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  2. Dose–response relationship - Wikipedia

    en.wikipedia.org/wiki/Doseresponse_relationship

    The doseresponse relationship, or exposure–response relationship, describes the magnitude of the response of an organism, as a function of exposure (or doses) to a stimulus or stressor (usually a chemical) after a certain exposure time. [1] Doseresponse relationships can be described by doseresponse curves. This is explained further ...

  3. EC50 - Wikipedia

    en.wikipedia.org/wiki/EC50

    The EC 50 of a quantal dose response curve represents the concentration of a compound where 50% of the population exhibit a response, [5] after a specified exposure duration. For clarification, a graded dose response curve shows the graded effect of the drug (y axis) over the dose of the drug (x axis) in one or an average of subjects.

  4. Hormesis - Wikipedia

    en.wikipedia.org/wiki/Hormesis

    Hormesis is a biological phenomenon where a low dose of a potentially harmful stressor, such as a toxin or environmental factor, stimulates a beneficial adaptive response in an organism. In other words, small doses of stressors that would be damaging in larger amounts can actually enhance resilience, stimulate growth, or improve health at lower ...

  5. Bradford Hill criteria - Wikipedia

    en.wikipedia.org/wiki/Bradford_Hill_criteria

    Temporality: The effect has to occur after the cause (and if there is an expected delay between the cause and expected effect, then the effect must occur after that delay). Biological gradient (doseresponse relationship): Greater exposure should generally lead to greater incidence of the effect. However, in some cases, the mere presence of ...

  6. Pharmacodynamics - Wikipedia

    en.wikipedia.org/wiki/Pharmacodynamics

    Pharmacodynamics places particular emphasis on doseresponse relationships, that is, the relationships between drug concentration and effect. [1] One dominant example is drug-receptor interactions as modeled by +

  7. Pharmacokinetics - Wikipedia

    en.wikipedia.org/wiki/Pharmacokinetics

    Pharmacokinetics is based on mathematical modeling that places great emphasis on the relationship between drug plasma concentration and the time elapsed since the drug's administration. Pharmacokinetics is the study of how an organism affects the drug, whereas pharmacodynamics (PD) is the study of how the drug affects the organism.

  8. Today's Wordle Hint, Answer for #1271 on Wednesday, December ...

    www.aol.com/todays-wordle-hint-answer-1271...

    If you’re stuck on today’s Wordle answer, we’re here to help—but beware of spoilers for Wordle 1271 ahead. Let's start with a few hints.

  9. Linear no-threshold model - Wikipedia

    en.wikipedia.org/wiki/Linear_no-threshold_model

    The linear no-threshold model (LNT) is a dose-response model used in radiation protection to estimate stochastic health effects such as radiation-induced cancer, genetic mutations and teratogenic effects on the human body due to exposure to ionizing radiation. The model assumes a linear relationship between dose and health effects, even for ...