Cystic Fibrosis Methods and Protocols

  • William R. Skach

Part of the Methods in Molecular Medicine™ book series (MIMM, volume 70)

Table of contents

  1. Front Matter
    Pages i-xvi
  2. Genetics of Cystic Fibrosis

    1. Front Matter
      Pages 1-1
    2. Julian Zielenski, Isabel Aznarez, Tuncer Onay, John Tzounzouris, Danuta Markiewicz, Lap-Chee Tsui
      Pages 3-19
    3. Meera Srivastava, Ofer Eidelman, Harvey B. Pollard
      Pages 21-29
    4. Jeffrey J. Wine, Michael Dean, Damjan Glavac
      Pages 31-46
  3. CFTR structure and Function:

    1. Front Matter
      Pages 47-47
    2. Structure, Gating, and Regulation

      1. Allan Powe, Zhen Zhou, Tzyh-Chang Hwang, Georg Nagel
        Pages 67-98
      2. Tang Zhu, Deborah A. R. Hinkson, David Dahan, Alexandra Evagelidis, John W. Hanrahan
        Pages 99-109
      3. Ashvani K. Singh, Sangeeta Singh, Daniel C. Devor, Raymond A. Frizzell, Willy van Driessche, Robert J. Bridges
        Pages 129-142
      4. Ilana Kogan, Mohabir Ramjeesingh, Canhui Li, Christine E. Bear
        Pages 143-157
      5. Alan S. Verkman, Sujatha Jayaraman
        Pages 187-196
    3. Expression, Folding, and Degradation

      1. Mohamed Benharouga, Manu Sharma, Gergely L. Lukacs
        Pages 229-243
      2. Geoffrey C. Meacham, Douglas M. Cyr
        Pages 245-256
      3. Yimao Zhang, Susan Michaelis, Jeffrey L. Brodsky
        Pages 257-265

About this book

Introduction

Since the cloning of the cystic fibrosis transmembrane conductance regulator (CFTR) nearly a decade ago, cystic fibrosis researchers, clinicians, and patients have come to rely increasingly on a diverse array of fundamental techniques to understand the molecular basis of this complex disease. Cystic Fibrosis Methods and Protocols consolidates a broad range of detailed and readily reproducible in vitro, cellular, and whole animal laboratory protocols into an indispensable resource. From electrophysiology and cell biology, to animal models and gene therapy, this comprehensive set of methods provides the step-by-step instructions needed for investigators to incorporate new approaches into their research programs. Specific protocols describe new techniques for diagnosis, in vitro methods for the expression and functional analysis of CFTR, novel biochemical and cellular systems to determine how mutations subvert CFTR function, and in vivo protocols to examine how CFTR dysfunction produces multisystem pathology in human and animal models.
Comprehensive, multidisciplinary, and highly practical, Cystic Fibrosis Methods and Protocols makes accessible to today's cystic fibrosis investigator the powerful new scientific techniques required to investigate the basic science of the disease and to translate this into effective clinical solutions.

Editors and affiliations

  • William R. Skach
    • 1
  1. 1.Division of Molecular MedicineOregon Health Sciences UniversityPortland

Bibliographic information

  • DOI https://doi.org/10.1385/1592591876
  • Copyright Information Humana Press 2002
  • Publisher Name Humana Press
  • eBook Packages Springer Protocols
  • Print ISBN 978-0-89603-897-4
  • Online ISBN 978-1-59259-187-9
  • Series Print ISSN 1543-1894
  • Series Online ISSN 1940-6037
  • About this book
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