Showing 1,281 - 1,300 results of 34,749 for search '(( 50 ((((ng decrease) OR (nn decrease))) OR (a decrease)) ) OR ( 5 point decrease ))', query time: 0.93s Refine Results
  1. 1281

    A-p50 affects A549 cell survival through inhibition of NF-κB-mediated transcriptional activation by Jing Mi (18654)

    Published 2011
    “…Ad-A-p50 virus-injected tumor tissues show a decrease in Ki67 protein expression compared with Ad-siNT-injected tumor tissues (×100 magnification, brownish red nuclear stain), consistent with a decrease in cell proliferation. …”
  2. 1282
  3. 1283

    Structural and Co-conformational Effects of Alkyne-Derived Subunits in Charged Donor−Acceptor [2]Catenanes by Ognjen Š. Miljanić (2485972)

    Published 2007
    “…The barriers for the three processes were found to be successively 14.4, 14.5−17.5, and 13.1−15.8 kcal mol<sup>-1</sup>. Within the limitations of the small dataset investigated, emergent trends in the barrier heights can be recognized:  the values decrease with the increasing size of the π-electron-donating macrocycle and tend to be lower in the sterically less encumbered series of [2]catenanes containing the 1,3-butadiyne moiety.…”
  4. 1284

    Structural and Co-conformational Effects of Alkyne-Derived Subunits in Charged Donor−Acceptor [2]Catenanes by Ognjen Š. Miljanić (2485972)

    Published 2007
    “…The barriers for the three processes were found to be successively 14.4, 14.5−17.5, and 13.1−15.8 kcal mol<sup>-1</sup>. Within the limitations of the small dataset investigated, emergent trends in the barrier heights can be recognized:  the values decrease with the increasing size of the π-electron-donating macrocycle and tend to be lower in the sterically less encumbered series of [2]catenanes containing the 1,3-butadiyne moiety.…”
  5. 1285

    Structural and Co-conformational Effects of Alkyne-Derived Subunits in Charged Donor−Acceptor [2]Catenanes by Ognjen Š. Miljanić (2485972)

    Published 2007
    “…The barriers for the three processes were found to be successively 14.4, 14.5−17.5, and 13.1−15.8 kcal mol<sup>-1</sup>. Within the limitations of the small dataset investigated, emergent trends in the barrier heights can be recognized:  the values decrease with the increasing size of the π-electron-donating macrocycle and tend to be lower in the sterically less encumbered series of [2]catenanes containing the 1,3-butadiyne moiety.…”
  6. 1286

    Structural and Co-conformational Effects of Alkyne-Derived Subunits in Charged Donor−Acceptor [2]Catenanes by Ognjen Š. Miljanić (2485972)

    Published 2007
    “…The barriers for the three processes were found to be successively 14.4, 14.5−17.5, and 13.1−15.8 kcal mol<sup>-1</sup>. Within the limitations of the small dataset investigated, emergent trends in the barrier heights can be recognized:  the values decrease with the increasing size of the π-electron-donating macrocycle and tend to be lower in the sterically less encumbered series of [2]catenanes containing the 1,3-butadiyne moiety.…”
  7. 1287

    Reduced skin lipid content in obese Japanese women mediated by decreased expression of rate-limiting lipogenic enzymes by Yoshiko Horie (4923043)

    Published 2018
    “…Both skin cholesterol and fatty acid levels exhibited an “inverted-U” relationship with BMI, suggesting that there is an optimal BMI for peak lipid content and barrier function. Decreased lipid levels at higher BMI were accompanied by downregulated expression of <i>PPARδ</i> and other genes related to lipid metabolism, including those encoding acetyl-CoA carboxylase and HMG-CoA reductase, the rate-limiting enzymes for fatty acid and cholesterol synthesis, respectively. …”
  8. 1288
  9. 1289
  10. 1290
  11. 1291
  12. 1292
  13. 1293
  14. 1294

    DataSheet1.docx by Rui Hong Guo (4963240)

    Published 2018
    “…Interestingly, host contact increased the expression and secretion of V. vulnificus RtxA1 toxin, which was decreased and delayed by the rpoS mutation. …”
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  17. 1297
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  19. 1299
  20. 1300

    Lowering Melting Points in Asymmetrically Substituted Salen-Copper(II) Complexes Exhibiting Mesomorphic Behavior. Structure of the Mesogen Cu(5-hexyloxySalen) by Reinhard Paschke (553784)

    Published 2002
    “…In comparison with their symmetrical analogues, unsymmetrically substituted Cu−Salen complexes show mesophases with lowered melting points. For terminally substituted complexes, symmetrical ones (R<sup>1</sup> = R<sup>2</sup>) have only an S<sub>A</sub> phase, while for unsymmetrical alkoxy substitution a monotropic S<sub>E</sub> phase occurs and the melting temperature decreases with no loss in mesophase stability. …”