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  • Book
  • © 2005

Gap Junctions in Development and Disease

  • First book to connect changes of gap junction proteins with disease

  • Brilliant color illustrations

  • Contributions by experienced authors

  • Includes supplementary material: sn.pub/extras

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Table of contents (12 chapters)

  1. Front Matter

    Pages I-XVII
  2. Connexin and Pannexin Genes in the Mouse and Human Genome

    • Klaus Willecke, Jürgen Eiberger, Julia von Maltzahn
    Pages 1-12
  3. Connexins in Cardiac Development: Expression, Role, and Transcriptional Control

    • Daniel B. Gros, Sébastien Alcoléa, Laurent Dupays, Sonia Meysen, Magali Théveniau-Ruissy, Birgit E.J. Teunissen et al.
    Pages 29-55
  4. Gap Junction and Connexin Remodeling in Human Heart Disease

    • Nicholas J. Severs, Emmanuel Dupont, Riyaz Kaba, Neil Thomas
    Pages 57-82
  5. Gap Junction Expression in Brain Tissues with Focus on Development

    • Rolf Dermietzel, Carola Meier
    Pages 83-110
  6. Connexins Responsible for Hereditary Deafness — The Tale Unfolds

    • Martine Cohen-Salmon, Francisco J. del Castillo, Christine Petit
    Pages 111-134
  7. Intercellular Communication in Lens Development and Disease

    • Adam M. DeRosa, Francisco J. Martinez-Wittinghan, Richard T. Mathias, Thomas W. White
    Pages 173-195
  8. Connexin Modulators of Endocrine Function

    • Philippe Klee, Nathalie Boucard, Dorothée Caille, José Cancela, Anne Charollais, Eric Charpantier et al.
    Pages 197-221
  9. Placental Connexins of Mice and Men

    • Caroline Dunk, Mark Kibschull, Alexandra Gellhaus, Elke Winterhager, Stephen Lye
    Pages 239-252
  10. Connexins in Growth Control and Cancer

    • Christian C. Naus, Gary S. Goldberg, Wun Chey Sin
    Pages 253-273
  11. Back Matter

    Pages 275-279

About this book

Communication between cells via intercellular channels – gap junctions – appears essential to certain developmental processes and appropriate organ function. Gap Junctions in Development and Disease 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.

Editors and Affiliations

  • Medical Faculty of the University Duisburg-Essen, Essen, Germany

    Elke Winterhager

Bibliographic Information

Buy it now

Buying options

eBook USD 129.00
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book USD 169.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book USD 169.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Other ways to access