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Sinus hypoplasia in the cystic fibrosis rat resolves in the absence of chronic infection.

Jessica GraysonKiranya E TipirneniDaniel F SkinnerMatthew FortDo-Yeon ChoShaoyan ZhangAndrew C PrinceDong-Jin LimCalvin MackeyBradford A Woodworth
Published in: International forum of allergy & rhinology (2017)
CF rat sinuses are smaller at birth, but develop volumes similar to wild-type rats with maturation. This suggests that loss of CFTR may confer sinus hypoplasia at birth, but normal development ensues without chronic sinus infection.
Keyphrases
  • cystic fibrosis
  • wild type
  • pseudomonas aeruginosa
  • lung function
  • oxidative stress
  • gestational age
  • drug induced
  • chronic obstructive pulmonary disease
  • pregnant women