Titlebook: Individualität und psychologische Gruppenbildung; Eine sozialpsycholog Claudia Kampmeier Book 2001 Springer Fachmedien Wiesbaden 2001 Grupp

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ression or protein–protein interaction networks. Also, approaches to reverse engineer gene networks or methods that seek to identify novel interactions between genes are described. Given the relatively small sample numbers typically available, these reverse engineering approaches are generally usefu

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Claudia Kampmeierss, statistical methods that be used to build QSAR models as well as methods to validate the models that are developed. Most of the methods described in this chapter can be used to develop models for health endpoints other than developmental toxicity as well.

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Claudia Kampmeiertter success has been achieved with ligand-based modeling methods including quantitative structure–activity relationship (QSAR) analysis, pharmacophore modeling and machine learning that use appropriate descriptors to account for the diversity of the ligand classes that bind to PXR. These combined c

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Claudia Kampmeierhe use of computational techniques and databases to predict chemical properties and toxicity, as well as an overview of molecular dynamics.  The final section is a compilation of the key elements and main approaches used in pharmacokinetic and pharmacodynamic modeling, including the modeling of abso

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Claudia Kampmeiertter success has been achieved with ligand-based modeling methods including quantitative structure–activity relationship (QSAR) analysis, pharmacophore modeling and machine learning that use appropriate descriptors to account for the diversity of the ligand classes that bind to PXR. These combined c

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Claudia Kampmeierty, as well as an overview of molecular dynamics.  The final section is a compilation of the key elements and main approaches used in pharmacokinetic and pharmacodynamic modeling, including the modeling of abso978-1-4939-5897-9978-1-62703-050-2Series ISSN 1064-3745 Series E-ISSN 1940-6029