The identification of the cystic fibrosis transmembrane conductance regulator gene (CFTR)
in 1989 represents a landmark accomplishment in human genetics. Since that time, there …

Abstract A 13.5-kb genomic fragment of the mouse cystic fibrosis transmembrane
conductance regulator (CFTR) gene was isolated from a C 57 BL 6 J liver DNA library, using …

Cloning and characterization of the cystic fibrosis transmembrane conductance regulator
(CFTR) gene led to the identification and isolation of cDNA and genomic sequences that …

To help elucidate the function of the cystic fibrosis transmembrane conductance regulator
(CFTR), we have undertaken a cross-species analysis of the DNA sequence which encodes …

The cystic fibrosis transmembrane conductance regulator (CFTR) gene exhibits a tightly
regulated pattern of expression in human epithelial cells. The mechanism of this regulation …

Expression of the gene encoding the cystic fibrosis transmembrane conductance regulator
(CFTR) is tightly regulated. Using a panel of cell lines expressing different levels of CFTR …

More than 400 sequence alterations have been identified in the whole coding sequence of
the cystic fibrosis transmembrane conductance regulator (CFTR) gene corresponding to the …

The in vivo transcription start sites of the human cystic fibrosis transmembrane conductance
regulator gene (CFTR) and its murine homologue (Cftr) have been mapped in a range of …

The gene responsible for cystic fibrosis, the most common severe autosomal recessive
disorder, is located on the long arm of human chromosome 7, region q31–q32. The gene …

The cystic fibrosis transmembrane conductance regulator (CFTR) gene, the gene
responsible for the lethal hereditary disorder cystic fibrosis, codes for a membrane protein …