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DELIVERY OF
BOOKS
The delivery time for books varies with the different
suppliers, so we are unable to give a specific delivery time. If
in stock it will be approximately 5 days, if not in stock 2 to 3
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The
Applied Genetics of
Humans, Animals, Plants and Fungi
by Bernard C. Lamb |
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Cat.# DA-GEN1 |
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Published: 2007
ISBN: 9781860946103 |
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A concise, clear writing style and a detailed and rich
coverage of topics are the reasons that students found the
first edition of the book so engaging and useful.
- Wide coverage of and clear descriptions of the
applied genetics of humans, animals, plants and fungi
- Describes the theory and practice of the applied
genetics of all the groups, with diagrams, many examples
and photos
- Brightly illustrated with 65 colour photos,
including some latest methods in medical genetics
Riding on this wave, all chapters within the second
edition of this popular book have been thoroughly
updated and expanded, especially the human and animal
materials. A wider range of animals is covered,
including dogs and cats as well as farm animals. The use
of cord blood for therapy, pre-implantation genetic
diagnosis and animal cloning are also explored and dealt
with. |
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Biological Aging, Methods & Protocols,
with CD-ROM
by Trygve O. Tollefsbol |
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Cat.# DA-GEN2 |
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Published: 2007
ISBN: 9781588296580 |
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"Biological Aging: Methods and Protocols"
investigates the various processes that are affected by
the age of an organism. Several new tools for the analysis
of biological aging have been introduced recently, and
this volume provides methods and protocols for these new
techniques in addition to its coverage of established
procedures. The editors have carefully selected only those
topics that are considered mainstays of the field or are
showing promise in revolutionizing this relatively new
science.
- New and novel techniques in biological aging
research
- Cutting-edge applications of proteomics and
metabolomics
- Identifying genes that extend lifespan using
high-throughput screening systems
The three main areas of focus in this cutting-edge
compendium of biological aging research are: methods
that are basic to understanding the fundamental
mechanisms of cellular aging; techniques used to
intervene in the aging process; and approaches to
analyzing the many molecular processes of biological
aging. Researchers seeking new technology and techniques
will find this volume of tremendous benefit as they move
towards new directions in the exciting and expanding
field of biological aging. |
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Genetically Engineered Food:
Methods and Detection (Ed.2)
by Knut J. Heller
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Cat.# JW-GEN1 |
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Published: 2007
ISBN: 9783527313938 |
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Continuing the very successful first edition, this book
reviews the most recent changes to the legal situation in
Europe concerning genetically engineered food and
labelling.
Due to the extremely rapid developments in green
biotechnology, all the chapters have been substantially
revised and updated.
Divided into three distinct parts, the text begins by
covering applications and perspectives, including
transgenic modification of production traits in farm
animals, fermented food production and the production of
food additives using filamentous fungi. The second section
is devoted to legislation, while the final part examines
methods of detection, such as DNA-based methods, and
methods for detecting genetic engineering in composed and
processed foods.
From the reviews of the first edition:
"This work promises to be a standard reference in the
detection of genetically engineered food. I believe this
work will find a valued place for any scientist, regulator
or technical library that deals with biotechnology or
detection of genetically engineered food organisms."
—James J. Heinis, Journal of Agricultural & Food
Information
Table of Contents:
Preface
List of Contributors
Part I Application and Perspectives
1. Transgenic Modification of Production Traits in Farm
Animals
1.1 Introduction
1.2 The Creation of Transgenic Animals
1.3 Gene Transfer in Poultry
1.4 Gene Transfer in Fish
1.5 Transgenes – Gene Constructs
1.6 Transgenic Animals with Agricultural Traits
1.7 Improved Growth Rate, Carcass Composition, and Feed
Efficiency
1.8 Alteration of the Composition of Milk
1.9 Improved Animal Health
1.10 Improved Biochemical Pathways
1.11 Improved Wool Production
1.12 Transgenic Farm Animals, Biosafety Issues, Animal Welfare,
and Ethics
1.13 Conclusion
References
2. Genetically Modified Plants
2.1 Methods for Establishing Genetically Modified Plants
2.2 GM Plants Already on the Market (EU, USA, Canada, Japan)
2.3 GM Plants “In the Pipeline”
2.4 Outlook
References
3. Fermentation of Food by Means of Genetically Modified
Yeast and Filamentous Fungi
3.1 Introduction
3.2 Yeast
3.3 Filamentous Fungi
3.4 Prospects
Acknowledgements
References
4. Production of Food Additives Using Filamentous Fungi
4.1 Filamentous Fungi in Food Production
4.2 Additives for the Food Industry
4.3 Design of Genetically Modified Microorganisms for
Production of Food Additives and Processing Aids
4.4 Industrial Enzyme Production Processes
References
5. Genetic Engineering of Bacteria Used in Food
Fermentation
5.1 Introduction
5.2 Lactic Acid Bacteria
5.3 Perspectives and Objectives
5.4 Methods
5.5 Conclusions
References
Part II Legislation in Europe.
