Showing 19,721 - 19,740 results of 105,424 for search '(( i de decrease ) OR ( 5 ((point decrease) OR (((nn decrease) OR (a decrease)))) ))', query time: 1.83s Refine Results
  1. 19721
  2. 19722

    Changes in the frequency of theta oscillation during REM sleep after SD are associated with <i>Cyp4a32</i>. by Shanaz Diessler (5617589)

    Published 2018
    “…(D) Effects of SD and genotype on liver <i>Cyp4a32</i> expression. Carrying a <i>B6-</i>allele at the <i>Cyp4a32 cis-e</i>QTL–associated marker greatly decreased its expression. …”
  3. 19723
  4. 19724

    Knockdown of HuD induces apoptosis in N2a cells. by Naina Gaikwad (20435889)

    Published 2024
    “…<p>Control siRNA and HuD siRNA were transfected in N2a cells after 48 hours of transfection cells were trypsinised and stained with Annexin-V conjugated FITC and Propidium Iodide. …”
  5. 19725

    Clearance of rAd5 from mouse blood circulation. by Latha P. Ganesan (203662)

    Published 2011
    “…In order to generate a complete concentration-time profile of viral clearance up to 30 min, the concentrations at later time points (10, 20, and 30 min), previously obtained (Panel A insert, 1.6×10<sup>10</sup>), were normalized to the mean concentration at 5 min using the concentration-decay ratio among time points. …”
  6. 19726

    Quantifying the demographic cost of human-related mortality to a raptor population by W. Grainger Hunt (375336)

    Published 2017
    “…Occupancy surveys 5 and 13 years later (2005 and 2013) showed that the nesting population remained intact, and no upward trend was apparent in the proportion of subadult eagles as pair members, a condition that would have suggested a deficit of adult replacements. …”
  7. 19727

    Charge Distribution in Cationic Molybdenum Imido Alkylidene <i>N</i>‑Heterocyclic Carbene Complexes: A Combined X‑ray, XAS, XES, DFT, Mössbauer, and Catalysis Approach by Mathis Benedikter (9726148)

    Published 2020
    “…The binding situation in the corresponding cationic complexes Mo­(<i>N</i>-2,6-Me<sub>2</sub>C<sub>6</sub>H<sub>3</sub>)­(CHCMe<sub>2</sub>Ph)­(NHC)­(OC­(CF<sub>3</sub>)<sub>3</sub>)<sup>+</sup> B­(Ar<sup>F</sup>)<sub>4</sub><sup>–</sup> (NHC = IMes (<b>1</b>), IMesCl<sub>2</sub> (<b>2</b>), IMesMe<sub>2</sub> (<b>3</b>), and IMesH<sub>2</sub> (<b>4</b>) was compared to that of the analogous neutral Schrock catalyst Mo­(<i>N</i>-2,6-Me<sub>2</sub>C<sub>6</sub>H<sub>3</sub>)­(CHCMe<sub>2</sub>Ph)­((OC­(CF<sub>3</sub>)<sub>3</sub>))<sub>2</sub> (<b>5</b>). Single-crystal X-ray data were used as a starting point for the optimization of the geometries of the catalysts at the PBE0-D3BJ/def2-SVP level of theory; the obtained data were compared to those obtained from X-ray absorption (XAS) and emission spectroscopy (XES). …”
  8. 19728

    Charge Distribution in Cationic Molybdenum Imido Alkylidene <i>N</i>‑Heterocyclic Carbene Complexes: A Combined X‑ray, XAS, XES, DFT, Mössbauer, and Catalysis Approach by Mathis Benedikter (9726148)

    Published 2020
    “…The binding situation in the corresponding cationic complexes Mo­(<i>N</i>-2,6-Me<sub>2</sub>C<sub>6</sub>H<sub>3</sub>)­(CHCMe<sub>2</sub>Ph)­(NHC)­(OC­(CF<sub>3</sub>)<sub>3</sub>)<sup>+</sup> B­(Ar<sup>F</sup>)<sub>4</sub><sup>–</sup> (NHC = IMes (<b>1</b>), IMesCl<sub>2</sub> (<b>2</b>), IMesMe<sub>2</sub> (<b>3</b>), and IMesH<sub>2</sub> (<b>4</b>) was compared to that of the analogous neutral Schrock catalyst Mo­(<i>N</i>-2,6-Me<sub>2</sub>C<sub>6</sub>H<sub>3</sub>)­(CHCMe<sub>2</sub>Ph)­((OC­(CF<sub>3</sub>)<sub>3</sub>))<sub>2</sub> (<b>5</b>). Single-crystal X-ray data were used as a starting point for the optimization of the geometries of the catalysts at the PBE0-D3BJ/def2-SVP level of theory; the obtained data were compared to those obtained from X-ray absorption (XAS) and emission spectroscopy (XES). …”
  9. 19729

    Charge Distribution in Cationic Molybdenum Imido Alkylidene <i>N</i>‑Heterocyclic Carbene Complexes: A Combined X‑ray, XAS, XES, DFT, Mössbauer, and Catalysis Approach by Mathis Benedikter (9726148)

