Showing 13,501 - 13,520 results of 103,675 for search '(( a step decrease ) OR ( 5 ((((we decrease) OR (a decrease))) OR (nn decrease)) ))', query time: 1.42s Refine Results
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    Impact of Weak Agostic Interactions in Nickel Electrocatalysts for Hydrogen Oxidation by Christina M. Klug (4107286)

    Published 2017
    “…However, the decrease in catalytic rate is accompanied by a beneficial 130 mV decrease in overpotential.…”
  4. 13504

    Baseline characteristics of the study population. by Hae In Jung (18137024)

    Published 2024
    “…</p><p>Conclusions</p><p>As problems indicated by EQ-5D worsened, there was a consistent decrease in handgrip strength (HGS) across both genders. …”
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    A bivalent live-attenuated vaccine candidate elicits protective immunity against human adenovirus types 4 and 7 by Jingao Guo (11034885)

    Published 2021
    “…<p>Human adenovirus types 4 (HAdV4) and 7 (HAdV7) often lead to severe respiratory diseases and occur epidemically in children, adults, immune deficiency patients, and other groups, leading to mild or severe symptoms and even death. …”
  8. 13508
  9. 13509

    Decreased myofibroblasts in the peritumoral region and high expression of MMP-7 in Pan02 S.C. tumor of <i>S100a4-Cre; Ext1</i><sup><i>f/f</i></sup> mice. by Ayumi Niwa (6256790)

    Published 2023
    “…Alcian blue staining (pH = 2.5) in the peritumoral region of Pan02 S.C. pancreatic tumors in <i>S100a4-Cre; Ext1</i><sup><i>f/f</i></sup> and control mice (middle). …”
  10. 13510

    Controlling the Conformational Energy of a Phenyl Group by Tuning the Strength of a Nonclassical CH···O Hydrogen Bond: The Case of 5‑Phenyl-1,3-dioxane by William F. Bailey (1617169)

    Published 2016
    “…Acid-catalyzed equilibration of a series of anancomeric 2-<i>tert</i>-butyl-5-aryl-1,3-dioxane isomers demonstrates that remote substituents on the phenyl ring affect the conformational energy of a 5-aryl-1,3-dioxane: electron-withdrawing substituents decrease the conformational energy of the aryl group, while electron-donating substituents increase the conformational energy of the group. …”
  11. 13511

    Controlling the Conformational Energy of a Phenyl Group by Tuning the Strength of a Nonclassical CH···O Hydrogen Bond: The Case of 5‑Phenyl-1,3-dioxane by William F. Bailey (1617169)

    Published 2016
    “…Acid-catalyzed equilibration of a series of anancomeric 2-<i>tert</i>-butyl-5-aryl-1,3-dioxane isomers demonstrates that remote substituents on the phenyl ring affect the conformational energy of a 5-aryl-1,3-dioxane: electron-withdrawing substituents decrease the conformational energy of the aryl group, while electron-donating substituents increase the conformational energy of the group. …”
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