GFP-tagged CFTR transgene is functional in the G551D cystic fibrosis mouse colon.

Oceandy, D; McMorran, B; Schreiber, R; Wainwright, B J; Kunzelmann, K

Oceandy, D; McMorran, B; Schreiber, R; Wainwright, B J; Kunzelmann, K.

Affiliation

Oceandy D; Institute for Molecular Biosciences, The University of Queensland, St. Lucia QLD 4072, Australia.

J Membr Biol ; 192(3): 159-67, 2003 Apr 01.

Article in En | MEDLINE | ID: mdl-12820661

Subject(s)

Colon/metabolism; Cystic Fibrosis Transmembrane Conductance Regulator/metabolism; Cystic Fibrosis/metabolism; Intestinal Mucosa/metabolism; Animals; Cystic Fibrosis/genetics; Cystic Fibrosis/pathology; Cystic Fibrosis/therapy; Cystic Fibrosis Transmembrane Conductance Regulator/genetics; Gene Expression Regulation; Genetic Therapy/methods; Intestinal Mucosa/pathology; Mice; Mice, Inbred CFTR; Mice, Transgenic; Recombinant Fusion Proteins/genetics; Recombinant Fusion Proteins/metabolism; Respiratory Mucosa/metabolism; Respiratory Mucosa/pathology; Trachea/metabolism; Trachea/pathology

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Collection: 01-internacional Database: MEDLINE Main subject: Colon / Cystic Fibrosis Transmembrane Conductance Regulator / Cystic Fibrosis / Intestinal Mucosa Limits: Animals Language: En Journal: J Membr Biol Year: 2003 Type: Article Affiliation country: Australia

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