    Published 2020
    “…The binding situation in the corresponding cationic complexes Mo­(<i>N</i>-2,6-Me<sub>2</sub>C<sub>6</sub>H<sub>3</sub>)­(CHCMe<sub>2</sub>Ph)­(NHC)­(OC­(CF<sub>3</sub>)<sub>3</sub>)<sup>+</sup> B­(Ar<sup>F</sup>)<sub>4</sub><sup>–</sup> (NHC = IMes (<b>1</b>), IMesCl<sub>2</sub> (<b>2</b>), IMesMe<sub>2</sub> (<b>3</b>), and IMesH<sub>2</sub> (<b>4</b>) was compared to that of the analogous neutral Schrock catalyst Mo­(<i>N</i>-2,6-Me<sub>2</sub>C<sub>6</sub>H<sub>3</sub>)­(CHCMe<sub>2</sub>Ph)­((OC­(CF<sub>3</sub>)<sub>3</sub>))<sub>2</sub> (<b>5</b>). Single-crystal X-ray data were used as a starting point for the optimization of the geometries of the catalysts at the PBE0-D3BJ/def2-SVP level of theory; the obtained data were compared to those obtained from X-ray absorption (XAS) and emission spectroscopy (XES). …”
  10. 19730

    Charge Distribution in Cationic Molybdenum Imido Alkylidene <i>N</i>‑Heterocyclic Carbene Complexes: A Combined X‑ray, XAS, XES, DFT, Mössbauer, and Catalysis Approach by Mathis Benedikter (9726148)

    Published 2020
    “…The binding situation in the corresponding cationic complexes Mo­(<i>N</i>-2,6-Me<sub>2</sub>C<sub>6</sub>H<sub>3</sub>)­(CHCMe<sub>2</sub>Ph)­(NHC)­(OC­(CF<sub>3</sub>)<sub>3</sub>)<sup>+</sup> B­(Ar<sup>F</sup>)<sub>4</sub><sup>–</sup> (NHC = IMes (<b>1</b>), IMesCl<sub>2</sub> (<b>2</b>), IMesMe<sub>2</sub> (<b>3</b>), and IMesH<sub>2</sub> (<b>4</b>) was compared to that of the analogous neutral Schrock catalyst Mo­(<i>N</i>-2,6-Me<sub>2</sub>C<sub>6</sub>H<sub>3</sub>)­(CHCMe<sub>2</sub>Ph)­((OC­(CF<sub>3</sub>)<sub>3</sub>))<sub>2</sub> (<b>5</b>). Single-crystal X-ray data were used as a starting point for the optimization of the geometries of the catalysts at the PBE0-D3BJ/def2-SVP level of theory; the obtained data were compared to those obtained from X-ray absorption (XAS) and emission spectroscopy (XES). …”
  11. 19731

    Charge Distribution in Cationic Molybdenum Imido Alkylidene <i>N</i>‑Heterocyclic Carbene Complexes: A Combined X‑ray, XAS, XES, DFT, Mössbauer, and Catalysis Approach by Mathis Benedikter (9726148)

    Published 2020
    “…The binding situation in the corresponding cationic complexes Mo­(<i>N</i>-2,6-Me<sub>2</sub>C<sub>6</sub>H<sub>3</sub>)­(CHCMe<sub>2</sub>Ph)­(NHC)­(OC­(CF<sub>3</sub>)<sub>3</sub>)<sup>+</sup> B­(Ar<sup>F</sup>)<sub>4</sub><sup>–</sup> (NHC = IMes (<b>1</b>), IMesCl<sub>2</sub> (<b>2</b>), IMesMe<sub>2</sub> (<b>3</b>), and IMesH<sub>2</sub> (<b>4</b>) was compared to that of the analogous neutral Schrock catalyst Mo­(<i>N</i>-2,6-Me<sub>2</sub>C<sub>6</sub>H<sub>3</sub>)­(CHCMe<sub>2</sub>Ph)­((OC­(CF<sub>3</sub>)<sub>3</sub>))<sub>2</sub> (<b>5</b>). Single-crystal X-ray data were used as a starting point for the optimization of the geometries of the catalysts at the PBE0-D3BJ/def2-SVP level of theory; the obtained data were compared to those obtained from X-ray absorption (XAS) and emission spectroscopy (XES). …”
  12. 19732

    Charge Distribution in Cationic Molybdenum Imido Alkylidene <i>N</i>‑Heterocyclic Carbene Complexes: A Combined X‑ray, XAS, XES, DFT, Mössbauer, and Catalysis Approach by Mathis Benedikter (9726148)

    Published 2020
    “…The binding situation in the corresponding cationic complexes Mo­(<i>N</i>-2,6-Me<sub>2</sub>C<sub>6</sub>H<sub>3</sub>)­(CHCMe<sub>2</sub>Ph)­(NHC)­(OC­(CF<sub>3</sub>)<sub>3</sub>)<sup>+</sup> B­(Ar<sup>F</sup>)<sub>4</sub><sup>–</sup> (NHC = IMes (<b>1</b>), IMesCl<sub>2</sub> (<b>2</b>), IMesMe<sub>2</sub> (<b>3</b>), and IMesH<sub>2</sub> (<b>4</b>) was compared to that of the analogous neutral Schrock catalyst Mo­(<i>N</i>-2,6-Me<sub>2</sub>C<sub>6</sub>H<sub>3</sub>)­(CHCMe<sub>2</sub>Ph)­((OC­(CF<sub>3</sub>)<sub>3</sub>))<sub>2</sub> (<b>5</b>). Single-crystal X-ray data were used as a starting point for the optimization of the geometries of the catalysts at the PBE0-D3BJ/def2-SVP level of theory; the obtained data were compared to those obtained from X-ray absorption (XAS) and emission spectroscopy (XES). …”
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  19. 19739
  20. 19740