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991.
Darin J. Gustin Yihong Li Matthew L. Brown Xiaoshan Min Mike J. Schmitt Malgorzata Wanska Xiaodong Wang Richard Connors Sheere Johnstone Mario Cardozo Alan C. Cheng Shawn Jeffries Brendon Franks Shyun Li Shanling Shen Mariwil Wong Holger Wesche Guifen Xu Zhulun Wang 《Bioorganic & medicinal chemistry letters》2013,23(16):4608-4616
Sphingosine-1-phosphate (S1P) signaling plays a vital role in mitogenesis, cell migration and angiogenesis. Sphingosine kinases (SphKs) catalyze a key step in sphingomyelin metabolism that leads to the production of S1P. There are two isoforms of SphK and observations made with SphK deficient mice show the two isoforms can compensate for each other’s loss. Thus, inhibition of both isoforms is likely required to block SphK dependent angiogenesis. A structure based approach was used to design and synthesize a series of SphK inhibitors resulting in the identification of the first potent inhibitors of both isoforms of human SphK. Additionally, to our knowledge, this series of inhibitors contains the only sufficiently potent inhibitors of murine SphK1 with suitable physico-chemical properties to pharmacologically interrogate the role of SphK1 in rodent models and to reproduce the phenotype of SphK1 (?/?) mice. 相似文献
992.
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993.
Kollmus Heike Fuchs Helmut Lengger Christoph Haselimashhadi Hamed Bogue Molly A. stereicher Manuela A. Horsch Marion Adler Thure Aguilar-Pimentel Juan Antonio Amarie Oana Veronica Becker Lore Beckers Johannes Calzada-Wack Julia Garrett Lillian Hans Wolfgang Hlter Sabine M. Klein-Rodewald Tanja Maier Holger Mayer-Kuckuk Philipp Miller Gregor Moreth Kristin Neff Frauke Rathkolb Birgit Rcz Ildik Rozman Jan Spielmann Nadine Treise Irina Busch Dirk Graw Jochen Klopstock Thomas Wolf Eckhard Wurst Wolfgang Yildirim Ali nder Mason Jeremy Torres Arturo Balling Rudi Mehaan Terry Gailus-Durner Valerie Schughart Klaus Hrab de Angelis Martin 《Mammalian genome》2020,31(1):30-48
Mammalian Genome - The collaborative cross (CC) is a large panel of mouse-inbred lines derived from eight founder strains (NOD/ShiLtJ, NZO/HILtJ, A/J, C57BL/6J, 129S1/SvImJ, CAST/EiJ, PWK/PhJ, and... 相似文献
994.
Markus Fischer Meike Luck Maximilian Werle Holger A. Scheidt Peter Müller 《Biochemistry and Biophysics Reports》2020
Ruxolitinib is a small-molecule protein kinase inhibitor, which is used as a therapeutic agent against several diseases. Due to its anti-inflammatory impact, ruxolitinib has also been considered recently for usage in the treatment of Covid-19. While the specific effects of ruxolitinib on Janus kinases (JAK) is comparatively well investigated, its (unspecific) impact on membranes has not been studied in detail so far. Therefore, we characterized the interaction of this drug with lipid membranes employing different biophysical approaches. Ruxolitinib incorporates into the glycerol region of lipid membranes causing an increase in disorder of the lipid chains. This binding, however, has only marginal influence on the structure and integrity of membranes as found by leakage and permeation assays. 相似文献
995.
Stepan H Philipp A Roth I Kralisch S Jank A Schaarschmidt W Lössner U Kratzsch J Blüher M Stumvoll M Fasshauer M 《Regulatory peptides》2011,168(1-3):69-72
Preeclampsia is a serious cardiovascular complication in pregnancy which is associated with an increased future metabolic and cardiovascular risk for mother and newborn. Recently, chemerin was introduced as a novel adipokine inducing insulin resistance in vitro and in vivo. In the current study, we investigated serum concentrations of chemerin by ELISA in control and preeclampsia patients during pregnancy (Control: n=37, preeclampsia: n=37) and 6 months after delivery (Control: n=35, preeclampsia: n=36). Furthermore, the association between chemerin and markers of renal function, glucose and lipid metabolism, as well as inflammation was studied in pregnant patients. Median maternal chemerin concentrations were significantly elevated in preeclampsia patients (249.5 [range: 123.1-366.9] μg/l) as compared to controls (204.8 [138.5-280.8] μg/l) (p<0.001). Furthermore, chemerin serum levels positively correlated with blood pressure, creatinine, free fatty acids, cholesterol, triglycerides (TG), leptin, adiponectin, and C-reactive protein in univariate analyses. In multivariate analyses, TG and leptin remained independently associated with circulating chemerin. Interestingly, median chemerin concentrations 6 months after delivery remained significantly higher in former preeclampsia patients (196.0 [119.8-368.7] μg/l) as compared to controls (152.2 [102.8-216.4] μg/l). Taken together, maternal chemerin serum concentrations are significantly increased in preeclampsia during and after pregnancy. Furthermore, TG and leptin are independent predictors of circulating chemerin during pregnancy. 相似文献
996.