6. The Legal Situation for Genetically Engineered Food in
Europe
6.1 Introduction
6.2 The Law Applicable to Genetically Modified Food
References
Part III Methods of Detection
7. Detection of Genetic Modifications – Some Basic
Considerations
7.1 The Conversion of Genetic Information from DNA to
Phenotypes
7.2 DNA, Protein, and Phenotypes as Targets for Detection
Assays
7.3 Food-grade Modifications
7.4 Detection of Unknown Modifications
8. DNA-based Methods for Detection of Genetic
Modifications
8.1 Introduction
8.2 Recent DNA Methodology
8.3 Specific Detection of Genetic Material
8.4 Nucleic Acid Amplification Methods using PCR
8.5 Alternative and Promising DNA Detection Techniques
8.6 Conclusions and Future Prospects for GMO Detection by DNA
Analysis
References
9. Genetic Engineering of Fish, and Methods of Detection
9.1 Introduction
9.2 Development and Production of Transgenic Fish
9.3 Examples of Successful Production of Transgenic Fish
9.4 Methods of Detecting Processed Transgenic Fish
9.5 Food Safety of Transgenic Fish
References
10. Detection Methods for Genetically Modified Crops
10.1 Introduction
10.2 Isolation of plant DNA
10.3 Detection Strategies
10.4 Outlook, Conclusions
References
11. Methods for Detection of Genetically Modified
Organisms in Composite and Processed Foods
11.1 Introduction
11.2 Challenges Specific to the Detection of GMO in Composite and
Processed Foods
11.3 Degradation of Proteins and DNA
11.4 Analytical Methods
11.5 Conclusions
References
12. Mutations in Lactococcus lactis and their Detection
Summary
12.1 Introduction
12.2 The Composition of the Genome of Lactococcus lactis
12.3 Flexibility in the Genome of Lactococcus lactis
12.4 Conjugation
12.5 Transduction
12.6 Transformation
12.7 IS Elements and Transposons
12.8 Lactococcal Phages as Sources of Genetic Plasticity
12.9 An Example of Natural Genetic Flexibility: The L. lactis
NCDO712 Family
12.10 Mutations in Lactococcus lactis as a Consequence of
Environmental Factors and DNA Metabolism
12.11 Methods of Mutating the Genome of L. lactis
12.12 Genetic Engineering of Lactococcus lactis
12.13 Strategies for Detection of Genetically Modified Lactococcus
lactis
12.14 Sample Preparation
12.15 DNA-based Procedures
12.16 Protein-based Procedures
12.17 Conclusions
References
13. Methods for Detection of Genetically Modified
Microorganisms used in Food Fermentation Processes
13.1 Introduction
13.2 Current Methods for Detection of GMM
13.3 DNA Isolation
13.4 DNA Stability
13.5 Organism-specific Detection of the GMM
13.6 Conclusion
References
Index
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Flow Cytometry with Plant
Cells:
Analysis of Genes, Chromosomes and
Genomes
by Jaroslav Dolezel, Johann Greilhuber,
and Jan Suda |
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Cat.# JW-GEN2 |
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Published: 2007
ISBN: 9783527314874 |
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Targeted at beginners as well as experienced users,
this handy reference explains the benefits and uses of
flow cytometery in the study of plants and their genomes.
