Mechanisms of disease: Cystic fibrosis

[1] PURIFICATION AND FUNCTIONAL RECONSTITUTION OF THE CYSTIC-FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR (CFTR) [J]. CELL, 1992, 68 (04) : 809 - 818

[2] Mammalian ABC transporters in health and disease [J]. ANNUAL REVIEW OF BIOCHEMISTRY, 2002, 71 : 537 - 592

[3] MUTATIONS IN THE CYSTIC-FIBROSIS GENE IN PATIENTS WITH CONGENITAL ABSENCE OF THE VAS-DEFERENS [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1995, 332 (22) : 1475 - 1480

[4] Evidence that systemic gentamicin suppresses premature stop mutations in patients with cystic fibrosis [J]. AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2001, 163 (07) : 1683 - 1692

[5] Relation between mutations of the cystic fibrosis gene and idiopathic pancreatitis [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1998, 339 (10) : 653 - 658

[6] *CYST FIBR FDN, 2004, CYST FIBR FDN NAT PA

[7] DETERDING RR, 2004, PEDIATR PULM, V38, P249

[8] Curcumin, a major constituent of turmeric, corrects cystic fibrosis defects [J]. SCIENCE, 2004, 304 (5670) : 600 - 602

[9] SUBMUCOSAL GLANDS ARE THE PREDOMINANT SITE OF CFTR EXPRESSION IN THE HUMAN BRONCHUS [J]. NATURE GENETICS, 1992, 2 (03) : 240 - 248

[10] α1-antitrypsin deficiency alleles in cystic fibrosis lung disease [J]. AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 2003, 29 (03) : 390 - 396

[1] PURIFICATION AND FUNCTIONAL RECONSTITUTION OF THE CYSTIC-FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR (CFTR) [J]. CELL, 1992, 68 (04) : 809 - 818

[2] Mammalian ABC transporters in health and disease [J]. ANNUAL REVIEW OF BIOCHEMISTRY, 2002, 71 : 537 - 592

[3] MUTATIONS IN THE CYSTIC-FIBROSIS GENE IN PATIENTS WITH CONGENITAL ABSENCE OF THE VAS-DEFERENS [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1995, 332 (22) : 1475 - 1480

[4] Evidence that systemic gentamicin suppresses premature stop mutations in patients with cystic fibrosis [J]. AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2001, 163 (07) : 1683 - 1692

[5] Relation between mutations of the cystic fibrosis gene and idiopathic pancreatitis [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1998, 339 (10) : 653 - 658

[6] *CYST FIBR FDN, 2004, CYST FIBR FDN NAT PA

[7] DETERDING RR, 2004, PEDIATR PULM, V38, P249

[8] Curcumin, a major constituent of turmeric, corrects cystic fibrosis defects [J]. SCIENCE, 2004, 304 (5670) : 600 - 602

[9] SUBMUCOSAL GLANDS ARE THE PREDOMINANT SITE OF CFTR EXPRESSION IN THE HUMAN BRONCHUS [J]. NATURE GENETICS, 1992, 2 (03) : 240 - 248

[10] α1-antitrypsin deficiency alleles in cystic fibrosis lung disease [J]. AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 2003, 29 (03) : 390 - 396