Showing 80,021 - 80,040 results of 113,932 for search '(( 5 ((a decrease) OR (mean decrease)) ) OR ( a ((fold decrease) OR (point decrease)) ))', query time: 1.36s Refine Results
  1. 80021
  2. 80022
  3. 80023
  4. 80024
  5. 80025
  6. 80026
  7. 80027
  8. 80028
  9. 80029
  10. 80030
  11. 80031

    Brain AKI by Shaimaa Amin (10114513)

    Published 2023
    “…Dipeptidyl peptidase 4 (DPP-4) inhibitors decrease the degradation of glucagon-like peptide-1 (GLP-1) improving glycemic control. …”
  12. 80032

    Effect of annealing on structural and optical properties of copper sulphide thin films by Fahd Elmourabit (20287004)

    Published 2024
    “…The optical band gap is found to decrease from 2.70 to 2.55 eV by annealing.</p>…”
  13. 80033

    Chiral Induction in Quinoline-Derived Oligoamide Foldamers:  Assignment of Helical Handedness and Role of Steric Effects by Christel Dolain (2302942)

    Published 2005
    “…Upon assigning an <i>R</i><sup>s</sup> or <i>S</i><sup>s</sup> chirality to the stereogenic center using a nomenclature where the four substituents are ranked according to decreasing sizes, it is observed that <i>R</i><sup>s</sup> chirality always favors left-handed helicity and <i>S</i><sup>s</sup> chirality favors right-handed helicity (P). …”
  14. 80034

    Empirical measurements of tissue Na<sup>+</sup> and K<sup>+</sup> contents across different durations of salinity stress as measured by flame photometry analysis. by Isaiah Catalino M. Pabuayon (9554981)

    Published 2022
    “…This trend implies that the difference in Na<sup>+</sup> content started before the earliest sampling time-point (6 DAS). All genotypes showed a decreasing trend in K<sup>+</sup> accumulation. …”
  15. 80035

    Chiral Induction in Quinoline-Derived Oligoamide Foldamers:  Assignment of Helical Handedness and Role of Steric Effects by Christel Dolain (2302942)

    Published 2005
    “…Upon assigning an <i>R</i><sup>s</sup> or <i>S</i><sup>s</sup> chirality to the stereogenic center using a nomenclature where the four substituents are ranked according to decreasing sizes, it is observed that <i>R</i><sup>s</sup> chirality always favors left-handed helicity and <i>S</i><sup>s</sup> chirality favors right-handed helicity (P). …”
  16. 80036

    Effects of normal saline on hemodynamic and metabolic function during hemorrhagic shock. by Raúl J. Gazmuri (653679)

    Published 2015
    “…Numbers in brackets indicate when the number of animals decreased from the preceding time point. Values are shown as mean ± SEM. …”
  17. 80037

    Effects of vasopressin on hemodynamic and metabolic function during hemorrhagic shock. by Raúl J. Gazmuri (653679)

    Published 2015
    “…Numbers in brackets indicate when the number of animals decreased from the preceding time point. Values are shown as mean ± SEM. …”
  18. 80038

    Chiral Induction in Quinoline-Derived Oligoamide Foldamers:  Assignment of Helical Handedness and Role of Steric Effects by Christel Dolain (2302942)

    Published 2005
    “…Upon assigning an <i>R</i><sup>s</sup> or <i>S</i><sup>s</sup> chirality to the stereogenic center using a nomenclature where the four substituents are ranked according to decreasing sizes, it is observed that <i>R</i><sup>s</sup> chirality always favors left-handed helicity and <i>S</i><sup>s</sup> chirality favors right-handed helicity (P). …”
  19. 80039

    Effect of PD-L1/2 blockade on CD4<sup>+</sup> T-cell expansion. by Bijan Raziorrouh (619846)

    Published 2014
    “…<p>Induction of CD4<sup>+</sup> T-cell proliferation in chronic HBV (n = 23) from h0 (<i>left</i>) to antigenic stimulation (<i>middle</i>) and PD-L1/2 blockade (<i>right</i>) illustrated as point to point graphs from (<b>A</b>) PD-L1/2 responders (n = 9) and (<b>B</b>) Non-responders (n = 14). …”
  20. 80040

    Chiral Induction in Quinoline-Derived Oligoamide Foldamers:  Assignment of Helical Handedness and Role of Steric Effects by Christel Dolain (2302942)

    Published 2005
    “…Upon assigning an <i>R</i><sup>s</sup> or <i>S</i><sup>s</sup> chirality to the stereogenic center using a nomenclature where the four substituents are ranked according to decreasing sizes, it is observed that <i>R</i><sup>s</sup> chirality always favors left-handed helicity and <i>S</i><sup>s</sup> chirality favors right-handed helicity (P). …”