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Gap junctions in development and disease

Author: Elke Winterhager
Publisher: Berlin ; New York : Springer, ©2005.
Edition/Format:   eBook : Document : EnglishView all editions and formats
Publication:Springer e-books
Summary:
"The main objective of Gap Junctions in Development and Disease is to describe the molecular events that cause impairments in development and disease. Communication between cells via intercellular channels, so called gap junctions, appears to be essential for certain developmental processes and appropriate organ function. Starting with a comprehensive review of the various mouse and human genes encoding the  Read more...
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Genre/Form: Electronic books
Additional Physical Format: Print version:
Gap junctions in development and disease.
Berlin ; New York : Springer, ©2005
(DLC) 2005926503
(OCoLC)61219180
Material Type: Document, Internet resource
Document Type: Internet Resource, Computer File
All Authors / Contributors: Elke Winterhager
ISBN: 9783540286219 3540286217 3540261567 9783540261568
OCLC Number: 262680796
Description: 1 online resource (xvii, 279 pages) : illustrations
Contents: Connexin and Pannexin Genes in the Mouse and Human Genome --
Essential Role of Gap Junctions During Development and Regeneration of Skeletal Muscle --
Connexins in Cardiac Development: Expression, Role, and Transcriptional Control --
Gap Junction and Connexin Remodeling in Human Heart Disease --
Gap Junction Expression in Brain Tissues with Focus on Development --
Connexins Responsible for Hereditary Deafness --
The Tale Unfolds --
Human Connexins in Skin Development and Skin Disorders --
Intercellular Communication in Lens Development and Disease --
Connexin Modulators of Endocrine Function --
Roles of Gap Junctions in Ovarian Folliculogenesis: Implications for Female Infertility --
Placental Connexins of Mice and Men --
Connexins in Growth Control and Cancer.
Responsibility: Elke Winterhager (ed.).
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Abstract:

Reviewing various mouse and human genes encoding the channel-forming connexins, this book also describe several connexin mutations associated with human diseases such as hereditary deafness and  Read more...

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