يعرض 14,081 - 14,100 نتائج من 105,824 نتيجة بحث عن '(( i x decrease ) OR ( 5 ((((ng decrease) OR (a decrease))) OR (nn decrease)) ))', وقت الاستعلام: 1.70s تنقيح النتائج
  1. 14081

    Effect of 4‑HNE Modification on ZU5-ANK Domain and the Formation of Their Complex with β‑Spectrin: A Molecular Dynamics Simulation Study حسب Antistio Alviz-Amador (8174016)

    منشور في 2019
    "…However, effects at the atomic level of this carbonylation on structure and function of modified protein are not yet fully understood. We present a study based on molecular dynamics simulations of nine 4-HNE modified residues of the ZU5-ANK ankyrin domain with β-spectrin and their binding energy profiles. …"
  2. 14082

    Effect of 4‑HNE Modification on ZU5-ANK Domain and the Formation of Their Complex with β‑Spectrin: A Molecular Dynamics Simulation Study حسب Antistio Alviz-Amador (8174016)

    منشور في 2019
    "…However, effects at the atomic level of this carbonylation on structure and function of modified protein are not yet fully understood. We present a study based on molecular dynamics simulations of nine 4-HNE modified residues of the ZU5-ANK ankyrin domain with β-spectrin and their binding energy profiles. …"
  3. 14083

    Data_Sheet_1_Decreased Intrinsic Functional Connectivity in First-Episode, Drug-Naive Adolescents With Generalized Anxiety Disorder.docx حسب Fan Yang (1413)

    منشور في 2019
    "…Moreover, the disrupted intra-network connectivity (i.e., the SMG-based network and the SPG-based network) and inter-network connectivity between the SMG-based network and the SPG-based network accounted for 25.5% variance of the State and Trait Anxiety Inventory (STAI) and 39.5% variance of the trait subscale of STAI. …"
  4. 14084
  5. 14085

    Both WD and AD cross-modally provoke a potentiation of the visual OKR. حسب Manuel Teichert (6443960)

    منشور في 2019
    "…Subsequently, spatial frequency sensitivity slightly decreased until day 5 after AD and remained at a stable level above control values until 10 days after AD. …"
  6. 14086
  7. 14087

    HuR specifically represses translation through the IGF-IR 5′-UTR in a concentration-dependent manner حسب Zheng Meng (9293)

    منشور في 2011
    "…The FLuc RNA (5 ng) was used as a control. The results are expressed relative to the control reactions without HuR. () translation with recombinant HuR protein. …"
  8. 14088
  9. 14089
  10. 14090

    Shear stress and MT depolymerization are associated with decreased airway epithelial paracellular permeability and shear stress results in increased MT depolymerization. حسب Venkataramana K. Sidhaye (319946)

    منشور في 2013
    "…NHBE cells exposed to nocodazole (20 µM) had a decrease in FITC-dextran permeability, similar to that seen after exposure to shear stress. …"
  11. 14091
  12. 14092

    Human preterm infants diagnosed with IUGR have decreased Paneth cell counts compared to preterm non-IUGR control infants. حسب Camille M. Fung (844334)

    منشور في 2016
    "…(A) IUGR infants had similar numbers of goblet cells per 100 epithelial cells compared to non-IUGR infants (p = 0.5). …"
  13. 14093
  14. 14094

    Effects of RSV and FIDAS on AR/Q640X-signalling under androgen deprived conditions. حسب Wolfgang Streicher (571178)

    منشور في 2014
    "…Data are expressed in fold AR basal activity which was set to 1. As depicted, RSV and FIDAS significantly decreased PSA-promoter mediated reporter gene activity in Q640X and AR co-expressing cells, *p>0.05.…"
  15. 14095
  16. 14096

    Glibenclamide Decreases ATP-Induced Intracellular Calcium Transient Elevation via Inhibiting Reactive Oxygen Species and Mitochondrial Activity in Macrophages حسب Duo-ling Li (523730)

    منشور في 2014
    "…The transient elevation was inhibited by an ROS scavenger (tiron) and mitochondria inhibitor (rotenone). Glibenclamide and 5-hydroxydecanoate (5-HD) also decreased ATP-induced [Ca<sup>2+</sup>]<sub>i</sub> transient elevation, but pinacidil and other unselective K<sup>+</sup> channel blockers had no effect. …"
  17. 14097
  18. 14098
  19. 14099
  20. 14100