the F0 sector. This proton conductance, which is not coupled to phosphorylation, is exquisitely sensitive to inhibition by oligomycin. Nevertheless, the oxidative phosphorylation capacity of these mitochondria from cells expressing OSCP variants was no different to that of the control. These results suggest that the incorporation of OSCP variants into functional ATP synthase complexes can display effects in the control of proton flux through the F0 sector, most likely mediated through altered protein—protein contacts within the enzyme complex. This conclusion is supported by data indicating impaired stability of solubilized mtATPase complexes that is not, however, reflected in the assembly of functional enzyme complexes in vivo. Given a location for OSCP atop the F1-33 hexamer that is distant from the proton channel, then the modulation of proton flux by OSCP must occur at a distance. We consider how subtle conformational changes in OSCP may be transmitted to F0. 相似文献
56.
Anirban Ghosh Michelle Davey Ian C. Chute Steven G. Griffiths Scott Lewis Simi Chacko David Barnett Nicolas Crapoulet Sébastien Fournier Andrew Joy Michelle C. Caissie Amanda D. Ferguson Melissa Daigle M. Vicki Meli Stephen M. Lewis Rodney J. Ouellette 《PloS one》2014,9(10)
Recent studies indicate that extracellular vesicles are an important source material for many clinical applications, including minimally-invasive disease diagnosis. However, challenges for rapid and simple extracellular vesicle collection have hindered their application. We have developed and validated a novel class of peptides (which we named venceremin, or Vn) that exhibit nucleotide-independent specific affinity for canonical heat shock proteins. The Vn peptides were validated to specifically and efficiently capture HSP-containing extracellular vesicles from cell culture growth media, plasma, and urine by electron microscopy, atomic force microscopy, sequencing of nucleic acid cargo, proteomic profiling, immunoblotting, and nanoparticle tracking analysis. All of these analyses confirmed the material captured by the Vn peptides was comparable to those purified by the standard ultracentrifugation method. We show that the Vn peptides are a useful tool for the rapid isolation of extracellular vesicles using standard laboratory equipment. Moreover, the Vn peptides are adaptable to diverse platforms and therefore represent an excellent solution to the challenge of extracellular vesicle isolation for research and clinical applications. 相似文献
57.
IL-1beta suppresses prolonged Akt activation and expression of E2F-1 and cyclin A in breast cancer cells 总被引:1,自引:0,他引:1
Shen WH Jackson ST Broussard SR McCusker RH Strle K Freund GG Johnson RW Dantzer R Kelley KW 《Journal of immunology (Baltimore, Md. : 1950)》2004,172(12):7272-7281
Cell cycle aberrations occurring at the G(1)/S checkpoint often lead to uncontrolled cell proliferation and tumor growth. We recently demonstrated that IL-1beta inhibits insulin-like growth factor (IGF)-I-induced cell proliferation by preventing cells from entering the S phase of the cell cycle, leading to G(0)/G(1) arrest. Notably, IL-1beta suppresses the ability of the IGF-I receptor tyrosine kinase to phosphorylate its major docking protein, insulin receptor substrate-1, in MCF-7 breast carcinoma cells. In this study, we extend this juxtamembrane cross-talk between cytokine and growth factor receptors to downstream cell cycle machinery. IL-1beta reduces the ability of IGF-I to activate Cdk2 and to induce E2F-1, cyclin A, and cyclin A-dependent phosphorylation of a retinoblastoma tumor suppressor substrate. Long-term activation of the phosphatidylinositol 3-kinase/Akt signaling pathway, but not the mammalian target of rapamycin or mitogen-activated protein kinase pathways, is required for IGF-I to hyperphosphorylate retinoblastoma and to cause accumulation of E2F-1 and cyclin A. In the absence of IGF-I to induce Akt activation and cell cycle progression, IL-1beta has no effect. IL-1beta induces p21(Cip1/Waf1), which may contribute to its inhibition of IGF-I-activated Cdk2. Collectively, these data establish a novel mechanism by which prolonged Akt phosphorylation serves as a convergent target for both IGF-I and IL-1beta; stimulation by growth factors such as IGF-I promotes G(1)-S phase progression, whereas IL-1beta antagonizes IGF-I-induced Akt phosphorylation to induce cytostasis. In this manner, Akt serves as a critical bridge that links proximal receptor signaling events to more distal cell cycle machinery. 相似文献
58.
59.
Su-Ping Li Ryszard Ochyra Peng-Cheng Wu Rodney D. Seppelt Ming-Hong Cai Hai-Ying Wang Cheng-Sen Li 《Polar Biology》2009,32(10):1415-1425
Drepanocladus longifolius (Mitt.) Paris is recorded for the first time from King George Island, South Shetland Islands, in the maritime Antarctic.
It was collected in West Lake during the 23rd Chinese National Antarctic Research Expedition in 2006–2007. The moss was found
at a depth of 5–6 m attached to the bed of the lake. The stems of the moss are about 1–1.5 m in length. The moss exhibits
seasonal growth patterns, with shorter branch internodes, more widely spaced leaves and more branches in summer than in winter.
Most of the branches are initiated in summer. The annual shoot extension is about 3–6 cm, which implies that the plants must
be at least 15 years of age. The distribution of aquatic moss species and records in Antarctica is outlined and discussed
and the nomenclature of previous reports clarified. 相似文献
60.