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Genomics Drug Discovery
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Genomics Drug Discovery Hardback - 2008 - 1st Edition

by Dimitri Semizarov; Eric Blomme

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Reader reviews for Genomics Drug Discovery

From the publisher

Early characterization of toxicity and efficacy would significantly impact the overall productivity of pharmaceutical R&D and reduce drug candidate attrition and failure. By describing the available platforms and weighing their relative advantages and disadvantages, including microarray data analysis, Genomics in Drug Discovery and Development introduces readers to the biomarker, pharmacogenomic, and toxicogenomics toolbox. The authors provide a valuable resource for pharmaceutical discovery scientists, preclinical drug safety department personnel, regulatory personnel, discovery toxicologists, and safety scientists, drug development professionals, and pharmaceutical scientists.

From the rear cover

New, effective strategies for early assessment of drug toxicity and efficacy

Genomics in Drug Discovery and Development introduces readers to the biomarker, pharmacogenomic, pharmacogenetic, and toxicogenomic toolboxes, four promising and rapidly growing areas of genomics research that have begun opening the door to personalized medicine solutions. The authors thoroughly review and analyze all relevant technologies and analytical methods necessary for the competent design and execution of biomarker, pharmacogenomic, pharmacogenetic, and toxicogenomic studies. Moreover, by emphasizing the synergies among these areas, they arm pharmaceutical discovery scientists and drug development professionals with state-of-the-art strategies for reducing drug development time and costs, expediting a drug's approval, and improving its life cycle. Academic researchers will find in this book authoritative and integrated coverage of these rapidly developing and popular areas of genomic research.

Readers involved in laboratory, clinical, or modeling studies who are seeking to assess the toxicity and efficacy of drug candidates as early as possible can rely on this book to help guide their experiments. Topics include:

  • Weighing the relative advantages and disadvantages of available genomic technology platforms

  • Using pharmacogenomics and pharmacogenetics to position drug studies in the context of clinical trials

  • Identifying and validating biomarkers

  • Predicting and characterizing the toxicity of drugs

  • Applying study findings to improve the productivity of drug discovery

Today's pharmaceutical industry is characterized by exponentially rising R&D costs and a steadily decreasing percentage of approved drugs. Pharmaceutical discovery scientists therefore should take advantage of this book's unique integrated coverage of biomarkers, toxicogenomics, and pharmacogenomics in order to make their own discovery efforts as fruitful as possible.

Details

  • Title Genomics Drug Discovery
  • Author Dimitri Semizarov; Eric Blomme
  • Binding Hardback
  • Edition number 1st
  • Edition 1
  • Pages 496
  • Volumes 1
  • Language ENG
  • Publisher Wiley, New Delhi
  • Publication date 2008-11-01
  • Features Bibliography, Index, Table of Contents
  • ISBN 9780470096048 / 0470096047
  • Weight 1.85 lbs (0.84 kg)
  • Dimensions 9.3 x 6.1 x 1.1 in (23.62 x 15.49 x 2.79 cm)
  • Category Medical / Nursing
  • Library of Congress subjects Pharmacogenomics, Drug Design
  • Library of Congress Catalogue Number 2008021434
  • Dewey Decimal Code 615.19

Media reviews

Citations

  • Scitech Book News, 03/01/2009, Page 126

About the author

Dimitri Semizarov, PhD, is a Senior Group Leader in the Cancer Research Department of Abbott Laboratories' Global Pharmaceutical R&D. Dr. Semizarov leads cancer genomics research at Abbott, applying genomics technologies to enable personalization of cancer therapy. He is author or coauthor of more than twenty scientific articles and eight patent applications, as well as three book chapters (including two chapters in Wiley's Preclinical Development Handbook).

Eric Blomme, DVM, PhD, Diplomate, American College of Veterinary Pathologists, is a Senior Project Leader for Cellular, Molecular, and Exploratory Toxicology in Global Pharmaceutical R&D at Abbott Laboratories. He has extensive drug discovery, toxicology, and screening experience working for Abbott, Pharmacia, Monsanto, Searle, Ohio State University, and Cornell University. Dr. Blomme has written over fifty journal articles and eight book chapters, and is a reviewer for multiple scientific journals in the fields of toxicology and pathology.

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Genomics in Drug Discovery and Development

by Semizarov, Dimitri

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