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Autor: Patrizia Ferretti
ISBN-13: 9780470090114
Einband: E-Book
Seiten: 562
Sprache: Englisch
eBook Typ: PDF
eBook Format: E-Book
Kopierschutz: Adobe DRM [Hard-DRM]
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Embryos, Genes and Birth Defects

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The first edition of Embryos, Genes and BirthDefects, edited by the late Peter Thorogood, was a radicalnew book aimed at bridging the gap between the medical disciplinesof embryology and dysmorphology, and recent advances in cellular,molecular and developmental biology. This new edition remainsunique in its breadth and brings up to date our understanding ofbirth defects and of the strategies utilized to gain suchknowledge. It features new chapters on human cytogenetics,mutagenesis and the eyes and ears.
The book presents key topics in developmental biology andexplains how they provide the foundations for understandingclinical birth defects. The first six chapters introduce conceptsand strategies adopted to elucidate developmental anomalies leadingto birth defects. The book then focuses on specific organs andreviews the cellular and molecular mechanisms affecting theirdevelopment and how disruption of these mechanisms by genetic orenvironmental factors may underlie certain birth defects. Thechapters are concise and provide up-to-date coverage of topics in aformat that is easily accessible and yet at the forefront ofresearch.

Written primarily for paediatricians, obstetricians, clinicalgeneticists and allied workers, this book guides the reader throughthe contribution of modern molecular biology to our understandingof human development. Developmental and cellular biologists willlearn how errors in the cellular and genetic mechanism can lead toclassical disorders, diseases and syndromes.
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InhaltsangabePreface to the First Edition.

Preface to the Second Edition.

Contributors.

                                                                                                                                                                                                                                                                                                                                                                                                           &am                                                                                                                         1.1. 1. The Relationship between Genotype and Phenotype: Some Basic Concepts (Philip Stanier and Gudrun Moore).

Introduction.

The relationship between genotype and phenotype.

The role of ‘model systems’.

The changing concept of homology.

2. Uses of Databases in Dysmorphology (Michael Baraitser).

What is a syndrome?.

Some of these problems are addressed by dysmorphology databases.

Where databases do not help.

Dysmorphology databases.

How databases work.

3. Human Cytogenetics  (J. D. A. Delhanty).

Introduction.

Population cytogenetics.

Structural anomalies.

The genesis of chromosome abnormalities.

Embryo survival.

The cause of high levels of chromosome abnormality in human embryos.

Relative parental risks – age, translocations, inversions, gonadal and germinal mosaics.

4. Identification and Analysis of Genes Involved in Congenital Malformation Syndromes (Peter J. Scambler).

Gene identification.

Biological analysis of genes implicated in birth defect syndromes.

Animal models.

Why study rare human birth defect syndromes?.

5. Transgenic Technology and Its Role in Understanding Normal and Abnormal Mammalian Development (Valerie Vidal and Andreas Schedl).

Introduction.

Transgenic mice.

Genetic manipulation using gene targeting in ES cells.

Outlook and future developments.

6. Chemical Teratogens: Hazards, Tools and Clues (Nigel A. Brown) (with revisions by Cheryll Tickle).

Introduction.

Teratogens and human malformations.

General strategy in chemical teratogenesis.

Valproic acid.

Gene–teratogen interaction.

Teratogens and phenocopies.

Teratogens as manipulative tools.

Teratogens as clues.

Final comments.

7. The Limbs (Patrizia Ferretti and Cheryll Tickle).

Developmental anatomy of the human limb.

Main classes of limb defects.

Contemporary studies on mechanisms of limb development.

Limb regeneration.

How, when and where experimental studies elucidate abnormal development.

Agenda for the future.

8. Brain and Spinal Cord Andrew J. Copp.

Introduction.

Overview of nervous system development.

Defects of CNS development: towards a genetic and developmental understanding.

Agenda for the future.

endolymph homeostasis.

The future.

11. Development of the Enteric Nervous System in Relation to Hirschsprung’s Disease (Heather M. Young, Donald F. Newgreen and Alan J. Burns).

Introduction.

Anatomy and function of the ENS.

The best-characterized developmental defect of the ENS – Hirschsprung’s disease.

Cell biology of ENS development.

Molecular biology of ENS development and Hirschsprung-like dysplasias.

HSCR: current and future treatments.

Conclusions.

12. The Head (Gillian M. Morriss-Kay).

Introduction.

Developmental anatomy.

Main classes of craniofacial defect.

Cellular and molecular mechanisms.

Agenda for the future.

13. The Heart (Deborah Henderson, Mary R. Hutson and Margaret L. Kirby).

Developmental anatomy.

Major cell populations needed for heart development.

Molecular regulation of heart development.

Cardiovascular defects.

The Future.

14. The Skin (Ahmad Waseem and Irene M. Leigh).

Introduction.

Developmental anatomy.

Main classes of skin defects.

Future perspectives.

15. The Vertebral Column (David Rice and Susanne Dietrich).

Introduction.

Developmental anatomy of the vertebral column.

Making the vertebral column.

Agenda for the future.

16. The Kidney (Paul J. D. Winyard).

Introduction.

Structure and function.

Developmental anatomy of nephrogenesis.

Transcription factors.

Growth factors and their receptors.

Survival/proliferation factors.

Cell adhesion molecules.

Other molecules.

Non-genetic causes of renal malformations.

Agenda for the future.

17. The Teeth (Irma Thesleff).

Developmental anatomy.

Main classes of defects.

Cellular and molecular mechanisms affecting development.

How cellular and molecular developmental mechanisms assist in elucidating the causes of abnormal development.

Agenda for the future.

Index.


Editiert von: Patrizia Ferretti, Andrew Copp, Cheryll Tickle, Gudrun Moore
Dr. Patrizia Ferretti.Developmental Biology Unit, Institute of Child Health, University College London.

Prof. Andrew Copp (Dean of Institute).Neural Development Unit, Institute of Child Health, University College London.

Prof. Cheryll Tickle.Professor of Anatomy&Physiology, The Wellcome Trust Building, University of Dundee.

Prof. Gudrun Moore.Institute of Child Health, University College London.

The editors are all distinguished developmental biologists with a broad range of expertise in human birth defects. Andrew Copp holds an endowed chair in Developmental Neurobiology at University College London and is Dean of the world-renowned Institute of Child Health.

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Autor: Patrizia Ferretti
ISBN-13:: 9780470090114
ISBN: 0470090111
Verlag: John Wiley & Sons
Seiten: 562
Sprache: Englisch
Auflage 2, 2. Auflage
Sonstiges: Ebook