Following a brief introduction that highlights general
considerations when analyzing plant cells by flow
cytometric methods, the book goes on to discuss examples
of application in plant genetics, genomic analysis, cell
cycle analysis, marine organism analysis and breeding
studies. With its list of general reading and a glossary
of terms, this first reference on FCM in plants fills a
real gap by providing first-hand practical hints for the
growing community of plant geneticists.
Table of Contents:
- Development of flow cytometry
- Principles of flow cytometry
- Overview of plant flow cytometry
- Nuclear DNA content measurement
- Ploidy level estimation and its uses in plant
biosystematics
- Reproduction mode screening
- Genome size
- Genome base composition
- Flow cytometry in agro science
- Protoplast analysis
- Flow cytometry of photosynthetic systems
- Flow cytometry of non-vascular plants
- Aquatic flow cytometry
- Cell cycle analysis
- Endopolyploidy
- Flow karyotyping and chromosome sorting
- Analysis of gene expression
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Bioinformatics for
Geneticists
by Michael R. Barnes |
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Cat.# JW-GEN3 |
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Published: 2007
ISBN: 9780470026199 |
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A Bioinformatics Primer for the
Analysis of Genetic Data (Ed.2) A fully revised version of the successful First
Edition, this one-stop reference book enables all
geneticists to improve the efficiency of their research.
The study of human genetics is moving into a challenging
new era. New technologies and data resources such as the
HapMap are enabling genome-wide studies, which could
potentially identify most common genetic determinants of
human health, disease and drug response. With these
tremendous new data resources at hand, more than ever care
is required in their use. Faced with the sheer volume of
genetics and genomic data, bioinformatics is essential to
avoid drowning true signal in noise. Considering these
challenges, Bioinformatics for Geneticists, Second Edition
works at multiple levels: firstly, for the occasional user
who simply wants to extract or analyse specific data;
secondly, at the level of the advanced user providing
explanations of how and why a tool works and how it can be
used to greatest effect. Finally experts from fields
allied to genetics give insight into the best genomics
tools and data to enhance a genetic experiment.
Hallmark Features of the Second Edition:
- Illustrates the value of bioinformatics as a
constantly evolving avenue into novel approaches to
study genetics
- The only book specifically addressing the
bioinformatics needs of geneticists
- More than 500f chapters are completely new
contributions
- Dramatically revised content in core areas of gene
and genomic characterisation, pathway analysis, SNP
functional analysis and statistical genetics
- Focused on freely available tools and web-based
approaches to bioinformatics analysis, suitable for
novices and experienced researchers alike
Praise for the First Edition:
”…a very valuable and important resource for bringing
bioinformatics into the work practice of geneticists… we
strongly recommend this book…” CLINICAL CHEMISTRY, 2004
”…a useful addition to the library of a seasoned
scientist… a useful resource in itself, cataloguing the
‘how’ and ‘why’…” BRIEFINGS IN BIOINFORMATICS, June 2004
Bioinformatics for Geneticists, Second Edition describes
the key bioinformatics and genetic analysis processes
that are needed to identify human genetic determinants.
The book is based upon the combined practical experience
of domain experts from academic and industrial research
environments and is of interest to a broad audience,
including students, researchers and clinicians working
in the human genetics domain. Table of Contents:
Foreword
Preface
Contributors
Glossary
SECTION I AN INTRODUCTION TO BIOINFORMATICS FOR THE
GENETICIST
1. Bioinformatics challenges for the geneticist
1.1 Introduction
1.2 The role of bioinformatics in genetics research
1.3 Genetics in the post-genome era
1.4 Conclusions
References
2. Managing and manipulating genetic data
2.1 Introduction
2.2 Basic principles
2.3 Data entry and storage
2.4 Data manipulation
2.5 Examples of code
2.6 Resources
2.7 Summary
References
SECTION II MASTERING GENES, GENOMES AND GENETIC
VARIATION DATA
3. The HapMap – A haplotype map of the human genome
3.1 Introduction
3.2 Accessing the data
3.3 Application of HapMap data in association studies
3.4 Future Perspectives
References
4. Assembling a view of the human genome
4.1 Introduction
4.2 Genomic sequence assembly
4.3 Annotation from a distance: the generalities
4.4 Annotation up close and personal: the specifics
4.5 Annotation: the next generation
References
5. Finding, delineating and analysing genes
5.1 Introduction
5.2 Why learn to predict and analyse genes in the complete genome
era?
