يعرض 41 - 60 نتائج من 17,741 نتيجة بحث عن '(( 50 ((teer decrease) OR (a decrease)) ) OR ((( 5 ng decrease ) OR ( 5 ht decrease ))))', وقت الاستعلام: 0.68s تنقيح النتائج
  1. 41

    ngLVA degradation kinetics. حسب Nicole A. Grieshaber (11175417)

    منشور في 2022
    "…Chloramphenicol treated sample showed a decrease of half max intensity 30 mins after treatment.…"
  2. 42
  3. 43
  4. 44
  5. 45
  6. 46
  7. 47
  8. 48

    Synthesis and Biological Evaluation of Peripheral 5HT<sub>2B</sub> Antagonists for Liver Fibrosis حسب Jihyeon Yoon (8705706)

    منشور في 2025
    "…Recent studies have shown that antagonizing 5-hydroxytryptamine receptor 2B (5HT<sub>2B</sub>) stimulates the apoptosis of activated hepatic stellate cells and inhibits their proliferation while concurrently regressing hepatocyte proliferation. …"
  9. 49

    Synthesis and Biological Evaluation of Peripheral 5HT<sub>2B</sub> Antagonists for Liver Fibrosis حسب Jihyeon Yoon (8705706)

    منشور في 2025
    "…Recent studies have shown that antagonizing 5-hydroxytryptamine receptor 2B (5HT<sub>2B</sub>) stimulates the apoptosis of activated hepatic stellate cells and inhibits their proliferation while concurrently regressing hepatocyte proliferation. …"
  10. 50
  11. 51
  12. 52
  13. 53
  14. 54
  15. 55
  16. 56
  17. 57
  18. 58

    Pharmacological Mechanism of the Non-hallucinogenic 5‑HT<sub>2A</sub> Agonist Ariadne and Analogs حسب Michael J. Cunningham (14267038)

    منشور في 2022
    "…Compared to DOM, Ariadne shows lower signaling potency and efficacy in multiple signaling pathways examined (G<sub>q</sub>, G<sub>11</sub>, and β-arrestin2) coupled to 5-HT<sub>2A</sub> receptors. We confirmed the shift in signaling for an α-propyl analog and provide a molecular docking rationale for the progressive decrease in signaling potency with the growing length of the α-substituent. …"
  19. 59

    Pharmacological Mechanism of the Non-hallucinogenic 5‑HT<sub>2A</sub> Agonist Ariadne and Analogs حسب Michael J. Cunningham (14267038)

    منشور في 2022
    "…Compared to DOM, Ariadne shows lower signaling potency and efficacy in multiple signaling pathways examined (G<sub>q</sub>, G<sub>11</sub>, and β-arrestin2) coupled to 5-HT<sub>2A</sub> receptors. We confirmed the shift in signaling for an α-propyl analog and provide a molecular docking rationale for the progressive decrease in signaling potency with the growing length of the α-substituent. …"
  20. 60