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180525s2018 mau o 000 0 eng d |
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|a 1038059188
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|a 615.7
|2 23
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|a Pharmacogenetics /
|c edited by Kim Brøsen, Per Damkier.
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|a First edition.
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|a Cambridge, MA :
|b Academic Press,
|c 2018.
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|a 1 online resource
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|a text
|b txt
|2 rdacontent
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|a computer
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|a online resource
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|a Advances in pharmacology ;
|v volume 83
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|a Online resource; title from PDF title page (EBSCO, viewed May 29, 2018)
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|a Front Cover; Pharmacogenetics; Copyright; Contents; Contributors; Preface; Section I: Cytochrome P450; Chapter One: Cytochrome P450 in Pharmacogenetics: An Update; 1. Introduction; 2. Genetic Variability of CYP Enzymes; 3. CYP1A Subfamily; 3.1. CYP1A2; 4. CYP2A and CYP2B Subfamilies; 4.1. CYP2A6; 4.2. CYP2B6; 5. CYP2C Subfamily; 5.1. CYP2C8; 5.2. CYP2C9; 5.3. CYP2C19; 6. CYP2D6; 7. CYP3A Subfamily; 7.1. CYP3A4; 7.2. CYP3A5; 8. Conclusion; Conflict of Interest; References; Chapter Two: Epigenetics and MicroRNAs in Pharmacogenetics; 1. Introduction; 2. Epigenetics in Pharmacogenetics
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|a 2.1. Polymorphisms Interacting With DMET Gene Methylation2.2. Polymorphisms Affecting Methylation Machinery; 3. miRNAs in Pharmacogenetics; 3.1. miR-SNPs Affecting Enzymes; 3.2. miR-SNPs Affecting Transporters; 3.3. miR-SNPs Affecting Regulators and miRNA Machinery; 4. Conclusion; Acknowledgments; Conflict of Interest; References; Chapter Three: Tamoxifen and CYP2D6: A Controversy in Pharmacogenetics; 1. Introduction; 1.1. Tamoxifen Metabolism; 1.2. Tamoxifen Transport; 2. CYP2D6 and Tamoxifen Metabolism; 2.1. Studies on Drug-Induced Inhibition of Tamoxifen Metabolism
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|a 2.2. Limitations of the Pharmacoepidemiological Drug-Drug Interaction Studies2.3. Studies on Pharmacogenetically Reduced Tamoxifen Metabolism; 2.4. Comprehensive Genotyping; 2.5. Use of Tumor-Infiltrated DNA for Genotyping; 3. Perspectives; 3.1. Comprehensive Genotyping; 3.2. Genetically Reduced CYP2D6 Activity May Have Greatest Impact on Tamoxifen Effectiveness in Premenopausal Breast Canc ... ; 3.3. Tamoxifen Transport; 3.4. Other Biomarkers May Impact Tamoxifen Effectiveness; 3.5. Tamoxifen Analogues; 4. Conclusion; Acknowledgments; Conflict of Interest; References; Section II: Methods
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|a Chapter Four: Imaging in Pharmacogenetics1. Introduction; 2. Imaging Modalities; 3. Absorption; 4. Distribution; 5. Metabolism; 6. Elimination; 7. Conclusion; Conflict of Interest; References; Chapter Five: Pharmacoepidemiology in Pharmacogenetics; 1. Introduction; 2. Study Design; 2.1. Experimental and Observational Cohort Studies; 2.1.1. Calculating Risk-Based Measures of Disease Frequency and Association; 2.1.2. Calculating Rate-Based Measures of Disease Frequency and Association; 2.2. Case-Control Studies; 2.2.1. Strategies for Sampling Controls
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|a 2.2.2. Calculating Associations in Case-Control Studies2.3. Assessing Interaction in Epidemiologic Studies; 2.3.1. Case-Only Studies; 2.3.2. Biologic Interaction; 3. Bias and Validity; 3.1. Confounding; 3.2. Selection Bias and Matching in Case-Control Studies; 3.3. Information Bias; 3.4. Reverse Causation; 4. Conclusion; Further Reading; Conflict of Interest; References; Section III: Special Themes; Chapter Six: Population Diversity in Pharmacogenetics: A Latin American Perspective; 1. Introduction; 2. Global Distribution of PGx Variants
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|a Pharmacogenetics.
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|a Pharmaceutical industry
|x Technological innovations.
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|a MEDICAL
|x Pharmacology.
|2 bisacsh
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|a Pharmaceutical industry
|x Technological innovations.
|2 fast
|0 (OCoLC)fst01060184
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650 |
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|a Pharmacogenetics.
|2 fast
|0 (OCoLC)fst01060243
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|a Electronic books.
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1 |
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|a Brøsen, Kim.
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700 |
1 |
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|a Damkier, Per.
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776 |
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|i Print version:
|t Pharmacogenetics.
|b First edition.
|d Cambridge, MA : Academic Press, 2018
|z 0128133813
|z 9780128133811
|w (OCoLC)1013515830
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830 |
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|a Advances in pharmacology (San Diego, Calif.) ;
|v 83.
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856 |
4 |
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|3 ScienceDirect
|u https://www.sciencedirect.com/science/bookseries/10543589/83
|z Full Text via HEAL-Link
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856 |
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|3 ScienceDirect
|u https://www.sciencedirect.com/science/book/9780128133811
|z Full Text via HEAL-Link
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