5.3 The evidence cascade for gene products
5.4 Dealing with the complexities of gene models
5.5 Locating known genes in the human genome
5.6 Genome portal inspection
5.7 Analysing novel genes
5.8 Conclusions and prospects
References
6. Comparative genomics
6.1 Introduction
6.2 The Genomic landscape
6.3 Concepts
6.4 Practicalities
6.5 Technology
6.6 Applications
6.7 Challenges and future directions
6.8 Conclusion
References
SECTION III BIOINFORMATICS FOR GENETIC STUDY DESIGN AND
ANALYSIS
7. Identifying mutations in single gene disorders
7.1 Introduction
7.2 Clinical Ascertainment
7.3 Genome-wide mapping of monogenic diseases
7.4 The nature of mutation in monogenic diseases
7.5 Considering epigenetic effects in mendelian traits
7.6 Summary
References
8. From Genome Scan Culprit Gene
8.1 Introduction
8.2 Theoretical and practical considerations
8.3 A stepwise approach to locus refinement and candidate
gene identification
8.4 Conclusion
8.5 A list of the software tools and Web links mentioned
in this chapter
References
9. Integrating Genetics, Genomics and Epigenomics to Identify
Disease Genes
9.1 Introduction
9.2 Dealing with the (draft) human genome sequence
9.3 Progressing loci of interest with genomic information
9.4 In silico characterization of the IBD5 locus – a case study
9.5 Drawing together biological rationale – hypothesis
building
9.6 Identification of potentially functional polymorphisms
9.7 Conclusions
References
10. Tools for statistical genetics
10.1 Introduction
10.2 Linkage analysis
10.3 Association analysis
10.4 Linkage disequilibrium
10.5 Quantitative trait locus (QTL) mapping in experimental
crosses
10.6 Closing remarks
Reference
SECTION IV MOVING FROM ASSOCIATED GENES TO DISEASE
ALLELES
11. Predictive functional analysis of polymorphisms: An overview
11.1 Introduction
11.2 Principles of predictive functional analysis of
polymorphisms
11.3 The anatomy of promoter regions and regulatory
elements
11.4 The anatomy of genes
11.5 Pseudogenes and regulatory mRNA
11.6 Analysis of novel regulatory elements and motifs in
nucleotide sequences
11.7 Functional analysis of non-synonymous coding
polymorphisms
11.8 Integrated tools for functional analysis of genetic
variation
11.9 A note of caution on the prioritization of in silico
predictions for further laboratory investigation
11.10 Conclusions
References
12. Functional in silico analysis of gene regulatory polymorphism
12.1 Introduction
12.2 Predicting regulatory regions
12.3 Modelling and predicting transcription factor-binding
sites
12.4 Predicting regulatory elements for splicing
regulation
12.5 Evaluating the functional importance of regulatory
polymorphisms
References
13. Amino-acid properties and consequences of
substitutions
13.1 Introduction
13.2 Protein features relevant to amino-acid behaviour
13.3 Amino-acid classifications
13.4 Properties of the amino acids
13.5 Amino-acid quick reference
13.6 Studies of how mutations affect function
13.7 A summary of the thought process
References
14. Non-coding RNA bioinformatics
14.1 Introduction
14.2 The non-coding (nc) RNA universe
14.3 Computational analysis of ncRNA
14.4 ncRNA variation in disease
14.5 Assessing the impact of variation in ncRNA
14.6 Data resources to support small ncRNA analysis
14.7 Conclusions
References
SECTION V ANALYSIS AT THE GENETIC AND GENOMIC DATA
INTERFACE
15. What are microarrays?
15.1 Introduction
15.2 Principles of the application of microarray technology
15.3 Complementary approaches to microarray analysis
15.4 Differences between data repository and research
database
15.5 Descriptions of freely available research database
packages
References
16. Combining quantitative trait and gene-expression data
16.1 Introduction: the genetic regulation of endophenotypes
16.2 Transcript abundance as a complex phenotype
16.3 Scaling up genetic analysis and mapping models for
microarrays
16.4 Genetic correlation analysis
16.5 Systems genetic analysis
16.6 Using expression QTLs to identify candidate genes for the
regulation of complex phenotypes
16.7 Conclusions
References
17. Bioinformatics and cancer genetics
17.1 Introduction
17.2 Cancer genomes
17.3 Approaches to studying cancer genetics
17.4 General resources for cancer genetics
17.5 Cancer genes and mutations
17.6 Copy number alterations in cancer
