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141.
Jie Dai Jun Zhou Hongmei Liu Kaixun Huang 《Journal of biological inorganic chemistry》2016,21(8):1037-1046
Selenite and ebselen supplementation has been shown to possess anti-cataract potential in some experimental animal models of cataract, however, the underlying mechanisms remain unclear. The present study was designed to evaluate the anti-cataract effects and the underlying mechanisms of selenite and ebselen supplementation on galactose induced cataract in rats, a common animal model of sugar cataract. Transmission electron microscopy images of lens fiber cells (LFC) and lens epithelial cells (LEC) were observed in d-galactose-induced experimental cataractous rats treated with or without selenite and ebselen, also redox homeostasis and expression of proteins such as selenoprotein R (SELR), 15kD selenoprotein (SEP15), superoxide dismutase 1 (SOD1), catalase (CAT), β-crystallin protein, aldose reductase (AR) and glucose-regulated protein 78 (GRP78) were estimated in the lenses. The results showed that d-galactose injection injured rat lens and resulted in cataract formation; however, selenite and ebselen supplementation markedly alleviated ultrastructural injury of LFC and LEC. Moreover, selenite and ebselen supplementation could mitigate the oxidative damage in rat lens and increase the protein expressions of SELR, SEP15, SOD1, CAT and β-crystallin, as well as decrease the protein expressions of AR and GRP78. Taken together, these findings for the first time reveal the anti-cataract potential of selenite and ebselen in galactosemic cataract, and provide important new insights into the anti-cataract mechanisms of selenite and ebselen in sugar cataract. 相似文献
142.
Rodolfo Jaffé Antonio Castilla Nathaniel Pope Vera Lucia Imperatriz-Fonseca Jean Paul Metzger Maria Cristina Arias Shalene Jha 《Conservation Genetics》2016,17(2):267-278
Pollination services are increasingly threatened by the loss and modification of natural habitats, posing a risk to the maintenance of both native plant biodiversity and agricultural production. In order to safeguard pollination services, it is essential to examine the impacts of habitat degradation on the population dynamics of key pollinators and identify potential “rescue pollinators” capable of persisting in these human-altered landscapes. Using a landscape genetic approach, we assessed the impact of landscape structure on genetic differentiation in the widely-distributed tropical stingless bee Trigona spinipes (Apidae: Meliponini) across agricultural landscape mosaics composed of coffee plantations and Atlantic forest fragments in southeastern Brazil. We genotyped 115 bees at 16 specific and highly polymorphic microsatellite loci, developed using next-generation sequencing. Our results reveal that T. spinipes is capable of dispersing across remarkably long distances, as we did not find genetic differentiation across a 200 km range, nor fine-scale spatial genetic structure. Furthermore, gene flow was not affected by forest cover, land cover, or elevation, indicating that reproductive individuals are able to disperse well through agricultural landscapes and across altitudinal gradients. We also found evidence of a recent population expansion, suggesting that this opportunistic stingless bee is capable of colonizing degraded habitats. Our results thus suggest that T. spinipes can persist in heavily-altered landscapes and can be regarded as a rescue pollinator, potentially compensating for the decline of other native pollinators in degraded tropical landscapes. 相似文献
143.
Lee CH 《Applied microbiology and biotechnology》2012,93(2):517-523
One of the primary limitations of cancer therapy is lack of selectivity of therapeutic agents to tumor cells. Current efforts
are focused on discovering and developing anticancer agents that selectively target only tumor cells and spare normal cells
to improve the therapeutic index. The use of preferentially replicating bacteria as an oncolytic agent is one of the innovative
approaches for the treatment of cancer. This is based on the observation that some obligate or facultative anaerobic bacteria
are capable of multiplying selectively in tumors and inhibiting their growth. Meanwhile, bacteria have been demonstrated to
colonize and destroy tumor, and have emerged as biological gene vectors to tumor microenvironment. To improve the efficacy
and safety of the bacterial therapy, a further understanding of bacteria between with immune system is required. Furthermore,
we want to evaluate how bacterial infection facilitates the “bystander effect” of chemotherapeutic agent and assess if it
can be used for additional antitumor effect when combined with chemotherapy. This study may not only evaluate therapeutic
efficacy of bacteria for the treatment of cancer but also elucidate the mechanisms underlying antitumor activities mediated
by bacteria, which involve host immune responses and the cellular molecular responses. 相似文献
144.
