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  • © 2017

The Role of Pendrin in Health and Disease

Molecular and Functional Aspects of the SLC26A4 Anion Exchanger

  • Written by experts in pendrin research

  • Provides readers with detailed knowledge about pendrin genetics, structure and pharmacology

  • Helps in understanding the molecular mechanisms of pendrin related disorders

  • Combines in the best way cutting-edge research with clinical aspects of pendrin function

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Softcover Book USD 169.99
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Table of contents (11 chapters)

  1. Front Matter

    Pages i-x
  2. Introduction

    • Silvia Dossena, Markus Paulmichl
    Pages 1-4
  3. The Role of Pendrin in the Inner Ear

    1. Front Matter

      Pages 5-5
    2. Mouse Models Reveal the Role of Pendrin in the Inner Ear

      • Philine Wangemann, Andrew J. Griffith
      Pages 7-22
    3. Pendrin-Linked Deafness in Humans

      • Sebastian Roesch, Miklós Tóth, Gerd Rasp
      Pages 37-60
    4. Genetic Diagnosis of Deafness

      • Sueli Matilde da Silva Costa, Priscila Zonzini Ramos, Fábio Tadeu Arrojo Martins, Edi Lúcia Sartorato
      Pages 61-81
  4. The Role of Pendrin in the Thyroid

    1. Front Matter

      Pages 83-83
    2. Hypothyroidism, Subclinical Hypothyroidism and Related Diagnostic Tools

      • Gregor Schweighofer Zwink, Christian Pirich
      Pages 85-105
  5. The Role of Pendrin in the Kidney

    1. Front Matter

      Pages 119-119
  6. The Role of Pendrin in the Airways

    1. Front Matter

      Pages 139-139
    2. The Role of Pendrin in the Airways: Links with Asthma and COPD

      • Kenji Izuhara, Shoichi Suzuki, Charity Nofziger, Masahiro Ogawa, Shoichiro Ohta, Yasuhiro Nanri et al.
      Pages 141-154
  7. The Pendrin Gene and Protein

    1. Front Matter

      Pages 155-155
    2. Transcriptional Regulation and Epigenetics of Pendrin

      • Julia Rozenfeld, Charity Nofziger, Orly Kladnitsky, Seth L. Alper, Israel Zelikovic
      Pages 157-185
    3. The Pendrin Polypeptide

      • Silvia Dossena, Emanuele Bernardinelli, Alok K. Sharma, Seth L. Alper, Markus Paulmichl
      Pages 187-220
  8. Back Matter

    Pages 221-226

About this book

This book reviews the current state of knowledge on the genetics, molecular biology and physiology of pendrin, with a particular focus on pendrin dysfunction and the consequences for human health. 


Pendrin is a membrane transport protein expressed in the thyroid, inner ear, kidney and airways, and was recently found in a variety of other tissues and organs. Pendrin malfunction may cause a genetic disease called Pendred syndrome or non-syndromic deafness.


The book provides a thorough description of the multifaceted role of pendrin in human health and disease. As such, it offers an invaluable tool for physiology and pathology researchers, while also providing essential guidance for otorhinolaryngologists and endocrinologists in the diagnosis of Pendred syndrome and pendrin-related deafness.

Reviews

“The purpose is to summarize the current knowledge about the role of pendrin in normal physiology and disease pathology. The intended audience is predominantly researchers and physicians interested in a detailed description of the multifaceted function of pendrin. However, the book also could serve as a good source for undergraduate and graduate students and postgraduate trainees interested in thyroid physiology and pathology as well as physiology, pathology, and diagnosis of deafness in general.” (Partha Kasturi, Doody’s Book Reviews, June, 2017) 

Editors and Affiliations

  • Paracelsus Medical University Institute of Pharmacology and Toxicology, Salzburg, Austria

    Silvia Dossena

  • Paracelsus Medical University Institut of Pharmacology and Toxicology, Salzburg, Austria

    Markus Paulmichl

About the editors

Prof. Dr. Markus Paulmichl Institute of Pharmacology and Toxicology of the Paracelsus Medical University Salzburg, Austria

Silvia Dossena, PhD Institute of Pharmacology and Toxicology of the Paracelsus Medical University Salzburg, Austria

Bibliographic Information

  • Book Title: The Role of Pendrin in Health and Disease

  • Book Subtitle: Molecular and Functional Aspects of the SLC26A4 Anion Exchanger

  • Editors: Silvia Dossena, Markus Paulmichl

  • DOI: https://doi.org/10.1007/978-3-319-43287-8

  • Publisher: Springer Cham

  • eBook Packages: Biomedical and Life Sciences, Biomedical and Life Sciences (R0)

  • Copyright Information: Springer International Publishing Switzerland 2017

  • Hardcover ISBN: 978-3-319-43285-4Published: 10 March 2017

  • Softcover ISBN: 978-3-319-82780-3Published: 20 July 2018

  • eBook ISBN: 978-3-319-43287-8Published: 02 March 2017

  • Edition Number: 1

  • Number of Pages: X, 226

  • Number of Illustrations: 10 b/w illustrations, 26 illustrations in colour

  • Topics: Molecular Medicine, Otorhinolaryngology, Endocrinology, Human Genetics

Buy it now

Buying options

eBook USD 129.00
Price excludes VAT (USA)
  • Available as EPUB and 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