Showing 12,301 - 12,320 results of 102,401 for search '(( a step decrease ) OR ( 5 ((teer decrease) OR (((nn decrease) OR (a decrease)))) ))', query time: 1.53s Refine Results
  1. 12301

    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. …”
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    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). …”
  9. 12309

    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. …”
  10. 12310

    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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