17.7 Loss of heterozygosity in cancer
17.8 Gene-expression data in cancer
17.9 Multiplatform gene target identification
17.10 The epigenetics of cancer
17.11 Tumour modelling
17.12 Conclusions
References
18. Needle in a haystack? dealing with 500 SNP genome scans
18.1 Introduction
18.2 Genome scan analysis issues
18.3 Ultra-high-density genome-scanning technologies
18.4 Bioinformatics for genome scan analysis
18.5 Conclusions
References
19. A bioinformatics perspective on genetics in drug
discovery and development
19.1 Introduction
19.2 Target genetics
19.3 Pharmacogenetics (PGx)
19.4 Conclusions: toward ‘personalized medicine’
References
Appendix I
Appendix II
Index |
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Developmental Genetics of
the Flower,
Volume 44
Advances in Botanical Research
by J. A. Callow |
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Cat.# EL-GEN1 |
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Published: 2006
ISBN: 9780120059447 |
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Current major interests in this area include the study
of higher level phylogenetic relationships and character
evolution in the angiosperms, floral evolution, the
genetic basis of key floral differences in basal
angiosperms, the genetic and genomic consequences of
polyploid speciation, conservation genetics of rare plant
species, and phylogeography. This book provides a series
of papers focused on the developmental genetics of
flowering as well as the genetic control of the timing of
flowering. Investigation of speciational mechanisms,
evolutionary relationships, and character evolution in
flowering plants and land plants utilizing a variety of
experimental approaches are discussed. The chapters are
excellent reviews of the current fast-moving area of
research. |
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The Mouse in Biomedical
Research 2e,
Volume 2
History, Genetics, and Wild Mice
by James G. Fox, Stephen Barthold,
Christian E. Newcomer, Abigail Smith, and Fred W. Quimby |
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Cat.# EL-GEN2 |
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Published: 2006
ISBN: 9780123694560 |
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History, Genetics, and Wild Mice provides
information about the history, biology and genomics of the
laboratory mouse (Mus musculus), as well as basic
information on maintenance and use of mouse stocks. Mouse
origins and relationships are covered in chapters on
history, evolutionary taxonomy and wild mice. Genetics and
genomics of the mouse are covered in chapters on genetic
nomenclature, gene mapping, cytogenetics and the molecular
organization of the mouse genome. Maintenance of
laboratory mice is described in chapters on breeding
systems for various types of strains and stocks and
genetic monitoring. Use of the mouse as a model system for
basic biomedical research is described in chapters on
chemical mutagenesis, gene trapping, pharmacogenetics and
embryo
manipulation. |
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Atlas of Mammalian
Chromosomes
by Stephen O'Brien, Joan Menninger,
and William Nash |
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Cat.# JW-GEN4 |
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Published: 2006
ISBN: 9780471350156 |
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A stunning visual collection of the banded metaphase
chromosome karyotypes from some 850 species of mammals,
the Atlas of Mammalian Chromosomes represents an
unabridged compendium of the state of this genomic art
form. Bringing together information currently scattered
throughout the cytogenetics literature for scores of
published and unpublished species, this atlas features
high-quality karyotype images for nearly every mammal
studied to date, making it the most comprehensive
assemblage of high-resolution chromosome photographs
available - a critically invaluable resource for today's
comparative genomics era.
For every available species, the Atlas of Mammalian
Chromosomes presents the best karyotype produced, the
common and Latin name of the species, the published
citation, and the contributing authors. Most karyotypes
are G-banded, revealing the chromosomal bar codes of
homologous segments among related species.
