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The Identification of the CF (Cystic Fibrosis) Gene

Recent Progress and New Research Strategies

  • Book
  • © 1991

Overview

Editors:
  1. Lap-Chee Tsui

    1. The Hospital for Sick Children, Toronto, Canada

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  2. Giovanni Romeo

    1. Istituto Giannina Gaslini, Genoa, Italy

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    You can also search for this editor in PubMed   Google Scholar

  3. Rainer Greger

    1. Albert-Ludwigs-Universität, Freiburg, Germany

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  4. Sergio Gorini

    1. Fondazione Internazionale Menarini, Florence, Italy

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Part of the book series: Advances in Experimental Medicine and Biology (AEMB, volume 290)

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Table of contents (50 chapters)

  1. Front Matter

    Pages i-xi
    Download chapter PDF

  2. Cystic Fibrosis — A Strategy for the Future

    • Robert Williamson
    Pages 1-7

  3. Molecular Genetics of Cystic Fibrosis

    • L.-C. Tsui, J. Rommens, B. Kerem, R. Rozmahel, J. Zielenski, D. Kennedy et al.
    Pages 9-18

  4. The CF Gene Product as a Member of a Membrane Transporter (TM6-NBF) Super Family

    • John R. Riordan, Noa Alon, Zbyszko Grzelczak, Steve Dubel, Shi-Zhang Sun
    Pages 19-29

  5. Genetic Analysis of Cystic Fibrosis

    • Xavier Estivill, Teresa Casals, Virginia Nunes
    Pages 31-38

  6. Molecular and Genetic Analyses at the CF Locus

    • K. W. Klinger, P. Stanislovitis, J. Merrill, G. T. Horn
    Pages 39-44

  7. Identification of Cystic Fibrosis Mutations

    • Michael Dean, Bernard Gerrard, Claudia Stewart, Leslie Krueger, Douglas Holsclaw, Lynne Quittell et al.
    Pages 45-51

  8. Mutation Analysis for Cystic Fibrosis in a North American Population

    • A. L. Beaudet, G. L. Feldman, K. Kobayashi, W. K. Lemna, S. D. Fernbach, M. R. Knowles et al.
    Pages 53-54

  9. Toward a Geographical History of the Predominant and Secondary Mutations in Europe

    • J. L. Serre
    Pages 55-62

  10. Origin and Diffusion of the Major CF Mutation in Europe

    • Marcella Devoto
    Pages 63-74

  11. Present State of DNA-Diagnosis for Cystic Fibrosis and Attitudes Concerning a Heterozygote Screening in the GDR

    • Ch. Coutelle, K. Grade, A. Speer, K. Will, Chr. Gille, R. Szibor et al.
    Pages 75-81

  12. Pros and Cons of Neonatal Screening for Cystic Fibrosis

    • Gerard J. te Meerman, Jeannette E. Dankert-Roelse
    Pages 83-95

  13. Genotype-Phenotype Correlations in Cystic Fibrosis Patients

    • Manfred Stuhrmann, Thilo Dörk, Michael Krawczak, Margarete Dueck, Ulrich Banholzer, Jutta Domagk et al.
    Pages 97-103

  14. Ion Transport in Normal and CF Airway Epithelia

    • Richard C. Boucher, Thierry Chinet, Niels Willumsen, Michael R. Knowles, M. Jackson Stutts
    Pages 105-118

  15. Aerosolized Amiloride as Treatment of Cystic Fibrosis Lung Disease: A Pilot Study

    • Michael R. Knowles, Nina L. Church, William E. Waltner, James R. Yankaskas, Peter Gilligan, Malcolm King et al.
    Pages 119-132

  16. Some Properties of Sodium and Chloride Channels in Respiratory Epithelia of CF- and Non-CF-Patients

    • J. Disser, A. Hazama, E. Frömter
    Pages 133-144

  17. Roles of Ca and cAMP on Cl Channel Activity in Cystic Fibrosis Sweat Clear Cells as Studied by Microsuperfusion and Cell Volume Analysis

    • K. Sato, M. Ohtsuyama, Y. Suzuki, G. Samman, K. T. Sato, F. Sato
    Pages 145-158

  18. Regulation of Absorption in the Human Sweat Duct

    • P. M. Quinton, M. M. Reddy
    Pages 159-172

  19. Altered Biochemical Regulation of Secretion in Cystic Fibrosis Epithelial Cells

    • M. A. McPherson, D. K. Shori, C. Lloyd Mills, M. C. Goodchild, R. L. Dormer
    Pages 173-186

  20. Chloride Ion Transport in Transformed Normal and Cystic Fibrosis Epithelial Cells

    • A. L. Cozens, M. J. Yezzi, L. Chin, E. M. Simon, D. S. Friend, D. C. Gruenert
    Pages 187-196
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Keywords

Editors and Affiliations

  • The Hospital for Sick Children, Toronto, Canada

    Lap-Chee Tsui

  • Istituto Giannina Gaslini, Genoa, Italy

    Giovanni Romeo

  • Albert-Ludwigs-Universität, Freiburg, Germany

    Rainer Greger

  • Fondazione Internazionale Menarini, Florence, Italy

    Sergio Gorini

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