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point decrease » point increase (Expand Search)
fold decrease » fold increase (Expand Search), fold increased (Expand Search)
a decrease » _ decrease (Expand Search), _ decreased (Expand Search), _ decreases (Expand Search)
point decrease » point increase (Expand Search)
fold decrease » fold increase (Expand Search), fold increased (Expand Search)
a decrease » _ decrease (Expand Search), _ decreased (Expand Search), _ decreases (Expand Search)
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15861
Baseline characteristics of the study population.
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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15862
Silencing of ATG5 gene.
Published 2012“…(A) Time-dependent decrease in ATG5 protein in siATG5-transfected cells. …”
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15863
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15864
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15865
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15866
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15867
A bivalent live-attenuated vaccine candidate elicits protective immunity against human adenovirus types 4 and 7
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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15868
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15869
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15870
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15871
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15872
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15873
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15874
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15875
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15876
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
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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15877
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
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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15878
DataSheet2_A comprehensive assessment of RCP4.5 projections and bias-correction techniques in a complex coastal karstic aquifer in the Mediterranean.docx
Published 2023“…Results of future climate projections show a decrease in precipitation of about 6% and an increase in temperature of 2°C until the end of this century, compared to the historical period (1971–2005). …”
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15879
DataSheet1_A comprehensive assessment of RCP4.5 projections and bias-correction techniques in a complex coastal karstic aquifer in the Mediterranean.docx
Published 2023“…Results of future climate projections show a decrease in precipitation of about 6% and an increase in temperature of 2°C until the end of this century, compared to the historical period (1971–2005). …”
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15880