Showing 6,801 - 6,820 results of 30,064 for search '(( 2 step decrease ) OR ( 50 ((((teer decrease) OR (nn decrease))) OR (a decrease)) ))', query time: 1.02s Refine Results
  1. 6801
  2. 6802

    Shock-Tube Study of the Ignition of Gas-Phase 1,3,5-Trimethylbenzene in Air by Fan Rao (1343973)

    Published 2015
    “…Lean mixtures are fastest to ignite at temperatures above 1390 K at 1.0 atm, whereas they are slowest to ignite below 1300 K at 20.0 atm, and the equivalence ratio does not have an evident effect on the ignition time at 5.0 atm. The global activation energy decreases dramatically as the pressure increases at all equivalence ratios. …”
  3. 6803

    Expression and autolysis of CAPN3 in quadriceps muscle of LGMD2A patients. by Mats I. Nilsson (606586)

    Published 2014
    “…Logically, a reduction in total CAPN3, obtained from Ca<sup>2+</sup>-free homogenates, equates to a decrease in <i>total autolytic capacity</i>. …”
  4. 6804
  5. 6805
  6. 6806
  7. 6807
  8. 6808
  9. 6809
  10. 6810
  11. 6811
  12. 6812
  13. 6813

    Transient expression of HIF1α(PP) inhibited intracranial tumor growth. by Hyunsung Choi (727224)

    Published 2015
    “…Tumor volumes, plotted in a log scale, decreased significantly from HIF1α(PP) in reference to β-gal. …”
  14. 6814
  15. 6815

    Structure–Activity Studies of 1<i>H</i>‑Imidazo[4,5‑<i>c</i>]quinolin-4-amine Derivatives as A<sub>3</sub> Adenosine Receptor Positive Allosteric Modulators by Lucas B. Fallot (14106171)

    Published 2022
    “…Although having low Caco-2 permeability and high plasma protein binding, hydrophobic 2-cyclohept-4-enyl-<i>N</i>-3,4-dichlorophenyl, MRS7788 <b>18</b>, and 2-heptan-4-yl-<i>N</i>-4-iodophenyl, MRS8054 <b>39</b>, derivatives were orally bioavailable in rat. 2-Heptan-4-yl-<i>N</i>-3,4-dichlorophenyl <b>14</b> and 2-cyclononyl-<i>N</i>-3,4-dichlorophenyl <b>20</b> derivatives and <b>39</b> greatly enhanced Cl-IB-MECA-stimulated [<sup>35</sup>S]GTPγS binding <i>E</i><sub>max</sub>, with only <b>12b</b> trending toward decreasing the agonist EC<sub>50</sub>. A feasible route for radio-iodination at the <i>p-</i>position of a 4-phenylamino substituent suggests a potential radioligand for allosteric site binding. …”
  16. 6816

    Structure–Activity Studies of 1<i>H</i>‑Imidazo[4,5‑<i>c</i>]quinolin-4-amine Derivatives as A<sub>3</sub> Adenosine Receptor Positive Allosteric Modulators by Lucas B. Fallot (14106171)

    Published 2022
    “…Although having low Caco-2 permeability and high plasma protein binding, hydrophobic 2-cyclohept-4-enyl-<i>N</i>-3,4-dichlorophenyl, MRS7788 <b>18</b>, and 2-heptan-4-yl-<i>N</i>-4-iodophenyl, MRS8054 <b>39</b>, derivatives were orally bioavailable in rat. 2-Heptan-4-yl-<i>N</i>-3,4-dichlorophenyl <b>14</b> and 2-cyclononyl-<i>N</i>-3,4-dichlorophenyl <b>20</b> derivatives and <b>39</b> greatly enhanced Cl-IB-MECA-stimulated [<sup>35</sup>S]GTPγS binding <i>E</i><sub>max</sub>, with only <b>12b</b> trending toward decreasing the agonist EC<sub>50</sub>. A feasible route for radio-iodination at the <i>p-</i>position of a 4-phenylamino substituent suggests a potential radioligand for allosteric site binding. …”
  17. 6817
  18. 6818
  19. 6819
  20. 6820