Showing 1 - 20 results of 4,520 for search '(( strain i decrease ) OR ( i ((large decrease) OR (marked decrease)) ))', query time: 0.57s Refine Results
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    Infection related impact of different <i>Schistosoma mansoni</i> strains on host pathology. by Tim A. Dannenhaus (19959583)

    Published 2024
    “…<p>(A) Liver and spleen pathology of mice infected with 100 cercariae of the BH, LB and PR strain; the bar corresponds to 1 cm. (B) Ratio of liver and spleen weight to body weight and organ cell counts; the PR strain had the highest ratio of organs to body weight, which also tended to be reflected in organ cell counts (D) Liver enzymes alanine aminotransferase (ALT) and aspartate aminotransferase (AST) were elevated during infection with all three strains, with the exception of AST in the PR group. …”
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    Conformational Role of Methyl in the Potency of Cyclohexane-Substituted Squaramide CCR6 Antagonists by Brian S. Gerstenberger (1936534)

    Published 2025
    “…Evidence generated through the characterization of conformationally restricted analogues supports the conclusion that the large potency enhancement is the result of the methyl substituent biasing the cyclohexane ring ground state conformation to favor that of the bound ligand and thus decreasing the ligand strain energy.…”
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    Conformational Role of Methyl in the Potency of Cyclohexane-Substituted Squaramide CCR6 Antagonists by Brian S. Gerstenberger (1936534)

    Published 2025
    “…Evidence generated through the characterization of conformationally restricted analogues supports the conclusion that the large potency enhancement is the result of the methyl substituent biasing the cyclohexane ring ground state conformation to favor that of the bound ligand and thus decreasing the ligand strain energy.…”
  17. 17

    Conformational Role of Methyl in the Potency of Cyclohexane-Substituted Squaramide CCR6 Antagonists by Brian S. Gerstenberger (1936534)

    Published 2025
    “…Evidence generated through the characterization of conformationally restricted analogues supports the conclusion that the large potency enhancement is the result of the methyl substituent biasing the cyclohexane ring ground state conformation to favor that of the bound ligand and thus decreasing the ligand strain energy.…”
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