Showing 1,721 - 1,740 results of 29,239 for search '(( 50 ((na decrease) OR (((nn decrease) OR (a decrease)))) ) OR ( 12 wt decrease ))', query time: 1.04s Refine Results
  1. 1721
  2. 1722

    Sema3a inhibits the differentiation of Raw264.7 cells to osteoclasts under 2Gy radiation by reducing inflammation by Bo Huang (30906)

    Published 2018
    “…Raw264.7 cells were divided into four groups: A, receiving no radiation; B, receiving no radiation + 50ngng/ml Sema3a; C, receiving 2Gy radiation; and D, receiving 2Gy radiation +50ngng/ml Sema3a. …”
  3. 1723
  4. 1724
  5. 1725
  6. 1726

    Data_Sheet_1_Curcumin, a Multi-Ion Channel Blocker That Preferentially Blocks Late Na+ Current and Prevents I/R-Induced Arrhythmias.zip by Lv Song (9265217)

    Published 2020
    “…It is first revealed that Cur is a multi-ion channel blocker that preferentially blocks I<sub>Na.L</sub> and may have potential antiarrhythmic property.…”
  7. 1727
  8. 1728
  9. 1729
  10. 1730
  11. 1731

    Protons cause a greater increase in persistent sodium current in C373F/E1784K Na<sub>V</sub>1.5. by Colin H. Peters (4430245)

    Published 2017
    “…<p><b>(A)</b> Sample persistent sodium current recordings at -20mV from C373F and C373F/E1784K Na<sub>V</sub>1.5 at pH 7.4 and pH 6.0. …”
  12. 1732
  13. 1733
  14. 1734
  15. 1735
  16. 1736
  17. 1737
  18. 1738

    Selective TASK‑1 Inhibitor with a Defined Structure–Activity Relationship Reduces Cancer Cell Proliferation and Viability by Bárbara Arévalo (4053358)

    Published 2022
    “…Mutation of seven residues to A (I118A, L122A, F125A, Q126A, L232A, I235A, and L239A) markedly decreased the F3-induced inhibition of TASK-1 channels, consistent with the molecular modeling predictions. …”
  19. 1739

    Selective TASK‑1 Inhibitor with a Defined Structure–Activity Relationship Reduces Cancer Cell Proliferation and Viability by Bárbara Arévalo (4053358)

    Published 2022
    “…Mutation of seven residues to A (I118A, L122A, F125A, Q126A, L232A, I235A, and L239A) markedly decreased the F3-induced inhibition of TASK-1 channels, consistent with the molecular modeling predictions. …”
  20. 1740