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Gap Junctions in Development and Disease

Winterhager, Elke
Gap Junctions in Development and Disease Cover Image
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Book Information
Edition: 1st
Publisher: Springer Nature
ISBN: 3-540-26156-7 (3540261567)
ISBN-13: 978-3-540-26156-8 (9783540261568)
Binding: Hardcover
Copyright: 2006
Publish Date: 09/05
Weight: 1.42 Lbs.
Pages: 279
Subject Class: SCI (Medical Science and Research)
Remarks:
Print on Demand. Please allow additional time for delivery.
Return Policy: Returns accepted up to 12 months provided no other recalls or return restrictions apply.
Table Of Contents: View
Contributing Authors: View
 
Class Specifications
Discipline: Biology
Subject Definition: Gap Junctions-Physiology
NLM Class: QH 603
LC Class: QH603
Abstract: This book aims to describe the molecular events underlying impaired development and disease. Beginning with a comprehensive review of various mouse and human genes encoding the channel-forming connexins, later chapters describe several connexin mutations associated with human diseases such as hereditary deafness and female infertility. Erroneous signaling mediated by the interaction of mutant connexins with other proteins, thought to be responsible for dysfunction of organs such as heart, muscle, brain, skin, lens, placenta, and endocrine tissue in both mice and men, is also addressed. Although the question of why some mutations in gap-junction proteins lead to specific phenotypes remains to be answered, the reviews in this book provide an intriguing insight into the future direction of this research field.

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