Showing 8,481 - 8,500 results of 32,320 for search '(( 50 ((nn decrease) OR (((we decrease) OR (a decrease)))) ) OR ( e point decrease ))', query time: 1.14s Refine Results
  1. 8481
  2. 8482

    Effect of fenretinide and its metabolites on SCD expression and activity. by Eugenia Poliakov (116500)

    Published 2017
    “…<p>A) SCD1 protein expression is decreased after treatment with fenretinide, and its metabolite 3-keto-HPR. …”
  3. 8483
  4. 8484
  5. 8485

    Down-regulation of BjsR4 under tellurite and iron stresses, and impact of this down-regulation on survival at high iron concentration. by Julia Hahn (3279486)

    Published 2016
    “…<p><b>A)</b> The steady-state level of BjsR4 is decreased upon addition of tellurite. …”
  6. 8486

    Analgesic effect of a cholinergic agonist (carbachol) in a sural nerve ligation-induced hypersensitivity mouse model by Nodoka Kato (18298748)

    Published 2024
    “…</p> <p>SN ligation resulted in a significant decrease in pain threshold for mechanical stimulation 1 day after ligation. …”
  7. 8487

    Discovery of <i>N</i>‑(1,3,4-Thiadiazol-2-yl)amide Derivatives as Uncompetitive Inhibitors of 6‑Phosphogluconate Dehydrogenase by Rong Zhang (44942)

    Published 2025
    “…Moreover, <b>19n</b> treatment could result in a decrease of NADPH and Ru-5-P production as well as DNA synthesis in A549 cells. …”
  8. 8488
  9. 8489
  10. 8490
  11. 8491

    Synthesis and Characterization of the First Azastibatranes and Azabismatranes by Pavel L. Shutov (2967693)

    Published 2002
    “…The structural data obtained from geometry optimizations on <b>6</b> and <b>8</b> reproduce experimental trends, i.e., a decrease in the E−N<sub>dat</sub> distance from Sb to Bi. …”
  12. 8492

    Synthesis and Characterization of the First Azastibatranes and Azabismatranes by Pavel L. Shutov (2967693)

    Published 2002
    “…The structural data obtained from geometry optimizations on <b>6</b> and <b>8</b> reproduce experimental trends, i.e., a decrease in the E−N<sub>dat</sub> distance from Sb to Bi. …”
  13. 8493

    Synthesis and Characterization of the First Azastibatranes and Azabismatranes by Pavel L. Shutov (2967693)

    Published 2002
    “…The structural data obtained from geometry optimizations on <b>6</b> and <b>8</b> reproduce experimental trends, i.e., a decrease in the E−N<sub>dat</sub> distance from Sb to Bi. …”
  14. 8494

    Synthesis and Characterization of the First Azastibatranes and Azabismatranes by Pavel L. Shutov (2967693)

    Published 2002
    “…The structural data obtained from geometry optimizations on <b>6</b> and <b>8</b> reproduce experimental trends, i.e., a decrease in the E−N<sub>dat</sub> distance from Sb to Bi. …”
  15. 8495

    Synthesis and Characterization of the First Azastibatranes and Azabismatranes by Pavel L. Shutov (2967693)

    Published 2002
    “…The structural data obtained from geometry optimizations on <b>6</b> and <b>8</b> reproduce experimental trends, i.e., a decrease in the E−N<sub>dat</sub> distance from Sb to Bi. …”
  16. 8496

    Synthesis and Characterization of the First Azastibatranes and Azabismatranes by Pavel L. Shutov (2967693)

    Published 2002
    “…The structural data obtained from geometry optimizations on <b>6</b> and <b>8</b> reproduce experimental trends, i.e., a decrease in the E−N<sub>dat</sub> distance from Sb to Bi. …”
  17. 8497

    Synthesis and Characterization of the First Azastibatranes and Azabismatranes by Pavel L. Shutov (2967693)

    Published 2002
    “…The structural data obtained from geometry optimizations on <b>6</b> and <b>8</b> reproduce experimental trends, i.e., a decrease in the E−N<sub>dat</sub> distance from Sb to Bi. …”
  18. 8498

    An Analysis of Porphyrin Molecular FlexibilityUse of Porphyrin Diacids by Beisong Cheng (2970567)

    Published 1997
    “…Molecular mechanics calculations, using a modified version of MM2(87) and a newly developed force field for porphyrin diacids, correctly predict that the flexibility of <i>meso</i>-tetraaryl porphyrin diacids decreases as the steric bulk of the peripheral substituents increases:  [H<sub>4</sub>TPyP]<sup>2+</sup> ≈ [H<sub>4</sub>TPP]<sup>2+</sup> > [H<sub>4</sub>T-2,6-(OH)<sub>2</sub> PP]<sup>2+</sup> ≈ [H<sub>4</sub>T-2,6-F<sub>2</sub> PP]<sup>2+</sup> > [H<sub>4</sub>T-2,6-Cl<sub>2</sub> PP]<sup>2+</sup> ≈ [H<sub>4</sub>TMP]<sup>2+</sup>. …”
  19. 8499
  20. 8500