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Pharmacological modulation of cGMP levels by phosphodiesterase 5 inhibitors as a therapeutic strategy for treatment of respiratory pathology in cystic fibrosis.

  • Hongwei D. Yu
  • , Jens F. Poschet
  • , Graham S. Timmons
  • , Jennifer L. Taylor-Cousar
  • , Wojciech Ornatowski
  • , Joseph Fazio
  • , Elizabeth Perkett
  • , Kari R. Wilson
  • , Hugo R. de Jonge
  • , Vojo Deretic

Research output: Contribution to journalArticlepeer-review

Original languageAmerican English
JournalBiochemistry and Microbiology
StatePublished - Sep 1 2007

Keywords

  • cystic fybrosis
  • treatment
  • drug therapy
  • metabolism

Disciplines

  • Chemicals and Drugs
  • Congenital, Hereditary, and Neonatal Diseases and Abnormalities
  • Diseases
  • Medicine and Health Sciences
  • Pharmacy and Pharmaceutical Sciences
  • Respiratory Tract Diseases

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