Search alternatives:
significant implications » significant associations (Expand Search)
inter decrease » linear decrease (Expand Search), water decreases (Expand Search), teer decrease (Expand Search)
nn decrease » _ decrease (Expand Search), a decrease (Expand Search), mean decrease (Expand Search)
significant implications » significant associations (Expand Search)
inter decrease » linear decrease (Expand Search), water decreases (Expand Search), teer decrease (Expand Search)
nn decrease » _ decrease (Expand Search), a decrease (Expand Search), mean decrease (Expand Search)
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Intra- and inter-day precision and accuracy.
Published 2025“…<div><p>Purpose</p><p>Statins are the most commonly used drugs worldwide. Besides a significant decrease in cardiovascular diseases (CVDs) risk, the use of statins is also connected with a broad beneficial pleiotropic effect. …”
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The table shows the significant and non-significant altered group with different parameters.
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Juvenile demyelination leads to a decrease in axonal complexity of PFC PV interneurons.
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Global Land Use Change Impacts on Soil Nitrogen Availability and Environmental Losses
Published 2025“…In contrast, reversing managed to natural ecosystems significantly increased NNM by 20% (9.7, 25.4%) and decreased NN by 89% (−125, −46%), indicating increasing N availability while decreasing potential N loss. …”
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Sensitivity analysis for inter-shift subscale.
Published 2025“…Studies have consistently linked occupational fatigue to decreased productivity, heightened error rates, and compromised decision-making abilities, posing significant risks to both individual nurses and healthcare organizations. …”
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IRE1 depletion decreases heterochromatin, DNA, and H3K9me3 methylation, and UHRF1.
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IRE1 depletion decreases heterochromatin, DNA and H3K9me3 methylation, and UHRF1.
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Table 1_Dual variants of uncertain significance in a case of hyper-IgM syndrome: implications for diagnosis and management.docx
Published 2025“…</p>Objective<p>This study aims to elucidate the clinical implications of concurrent AICDA and IKBKB homozygous variants in a pediatric patient diagnosed with hyper-IgM syndrome.…”
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