Frontiers in Research on Cystic Fibrosis: Understanding Its Molecular and Chemical Basis and Relationship to the Pathogenesis of the Disease Young Hee KoPeter L. Pedersen OriginalPaper Pages: 417 - 427
Cystic Fibrosis: Channel, Catalytic, and Folding Properties of the CFTR Protein Fabian S. SeibertTip W. LooJohn R. Riordan OriginalPaper Pages: 429 - 442
CFTR: Domains, Structure, and Function Sreenivas DevidasWilliam B. Guggino OriginalPaper Pages: 443 - 451
Probing the Structural and Functional Domains of the CFTR Chloride Channel Myles H. AkabasMin CheungRomain Guinamard OriginalPaper Pages: 453 - 463
Coupling of ATP Hydrolysis with Channel Gating by Purified, Reconstituted CFTR Christine E. BearCanhui LiMohabir Ramjeesingh OriginalPaper Pages: 465 - 473
Purification, Characterization, and Expression of CFTR Nucleotide-Binding Domains J. P. ClancyZs. BebökE. J. Sorscher OriginalPaper Pages: 475 - 482
Cystic Fibrosis: A Disease of Altered Protein Folding Bao-He QuElizabeth StricklandPhilip J. Thomas OriginalPaper Pages: 483 - 490
Strategies for Correcting the AF508 CFTR Protein-Folding Defect C. Randell BrownLy Q. Hong-BrownWilliam J. Welch OriginalPaper Pages: 491 - 502
Modeling of Nucleotide Binding Domains of ABC Transporter Proteins Based on a F1-ATPase/recA Topology: Structural Model of the Nucleotide Binding Domains of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Mario A. BianchetYoung Hee KoPeter L. Pedersen OriginalPaper Pages: 503 - 524