Heller C Kühn MC Mülders-Opgenoorth B Schott M Willenberg HS Scherbaum WA Schinner S 《American journal of physiology. Endocrinology and metabolism》2011,301(5):E864-E872
The Wnt-signaling pathway regulates β-cell functions. It is not known how the expression of endogenous Wnt-signaling molecules is regulated in β-cells. Therefore, we investigated the effect of antidiabetic drugs and glucose on the expression of Wnt-signaling molecules in β-cells. Primary islets were isolated and cultured. The expression of Wnt-signaling molecules (Wnt-4, Wnt-10b, Frizzled-4, LRP5, TCF7L2) and TNFα was analyzed by semiquantitative PCR and Western blotting. Transient transfections were carried out and proliferation assays of INS-1 β-cells performed using [(3)H]thymidine uptake and BrdU ELISA. Insulin secretion was quantified. A knockdown (siRNA) of Wnt-4 in β-cells was carried out. Exendin-4 significantly increased the expression of Wnt-4 in β-cells on the mRNA level (2.8-fold) and the protein level (3-fold) (P < 0.001). The effect was dose dependent, with strongest stimulation at 10 nM, and it was maintained after long-term stimulation over 4 wk. Addition of exd-(9-39), a GLP-1 receptor antagonist, abolished the effect of exendin-4. Treatment with glucose, insulin, or other antidiabetic drugs had no effect on the expression of any of the examined Wnt-signaling molecules. Functionally, Wnt-4 antagonized the activation of canonical Wnt-signaling in β-cells. Wnt-4 had no effect on glucose-stimulated insulin secretion or insulin gene expression. Knocking down Wnt-4 decreased β-cell proliferation to 45% of controls (P < 0.05). In addition, Wnt-4 and exendin-4 treatment decreased the expression of TNFaα mRNA in primary β-cells. These data demonstrate that stimulation with exendin-4 increases the expression of Wnt-4 in β-cells. Wnt-4 modulates canonical Wnt signaling and acts as regulator of β-cell proliferation and inflammatory cytokine release. This suggests a novel mechanism through which GLP-1 can regulate β-cell proliferation. 相似文献
997.
Huesgen PF Miranda H Lam X Perthold M Schuhmann H Adamska I Funk C 《The Biochemical journal》2011,435(3):733-742
Cyanobacteria require efficient protein-quality-control mechanisms to survive under dynamic, often stressful, environmental conditions. It was reported that three serine proteases, HtrA (high temperature requirement A), HhoA (HtrA homologue A) and HhoB (HtrA homologue B), are important for survival of Synechocystis sp. PCC 6803 under high light and temperature stresses and might have redundant physiological functions. In the present paper, we show that all three proteases can degrade unfolded model substrates, but differ with respect to cleavage sites, temperature and pH optima. For recombinant HhoA, and to a lesser extent for HtrA, we observed an interesting shift in the pH optimum from slightly acidic to alkaline in the presence of Mg2+ and Ca2+ ions. All three proteases formed different homo-oligomeric complexes with and without substrate, implying mechanistic differences in comparison with each other and with the well-studied Escherichia coli orthologues DegP (degradation of periplasmic proteins P) and DegS. Deletion of the PDZ domain decreased, but did not abolish, the proteolytic activity of all three proteases, and prevented substrate-induced formation of complexes higher than trimers by HtrA and HhoA. In summary, biochemical characterization of HtrA, HhoA and HhoB lays the foundation for a better understanding of their overlapping, but not completely redundant, stress-resistance functions in Synechocystis sp. PCC 6803. 相似文献
998.