Addressing the mandate of the Human Genome Project to
annotate the genomes of other organisms as well, the Atlas
of Mammalian Chromosomes offers a step forward in our
understanding of species formation, of genome
organization, and of DNA script for natural selection. It
is an invaluable resource for geneticists, mammalogists,
and biologists interested in comparative genomics,
systematics, and chromosome structure. Table of
Contents: Foreword
Preface
Acknowledgments
MONOTREMATA
Order Monotremata
MARSUPIALIA
Order Didelphimorphia
Order Paucituberculata
Order Microbiotheria
Order Dasyuromorphia
Order Peramelemorphia
Order Notoryctemorphia
Order Diprotodontia
AFROTHERIA
Order Afrosoricida
Order Macroscelidea
Order Sirenia
Order Proboscidea
Order Hyracoidea
Order Tubulidentata
XENARTHRA
Order Xenarthra
EUARCHONTOGLIRES
Order Scandentia
Order Dermoptera
Order Primates
Order Rodentia
Order Lagomorpha
LAURASIATHERIA
Order Eulipotyphla
Order Chiroptera
Order Carnivora
Order Pholidota
Order Cetartiodactyla
Order Perissodactyla |
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Diagnostic Techniques in
Genetics
by Jean-Louis Serre, Isabelle Heath, and Simon
Heath |
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Cat.# JW-GEN5 |
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Published: 2006
ISBN:
9780470870259 |
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Recent developments within molecular biology and
genetic engineering have led to huge advances and changes
within the biological sciences especially within the field
of human genetics. Diagnostic Techniques in Genetics
offers an important overview of how DNA or RNA technology
may be applied to a large set of genetic diagnoses.
The first part of the book focuses on DNA/RNA applications
and includes many of the latest developments in the field
combined with routine procedures of genetic diagnoses, for
example cloning and sequencing DNA. The DNA applications
presented in the first chapter are then each applied to a
specific kind of genetic diagnosis and the text concludes
with a chapter devoted to population genetics.
First published in French by Dunod in 2002, this book is
an excellent reference for students taking courses in
molecular biology, medicine and medical genetics. It is
also a useful introduction for postgraduate students and
researchers in the field who require a general overview of
genetic diagnoses. |
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Gene-Environment Interactions:
Fundamentals of Ecogenetics
by Lucio G. Costa, and David L. Eaton |
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Cat.# JW-GEN6 |
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Published: 2006
ISBN: 9780471467816 |
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Understanding the play between heredity and
environment, and relating it to disease causation, is the
task of ecogenetics. Gene-Environment Interactions:
Fundamentals of Ecogenetics presents the first
comprehensive survey of this discipline, reflecting its
relationship with toxicology, epidemiology, pharmacology,
public health, and other medical and biological fields.
Divided into four sections, the text elucidates key basic
and advanced topics:
- Section 1 covers fundamentals, including the history
of the discipline, a discussion of the molecular
laboratory tools currently available to assess
genotypes, using such measurements in molecular
epidemiology studies, and the statistical issues
involved in their analysis.
- Section 2 focuses on a number of key genetic
polymorphisms relevant for ecogenetics, including
enzymes of phase I and phase II metabolism, enzymes
involved in DNA repair, as well as receptors and ion
channels. This highlights characteristics of selected,
widely studied genotypic/phenotypic differences, and
allows discussion of how given genetic variations can
influence responses to exogenous chemicals.
- Section 3 examines gene-environment interactions
through a disease-based approach, addressing how genetic
polymorphisms can influence susceptibility to various
diseases. Chapters cover important disease conditions
such as various types of cancer, neurodegenerative
diseases, cardiovascular disease, chronic pulmonary
diseases, infectious diseases, diabetes, and obesity.
- The final section discusses the ethical, legal, and
social issues that arise when investigating and
evaluating genetic polymorphisms in human populations,
as well as the impact of ecogenetics on risk assessment,
regulatory policies, and medicine and public health.
Packed with clear examples illustrating concepts, as
well as numerous tables and figures, Gene-Environment
Interactions: Fundamentals of Ecogenetics is a unique
resource for a wide range of physicians, students, and
other specialists. Table of Contents:
Foreword
Acknowledgments
Cont | | |