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61.
Langlois MJ Bergeron S Bernatchez G Boudreau F Saucier C Perreault N Carrier JC Rivard N 《PloS one》2010,5(12):e15742
Background
The PTEN phosphatase acts on phosphatidylinositol 3,4,5-triphosphates resulting from phosphatidylinositol 3-kinase (PI3K) activation. PTEN expression has been shown to be decreased in colorectal cancer. Little is known however as to the specific cellular role of PTEN in human intestinal epithelial cells. The aim of this study was to investigate the role of PTEN in human colorectal cancer cells.Methodology/Principal Findings
Caco-2/15, HCT116 and CT26 cells were infected with recombinant lentiviruses expressing a shRNA specifically designed to knock-down PTEN. The impact of PTEN downregulation was analyzed on cell polarization and differentiation, intercellular junction integrity (expression of cell-cell adhesion proteins, barrier function), migration (wound assay), invasion (matrigel-coated transwells) and on tumor and metastasis formation in mice. Electron microscopy analysis showed that lentiviral infection of PTEN shRNA significantly inhibited Caco-2/15 cell polarization, functional differentiation and brush border development. A strong reduction in claudin 1, 3, 4 and 8 was also observed as well as a decrease in transepithelial resistance. Loss of PTEN expression increased the spreading, migration and invasion capacities of colorectal cancer cells in vitro. PTEN downregulation also increased tumor size following subcutaneous injection of colorectal cancer cells in nude mice. Finally, loss of PTEN expression in HCT116 and CT26, but not in Caco-2/15, led to an increase in their metastatic potential following tail-vein injections in mice.Conclusions/Significance
Altogether, these results indicate that PTEN controls cellular polarity, establishment of cell-cell junctions, paracellular permeability, migration and tumorigenic/metastatic potential of human colorectal cancer cells. 相似文献62.
Integrated gut/liver microphysiological systems elucidates inflammatory inter‐tissue crosstalk
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Wen L.K. Chen Collin Edington Emily Suter Jiajie Yu Jeremy J. Velazquez Jason G. Velazquez Michael Shockley Emma M. Large Raman Venkataramanan David J. Hughes Cynthia L. Stokes David L. Trumper Rebecca L. Carrier Murat Cirit Linda G. Griffith Douglas A. Lauffenburger 《Biotechnology and bioengineering》2017,114(11):2648-2659
A capability for analyzing complex cellular communication among tissues is important in drug discovery and development, and in vitro technologies for doing so are required for human applications. A prominent instance is communication between the gut and the liver, whereby perturbations of one tissue can influence behavior of the other. Here, we present a study on human gut‐liver tissue interactions under normal and inflammatory contexts, via an integrative multi‐organ platform comprising human liver (hepatocytes and Kupffer cells), and intestinal (enterocytes, goblet cells, and dendritic cells) models. Our results demonstrated long‐term (>2 weeks) maintenance of intestinal (e.g., barrier integrity) and hepatic (e.g., albumin) functions in baseline interaction. Gene expression data comparing liver in interaction with gut, versus isolation, revealed modulation of bile acid metabolism. Intestinal FGF19 secretion and associated inhibition of hepatic CYP7A1 expression provided evidence of physiologically relevant gut‐liver crosstalk. Moreover, significant non‐linear modulation of cytokine responses was observed under inflammatory gut‐liver interaction; for example, production of CXCR3 ligands (CXCL9,10,11) was synergistically enhanced. RNA‐seq analysis revealed significant upregulation of IFNα/β/γ signaling during inflammatory gut‐liver crosstalk, with these pathways implicated in the synergistic CXCR3 chemokine production. Exacerbated inflammatory response in gut‐liver interaction also negatively affected tissue‐specific functions (e.g., liver metabolism). These findings illustrate how an integrated multi‐tissue platform can generate insights useful for understanding complex pathophysiological processes such as inflammatory organ crosstalk. Biotechnol. Bioeng. 2017;114: 2648–2659. © 2017 Wiley Periodicals, Inc. 相似文献
63.
Leila Feiz Rosalind Williams‐Carrier Susan Belcher Monica Montano Alice Barkan David B. Stern 《The Plant journal : for cell and molecular biology》2014,80(5):862-869
Ribulose‐1,5‐bisphosphate carboxylase/oxygenase (Rubisco) plays a critical role in sustaining life by catalysis of carbon fixation in the Calvin–Benson pathway. Incomplete knowledge of the assembly pathway of chloroplast Rubisco has hampered efforts to fully delineate the enzyme's properties, or seek improved catalytic characteristics via directed evolution. Here we report that a Mu transposon insertion in the Zea mays (maize) gene encoding a chloroplast dimerization co‐factor of hepatocyte nuclear factor 1 (DCoH)/pterin‐4α‐carbinolamine dehydratases (PCD)‐like protein is the causative mutation in a seedling‐lethal, Rubisco‐deficient mutant named Rubisco accumulation factor 2 (raf2‐1). In raf2 mutants newly synthesized Rubisco large subunit accumulates in a high‐molecular weight complex, the formation of which requires a specific chaperonin 60‐kDa isoform. Analogous observations had been made previously with maize mutants lacking the Rubisco biogenesis proteins RAF1 and BSD2. Chemical cross‐linking of maize leaves followed by immunoprecipitation with antibodies to RAF2, RAF1 or BSD2 demonstrated co‐immunoprecipitation of each with Rubisco small subunit, and to a lesser extent, co‐immunoprecipitation with Rubisco large subunit. We propose that RAF2, RAF1 and BSD2 form transient complexes with the Rubisco small subunit, which in turn assembles with the large subunit as it is released from chaperonins. 相似文献
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Over a period of 3 years, five reproductively active female nurse sharks (Ginglymostoma cirratum) from a wild, actively mating population of nurse sharks were captured, confined, and periodically examined through the course of gestation to determine the gestation period and characterize paternity. In the final year of the study, candidate animals were first evaluated in the field by ultrasonography, and the selected animals were then transported from the study site to holding facilities at SeaWorld Adventure Parks in Orlando, Florida. Periodic monitoring of the animals was conducted by ultrasonography, endoscopy, and routine blood analysis. Gestation was determined to be a minimum of 131 days, multiple paternity was shown for two individual litters, and ultrasonography and endoscopy were shown to be useful adjuncts for assessing pregnancy and monitoring gestation in this species. Poor survival of offspring, and small litter size may be a consequence of handling and transporting the animals, and the use of invasive procedures such as endoscopy. Zoo Biol 22:179–187, 2003. © 2003 Wiley‐Liss, Inc. 相似文献
67.
Neil Carrier 《Ethnos》2013,78(3):415-437
This article examines the enormous variety evident in the ‘social life’ of Kenyan khat (miraa) and the role of this variety in the creation and manipulation of value. The article, after a discussion of the literature on value and its relevance to miraa, describes variables used in distinguishing the many different types of miraa, describes how consumers associate themselves with certain varieties and suggests why some varieties are more valued – culturally and economically – than others. The article then looks at the international trade in miraa, and how value is manipulated as exporters – well positioned to exploit different ‘fields of value’ – blend different varieties together to ensure a decent financial reward. It concludes by emphasising that understanding miraa requires an appreciation of its complex particularity. 相似文献
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