Cystic Fibrosis

Diagnosis and Protocols, Volume I: Approaches to Study and Correct CFTR Defects

  • Margarida D. Amaral
  • Karl Kunzelmann

Part of the Methods in Molecular Biology book series (MIMB, volume 741)

Table of contents

  1. Front Matter
    Pages i-xvi
  2. Strategies to Correct the Basic Defect in CF and Assess Efficacy in Human Clinical Trials

  3. RNA Methods to Approach CFTR Expression

    1. Front Matter
      Pages 109-109
    2. Anabela S. Ramalho, Luka A. Clarke, Margarida D. Amaral
      Pages 115-135
    3. Liat Linde, Batsheva Kerem
      Pages 137-154
    4. Elisa Goina, Eugenio Fernandez-Alanis, Franco Pagani
      Pages 155-169
    5. Lisa Giovannini-Chami, Nathalie Grandvaux, Laure-Emmanuelle Zaragosi, Karine Robbe-Sermesant, Brice Marcet, Bruno Cardinaud et al.
      Pages 171-191
    6. Christopher J. Ott, Ann Harris
      Pages 193-209
  4. CFTR Protein Biogenesis, Folding, Degradation, and Traffic

    1. Front Matter
      Pages 211-211
    2. Margarida D. Amaral, Gergely L. Lukacs
      Pages 213-218
    3. Diane E. Grove, Meredith F.N. Rosser, Richard L. Watkins, Douglas M. Cyr
      Pages 219-232
    4. Yoshihiro Matsumura, LeeAnn Rooney, William R. Skach
      Pages 233-253

About this book

Introduction

Despite the many milestones in cystic fibrosis (CF) research, progress towards curing the disease has been slow, and it is increasingly difficult to grasp and use the already wide and still growing range of diverse methods currently employed to study CF so as to understand it in its multidisciplinary nature.  Cystic Fibrosis: Diagnosis and Protocols aims to provide the CF research community and related researchers with a very wide range of high-quality experimental tools, as an easy way to grasp and use classical and novel methods applied to cystic fibrosis.  Volume I: Approaches to Study and Correct CFTR Defects focuses on the cystic fibrosis transmembrane conductance regulator (CFTR) and its expression, biogenesis, structure, and function in terms of the defects causing CF.  Written in the highly successful Methods in Molecular Biology™ series format, chapters include introductions to their respective topics, lists of the necessary materials and reagents, step-by-step, readily reproducible laboratory protocols, and tips on troubleshooting and avoiding known pitfalls.

 

Comprehensive and practical, Cystic Fibrosis: Diagnosis and Protocols will provide readers with optimal working tools to address pressing questions in the best technical way, while helping all of us, as a research and clinical community, to move faster hand-in-hand toward unravelling the secrets of this challenging disorder and cure it.

Keywords

CF CFTR expression Human clinical trials Protein biogenesis and folding RNA methods Structure and function Transmembrane conductance regulator

Editors and affiliations

  • Margarida D. Amaral
    • 1
  • Karl Kunzelmann
    • 2
  1. 1.Faculty of Sciences, Centre for Biodiversity & FunctionalUniversity of LisboaLisboaPortugal
  2. 2., Department of PhysiologyUniversity of RegensburgRegensburgGermany

Bibliographic information

  • DOI https://doi.org/10.1007/978-1-61779-117-8
  • Copyright Information Springer Science+Business Media, LLC 2011
  • Publisher Name Humana Press
  • eBook Packages Springer Protocols
  • Print ISBN 978-1-61779-116-1
  • Online ISBN 978-1-61779-117-8
  • Series Print ISSN 1064-3745
  • Series Online ISSN 1940-6029
  • About this book
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