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Optimal experimental designs for dose–response studies with continuous endpoints
In most areas of clinical and preclinical research, the required sample size determines the costs and effort for any project, and thus, optimizing sample size is of primary importance. An experimental design of dose–response studies is determined by the number and choice of dose levels as well as th...
Guardat en:
| Publicat a: | Arch Toxicol |
|---|---|
| Autors principals: | , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Springer Berlin Heidelberg
2014
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4655015/ https://ncbi.nlm.nih.gov/pubmed/25155192 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00204-014-1335-2 |
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