Immune suppression remains a consistent obstacle to successful anti-tumor immune responses. As tumors develop, they create
a microenvironment that not only supports tumor growth and metastasis but also reduces potential adaptive immunity to tumor
antigens. Among the many components of this tumor microenvironment is a population of dendritic cells which exert profound
immune suppressive effects on T cells. In this review, we discuss our recent findings related to these tumor-associated dendritic
cells and how targeting them may serve to generate more durable anti-tumor immune responses. 相似文献
145.
Jay G. Forsythe Sloane L. English Rachel E. Simoneaux Arthur L. Weber 《Origins of life and evolution of the biosphere》2018,48(2):201-211
A one-pot method was developed for the preparation of a series of β-alanine standards of moderate size (2 to ≥12 residues) for studies concerning the prebiotic origins of peptides. The one-pot synthesis involved two sequential reactions: (1) dry-down self-condensation of β-alanine methyl ester, yielding β-alanine peptide methyl ester oligomers, and (2) subsequent hydrolysis of β-alanine peptide methyl ester oligomers, producing a series of β-alanine peptide standards. These standards were then spiked into a model prebiotic product mixture to confirm by HPLC the formation of β-alanine peptides under plausible reaction conditions. The simplicity of this approach suggests it can be used to prepare a variety of β-peptide standards for investigating differences between α- and β-peptides in the context of prebiotic chemistry. 相似文献
146.
Agnes Simonyi Yan He Wenwen Sheng Albert Y. Sun W. Gibson Wood Gary A. Weisman Grace Y. Sun 《Molecular neurobiology》2010,41(2-3):73-86
Alzheimer’s disease (AD) is marked by an increase in the production of extracellular beta amyloid plaques and intracellular neurofibrillary tangles associated with a decline in brain function. Increases in oxidative stress are regarded as an early sign of AD pathophysiology, although the source of reactive oxygen species (ROS) and the mechanism(s) whereby beta amyloid peptides (Aβ) impact oxidative stress have not been adequately investigated. Recent studies provide strong evidence for the involvement of NADPH oxidase and its downstream oxidative signaling pathways in the toxic effects elicited by Aβ. ROS produced by NADPH oxidase activate multiple signaling pathways leading to neuronal excitotoxicity and glial cell-mediated inflammation. This review describes recent studies demonstrating the neurotoxic effects of Aβ in conjunction with ROS produced by NADPH oxidase and the downstream pathways leading to activation of cytosolic phospholipase A2 (PLA2) and secretory PLA2. In addition, this review also describes recent studies using botanical antioxidants to protect against oxidative damage associated with AD. Investigating the metabolic and signaling pathways involving Aβ NADPH oxidase and PLA2 can help understand the mechanisms underlying the neurodegenerative effects of oxidative stress in AD. This information should provide new therapeutic approaches for prevention of this debilitating disease. 相似文献
147.
Differential expression analysis for sequence count data 总被引:22,自引:0,他引:22
High-throughput sequencing assays such as RNA-Seq, ChIP-Seq or barcode counting provide quantitative readouts in the form
of count data. To infer differential signal in such data correctly and with good statistical power, estimation of data variability
throughout the dynamic range and a suitable error model are required. We propose a method based on the negative binomial distribution,
with variance and mean linked by local regression and present an implementation, DESeq, as an R/Bioconductor package. 相似文献
148.
