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Stoichiometry of TLR9-ligand complex in vivo.Binding stoichiometry of TLR9-GFP with CpG-Cy5 and non CpG-Cy5 calculated from the two-dimensional PCH analysis of fluorescence fluctuation data. Data is expressed as the mean with standard deviation (nâ=â10). Induction of isolated LARs by intradermal injection of peptides derived from FC1P. The mean percent changes in FEV1 after intradermal administration of FC1P (â¢) and during a control day (â) of 9 responders (left) and 31 nonresponders (right). AUC analysis to compare percent change in FEV1 on control and FC1P days in nine patients was statistically significant, at P = 0.0004. Error bars, SD. Significant negative correlation (râ=ââ0.270, P<0.05) of total sperm count with number of deletions in 78 normozoospermic men analysed by 244A array.P-value calculated on log-transformed total sperm counts. General scheme for synchronization and treatment of TM6 cells with Se-methylselenocysteine (MSC) including the collection times. The TM6 cells were plated at a density of 6.6 à 103 cells/cm2 in either 100 mm dishes or six-well plates. After 48 hours of growth the cells were starved in DMEM/F12 medium without growth factors and serum (minimal medium) for a further 48 hours. The cells were released from starvation with DMEM/F12 medium containing growth factors (5 ng/ml epidermal growth factor (EGF) and 10 μg/ml insulin) and serum (2% adult bovine serum). After a further 6 hours MSC was added at a final concentration of 50 to 400 μM (depending upon the experiment) to one set of cells. Untreated cells served as controls. The cells were collected after starvation (0 hours), then at 6 (before the addition of MSC), 9, 12, 16 and 24 hours time-points. Mean percent change in maximal walking distance over time among intermittent claudication patients randomized to cilostazol 100 mg 2Ã/day (n = 227), pentoxifylline 400 mg 3Ã/day (n = 232), or placebo (n = 239) for 24 weeks. MWD = maximal walking distance. Reprinted from Dawson, DL, Cutler BS, Hiatt WR, et al 2000. A comparison of cilostazol and pentoxifylline for treating intermittent claudication. Am J Med, 109:523â30. Copyright © 2000, with permission from Elsevier.
Molecular structure of the title compound with the atom labeling scheme. Displacement ellipsoids for non-H atoms are drawn at the 50% probability level. ORTEP-3 (Farrugia, 1997) drawing of (I) with displacement ellipsoids plotted at 50% probability level. The molecular structure and atom numbering scheme of the title compound. Displacement ellipsoids are drawn at the 30% probability level and H atoms are shown as small spheres of arbitrary radii. The molecular structure of I, with 30% probability displacement ellipsoids. Rabbits fed with fat-rich diet increased plasma cholesterol.Plasma cholesterol concentration from NCR (â¢) and HCR (â¡) during the 11 experimental months. Values are expressed as mean ± SEM. Arrowhead indicates fat intake start in HCR, and arrow indicates the moment from which HCR weight resulted significantly different from NCR, (p<0.001).
Domain structure of Eph receptors and ephrinA and ephrinB ligands. Eph receptors have an extracellular region an ephrin-binding domain and two fibronectin type III repeats, and an intracellular region containing a tyrosine kinase domain, a SAM domain and a PDZ binding domain. EphrinA ligands are attached to the extracellular cell membrane with a GPI anchor. EphrinB ligands are transmembrane proteins with a cytoplasmic tail and PDZ binding domain. Bi-directional signaling results in forward signaling through Eph receptors and reverse signaling through ephrin ligands. Enhanced mortality in S. mansoniâinfected μMT mice. Groups (n = 10) of WT and KO mice were infected percutaneously with 30 cercariae and animal survival was monitored. The hatched line indicates the 50% survival time point for B cell KO animals. As indicated, no mortality was observed in infected WT animals during the same period. The two experiments shown are representative of four performed. The number of myelinated fibers quantified in the median, radial and ulnar nerves pre-amputation and at 6 weeks post-amputation. (P-values provided in parentheses.) ORTEP-3 view (Farrugia, 1997) of the regular [CrIIIF6]3- octahedron and of the "independent" fluoride ion F1 connected to Pb1 and Pb2 completing the Pb2F(CrF6) formula (ellipsoids at the 50% probability level). Transformation of Azomycin Nucleoside α-15 into Precursor α-7
BlandâAltman plot of oral and rectal temperatures. To display the relationships between rectal (reference) and oral temperatures, the difference between the rectal and oral measurements (see vertical axis) was plotted as a function of the mean of the 2 measurements (see horizontal axis). Induction of bPG staining on ECs in response to cytokine treatment. (A) Levels of cell surface HA increase following treatment of SVEC4-10 cells with TNF-α or IL-15. Cells were incubated for 4 h with TNF-α (10 ng/ml), IL-15 (50 ng/ml), IL-2 (50 ng/ml), or IFN-γ (10 ng/ml), harvested in EDTA, stained with bPG-biotin plus SA-PE, and analyzed by FACS® for bPG binding. Untreated cells, which constitutively express some HA, bind background levels of bPG (solid line). After treatment with TNF-α or IL-15, cells show even greater levels of staining (stippled line), whereas IL-2 has no effect. As previously shown, binding to bPG was not increased by incubation with IFN-γ 4. Baseline staining of SVEC4-10 cells with SA-PE alone is indicated by the dashed line in the TNF-α panel. Preincubating TNF-αâtreated cells with soluble HA reduced bPG staining to near background levels (heavy line). (B) Expression of ICAM-1, VCAM, P-selectin, and E-selectin by SVEC4-10 cells before (stippled line) and after (solid line) IL-15 treatment. (C) TME-3H3, 1°LNEC, LEII, and HUVEC cells were treated with human IL-15 (top) or IL-2 (bottom), as in A. TME-3H3 and 1°LNEC respond to IL-15 treatment by expressing increased levels of HA, whereas LEII and HUVEC cells are not affected. In contrast to IL-15, IL-2 had no effect on any of the EC lines or primary ECs. Solid lines, untreated cells; stippled lines, treated cells. (D) Dose dependence of increased HA levels in response to IL-15 treatment. SVEC4-10 cells were incubated for 4 h with IL-15 or IL-2 at varying concentrations, as shown. Results are reported as the mean fluorescence intensity (MFI) of cells after staining with bPG-biotin plus SA-PE, as determined by FACS® analysis. IL-2 had no effect on HA expression by SVEC4-10 cells, even at 200 ng/ml, whereas IL-15 had a dose-dependent effect on levels of surface HA, with changes seen at 10 ng/ml. Data shown are the mean ± SD from three separate experiments. The molecular structure of the title molecule, with the atom-numbering scheme. Displacement ellipsoids are drawn at the 50% probability level. Molecular structure showing 30% probability displacement ellipsoids. Concentration of paeonol in plasma (n = 6, mean ± S.D.) following a single i.v. (â¦), i.n. (âª), or i.g. (â´) administration; calculated dosage of 4 mg·kgâ1 of paeonol in rats.
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