Showing 8,441 - 8,460 results of 34,782 for search '(( 50 ((mean decrease) OR (a decrease)) ) OR ( 5 ((point decrease) OR (nn decrease)) ))', query time: 0.64s Refine Results
  1. 8441
  2. 8442

    A combined algorithm to distinguish between IB and NC models based on the differences in binding kinetics and DynR temporal evolution. by Federico Sevlever (8934533)

    Published 2020
    “…In <b>Examples 5 and 7</b>, the time where the inflection point in the <b>DynR</b> curve occurs (t<sub>ip</sub>) is well described by the range predicted by the <b>NC</b> model, so it is concluded that these two examples correspond to the <b>NC</b> model. …”
  3. 8443
  4. 8444
  5. 8445

    Data Sheet 2_Screening of neurotransmitter receptor modulators reveals novel inhibitors of influenza virus replication.pdf by Yarou Gao (20620991)

    Published 2025
    “…We identified 20 candidate compounds with IC50 values below 20 μM, suggesting a critical role for these receptors in influenza replication. …”
  6. 8446
  7. 8447
  8. 8448
  9. 8449
  10. 8450
  11. 8451
  12. 8452

    DataSheet_1_Future changes in the seasonal habitat suitability for anchovy (Engraulis japonicus) in Korean waters projected by a maximum entropy model.docx by Minkyoung Bang (13521394)

    Published 2022
    “…The MaxEnt was constructed by anchovy presence points and five environmental variables (sea surface temperature, sea surface salinity, sea surface current speed, mixed layer depth, and chlorophyll-a concentration) from 2000–2015. …”
  13. 8453

    Synthesis, Evaluation, and Mechanism Study of Novel Indole-Chalcone Derivatives Exerting Effective Antitumor Activity Through Microtubule Destabilization in Vitro and in Vivo by Jun Yan (28467)

    Published 2016
    “…Among them, <b>14k</b> exhibited most potent activity, with IC<sub>50</sub> values of 3–9 nM against six cancer cells, which displayed a 3.8–8.7-fold increase in activity when compare with compound <b>2</b>. …”
  14. 8454

    Synthesis, Evaluation, and Mechanism Study of Novel Indole-Chalcone Derivatives Exerting Effective Antitumor Activity Through Microtubule Destabilization in Vitro and in Vivo by Jun Yan (28467)

    Published 2016
    “…Among them, <b>14k</b> exhibited most potent activity, with IC<sub>50</sub> values of 3–9 nM against six cancer cells, which displayed a 3.8–8.7-fold increase in activity when compare with compound <b>2</b>. …”
  15. 8455

    Synthesis, Evaluation, and Mechanism Study of Novel Indole-Chalcone Derivatives Exerting Effective Antitumor Activity Through Microtubule Destabilization in Vitro and in Vivo by Jun Yan (28467)

    Published 2016
    “…Among them, <b>14k</b> exhibited most potent activity, with IC<sub>50</sub> values of 3–9 nM against six cancer cells, which displayed a 3.8–8.7-fold increase in activity when compare with compound <b>2</b>. …”
  16. 8456

    Synthesis, Evaluation, and Mechanism Study of Novel Indole-Chalcone Derivatives Exerting Effective Antitumor Activity Through Microtubule Destabilization in Vitro and in Vivo by Jun Yan (28467)

    Published 2016
    “…Among them, <b>14k</b> exhibited most potent activity, with IC<sub>50</sub> values of 3–9 nM against six cancer cells, which displayed a 3.8–8.7-fold increase in activity when compare with compound <b>2</b>. …”
  17. 8457

    Synthesis, Evaluation, and Mechanism Study of Novel Indole-Chalcone Derivatives Exerting Effective Antitumor Activity Through Microtubule Destabilization in Vitro and in Vivo by Jun Yan (28467)

    Published 2016
    “…Among them, <b>14k</b> exhibited most potent activity, with IC<sub>50</sub> values of 3–9 nM against six cancer cells, which displayed a 3.8–8.7-fold increase in activity when compare with compound <b>2</b>. …”
  18. 8458

    Synthesis, Evaluation, and Mechanism Study of Novel Indole-Chalcone Derivatives Exerting Effective Antitumor Activity Through Microtubule Destabilization in Vitro and in Vivo by Jun Yan (28467)

    Published 2016
    “…Among them, <b>14k</b> exhibited most potent activity, with IC<sub>50</sub> values of 3–9 nM against six cancer cells, which displayed a 3.8–8.7-fold increase in activity when compare with compound <b>2</b>. …”
  19. 8459

    Synthesis, Evaluation, and Mechanism Study of Novel Indole-Chalcone Derivatives Exerting Effective Antitumor Activity Through Microtubule Destabilization in Vitro and in Vivo by Jun Yan (28467)

    Published 2016
    “…Among them, <b>14k</b> exhibited most potent activity, with IC<sub>50</sub> values of 3–9 nM against six cancer cells, which displayed a 3.8–8.7-fold increase in activity when compare with compound <b>2</b>. …”
  20. 8460

    Synthesis, Evaluation, and Mechanism Study of Novel Indole-Chalcone Derivatives Exerting Effective Antitumor Activity Through Microtubule Destabilization in Vitro and in Vivo by Jun Yan (28467)

    Published 2016
    “…Among them, <b>14k</b> exhibited most potent activity, with IC<sub>50</sub> values of 3–9 nM against six cancer cells, which displayed a 3.8–8.7-fold increase in activity when compare with compound <b>2</b>. …”