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Model Organisms in Drug Discovery

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Model Organisms in Drug Discovery Cover

 

Synopses & Reviews

Publisher Comments:

Fruit flies are "little people with wings" goes the saying in the scientific community, ever since the completion of the Human Genome Project and its revelations about the similarity amongst the genomes of different organisms. It is humbling that most signaling pathways which "define" humans are conserved in Drosophila, the common fruit fly. Feed a fruit fly caffeine and it has trouble falling asleep; feed it antihistamines and it cannot stay awake. A C. elegans worm placed on the antidepressant flouxetine has increased serotonin levels in its tiny brain. Yeast treated with chemotherapeutics stop their cell division. Removal of a single gene from a mouse or zebrafish can cause the animals to develop Alzheimer’s disease or heart disease. These organisms are utilized as surrogates to investigate the function and design of complex human biological systems.

Advances in bioinformatics, proteomics, automation technologies and their application to model organism systems now occur on an industrial scale. The integration of model systems into the drug discovery process, the speed of the tools, and the in vivo validation data that these models can provide, will clearly help definition of disease biology and high-quality target validation. Enhanced target selection will lead to the more efficacious and less toxic therapeutic compounds of the future.

This book will be of interest to geneticists, bioinformaticians, pharmacologists, molecular biologists and people working in the pharmaceutical industry, particularly genomics.

Book News Annotation:

Yeast, nematodes, fruit flies, zebrafish, and mice are all used by scientists as model organisms for studying drug reactions and most have the advantages of complete genome sequences and "forward" and "reverse" genetic tools for genome-wide functional discoveries. Carroll and Fitzgerald (applied genomics, Pharmaceutical Research Institute, Bristol-Myers Squibb) present a text that describes the technical advantages for each of these organisms in turn, as well as accounts of disease models in the organisms that have impacted understandings of human biology.
Annotation 2004 Book News, Inc., Portland, OR (booknews.com)

Synopsis:

Model organisms are becoming increasingly useful in a systematic approach to a broad array of disease-based questions. With the advanced genetic techniques that are available for the model organisms and the availability of their genome sequences, these organisms are poised to have a major impact in drug discovery, particularly in the critical area of protein target validation. This timely book details recent advances in bioinformatics, proteomics, genomics, biochemical and automation technologies as applied to simple organisms in an integrated drug discovery platform.

Table of Contents

List of contributors.

Acknowledgments.

1. Introduction to Model Systems in Drug Discovery (Kevin Fitzgerald and Pamela M. Carroll).

2. Growing Yeast for Fun and Profit: Use of Saccharomyces cerevisiae as a Model System in Drug Discovery (Petra Ross-Macdonald).

3. Caenorhabditis elegans Functional Genomics in Drug Discovery: Expanding Paradigms (Titus Kaletta, Lynn Butler and Thierry Bogaert).

4. Drosophila as a Tool for Drug Discovery (Hao Li and Dan Garza).

5. Drosophila – a Model System for Targets and Lead Identification in Cancer and Metabolic Disorders (Corina Schütt, Barbara Froesch and Ernst Hafen).

6. Mechanism of Action in Model Organisms: Interfacing Chemistry, Genetics and Genomics (Pamela M. Carroll, Kevin Fitzgerald and Rachel Kindt).

7. Gene tics and Genomics in the Zebrafish: from Gene to Function and Back (Stefan Schulte-Merker).

8. Lipid Metabolism and Signaling in Zebrafish (Shiu-Ying Ho, Steven A. Farber and Michael Pack).

9. Chemical Mutagenesis in the Mouse: a Powerful Tool in Drug Target Identification and Validation (Andreas Russ, Neil Dear, Geert Mudde, Gabriele Stumm, Johannes Grosse, Andreas Schröder, Reinhard Sedlmeier, Sigrid Wattler and Michael Nehls).

10. Saturation Screening of the Druggable Mammalian Genome (Hector Beltrandelrio, Francis Kern, Thomas Lanthorn, Tamas Oravecz, James Piggott, David Powell, Ramiro Ramirez-Solis, Arthur T. Sands and Brian Zambrowicz).

Index.

Product Details

ISBN:
9780470848937
Editor:
Carroll, Pamela M.
Editor:
Fitzgerald, Kevin
Editor:
Carroll, Pamela M.
Editor:
Carroll, Pamela
Editor:
Fitzgerald, Kevin
Author:
Fitzgerald, Kevin
Author:
Carroll, Pamela M.
Publisher:
John Wiley & Sons
Location:
Chichester, West Sussex, England
Subject:
Drugs
Subject:
Chemistry - Organic
Subject:
Research
Subject:
Pharmacology
Subject:
Pharmacy
Subject:
Biotechnology
Subject:
Pharmacogenetics.
Subject:
Disease models, Animal.
Subject:
Drug Design.
Subject:
Genomics
Subject:
Pharmacogenomics
Subject:
Life Sciences - Genetics & Genomics
Subject:
Drugs -- Research.
Subject:
Biotechnology (Life Sciences)
Subject:
Health and Medicine-Pharmacology
Subject:
Biotechnology (Life Scie
Subject:
nces
Copyright:
Edition Description:
WOL online Book (not BRO)
Series Volume:
#69
Publication Date:
20040420
Binding:
HARDCOVER
Grade Level:
Professional and scholarly
Language:
English
Illustrations:
Yes
Pages:
302
Dimensions:
253 x 178 x 22 mm 24 oz

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Related Subjects

Health and Self-Help » Health and Medicine » Pharmacology
Science and Mathematics » Biology » General
Science and Mathematics » Biology » Genetics
Science and Mathematics » Chemistry » Chemical Engineering

Model Organisms in Drug Discovery New Hardcover
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Product details 302 pages John Wiley & Sons - English 9780470848937 Reviews:
"Synopsis" by , Model organisms are becoming increasingly useful in a systematic approach to a broad array of disease-based questions. With the advanced genetic techniques that are available for the model organisms and the availability of their genome sequences, these organisms are poised to have a major impact in drug discovery, particularly in the critical area of protein target validation. This timely book details recent advances in bioinformatics, proteomics, genomics, biochemical and automation technologies as applied to simple organisms in an integrated drug discovery platform.
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