Roider E Jellbauer S Köhn B Berchtold C Partilla M Busch DH Rüssmann H Panthel K 《Cancer immunology, immunotherapy : CII》2011,60(3):371-380
We have developed a new vaccination strategy by using the Salmonella type III secretion system (T3SS) to translocate heterologous antigens into the cytosol of host cells. This leads to an efficient
antigen-specific CD8 T cell induction. Recently, we have demonstrated the use of Salmonella’s T3SS for the immunoprophylaxis of a solid tumor. The murine fibrosarcoma WEHI 164 was transfected with the DNA sequence
encoding the MHC class I-peptide p60217–225 from Listeria monocytogenes. In the present study, we used this tumor model to investigate the potential of vaccination with recombinant Salmonella in a therapeutic setting. BALB/c mice were subcutaneously challenged with WEHI-p60 cells. Simultaneously or 4 days later,
these mice received either an orogastric or intravenous immunization with Salmonella translocating p60. Interestingly, 71–80% of the intravenously and 50–52% of the orogastrically immunized mice showed a complete
tumor regression after 14 days. In addition, the distribution of tetramer-positive p60217–225-specific CD8 T cell subpopulations in blood and tumor tissue was analyzed. Co-staining with CD62L and CD127 revealed that
the frequencies of p60217–225-specific effector and effector memory CD8 T cells in blood and in fibrosarcoma tissue were related to the kinetics of tumor
regression. In summary, our study demonstrates that therapeutic vaccination with Salmonella leads to efficient induction of tumor-invading effector CD8 T cells that may result in significant tumor regression. 相似文献
999.
Holger Teichert Stefan D?tterl Gerhard Gottsberger 《Plant Systematics and Evolution》2011,291(1-2):25-33
Heterodichogamy in a natural population of an Annonaceae species from the rainforests of French Guiana is described for the first time. Anaxagorea prinoides had bisexual flowers and two floral morphs within the studied population were protogynous. The population under study comprised 7 mature trees belonging to one morph and 12 to the other. Statistical analyses showed that the two morphs were in a 50:50% ratio, and therefore the temporal sexual pattern of heterodichogamy is given. When anthesis of flowers in the male stage ended in one morph, anthesis started with flowers in the female stage in the complementary morph. Approximately 1?h before the end of anthesis in one morph, flowers of the reciprocal morph started to emit a fruit-like scent. The temporal separation of the female and the male stages of the two different morphs lasted only approximately 1?h. Six of the seven identified compounds in the banana-like floral scent were esters and one was an alcohol. The main compounds examined are known to be components of fruit scents. Nitidulidae beetles of the genus Colopterus were the pollinators of A. prinoides and during flowering were maintained within the population of this species. This was not only due to the fact that the beetles remained sheltered in the pollination chamber of the flowers, but also because upon release from individuals of male-stage flowers at the end of flower anthesis they were attracted by the odoriferous female-stage flowers of other individuals of the same population. Heterodichogamy of A. prinoides appears to be a means by which reproductive success is augmented. Attraction of beetle pollinators by ??fruit-imitating?? floral scent is not restricted to species of Anaxagorea, but occurs in many representatives of the Annonaceae. 相似文献
1000.
Stenzel D Lundkvist A Sauvaget D Busse M Graupera M van der Flier A Wijelath ES Murray J Sobel M Costell M Takahashi S Fässler R Yamaguchi Y Gutmann DH Hynes RO Gerhardt H 《Development (Cambridge, England)》2011,138(20):4451-4463
Fibronectin (FN) is a major component of the extracellular matrix and functions in cell adhesion, cell spreading and cell migration. In the retina, FN is transiently expressed and assembled on astrocytes (ACs), which guide sprouting tip cells and deposit a provisional matrix for sprouting angiogenesis. The precise function of FN in retinal angiogenesis is largely unknown. Using genetic tools, we show that astrocytes are the major source of cellular FN during angiogenesis in the mouse retina. Deletion of astrocytic FN reduces radial endothelial migration during vascular plexus formation in a gene dose-dependent manner. This effect correlates with reduced VEGF receptor 2 and PI3K/AKT signalling, and can be mimicked by selectively inhibiting VEGF-A binding to FN through intraocular injection of blocking peptides. By contrast, AC-specific replacement of the integrin-binding RGD sequence with FN-RGE or endothelial deletion of itga5 shows little effect on migration and PI3K/AKT signalling, but impairs filopodial alignment along AC processes, suggesting that FN-integrin α5β1 interaction is involved in filopodial adhesion to the astrocytic matrix. AC FN shares its VEGF-binding function and cell-surface distribution with heparan-sulfate (HS), and genetic deletion of both FN and HS together greatly enhances the migration defect, indicating a synergistic function of FN and HS in VEGF binding. We propose that in vivo the VEGF-binding properties of FN and HS promote directional tip cell migration, whereas FN integrin-binding functions to support filopodia adhesion to the astrocytic migration template. 相似文献