The genetics of cystic fibrosis lung disease

[1] AFZELIUS BA, 1997, LUNG SCI FDN, P2573

[2] CHLORIDE CHANNELS IN THE APICAL MEMBRANE OF NORMAL AND CYSTIC-FIBROSIS AIRWAY AND INTESTINAL EPITHELIA [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1992, 263 (01): : L1 - L14

[3] DEFECTIVE ACIDIFICATION OF INTRACELLULAR ORGANELLES IN CYSTIC-FIBROSIS [J]. NATURE, 1991, 352 (6330) : 70 - 73

[4] BORTHWICK DW, 1998, UNPUB MURINE SUBMUCO

[5] ALTERNATE TRANSLATION INITIATION CODONS CAN CREATE FUNCTIONAL FORMS OF CYSTIC-FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (20) : 11941 - 11946

[6] EXTENSIVE POSTTRANSCRIPTIONAL DELETION OF THE CODING SEQUENCES FOR PART OF NUCLEOTIDE-BINDING FOLD-1 IN RESPIRATORY EPITHELIAL MESSENGER-RNA TRANSCRIPTS OF THE CYSTIC-FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR GENE IS NOT ASSOCIATED WITH THE CLINICAL MANIFESTATIONS OF CYSTIC-FIBROSIS [J]. JOURNAL OF CLINICAL INVESTIGATION, 1992, 90 (03) : 785 - 790

[7] FIBROCYSTIC DISEASE OF THE PANCREAS IN THE NEWBORN [J]. ARCHIVES OF DISEASE IN CHILDHOOD, 1956, 31 (155) : 22 - 27

[8] CYSTIC-FIBROSIS - MOLECULAR-BIOLOGY AND THERAPEUTIC IMPLICATIONS [J]. SCIENCE, 1992, 256 (5058) : 774 - 779

[9] LUNG-DISEASE IN THE CYSTIC-FIBROSIS MOUSE EXPOSED TO BACTERIAL PATHOGENS [J]. NATURE GENETICS, 1995, 9 (04) : 351 - 357

[10] CFTR gene transfer reduces the binding of Pseudomonas aeruginosa to cystic fibrosis respiratory epithelium [J]. AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1997, 16 (06) : 657 - 663

[1] AFZELIUS BA, 1997, LUNG SCI FDN, P2573

[2] CHLORIDE CHANNELS IN THE APICAL MEMBRANE OF NORMAL AND CYSTIC-FIBROSIS AIRWAY AND INTESTINAL EPITHELIA [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1992, 263 (01): : L1 - L14

[3] DEFECTIVE ACIDIFICATION OF INTRACELLULAR ORGANELLES IN CYSTIC-FIBROSIS [J]. NATURE, 1991, 352 (6330) : 70 - 73

[4] BORTHWICK DW, 1998, UNPUB MURINE SUBMUCO

[5] ALTERNATE TRANSLATION INITIATION CODONS CAN CREATE FUNCTIONAL FORMS OF CYSTIC-FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (20) : 11941 - 11946

[6] EXTENSIVE POSTTRANSCRIPTIONAL DELETION OF THE CODING SEQUENCES FOR PART OF NUCLEOTIDE-BINDING FOLD-1 IN RESPIRATORY EPITHELIAL MESSENGER-RNA TRANSCRIPTS OF THE CYSTIC-FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR GENE IS NOT ASSOCIATED WITH THE CLINICAL MANIFESTATIONS OF CYSTIC-FIBROSIS [J]. JOURNAL OF CLINICAL INVESTIGATION, 1992, 90 (03) : 785 - 790

[7] FIBROCYSTIC DISEASE OF THE PANCREAS IN THE NEWBORN [J]. ARCHIVES OF DISEASE IN CHILDHOOD, 1956, 31 (155) : 22 - 27

[8] CYSTIC-FIBROSIS - MOLECULAR-BIOLOGY AND THERAPEUTIC IMPLICATIONS [J]. SCIENCE, 1992, 256 (5058) : 774 - 779

[9] LUNG-DISEASE IN THE CYSTIC-FIBROSIS MOUSE EXPOSED TO BACTERIAL PATHOGENS [J]. NATURE GENETICS, 1995, 9 (04) : 351 - 357

[10] CFTR gene transfer reduces the binding of Pseudomonas aeruginosa to cystic fibrosis respiratory epithelium [J]. AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1997, 16 (06) : 657 - 663