Corti A 《Cellular and molecular neurobiology》2010,30(8):1163-1170
Chromogranin A (CgA) is an acidic glycoprotein belonging to a family of regulated secretory proteins stored in the dense core
granules of the adrenal medulla and of many other neuroendocrine cells and neurons. This protein is frequently used as a diagnostic
and prognostic serum marker for a range of neuroendocrine tumors. Circulating CgA is also increased in patients with other
diseases, including subpopulations of patients with non-neuroendocrine tumors, with important prognostic implications. A growing
body of evidence suggests that CgA is more than a diagnostic/prognostic marker for cancer patients. Indeed, results of in
vitro experiments and in vivo studies in animal models suggest that this protein and its fragments can affect several elements
of the tumor microenvironment, including fibroblasts and endothelial cells. In this article, recent findings implicating CgA
as a modulator of the tumor microenvironment and suggesting that abnormal secretion of CgA could play important roles in tumor
progression and response to therapy in cancer patients are reviewed and discussed. 相似文献
149.
Degradation of proteins mediated by ubiquitin-proteasome pathway (UPP) plays important roles in the regulation of eukaryotic cell cycle. In this study, the functional roles and regulatory mechanisms of UPP in mouse oocyte meiotic maturation, fertilization, and early embryonic cleavage were studied by drug-treatment, Western blot, antibody microinjection, and confocal microscopy. The meiotic resumption of both cumulus-enclosed oocytes and denuded oocytes was stimulated by two potent, reversible, and cell-permeable proteasome inhibitors, ALLN and MG-132. The metaphase I spindle assembly was prevented, and the distribution of ubiquitin, cyclin B1, and polo-like kinase 1 (Plk1) was also distorted. When UPP was inhibited, mitogen-activated protein kinase (MAPK)/p90rsk phosphorylation was not affected, but the cyclin B1 degradation that occurs during normal metaphase-anaphase transition was not observed. During oocyte activation, the emission of second polar body (PB2) and the pronuclear formation were inhibited by ALLN or MG-132. In oocytes microinjected with ubiquitin antibodies, PB2 emission and pronuclear formation were also inhibited after in vitro fertilization. The expression of cyclin B1 and the phosphorylation of MAPK/p90rsk could still be detected in ALLN or MG-132-treated oocytes even at 8 h after parthenogenetic activation or insemination, which may account for the inhibition of PB2 emission and pronuclear formation. We also for the first time investigated the subcellular localization of ubiquitin protein at different stages of oocyte and early embryo development. Ubiquitin protein was accumulated in the germinal vesicle (GV), the region between the separating homologous chromosomes, the midbody, the pronuclei, and the region between the separating sister chromatids. In conclusion, our results suggest that the UPP plays important roles in oocyte meiosis resumption, spindle assembly, polar body emission, and pronuclear formation, probably by regulating cyclin B1 degradation and MAPK/p90rsk phosphorylation. 相似文献
150.
Rhamnolipids, produced by Pseudomonas aeruginosa, represent an important group of biosurfactants having various industrial, environmental, and medical applications. Current
methods for rhamnolipid quantification involve the use of strong hazardous acids/chemicals, indirect measurement of the concentration
of sugar moiety, or require the availability of expensive equipment (HPLC-MS). A safer, easier method that measures the whole
rhamnolipid molecules would significantly enhance strain selection, metabolic engineering, and process development for economical
rhamnolipid production. A semi-quantitative method was reported earlier to differentiate between the rhamnolipid-producing
and non-producing strains using agar plates containing methylene blue and cetyl trimethylammonium bromide (CTAB). In this
study, a rapid and simple method for rhamnolipid analysis was developed by systematically investigating the complexation of
rhamnolipids and methylene blue, with and without the presence of CTAB. The method relies on measuring the absorbance (at
638 nm) of the rhamnolipid−methylene blue complex that partitions into the chloroform phase. With P. aeruginosa fermentation samples, the applicability of this method was verified by comparison of the analysis results with those obtained
from the commonly used anthrone reaction technique. 相似文献